Title of Invention	COSMETIC COMPOSITION CONTAINING A NEUROPEPTIDE Y RECEPTOR ANTAGONIST
Abstract	Abstract 159/MAS/97 "COSMETIC COMPOSITION CONTAINING A NEUROPEPTIDE Y RECEPTOR ANTAGONIST" The present invention relates to a composition for the treatment of celluilte by topical application characterized in that it comprises an NPY-(neuropeptide Y) antagonist component consisting of a product of fermentation of the strain Streptomyces sp SEBR 2794, deposited with the CNCM of the Institut Pasteur under the number 1-1332, and an a 2-antagonist component consisting of a product of fermentation of the strain Bacillus licheniformis SEBR 2464, deposited with the CNCM of the Institut Pasteur under the number 1-1778, in combination with a cosmetically acceptable excipient, wherein the NPY-antagonist is selected from those of classes A, B and C and the a 2-antagonist component is selected from those of classes D & E as described herein.

Title of Invention

COSMETIC COMPOSITION CONTAINING A NEUROPEPTIDE Y RECEPTOR ANTAGONIST

Abstract

Abstract 159/MAS/97 "COSMETIC COMPOSITION CONTAINING A NEUROPEPTIDE Y RECEPTOR ANTAGONIST" The present invention relates to a composition for the treatment of celluilte by topical application characterized in that it comprises an NPY-(neuropeptide Y) antagonist component consisting of a product of fermentation of the strain Streptomyces sp SEBR 2794, deposited with the CNCM of the Institut Pasteur under the number 1-1332, and an a 2-antagonist component consisting of a product of fermentation of the strain Bacillus licheniformis SEBR 2464, deposited with the CNCM of the Institut Pasteur under the number 1-1778, in combination with a cosmetically acceptable excipient, wherein the NPY-antagonist is selected from those of classes A, B and C and the a 2-antagonist component is selected from those of classes D & E as described herein.

Full Text	The present invention relates to a cosmetic composition containing a neuropeptide Y receptor antagon¬ist. Neuropeptide Y, referred to hereinbelow as "NFY" for short, is a neuromediator which is involved in a certain number of physiological processes and for which an involvement in regulating lipolysis has been demonstrated (P. Valet and M. J. Clin. Invest. 1990, 85, 291-295). NPY receptor antagonists, hereinafter referred to as "NPY antagonists", have been described as medicines, but their efficacy in the treatment of any disease has not been proven to date. It has now been found that NPY antagonists can be used for the preparation of cosmetic compositions. More particularly, it has been found that cos¬metic compositions containing an NPY-antagonist component can be used as lypolysis/lypogenesis regulators in the skin without, however, interferring with the skin's natural functions. It has also been found, that cosmetic compositions containing an NPY-antagonist component and an ^-antagon¬ist component are particularly advantageous. Thus, according to one of its aspects, the present invention relates to a cosmetic composition containing at least one NPY-antagonist component mixed with a cosmetic excipient. The NPY antagonist contained in the cosmetic composition may be a non-pep tide com¬pound, a peptide, a cell or tissue extract of animal or plant origin or a product obtained by fermentation of a microorganism, for example a bacterium or a fungus. NPY antagonists which are advantageous in the cosmetic compositions of the present invention are those of groups A, B and C below. A. Synthetic products selected from groups (I) to (VIII) below are advantageous NPY-antagonist components. t. Compounds of formula (I) in which Ar2 represents naphthyl, phenyl, quinolyl or isoquinolyl, optionally substituted with CI, F, (C1-C4) alkyl, (Cj^C1alkoxy, hydroxyl or (Cj^C1dialkylamino; - Ar2 represents phenyl or thienyl, optionally substi¬tuted with CI, F, (Cx-C4) alkyl, {C1-C4}alJcoxy or hydroxyl; - Rx, R2 and R'2 represent, independently of each other, hydrogen, (C1-C4)alkyl or alternatively Rx represents nothing and N is attached to Ar2 and, optionally, R2 and R'2 form a double bond, or alternatively Rx or R2 is attached to Ar2 and repre¬sents (CJ^-CJ) alkylene; - R3 and R4, which are identical or different, represent hydrogen, (C1-C4) alkyl or form, with the nitrogen atom to which they are attached, a saturated C5-C7 heterocycle selectedfrom pyrrolidine, piperidine and hexahydroazepine; - zx represents (C1C1) alkylene interrupted or substi¬tuted optionally with {C5-C7)cycloalkyl or phenyl; - Q1 represents methyl, amino, {C1-C4)alkoxycarbonylamino, (C1C1) alkylamino, di (C1-C4) alkylamino, pyrrolidinyl, piperidino, morpholino, piperazinyl, (C1-C4)alkyl-4-piperazinyl, amidino, (C1-C4)alkylamidino, guanidino, (C1-C4)alkylguanidino, pyridyl, imidazolyl, pyrimidinyl, indolyl, hydroxyl, {C1-C4)alkoxy, (C2-Ca)alkoxycarbonyl, N- [amino {C1C1) alkyl] -N- [ (C1-C4) alkyl] amino, carbamoyl or phenyl optionally substituted with CI, F, (C1-C4)alkyl, (C1-C4)alkoxy or hydroxyl; - Q2 represents hydrogen or (C1-C4) alkyl; - Q-$ represents hydrogen or {CI-C4)alkyl or Qx and Q3 are linked to form a heterocycle and together represent (C2-C3) alkylene whereas Zx represents nothing, in the form of pure enantiomers or mixtures thereof in any proportions, as well as the addition salts thereof with acids; which can be prepared according to EP 614,911. II - Raloxifen analogues, in particular in which R4 and R5 are, independently, a (C1-C6)alkyl or constitute, with the nitrogen atom to which they are attached, a heterocyclic group selected from hexamethylene-iminyl, piperazino, heptamethyleneiminyl, 4-methyl-piperidyl, imidazolinyl, piperidyl, pyrrolidinyl or morpholinyl; - R° is a hydroxy 1, a halogen, a hydrogen, a (C3- C8)cycloalkyl, a (C2-C7) alkanoyloxy, a (C1-Cg) alkoxy or a phenyl, the said phenyl optionally being substituted with one, two or three substitutents selected, from groups consisting of (C1-C1 alkyl, (Cj-C1) alkoxy, nitro, chloro, fluoro, trif luoromethyl, -0S02- (Ci-Cj^) alkyl or -0-C(0) -NH-R°3; - RL is hydroxyl, halogen, hydrogen, (C3-C3)cycloalkyl, (C2-C7) alkanoyloxy, (C1-Cg) alkoxy or phenyl, it being possible for the said phenyl optionally to be substituted with one, two or three substituents selected from the group consisting of (C1-C1) alJcyl, (C1-C4) alkoxy, nitro, chloro, fluoro, trifluoromethyl, -0S02- (Cj-C1J alkyl or -0-C(0)-NH-R°3; in which each R°3 represents, independently, (C1-Cg) alkyl, (C3-C8)cycloalkyl, unsubstituted or substituted phenyl in which the substitutant is halogen, {Cj_-C6) alkyl or {C1-Cs)alkoxy; with the limitation that when X° is a bond and A* is -S-, then R° and R8^ are not both selected from the group consisting of hydroxyl, methoxy and (C2-C7)alkanoyloxy; as well as the salts or solvates thereof, which can be prepared according to WO 96/12489, in particular a compound selected from: • 3- (4-methoxyphenyl)-4-[4-(2-pyrrolidin-l-ylethoxy)-benzoyl]-1,2-dihydronaphthalene, • 3-phenyl-4-[4- (2-pyrrolidin-1-ylethoxy)benzoyl] -7-methoxy-1,2-dihydronaphthalene, • 3- (4-methoxyphenyl) -4- [4- [2- (piperid-1-yl)ethoxy]benzo¬yl] -1,2-dihydronaphthalene, ■ 3- (4-hydroxyphenyl) -4- [4- [2- (pyrrolidin-1-yl) ethoxy] - benzoyl]-1,2-dihydronaphthalene, • 3-(4-methoxyphenyl)-4-[4-[2-(hexamethyleneimin-1- yl)ethoxy]benzoyl]-1,2-dihydronaphthalene, ■ 3- (4-methoxyphenyl) -4- [4- [2- (piperid-l-yl)ethoxy]benzo- yl]-1,2-dihydronaphthalene, • 3- (4-methoxyphenyl) -4- [4- [2- (piperid-l-yl)ethoxy]benzo- yl]-7-methoxy-1,2-dihydronaphthalene, - 3- (4-methoxyphenyl) -4- [4- [2- (N-methyl-1-pyrrolidinium) -ethoxy]benzoyl] -1,2-dihydronaphthalene, • 3- (4-methoxyphenyl)-4-[4-(2-dimethylaminoethoxy)benzo¬yl] -1,2-dihydronaphthalene, • 3-(4-methoxyphenyl)-4-(4-diethylaminoethoxybenzoyl)-1,2-dihydronaphthalene, • 3- (4-methoxyphenyl) -4- (4-diisopropylaminoethoxybenzo-yl)-1,2-dihydronaphthalene, • 2-(4-hydroxyphenyl)-3-[4-[2-(hexamethyleneimin-1-yl)ethoxy]benzoyl]-6-hydroxybenzofuran, • 2- (4-hydroxyphenyl) -3- [4- [2- (piperid-1-yl)ethoxy]ben- zoyl]-6-hydroxybenzofuran, • 2- (4-hydroxyphenyl) -3- [4- [2 -pyrrolidin-1-yl) ethoxy] -benzoyl]-6-hydroxybenzofuran, • 2- (4-hydroxyphenyl)-3-[4-[2-(N,N-diethylamino)ethoxy]-benzoyl]-6-hydroxybenzofuran, • 2- (4-hydroxyphenyl) -3- [4- [2- (N,N-diisopropylamino) -ethoxy]benzoyl]-6-hydroxybenzofuran, ■ 2- (4-hydroxyphenyl) -3- [4- [2- (N,N-dimethylamino) ethoxyj - benzoyl]-6-hydroxybenzofuran, • l-ethyl-2- (4-methoxyphenyl) -3- [4- [2- (piperid-1-yl) -ethoxy]benzoyl]-6-hydroxyindole, • 2- (4-methoxyphenyl)-3-[4-[2-(hexamethyleneimin-1-yl)ethoxy]benzoyl]-6-methoxybenzofuran, • 2- (4-methoxyphenyl)-3-[4-[2-(piperid-1-yl)ethoxy]-benzoyl]-6-methoxybenzofuran, • 2- (4-methoxypbenyl) -3- [4- [2- (pyrrolidin-1-yl] ethoxy] -benzoyl]-6-methoxybenzofuran, • 2- (4-methoxyphenyl)-3-[4-[2-(N,N-dieChylamino>ethoxy]-benzoyl]-6-methoxybenzofuran, • 2- (4-methoxypbenyl) -3- [4- [2- (N,N-diisopropylamino) -ethoxy]benzoyl]-6-methoxybenzofuran, • 2- {4-methoxyphenyl) -3- [4- [2- (N,N-dimethylam±no)ethoxy] -benzoyl]-6-methoxybenzofuran, • l-ethyl-2-(4-methoxyphenyl)-3-[4-[2-(piperid-1-yl)ethoxy]benzoyl]-6-methoxyindole, • 2-(4-methoxyphenyl)-3-[4-[3-(hexamethyleneimin-1-yl)propoxy]benzoyl]benzo[b]thiophene, • 2- (4-methoxyphenyl)-3-[4-[2-(hexamethyleneimin-1-yl) ethoxy] benzoyl] benzo [b] thiophene, • 2- (4-methoxyphenyl) -3-[4-[3-(piperid-1-yl)propoxy]-benzoyl] benzo [b] thiophene, ■ 2- (4-methoxyphenyl) -3- [4- [2- (pyrrolidin-1-yl) ethoxy] - benzoyl] benzo [t>] thiophene, - 2- (4-methoxyphenyl) -3- [4- [2-(N,N-diethylamino) ethoxy] -benzoyl] benzo [b] thiophene, • 2- (4-methoxyphenyl) -3- [4- [2- (N,N-diisopropylamino) -ethoxy] benzoyl] benzo [b] thiophene, • 2- (4-methoxyphanyl) -3- [4- [2- (N,H-dimethylamino) ethoxy] -benzoyl]benzo[b]thiophene, • 2-(4-chlorophenyl)-3-[4-[2-(hexamethyleneimin-1-yl)-ethoxy]benzoyl]-6-hydroxybenzo Eb]thiophene, • 2- (4-hydroxyphenyl) -3- [4- [2- (piperid-1-yl) ethoxy] benzo¬yl] benzo[b]thiophene, • 2-(4-hydroxyphenyl)-3- [4- [2-(pyrrolidin-1-yl)ethoxy] -benzoyl]benzo[b]thiophene, ■ 2- (4-hydroxyphenyl) -3- [4- [2- • 2- (4-hydroxyphenyl) -3- [4- [2- (N,N-diisopropylamino) -ethoxy]benzoyl]benzo[b]thiophene, • 2- (4-hydroxyphenyl) -3- [4- [2- (N,N-dimethylamino)ethoxy] -benzoyl]benzo[b]thiophene, • 2-(4-chlorophenyl)-3-[4-[2-(pyxrolidin-1-yl)ethoxy]-benzoyl]benzo[b]thiophene 1-oxide, • 2- (4-chlorophenyl)-3-[4-[2-(piperid-1-yl)ethoxy]benzo¬yl] benzo [b] thiophene 1-oxide, - [S- (n-butylsulphonyl) -2- [4- (n-butylsulphonyl)phenyl] -benzo[b]thien-3-yl][4-[2-(1-piperidyl)ethoxy]phenyl-methanone, - [6- (n-pentylsulphonyl) -2- [4- (n-pentylsulphonyl)phenyl] -benzo [b] thien-3-yl] [4-[2-(1-piperidyl)ethoxy]phenyl]-methanone, • [6- (n-hexylsulphonyl) -2- [4- (n-hexylsulphonyl)phenyl] -benzo[b]thien-3-yl] [4-[2-(1-piperidyl)ethoxy]phenyl]-methanone, • [6- (n-butylsulphonyl) -2- [4- (n-butylsulphonyl)phenyl] -benzo[b]thien-3-yl][4-[3-(1-piperidyl)propyloxy]-phenyl]methanone, - [6- (n-butylsulphonyl) -2- [4- (n-butylsulphonyl) phenyl] - benzo[b]thien-3-yl]- [4- [2-(1-pyrrolidinyl)ethoxy]- phenyl]methanone, • [6-hydroxy-2- [4- (n-butylsulphonyl)phenyl]benzo[b] thien-3-yl]-[4-[2-(1-piperidyl)ethoxy]phenyl]methanone, • [6-n-butylsulphonyl-2- [4-hydroxyphenyl]benzo tbl thien-3-yl]-[4-[2-(1-piperidyl)ethoxy]phenyl]methanone, • [6- [N- (4-chlorophenyl)carbamoyl! -2- [4- [N- (4-chlorophen¬yl) carbamoyl]phenyl] benzo[b]thien-3-yl] [4- [2- (1-piperidyl)ethoxy]phenyl]methanone, • [6- (N-(n-butyl)carbamoyl] -2- [4- [N- (n-butyl) - carbamoyl]phenyl]benzo £b]thien-3-yl] [4- [2-(1-piperid¬yl) ethoxy]phenyl]methanone, ■ [S- (N-methylcarbamoyl) -2- [4- (N-methylcarbamoyl)phenyl] -benzo[b]thien-3-yl] [4-[2-(1-piperidyl)ethoxy]phenyl]-methanone, • [6- (N-ethylcarbamoyl) -2- [4- (N-ethylcarbamoyl)phenyl] - benzo[b]thien-3-yl] [4-[2-(1-piperidyl)ethoxy]phenyl]- methanone, • [6-(N-isopropylcarbamoyl)-2-[4-(N-isopropylcarbamoyl)-phenyl] benzo [b] thien-3-yl] [4- [2-(1-piperidyl)ethoxy]-phenyl]methanone, • [6- (N-cyclohexylcarbamoyl) -2- [4- (N-cyclohexylcarbamo-yl) phenyl] benzo [b] thienyl-3-yl] [4- [2- (1-piperidinyl) -ethoxy] phenyl] methanone and the salts and solvates thereof. in which R0 and R30 represent, independently, H, CH3, -C0-(Cj^-CgJalkyl or optionally substituted phenyl and R20 represents pyrrolidino, piperidino, hexamethyleneimino or the pharmaceutically acceptable salts or solvates thereof, NPY antagonists described in US 5,504,094, in particular the compound of formula (III) in which R0 and R30 are both hydrogen and R20 is pyrrolidino, as well as the salts and solvates thereof. Ill - Phenylsulphonylguinolines of formula (IV): in which R3y ia as defined above, - R2y is -HN2, -OH or -SH and salts thereof, described in US 5,552,411, in particular 8-amino-6-(2-isopropylphenylsulphonyl)-5-nitroquinoline known under the code PD-160170 and 8-amino-6-(4-aminophenylsulphonyl)-5-nitroquinoline, known under the coda PD-9262, which are described in Bioorganic and Medicinal Chemistry Letters, 1996, 6, 15, 1809-1814. IV - Benextramine and analogues thereof described in J. Med. Cham. 1993, 36, 272-279, in Eur. J. Pharmacology 1994, 37, 2242-2248 and in Current Pharmaceutical Design, 1995, I, 295-304, in particular SC3117, SC3199, CC217 and CC2137. V - Inositol phosphate derivatives, in particular: a) specific isomers of inositol triphosphate, in par¬ticular D-myoinositol 1,2,6-triphosphate. myoinositol 1,2,3-triphosphate and L-myoinositol 1,3,4-triphosphate, which are described as NPY antagonists in WO 92/00079 and US 5,128,332. b) Inositol monophosphate in acidic form and salts thereof, in particular the sodium, potassium, calcium or zinc salts, which are described as NPY antagonists in WO 92/00744. VI - Compounds of formula in which: - Ar' is phenyl, 2-, 3- or 4-pyridyl, 2- or 3-thienyl, 4-or 5-pyrimidinyl, each optionally being mono- or disub¬stituted with a halogen, a hydroxyl or a linear or branched lower alkyl chain having from 1 to 6 carbon atoms; - A', W, X', Y and T' are identical or different and represent a hydrogen, a halogen, a hydroxyl, a linear or branched lower alkoxy chain having 1 to 6 carbon atoms; - R'i and R'2 are identical or different and represent a hydrogen, a linear or branched lower alkyl chain having 1 to 6 carbon atoms; - R'3 and R'4 are identical or different and represent a hydrogen or a linear or branched lower alkyl chain having 1 to 6 carbon atoms; and - R'g represents a hydrogen, a linear or branched lower alkyl chain having 1 to 6 carbon atoms or a phenyl; and salts thereof, which can be prepared as described in WO 96/14307, in particular • 1-cyano-l-(4-phenylpiperazin-l-yl)cyclohexane, • 1-phenyl-l-(4-phenylpiperazin-l-yl)cyclohexane, • 1-(3-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)cyclo-hexane, • 1-{3-methoxyphanyl)-1-[4-(2-pyrimidinyl)piperazin-l-yl]cyclohexane, • 1- (3-methoxyphenyl)-1-[4-(2-pyridyl)piperazin-1-yl]cyclohexane, • 1- (3-methoxyphenyl) -1- [4- (2-fluorophenyl)piperazin-l-yl]cyclohexane, • 1- (3-methoxyphenyl) -1- [4- (4-£luorophenyl)piperazin-l-yl]cyclohexane, • 1-(3-hydroxypheayl)-1-(4-phenylpiperazin-l-yl)cyclo¬hexane , • 1 - (3 , 5-dimethoxyphenyl)-1-(4-phenylpiperazin-l-yl) cyclohexane, • 1- (3-ethoxyphenyl) -1- (4-phenylpiperazin-l-yl) cyclo¬hexane , • 1- (3-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-phenylcyclohexane, • 1- (3-n-butoxyphenyl) -1- (4-phenylpiperazin-l-yl)cyclo¬hexane, • 1-(3-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-methylcyclohexane dihydrochloride cis isomer and trans isomer, • 1-(4-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)cyclo¬hexane, • 1-(2-methoxyphenyl)-1-{4-phenylpiperazin-l-yl)cyclo¬hexane , • 1-(3,4-methylenedioxyphenyl)-1-(4-phenylpiperazin-l-yl) cyclohexane, • 1- (3-ethoxyphenyl) -1- (4-phenylpiperazin-l-yl) -4-methyl-cyclohexane cis isomer and trans isomer, • 1- (3-ethoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-ethyl-cyclohexane cis isomer and trans isomer, • 1-(3-isopropoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-methylcyclohexane cis isomer and trans isomer, • 1-(3-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)-3-methylcyclohexane cis isomer and trans isomer, • 1- (3-benzyloxyphenyl)-1-(4-phenylpiperazin-l-yl)cyclo- hexane, • 4- (3-ethoxyphenyl) -4- (4-phenylpiperazin-l-yl) tetra-hydropyran, • 4- (3-ethoxyphenyl)-4- (4-phenylpiperazin-l-yl)tetra-hydro thiopyran, • 1- (3-methoxymethoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-methylcyclohexane cis isomer and trans isomer/ • 1- (3-ethoxymethoxyphenyl) -1- (4-phenylpiperazin-l-yl) -4-methylcyclohexane cis isomer and trans isomer, • 1- (3-ethoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-methoxycyclohexana cis isomer and trans isomer. VII - Compounds of formula Ta-Za-NR1a- in which - na represents 0, 1, 2, 3, 4 or 5; - Ra represents a hydrogen atom or a phenyl or naphthyl group optionally mono- or disubstituted with identical or different substituents selected from a fluorine, chlorine, bromine or iodine atom, a cyano, alkyl, phenyl, hydroxyl, alkoxy, dialkylaminoalkoxy, hydroxyphenyl, phenylalkoxy, alkylcarbonyl, amino, alkylamino, dialkylamino, alkylsulphonylamino, alkylcarbonylamino, alkoxycarbonylamino, alkoxycarbonyloxy, carboxyl, alkoxycarbony1, aminocarbonyl, alkylaminocarbony1, dialkylaminocarbonyl, alkylcarbonyloxy, alkylsulphonyloxy, hydroxymethyl, hydroxyethyl, hydroxypropyl, hydroxybutyl, trifluoromathyl, trifluoromethoxy, trifluoromethylthio, aminoalkyl, alkylaminoalkyl, aminocarbonylaminoalkyl, benzoylamino, alkanoylaminoalkyl, a1koxycarbonylaminoalkyl, benzyloxycarbonylaminoalkyl, aminosulphonyl, alkylamino-sulphonyl, dialkylaminosulphonyl, aminosulphonylamino, alkylaminosulphonylamino, dialkylaminosulphonylamino, cyanamino, aminocarbonyl-amino, alkylaminocarbonylamino, dialkylaminocarbonyl-amino, aminosulphonylaminoalkyl, alky1aminosulphonyl- aminoalkyl, carboxyalkyl, alkoxycarbonylalkyl, amino-carbonylalkyl, alkylaminocarbonylalkyl, aminosulphonyl-alkyl, alkylaminosulphonylalkyl, alkylsulphonyl, amino-sulphonyloxy, alkylaminosulphonyloxy, dialkylamino-sulphonyloxy or cyanoguanidi.no group/ an aminophenyl or aminonaphthyl group disubstituted with a chlorine or bromine atom, wherein the substituents rfay be identical or different, or a hydroxyphenyl or hydroxynaphthyl group disubstituted with a chlorine or bromine atom or with alkyl or alkoxy groups, wherein the substituents may' be identical or different, a diphenylmethyl group, an aminocarbonylalkyl group substituted on the alkyl part with a hydroxyphenylalkyl , group or with a (2,2-diphenylethyl)amlnocarbonylamino-phenyl group, a 5-membered heteroaryl group attached via a carbon or nitrogen atom, the said heteroaryl comprising an imino group optionally substituted with a (Cj-Cg) alkyl group or a phenyl group and an oxygen, sulphur or nitrogen atom, or a 6-membered heteroaryl group attached via a carbon atom, the said heteroaryl comprising one or two nitrogen atoms, as well as the 5 - or 6 -membered heteroaromatic rings defined above which constitute a heteroaromatic bicyclic system with two neighbouring carbon atoms of the hetero¬aromatic ring and a 1,4-butadienylene group, and, furthermore, all the mono- or bicyclic heteroaryl groups mentioned above may be monosubstituted on the carbon skeleton with a fluorine, chlorine or bomine atom, with an alkyl, alkoxy, hydroxy1, phenyl, nitro, cyano, carbonyl, alkoxycarbonyl, aminocarbonyl, alkylamino-carbonyl, dialkylaminocarbonyl, fluoromethyl, difluoro-methyl, trifluoromethyl, alkanoyl, aminosulphonyl, alkylaminosulphonyl or dialkylaminosulphonyl group, or disubstituted with a fluorine, bromine or chlorine atom, with methyl, methoxy or hydroxyl groups, wherein the substituents nay, be identical or different. a phenyl group substituted with a (1,5-dihydro-2,4-dioxo-3ff-l,2,4-triazol-4-yl]alkyl residue, in which the imidazole or triazole part is substituted with l or 2 phenyl groups, a eycloalkyl group having from 4 to 8 carbon atoms optionally substituted with a hydroxy1, amino, alkylamino or dialkylamino group, therein the substituents described above are not attached to position 1 of the eycloalkyl residue when Y represents an oxygen atom, a 1-[[[5,ll-dihydro-6 or a hydroxy 1 group, when Y, is an oxygen atom or a group -NR4a- and na represents a figure between 2 and 5, - R3 is a hydrogen atom, a linear or branched {Cr~ C10)alkyl group, a eycloalkyl group having from 3 to 7 carbon atoms, a phenyl group optionally substituted with a hydroxy1 or hydroxyalkyl group, or a phenylmethyl group optionally substituted on the phenyl part with a hydroxyl or hydroxyalkyl group, - R23 is an unbranched (C1-C5)alkyl substituted in the u position with an amino or alky1amino group which is protected, by an amine-protecting group, with a dialkyl¬ amino, N-alkylbenzylamino, aminocarbonyl, aminocarbonyl- amino, aminoethylimine, aminoiminomethy1, amino(hydroxyimino)methyl, amino(alkoxyimino)methyl, guanidino, hydrazinoiminomethyl, amino(nitroimino)methyl, [amino(nitroimino)methyl]amino, amino(cyanimino)methyl, [amino (cyan imino) methyl] amino, [ (alky 1 amino) iminome thyl] - amino, [{alkylamino)(alkylimino)methyl]amino, [amino (alkylimino)methyl] amino, 2-aminoimidazol-l-yl, triazol-3-yl)methylamino, {3 -amino-1,2,4-oxadiazol-5 - yDamino or (5-amino-l,2,4-oxadiazol-3-yl)amino group or with an imidazol-4-yl, imidazol-2-yl, l-methylimidazol-2- yl, imidazol-2-ylamino, imidazol-2-ylmethylamino or (4,5- dihydro-lH-imidazol-2-yl)amino group, optionally substi¬tuted on the carbon with one or two methyl groups, or a phenyl or phenylmethyl group optionally substituted on the aromatic rings with a cyano, iminomethylamino, cyaniminometbylamino, (methylamino)methylideneamino, aminoiminomathy1, amino(hydroxyimino)methyl, amino(alkoxyimino)methyl, hydrazineiminomathy1, amino (cyanimino) methyl or guanidino group or with an imidazol-2-yl, 1-methylimidazol-2-yl or 4,5 -dihydro- 1H-imidazol-2-yl group, optionally substituted on the carbon atoms with one or two methyl groups, in which, in the aminoiminomethyl, amino(hydroxyimino)methyl and guanidino groups mentioned in the definition of R2a above, one or more hydrogen-, atoms connected to the nitrogen atom, independent of each other, may be replaced by alkyl groups, or in which two hydrogen atoms connected to different nitrogen atoms may be replaced by an alkyl bridge having from 2 to 4 carbon atoms and for which the hydrogen atom of an HN ♦ R15a is a (Cj-C1) alkyl group, a (C3-C7) cycloalkyl group, a phenyl group or a phenylalky1 group in which the alkyl is C1-Cj, ♦ R1* and R17 , which are identical or different, represent a hydrogen atom, a (C1-Cg) alkyl group or alternatively one of the residues Risa and R17a represents a (C3-C7) cycloalkyl group or a phenyl group, ♦ R18a and R19a, which are identical or different, represent a hydrogen atom, (^-C,,) alkyl groups, benzyl or phenyl groups, - R3a is a hydrogen atom, a (C1-C7)alkyl group or a (C4-C7) cycloalkyl group, - Ta is a hydrogen atom, a phenyl group or a 5-membered heteroaryl group attached via a carbon or nitrogen atom and comprising a nitrogen, oxygen or sulphur atom option¬ally substituted with an alkyl group, or comprising a nitrogen atom optionally substituted with an alkyl group as well as an additional sulphur, oxygen or nitrogen atom, or alternatively, when Za represents a bond, Ta is a protecting group for an amino group or the residues (T^T^U,) - (CH2)m- or T3,0-, in which ♦ T2a to T3a, which are identical or different, are phenyl or 6-membered heteroaryl groups attached via carbon atoms, which, depending on the case, comprise one or two nitrogen atoms, 5-membered heteroaryl groups attached via carbon or nitrogen atoms, comprising a nitrogen atom . optionally substituted with an alkyl group, sulphur or oxygen, or comprising a nitrogen atom optionally substituted with an alkyl group as well as an addi¬tional nitrogen, sulphur or oxygen atom, in which a 1,4-butadienylene bridge may be made between two neighbouring carbon atoms of the 5- or 6-membered heteroaryl groups mentioned above in the definition of the Ta residues; the bicyclic aromatic or heteroaromatic rings thus constituted may also be attached to a carbon atom of the 1,4-butadienylene group and, moreover, not only the phenyl groups and the 5- or 6-membered heteroaryl groups but also the bicyclic aromatic or heteroaromatic rings may be mono- or disubstituted on the carbon skeleton with fluorine, chlorine, bromine or iodine atoms or with cyano, hyroxyl, amino, dimethylamino, diethylamino, N-ethylmethylamino, trifluoromethyl, trifluoro-methoxy, trifluoromethylthio, acetylamino, propionylamino, methanesulphonylamino, methane-sulphonyloxy, phenyl, phenylmathoxy, 2-phenylethoxy, alkyl or alkoxy groups or trisubstituted with an amino or hydroxyl group and two chlorine or bromine atoms or with a hydroxyl group and two alkyl or alkoxy groups, the substituents being identical or different, and the alkvl and alkoxv Darts mentioned above comprising from 1 to 4 carbon atoms, hydrogen atoms, (C1-C1alkyl groups, cycloalkyl groups having from 3 to 10 carbon atoms, bicyclo-alkyl or tricycloalkyl groups having from 6 to 12 carbon atoms or ♦ Txa and T2a together represent a linear-chain (C3-C7)alkylene group, ♦ XJa is the group >CH in which the hydrogen atom may be replaced by an alkyl, phenyl, hydroxyl, alkoxy, alkanoyloxy, alkoxycarbonyl or alkanoylamino group, in which the alkyls or alkoxys mentioned above may comprise, depending on the case, from 1 to 3 carbon atoms and the alkanoyls mentioned above may comprise ' 2 or 3 carbon atoms, or alternatively the ?CHCH2- , group or a nitrogen atom, ♦ m represents 0, 1, 2 or 3 ♦ or alternatively Ta is a group (T^T^UJ - (CH2)M in which ♦ T1a, T2a, Ua and ma are as defined above, except that the mono- or bicyclic aromatic or betero-aromatic rings mentioned above for Txa and T2a are connected together by a bond or by a -CH2 -, -C{CH3)2-, -CH2CH2-, -CH»CH- or -NHCO- bridge, - Ya is an oxygen atom or a group -NRa in which R4a makes the definition mentioned above form R1a, it being pos¬sible for the residues of Rxa and of R4a to be identical or different, and - Za is a single bond defined by a -CO-, -CH2-, -SO- or -S02- group, and, except where otherwise mentioned, the alkyl and alkoxy parts mentioned above may comprise from 1 to 3 carbon atoms, and the tautomers, diastereomers, enantiomers, mixtures and salts described in WO 94/17035. Among these compounds, • (R) -N2-(diphenylacetyl)-N-(phenylmethyl)argininamide, • (R) -N2-(diphenylacetyl) -N- [ argininamide, • (R)-N-[2- • N- [ (4-aminocarbonylaminophenyl)methyl] -N2- (diphenyl-acetyl)argininamide, • (R)-N-[{4-hydroxyphenyl)methyl]-N2-[[5-(2-phanyl-ethoxy)-lff-indol-2-yl]carbonyl]argininamide, • (R) -N2- (diphenylacetyl) -N- [ (4-fluorophenyl)methyl] -argininamide, ■ (R)-N-[(4-bromophenyl)methyl-N2-(diphenylacetyl)argin¬ inamide/ • the optically active diastereoisomers of N2-(a-cyclo- pentylphenylacetyl) -N- [ (4-hydroxyphenyl)methyl] -D-argin- . inamide, • N-[[4-(dimethylamino)phenyl]methyl]-N2-(diphenyl¬ acetyl) argininamide, ■ (R) -N2- (diphenylacetyl) -N- [ [4- (hydroxymethyl)phenyl] - methyl]argininamide, • (R) -N2-(diphenylacetyl)-N-[[4-(1-oxoethyl)phenyl]meth¬yl] argininamide, • • (R) -N2- (diphenylacetyl) -N- [ [4- [ (mathylaminocarbonyl) - amino] phenyl] methyl] argininamide, . (R)-N-[(4-amino-3,5-dichlorophenyl)methyl]-N2-(diphenylacetyl)argininamide, • (R)-N- [(4-amino-3,5-dichlorophenyl)methyl]-N2-(3,3-dipheny1-1-oxopropyl)argininamide, • • N2-(diphenylacetyl)-N-[3-[1-[2-[5,ll-dihydro-6(6H)oxo-pyrido[2,3-b][l,4]benzodiazepin-5-yl]-2-oxoethyl]-4-piperidyl] propyl] argininamide, ■ N2- (diphenylacetyl) -N- [ (4-hydroxy-3-methoxyphenyl)meth-yl]argininamide, ■ H2- (diphenylacetyl) -N- [(3-hydroxy-4-methoxyphenyl)meth-yl] argininamide, • (R,S)-N-[(4-amino-3,5-dibromophenyl)methyl]-Ns- (aminoiminomethyl) -N2- (diphenylacetyl) lysinamide, ■ N-[(3,5-dimethyl-4-hydroxyphanyl)methyl]-N2-(diphenyl¬ acetyl) argininamide, • N- [(lff-benzimidazol-5-yl)methyl]-N2-(diphenyl¬acetyl) argininamide, • N2-(diphenylacetyl)-N-[(4-hydroxy-3-methylphenyl)meth-yl]argininamide, • N-[[4-(aminocarbonyl)phenyl]methyl]-N2-(diphenyl¬acetyl )argininamide, • • (R) -N- [ ■ N2- (diphenylacetyl) -N- [ (lff-indol-5-yl)methyl] arginin- . amide, • (R) -N- [ [4- (aminosulphonyl)phenyl]methyl] -N2- (diphenyl¬acetyl) argininamide, • (R) -N2-(diphenylacetyl)-N-[[4-methoxycarbonyl)phenyl)-methyl]argininamide, • (R)-N2- (diphenylacetyl) -N- [ (4 -pyridyl) methyl] arginin¬amide , • (R)-N- [(4-amino-3,5-dibromophenyl)methyl]-N2- (diphenyl¬acetyl) argininamide, • (R)-H2-(diphenylacetyl)-N-[(2-thienyl)methyl]-N2- (2- naphthoyl)argininamide, • (R)-N-[(4-amino-3,5-dichlorophenyl)methyl]-N2-(2-naphthoyl)argininamide, • (R,S) -N5- (4, 5-dihydro-lJr-imidazol-2-yl) -N2- (diphenyl¬acetyl) -N-[(4-hydroxyphenyl)methyl]ornithinamide, • (R,S) -N2-(diphenylacetyl)-N-[(4-hydroxyphenyl)methyl] -N5-(lff-imidazol-2-yl)ornithinamide, • (R)-N- [[3- [(l,2-dihydro-3,5(4H)dioxo-l,2-diphenyl-3ff-l,2,4-triazol-4-yl)methyllphenyl]-N2-diphenylacetyl)-argininamide, • N2- (diphenylacetyl) -N- [ (3-hydroxyphenyl)methyl]arginin-amide, ■ (R)-N- [[3-[(4,5-dihydro-2,4 imidazol-3-yDmethyl] phenyllmethyl] -N2- (diphenyl¬ acetyl) argininamide. • (R)-N2-(diphenylacetyl)-N-[(4-hydroxyphenyl)methyl]- argininamide, known under the code BIBP3226, ■ ^-(diphenylacetyl) -N- [2- (4-hydroxyphenyl) ethyl] argin¬ inamide, • N2-(diphenylacetyl)-[(4'-hydroxy-[1,1'-biphenyl]-4-y1)me thy1]argininamide, • N- [[4- t(l,2-dihydro-3,5(4tf)dioxo-l,2-diphenyl-3if-l,2,4-triazol-4-yl)methyl]phenyl]methyl]-N2-(diphenyl¬acetyl) argininamide, • N2- (diphenylacetyl) -N- E (4-methoxyphenyl)methyl] arginin¬amide, ■ N2-(diphenylacetyl)-K-[2-(4-methoxyphenyl)ethyl]arg¬ ininamide, • N2-(diphenylacetyl)-N-[2-(3-methoxyphenyl)ethyl]arg¬ ininamide, - N2- (diphenylacetyl) -N- [(3-methoxyphenyl)methyl] arginin¬amide, ■ (R,S) -3- [4- (aminoiminomethyl) phenyl] -N2- (diphenyl¬ acetyl) -N- [ (4-hydroxyphenyl)methyl] alaninamide, • (R,S)-3-[3- (amino iminomethyl) phenyl] -N2- (diphenyl¬acetyl) -N- [ (4-methoxyphenyl)methyl] alaninamide, • (R,S)-3-[3- (aminoiminomethyl) phenyl] -N2- (diphenyl¬acetyl) -N- [ (4-hydroxyphanyl)methyl] alaninamide, • (R) -N2-[bis(4-bromophenyl)acetyl]-N-[(4-hydroxy¬phenyl) methyl] argininamide, • (R) -N2-(diphenylacetyl)-N-[(4-ethoxyphenyl)methyl]-argininamide, • (R) -N2-(diphenylacetyl)-N-[(4-hydroxyphenyl)methyl]-N-metnylargininamide, ■ (R,S)-N-[(4-amino-3,5-dibromophenyl)methyl]-3-[3- (aminoiminomethyl)phenyl] -N2- (diphenylacetyl) alanin¬ amide, • (R) -N- [ (4-hydroxyphenyl)mathyl] -N2- (2-naphthoyl)argin¬inamide, • (R) -N- [ (4-hydroxyphenyl)methyl] -N2- (2-naphthoyl) argin¬inamide , • (R)-N2-(2,2-diphenyl-2-hydroxyacetyl)-N-[(4-hydroxy¬ phenyl) methyl] argininamide, ■ (R,S)-M2-(diphenylacetyl)-N5-(lH-imidazol-2-yl)-M-[(4- methoxyphenyDmethyl] ornithinamide, • methyl) amino] carbonyl] -N- [(4-hydroxyphenyl)methyl]alan- inamide, • (R,S) -N2- (diphenylacetyl) -N5- (lff-imidazol-2 -yl) -K- (phenylmethyl)ornithinamine, ■ (R,S)-N-[(4-amino-3,5-dichlorophenyl)methyl]-N2- (diphenylacetyl) -N5- {lff-imidazol-2-yl)omithinamide, • (R,S) -N-[(4-hydroxyphenyl)methyl]-N5-{lH-imidazol-2- yl) -N2- (2-naphthoyl)ornithinamide, ■ (R,S) -N2-[ [(diphenylmathyl)amino]carbonyl]-N-[(4-hy- droxyphenyDmethyl] -N5- (LH-imidazol-2-yl)ornithinamide, • (R,S)-N- [(4-hydroxyphenyl)methyl] -N5- (li-imidazol-2-yl)-N2-[(2-naphthyl)acetyl]ornithinamide, • (R,S)-N-[(4-hydroxyphenyl)methyl]-N5-(lff-imidazol-2-yl)-N2-[[(2-naphthyl)amino]carbonyl]ornithinamide, • (R,S)-N-[(4-hydroxyphenyl)methyl]-N5-(ltf-imidazol-2-yl) -N2- [ (1,2,3,4-tetrahydroquinolin-3-yl)carbonyl]-orni thinamide, • (R,S)-N-[(4-hydroxyphenyl)methyl]-N5-(lH-imidazol-2-yl) -N2-[(1,2,3, 4-tetrahydroquinolin-2-yl)carbonyl]-ornithinamide, • (R) -N- [ (4-aminosulphonylaminophenyl)methyl] -N2- (diphen¬ylacetyl) argininamide, ■ (R) -H- [ (4-aminophenyl)methyl] -N2- (diphenylacetyl) argin¬ inamide/ - (R)-N-[(6-quinolinyl)methyl]-N2-(diphenylacetyl)argin¬inamide, • (R)-N2-[(3,4-dichlorophenyl)acetyl]-N-[(4-hydroxy-phenyl )me thyl]argininamide, • (R)-N2-(diphenylacetyl)-N-[[4-(2-hydroxyethyl)phenyl]-methyl]argininamide, ■ (R,S) -Ns- (3-amino-l,2,4-oxadiazol-5-yl) -N2- (diphenyl¬acetyl) -N-[(4-hydroxyphenyl)methyl]ornithinamide, ■ (R)-N2-[(9-fluorenyl)carbonyl]-N-[(4-hydroxyphenyl)-methyl] argininamide, • (R,S) -6-(aminoiminomethyl) -H2- (diphenylacetyl) -N- [(4-hydroxyphenyl)methyl]norleucinamide, • (R,S)-3-[4- (diphenylacetyl) -N- [ (4 -hydroxyphenyl) methyl] alanin-amide, • (R,S)-3 - [3 - (aminoiminomethyl)phenyl] -N2- (diphenyl-acetyl)-N-[ (4-ethoxycarbonyloxyphenyl)methyl]alanin-amide, • ■ (R,S)-H2-(diphanylacetyl)-N-[(4-hydroxyphenyl)methyl]-2-methylarglninamlde, • (R,S)-N2-(diphanylacetyl)-H-[ [4-(3-hydroxypropyl)-phenyl] methyl] argininamide, • (R)-N- [ [4- [(4,5-dihydro-5,5-dimethyl-2,4(3H)dioxo-lH-imidazol-3-yl)methyl]phenyl]methyl]-N2-(diphenyl-acetyl)argininamide, are advantageous, BIBP 3226 being preferred, in which R'^ represents a phenyl group unsubstituted or substituted with one or two halogen atoms, a (C1-Cjjalkyl group or a pyridyl group unsubstitutad or substituted with one or two halogen atoms, a (Cj-Cjialkyl group or a (ci-c3) alkoxy group, - R'2 represents a hydrogen atom, a (C1-C3)alkyl group, a phenyl group optionally substituted with one or two halogen atoms or with a (C1-Cj) alkyl group or with a (C1-C3)alkoxy group, a benzyl or heteroaryl group uneubstitu¬ted or substituted with one or two halogen atoms or a (C1-C3)alkyl or (C1-Cj)alkoxy group. - n' represents 1, 2, 3 or 4 or in which R' is defined by the formula: in which R'3 represents a pyridyl ring unsubstituted or substituted with one or two halogen atoms, with a (C1-C3)alkyl or (Cj^-Cjjalkoxy group, R"4 represents a hydro¬gen atom or a phenyl group optionally substituted with one or two halogen atoms or with a (C1-C3)alkyl group or with a (C1-C3)allcoxy group, R' 's represents a hydrogen , atom or a methyl or hyroxyl group and Z' ' represents a single bond, an oxygen atom or a sulphur atom and p' represents 1, 2 or 3, mf' represents 1, 2 or 3 and R'0 represents a hydrogen atom or a methyl group, as well as the pharmaceutically acceptable salts thereof, the NPY-antagonist effect of which is described in EP 448,765. Among these compounds, those of formula (VII) in which m" is 3, R"0 is hydrogen and R" is 2- (3-pyridyl-methylthio) ethyl, 3,3-diphenylpropyl, 2- (2-pyridylamino) -ethyl, 2 -(5-bromo-3-methyl-2-pyridylamino)ethyl, 2-(diphenylmethoxy)ethyl, 3-(3,5-difluorophenyl)-3-(2-pyridyl)propyl, 2-[N-{5-bromo-3-methyl-2-pyridyl)-H-benzylamino]ethyl or 2-(5-bromo-3-methyl-2-pyridyl)ethyl and the salts thereof are particularly advantageous, 1- [3- (3, 5-difluorophenyl) -3-(2-pyridyl)]propyl-3- [4- (Iff) -imidazolyl]guanidine trihydrochloride (Be 90481) being preferred. IX - Dihydropyridines of formula: the solid or dotted lines representing a single or double bond, as well as the additional salts or solvates thereof described in US 5,554,621. B. Other NPY antagonists which are advantageous in the cosmetic compositions of the present invention are peptides chosen from those of groups IX to XII below. X - Compounds of formula Tyr-Pro-Ser-Lys-Pro-Asp-D-Cya-NH- (CH2) BC0-Xxx2 (IX) -Arg-Cys-Tyr-Xxx3-Ala-Leu-Arg-His-Tyr-Xxx4 -Asn-Leu-Xxxs-Thr-Arg-Ile-Arg-Tyr-Tc in which - Xxx2 and Xxx3 are Ser or Ala, Xxx4 and Xxxs are Leu, lie. Met, Nle (norleucine) or Val - Tc is OH, 0(C1-C4)«lfcyl, NH2 or NHK^-C1 alkyl, - s is an integer from 1 to 11, and the salts thereof, described in EP 355,794. Among these compounds, that of formula (IX), in which s is 7, Xxx2 is Ala, Xxx3 is Ser, Xxx4 and Xxx5 are both lie and Tc is NH2, and the salts thereof, are advantageous. XI - Compounds of formula 8b-ia-Bka-B»k3-l>fc4-«kB-»M-0fc7-DP-Tlir-BP'-01u (X) -BP'-K-NH2 in which klr k2, k3, k4, k5, k6 and k7 represent zero or 1, their sum being at least 1, A is Phe or Tyr; B is Pro, Ser, Ala, Gly, Abu, Cys, Pro-Ser, Cys-Sar, Ala-Ser, Gly-Ser, Abu-Ser or Pro-Ala, Abu being 2-aminobutyrie acid; BP, BP' and BP' are amino acids with a basic side chain; D is Pro or Cys; E is NH- Among these compounds, those of Formula (X) in which BP is Lys or Arg; E is MH-(CH2) t-CO, with t = 1-7; tr is where t' is 0, 1 or 2, and the salts thereof, are advan¬tageous , the compound of formula H-Tyr-Abu-Ser-Lys-Aoc-Abu-Ile-Asn-Leu-Ile- (X') Thr-Arg-Gln-Arg-Tyr-NH2 where Aoc represents 8-aminooctanoic acid being particu¬larly preferred. XII - Cyclic or linear compounds of formula (Xxxa-Xxxb-Xxxc-Xxxd-Xxx,-Xxxf-Xxxg-Xxxh-Xxx1-Xxxj)n (XI) in which Xxxa, Xxxb, Xxxc and XxXj either do not exist, or alternatively Xxxa is Px or Cys; Xxxj, is Cys, Px or one or two amino acids; Xxxc is P1# Cys, Ser, Thr, Ala or Gly; Xxxd is Rx, Cys, Ser, Thr, Ala or Gly; Xxxm is Leu, lie, Val or Nle; Xxx is Arg, Lye or His; Hxx is Arg, Lys, His, Val, Leu, lie or Nle; Xxxb is Tyr, Pha, Trp, His, Lys or Arg; Xxx^ represents an NH2 group or an ester group or alternatively one or two amino acids; XXXJ is Cys or P2; 2X is hydrogen or a group P-CO where P is hydrogen, a glycosyl, nucleosyl or lipolyl radical or a (C1CjoJalkyl group, optionally containing double bonds and substituents selected from halogens and the H02, NH2, OH, sulpho, phospho, carboxy1 and alkyl groups; P2 is a group NP12P13 or OP14 in which P12 and P13 represent hydrogen or an alkyl, cycloalkyl, N-glycosyl, N-lipolyl, aralkyl or aryl group, optionally substituted with a halogen or with an H02, NH2, OH, sulpho, phospho, carboxyl or alkyl group; and P14 represents hydrogen or an alkyl, cycloalkyl, aralkyl, -O-glycosyl, -O-lipolyl, aralkyl or aryl group, optionally subsitituted with a halogen or wi tb an N02, NH2, OH, sulpho, phospho, carboxyl or alkyl group, with the limitation that - when Xxxb does not exist or represents Cys or Px, then Xxxa is nonexistent, - when Xxxd is Cya or Px, then Xxxc is nonexistent, - when Xxxi is NH2 or an ester, then XxXj is nonexistent. These compounds are described in WO 93/12139. Among these, the peptide of formula: Ser-Ala-Leu-Arg-His-Tyr-NH2 (XI') known under the code number BRC 672, is particularly advantageous. XXII - Compounds of formula H-Tyr-Pro-Ser-Lys-Pro-Asp-Asn-Pro-Gly-Glu- (XII) Asp-Ala-Pro-Ala-Glu-Asp-Xxxs-Ala-Arg-Tyr-Tyr-Ser-Ala-Leu-Arg-His-Tyr-He-Asn-Leu-Ile-Thr-Arg-Xxx7-Xxx8-Ll-(CH2)B-P3 in which z is 0, 1 or 2, Xxx6 is Mat or Leu; Xxx7 is Glu, (R)-Glu, Pro or (R)-Pro; Xxx8 is Arg, (R)-Arg or -Arg; h1 is O or NP', P' being H or alkyl; and P3 is a phenyl or naphthyl group which is unsubstituted or substituted with one or two P, CI, Br, alkyl, phenyl, OH, (phenyl)alkoxy, alkylcarbonyl, NH2 (optionally substituted with one or two alkyls), alkylsulphonyl, alkyl- or alkoxycarbonylamino, COOH, alkoxycarbonyl, NH2C0 (optionally substituted with one or two alkyls), alkylcarbonyloxy, alkylsul-phonyloxy, CH2OH, 1 - or 2-hydroxyethyl, (alkyl)-aminosulphonyl, cyanamino, aminocarbonylamino (optionally substituted with one or two alkyls) or NH2C(-N.CN)NH; a S-membered aromatic heterecycle containing oxygen, sulphur or nitrogen, an imino group or an imino group containing oxygen, sulphur or nitrogen; a 6-membered aromatic heterocycle with one or two nitrogen atoms; it being possible for the said heterocycles to be C-substituted with (C1-C6)alkyl or with phenylalkyl and optionally fused with ben¬zene and optionally also substituted either with an F, CI, Br, (Cj-Cg) alkyl, alkoxy, OH, phenyl, N02, NH2 (optionally substituted with one or two alkyls or with an allcanoyl) , CN, COOH, alkoxycarbonyl, NH2CO (optionally substituted with one or two alkyls), CH2F, CHF2, CF3, alkanoyl or NH2S02 (optionally substituted with one or two alkyls), or with two F, CI, Br, methyl, methoxy or OH; a phenyl group substituted with a [1,5-dihydro-2,4 (3ff)dioxoimidazol-3-yl] alkyl group or with a [dihydro-3,5 These compounds are illustrated in DE 4,311,756. C. NPY-antagonist products, in particular extracts with NFY-antagonist activity, which can be obtained by extrac¬tion of cells or tissues of animal or plant origin or by fermentation of microorganisms, in particular bacteria and fungi, for example yeasts, are advantageous NPY-antagonist components in the cosmetic compositions of the present invention. Particularly advantageous and even preferred products of this class are the products of groups XV, XVI and XVII illustrated below. XV - Extracts with NPY-antagonist activity obtained by extraction of a sponge, Orina. sp. Gray (or Gelliua sp.), in particular the indole compounds described in J. Nat. Products, 1994, 57, 1294-1299 and ibid. 1995, 58, 8, 1254-1260, or mixtures thereof, more particularly gelliusine A, gelliusine B, 2-[5-hydroxy-3-(2-amino- ethyl)]indol-2-yl-6-bromo-3- indolethanamine and 2-[S-bromo-3-(2-aminoethyl]indol-2-yl-6-bromo-3-indol- ethanamine, and the salts and mixtures thereof. XVI - Extracts from fermentation of Aspergillus strains, for example of Aspergillus niger with NPY-antagonist activity, in particular the compound known under the code name BMS-192548, which can be prepared by extraction of the culture medium of Aspergillus niger WB 2346, as described in J. Antibiotics, 1995, 48, 10, 1055-1059, having the formula (XV) XVII - Products, in particular extracts obtained by fermentation of Actinomycetaceae strains, having NPY- antagonist activity. More particularly, extracts obtained from a novel strain of actinomycetes having a parti¬ cularly advantageous activity as NPY-receptor antagonists are particularly preferred NPY-antagonist components. Fractions with NPY receptor antagonist activity are obtained from the fermentation broths of this strain, by filtration of the supernatant, optionally followed by steps of concentration, purification and/or lyophilization, these fractions being devoid of genotoxi¬city and having a stability which is sufficient to allow them to be formulated in the cosmetic compositions of the present invention. The supernatant of the fermentation broth can also be used as it is. These novel extracts constitute a subsequent and particularly advantageous aspect of the present inven¬tion. The organism producing the extracts with NPY receptor antagonist activity according to this specific aspect of the present invention is an actinomycetes strain which has been isolated from a sample of grassland taken from the Haute Garonne (France) , which has been assigned the in-house number SEBR 2794. A sample of this microorganism was deposited on 13 July 1993 at the CNCM of the Pasteur Institute where it was registered under the reference I 1332. The biochemical characteristics of this micro¬organism were determined on API 50 CH (specific for sugars) , API 50 AO (specific for organic acids) and API 50 AA (specific for amino acids) kits, (marketed by BioMerieux for API 50 CH and by the API Research Labora¬tory for the others) . It was thus determined that this microorganism belongs to the family of Sfcreptomycefcaceae, genua Streptomycaa. This is a polymorphous, filamentous micro¬organism. It grows well at 28°C on an ISP2 culture medium (agar yeast malt extract), the colour of its vegetative mycelium being pinkish-grey. This organism, which has properties that did not allow it to be identified as a species already described, must be considered as a novel species and it has been designated as Stxaptomycea ap SEBR 2794. The strain Streptomyces ap SEBR 2794, deposited at the CNCM of the Pasteur Institute under the number I 1332, and productive mutants thereof, also constitute a subject of the present invention. This noval strain was isolated according to the usual method, which consists in placing a small amount of soil in suspension in distilled water, in diluting the suspension to different concentrations and in plating out a small volume of each dilution on the surface of a Petri dish containing » nutrient agar medium. After incubating for a few days at 28°C, which allows the microorganisms to grow, the various colonies are taken separately and subcultured on nutrient agar so as to obtain more abundant cultures therefrom. After culturing on nutrient agar medium and subculturing several times successively, which makes it possible to obtain an abundant and pure culture of the strain of interest, a batch 0 for storage of the parent strain is manufactured, followed by primary and secondary inoculation batches. For this, a suspension of spores is prepared from a culture on nutrient agar medium in a Petri dish and from maintenance medium; this medium contains a cryo-protective agent making it possible to ensure good viability of the spores during conservation by freezing. The suspension of spores obtained is divided into cryotubes which will be stored at - 80 °C; these tubes constitute the batch 0. Following the same procedure, but starting with a tube from batch 0, a primary inoculation batch is prepared. Next, still according to the same procedure, a secondary inoculation batch is prepared from a cryotube of the primary inoculation batch. The manufacture of the inoculation batches 0, 1 and 2 ensures long-lasting accessibility of the strain and thus of the desired activity. The process for preparing the extracts with NPY receptor antagonist activity consists essentially in cultivating the novel strain SEBR 2794, or productive mutants thereof, on a suitable medium and under suitable culture conditions and in then extracting from the fermentation broth the active fraction produced during the culturing; this active fraction is found in the supernatant. Streptomycma ap SEBR 2794 can be cultured by any aerobic culture method. For this purpose, the various types of apparatus which are in common use in the fermen¬tation industry are used. It is possible, in particular, to adopt the following approach for carrying out the operations. Starting with a tube of the secondary inoculation batch, Petri dishes are seeded and, after incubating for five days, these provided a suspension of spores. This suspension of spores is used to seed stirred conical flasks containing a suitable medium. The stirred flask can also be seeded directly with a tube of the inoculation batch. The culturing in stirred flasks can last for two to seven days but a duration of three to five days is preferred. The production of activity is observed in the supernatant, from the first stage and onwards of cultur¬ing in flasks, but it may be advantageous to perform two successive culturing stages: a first stage for propagat¬ing the biomass, a second for production. In the latter case, a duration of one or two days is sufficient for the first stage. The antagonist activity contained in the flask culture supernatants is expressed as ID50 (50% inhibitory dilution, namely the dilution which inhibits binding of the ligand to its receptors by 50%); the ID50 is generally between 1/200 and 1/1000. The NPY receptor antagonist activity is obtained in the supernatant of the flask cultures, but it appears to be advantageous, in order to obtain a higher activity, to perform culturing in a fermenter and then to extract the supernatant therefrom. The fermenter is seeded with a one- or two-day-old stirred flask culture. In the fermenter, depending on the culture medium used, the antagonist activity may be observed in the supernatant from the first day onwards, but it is advantageous to prolong the culturing beyond three days in order to obtain an optimal production. Culturing SEBR 2794 in a fermenter makes it possible to control better the culture conditions which are described below, such as, for example, the pH or the aeration. The antagonist activity obtained in the fermenter supernatants, before concentrating, may vary, according to the culture conditions applied, between an ID50 of 1/500 and an ID50 of 1/10000. The culture medium used in the fermentation process must contain at least one assimilable carbon source, an assimilable nitrogen source and mineral elements. Assimilable carbon sources which may be used are carbohydrates such as glucose, mannose, maltose, dextrine, glycerol, amino acids and proteins. Assimilable carbon sources which may also be used are acetic? acid, suberic acid, citric acid, propionic acid, succinic acid and 2-ketoglutaric acid or certain animal or plant oils. Proteins, peptones and amino acids are among the best sources of assimilable nitrogen. These sources comprise, for example, casein, lactalbumin, gluten and hydrolysates thereof, fish meal, yeast extracts and peptones. The production of biomass may be increased by the addition, during culturing, of one and/or the other of these two main substrates. Potassium, sodium, iron, magnesium, calcium and manganese salts are among the mineral elements added to the culture medium to ensure growth of the microorganism and to optimize the assimilation of the carbon and nitrogen sources by the cells of the microorganism, as well as phosphorus compounds such as phosphates and trace elements. To grow the SEBR 2794 source on a medium contain¬ing these components, the process of culturing under aeration and with stirring, in which a liquid medium is used, is advantageous, although culturing on an agar medium can also be used. The temperature, the duration of incubation, the aeration and the pH of the medium must be such that they give rise to maximum growth of the microorganism used and a maximum yield of extracts with NPY receptor antagonist activity; a culture stirred for about 2 to 7 days is usually advantageous. The pH of the culture medium is preferably maintained at a more or less neutral or very weakly basic value and the optimum incubation temperature is between about 23°C and 35°C, the preferred range being 25°C to 33°C. The culture conditions, such as the composition and pH of the medium/ the incubation temperature, the stirring speed and the aeration of the fermentation may vary within a wide range and should obviously be chosen so as to obtain the best possible results. In order to obtain extracts of the NPY receptor antagonists produced during the culturing, the supernatant is separated from the mycelium after the fermentation broth has or has not been frozen. For this separation, centrifugation, filter-press filtration or clarifying filtration, that is to say filtration in the presence of a filtering adjuvant, or any other technique usually used to extract an extracellular product from a fermentation broth can be used. The active extract for cosmetic use is prepared from the culture supernatant obtained. The supernatant may be concentrated by a membrane technique or by any other concentration method so as to facilitate the packaging or the use of the active solution. It is thus possible to obtain activities with ID50 values ranging from 1/250 to 1/50000. Whether it has been concentrated or not, the supernatant may be diluted in various solvents which are compatible with cosmetological use. The extract thus obtained according to this specific aspect of the present invention is filtered through a 0.2 pm filter in order to remove all trace of residual biomass and to ensure microbiological cleanliness: it is then packaged asaptically in sterile bottles and the active solution which can be used in cosmetology is obtained. Fluids containing the NFY-antagonist extracts of the present invention in a glycol, preferably in propylene glycol, constitute another very advantageous aspect of the present invention. If it is desired to obtain a powder instead of an active solution, the filtrate can simply be lyophilized. An assay of NPY receptor antagonist activity carried out on an aliquot makes it possible to evaluate the activity of the active solution and to check the reproducibility of the process. On the supernatant or the lyophilizate, the extract of the invention may be purified in a more or less thorough manner according to the conventional techniques for purifying "biomolecules", polymers, protein substances or the like, such as, for example, gel permeation chromatography, ultrafiltration, adsorption chromatography, countercurrent chromatography or electro-focalization. The extracts obtained from this novel strain have a very advantageous NPY receptor antagonist activity. Their strong affinity for these receptors, both for the Yl and Y2 subtypes, has been demonstrated in dog adipo¬cytes, this model displaying great homology with human adipocyte. More particularly, the adipocyte membranes were obtained from omental adipose tissue taken from dogs, essentially used in the technique described by Taouis et al., J. Pharmacol. Exp. Ther {1987), 242, 1041-1049. The binding studies were performed according to the known conventional techniques. In particular, the adipocyte membranes (200 jj.g/ml) are incubated for 60 minutes at 30°C in a buffered binding medium (20 mM Krebs-Ringer Hepes solution, pH-7.4, 1% bovine serum albumin, 0.25 mg/ml bacitracin) with 0.08 nM of [125I] -NPY labelled with the Bolton-Hunter reagent (Amersham IM 170.2000 Ci/mmol) in the presence or absence of 0.3 /iM pig NPY. The incubation is stopped by filtration using Whatman GF/C filters and the radioactivity retained by the filter is evaluated with a gamma counter. The non-specific binding, measured in the presence of 0.3 /xH unlabel led NPY, represents 25% of the total binding. The dog adipocyte membrane preparation carries Y1 and Y2 receptors which may be distinguished on the basis of the selective affinity of the NPY fragment (13-36) for the Y2 receptors. The extracts according to the present invention demonstrated good affinity for the NPY receptors of this tissue, by displacing the [125I] -NPY bound to the adipocyte membranes in a dose-dependent manner with IC50 values (that is to say concentrations which inhibit the specific binding of [125I] -NPY by 50%) which depend on the degree of purification of the extracts and which, in the case of the crude extracts obtained directly from the fermentation supernatanta by lyophilization, are at least about 10"2 mg/ml. The NPY-antagonist nature of the extracts accord¬ing to this specific aspect of the present invention was demonstrated by studies on isolated organs and more particularly in the model of rat "vas deferens", The . extracts showed antagonist properties towards the effects of NPY in Y2 models of rat vas deferens and were studied according to the procedure described in Regulatory Peptides 1986, 13, 307-318. This activity was confirmed on human adipocytes isolated from subcutaneous adipose tissue, by assaying the release of fatty acids into the culture medium and comparing it with the control (incubation without product). 50% (w/w) solutions of these extracts in propylene glycol are particularly preferred. The aseptic preparation of these solutions makes It possible to avoid the addition of preserving agent. In the preparation of the compositions according to the present invention, the extracts with NPY receptor antagonist activity are mixed with aqueous or non-aqueous solvents and with conventional diluents which are compatible with topical use, as well as with the active components of the composition itself. Suitable solvents and/or diluents will be chosen according to their capac¬ity to transport the active component from the extfact of the invention into the subcutaneous adipose layer. These compositions generally contain excipients or additives chosen from the ingredients usually used in compositions intended for local application according to the need for the specific formulations envisaged. They may contain, for example, thickeners, softeners, emollients, stabilizers, preserving agents, anti-foaming agents, surfactants, antioxidants, dyes and/or pigments, and fragrances. They may also contain other active components having either an effect of the same type, for example products which contribute towards controlling lipolysis/ lipogenesis or products which are useful in this type of composition, such as collagen synthesis stimulators, collagenase or elastase inhibitors, and vasoprotectors. The preferred cosmetic compositions according to the present invention contain, besides the NPY antagonist, an ct2-antagonist which may itself also be a . non-peptide synthetic compound, a peptide or a product obtained by fermentation of a microorganism, for example a bacterium or a fungus, or by extraction of cells or tissues of plant or animal origin. a2-Antagonists which are advantageous to use as additional components, along with the NPY antagonist, are those of classes D and E below. D. Synthetic products chosen from those of groups XVIII to XXV below. XVIII - The compounds described in BE 840,363, in par¬ ticular mirtazapine. XIX - The compounds described in DE 2,603,407, in par¬ticular eetiptiline and structural analogues thereof. XX - The compounds described in ITS 4,337,260, in particular mosapramine XXI - The compounds described in US 2,979,511, in par¬ticular idazoxan. XXII - The compounds described in WO 92/13856, in par¬ ticular 5-thiazolyl-N,N-dimethyltryptaminea including CP 93393. t XXIII - The compounds described in US 4,229,449, in particular reboxetine. XXIV - The compounds described in GB 2,157,631, in particular fluparoxan. XXV - The compounds described in GB 2,167,408, in par¬ ticular altipamezole. E. e2 -Antagonist products obtained by extraction of cells or tissues of animal or plant origin or by fermentation of microorganisms, in particular bacteria and fungi, for example yeasts. Examples of products of this class, also including semisynthetic products, are the products of . groups XXVI and XXVII below. XXVI - Extracts of ergot, components and semisynthetic compounds thereof, having an c2-antagonist action, in particular nicegoline. XXVII - Products, in particular extracts obtained from the fermentation of strains of Bacillus lichenifonnis, with antagonist activity towards the a2 receptor, in particular from the strain SEBR 2464. These products, in particular the extracts belonging to this group, represent another specific aspect of the present invention. The productive organism according to this speci¬fic aspect of the present invention is a strain of Bacillus lichenlformla which has been isolated and has been given the code number SEBR 2464. A sample of this microorganism was deposited on 22 October 1996 at the CNCM of the Pasteur Institute, where it was registered under the reference 1-1778. The characteristics of this microorganism were determined on API 20B, API 50 CHB, 50 CH, 50 AA, 50AO and 20E API kits. This is a bacterium in uniformly shaped mobile rod form, from 2 to 10 (no. in length and from 0.5 to 1 /JM in width, individually or in short chains. As with most Bacilli, this bacterium is gram+, facultative anaerobic, catalase positive, oxidase nega¬tive and has the characteristic of sporulating under certain conditions. It grows well at pH 5 to 7, at temperatures between 15 and 55°C and for salinities (MaCl) of up to 7%. This strain was isolated as a contaminant, during experiments using columns of sand, according to the conventional microbiological techniques known to those skilled in the art. This particular strain, along with productive mutants thereof, therefore constitutes a further subject of the present invention. After culturing on nutrient agar medium and subculturing several times successively, which make it possible to obtain an abundant and pure culture of the strain of interest, a batch 0 is manufactured for storage of the parent strain, followed by primary and secondary inoculation batches. For this, a suspension of spores is prepared from a culture on nutrient agar medium in a Petri dish and from a maintenance medium; this medium contains a cryo-protective agent making it possible to ensure good viability of the spores during storage by freezing. The suspension of spores obtained is divided into cryotubes which will be stored at -80°C: these tubes constitute batch 0. Following the same procedure, but starting with a tube from batch 0, a primary inoculation batch is prepared. Next, still according to the same procedure, a secondary inoculation batch is prepared from a cryotube of the primary inoculation batch. The manufacture of the inoculation batches 0, 1 and 2 ensures long-lasting accessibility of the strain and thus of the desired activity. The process for preparing the extracts with or2-receptor antagonist activity consists essentially in growing the novel strain SEBR 2464, or productive mutants thereof, on a suitable medium and under suitable culture conditions and in then extracting the active fraction from in the culture supernatant. This supernatant may be concentrated until a dry extract is obtained. The Bacillus lichenlformiB SEBR 2464 can be cultured by any aerobic culture method and in various types of apparatus usually used in the fermentation industry. It is possible, in particular, to adopt the following approach for carrying out the operations. Starting with a tube of the secondary inoculation batch, Petri dishes are seeded and, after incubating for . two days, these allow stirred conical flasks containing a suitable medium to be inoculated. A stirred flask can also be seeded directly with a tube of the inoculation batch. In this case, the duration of culturing will be longer for the same medium. The antagonist activity is obtained in the flask cultures within 10 hours to 48 hours depending on the culture conditions used. The a2-receptor antagonist activity is extracted from the culture supernatants. The activity of the extracts is expressed as ID50 (50% inhibitory dilution); one litre of culture makes it possible to obtain 10 ml of extract having an ID50 value of between 1/2500 and 1/10,000. The a2-receptor antagonist activity may be obtained by extracting the supernatant of the flask cultures, but it appears to be advantageous, in order to obtain a higher activity, to perform culturing in a fermenter and then to extract the supernatant therefrom. The fermenter is seeded with a 1- to 2-day-old culture in a stirred flask; it is preferable for the culture not to have begun to sporulate. In the fermenter, according to the culture conditions used, the antagonist activity may be observed from the first hours of culturing and onwards, but it is advantageous to wait until the stationary growth phase has been reached before extracting. Culturing SEBR 2464 in a fermenter allows better control of the culture conditions which are described below, for example the pH and the aeration. The a2-receptor antagonist activity obtained in the fermenter may vary, depending on the culuture condi¬tions applied. One litre of culture makes it possible to obtain from the supernatant, after extraction, 10 ml of extract having an ID50 of between 1/3000 and 1/15,000. The characteristics of the medium are identical to those described above for the strain SEBR 2794. In order to grow the strain SEBR 2464 on a medium containing these components, the process of culturing under aeration and with stirring, in which a liquid medium is used, is advantageous, although culturing on an agar medium can also be used. The temperature, the duration of incubation, the aeration and the pH of the medium must be such that they give rise to a maximum growth of the microorganism used and a maximum yield of extract with a2-receptor antagon¬ist activity. A culture stirred and aerated for about 10 hours to 48 hours is usually advantageous. The pH of the culture medium is preferably maintained at a more or less neutral or very weakly acidic value and the optimum incubation temperature is between 25°C and 50°C. The culture conditions, such as the composition and pH of the medium, the incubation temperature, the stirring speed and the aeration of the fermentation, may vary within a wide range and should obviously be chosen so as to obtain the best possible results. The production of an extract having a high a2-receptor antagonist activity requires several extraction steps. A first step consists in eliminating the biomass. For this, centrifugation, tangential microfiltration, clarifying filtration, that is to say a filtration in the presence of a filtering adjuvant, or any other method usually used to extract an extracellular product from a fermentation broth may be used. The supernatant is then placed in contact overnight with a hydrophobic resin preferably made of polystyrene-divinylbenzene, for example such as Amberlite XAD2 resin (Rohm & Haas) or CHP20P resin (Mitsubishi). The loaded resin is then separated by frontal filtration and the filtrate is removed. The resin undergoes several successive extrac¬tions with different solvents, allowing molecules of a hydrophobic nature to be extracted. After each extrac¬tion, the resin is separated from the organic phase by filtration. The various organic phases are then evaporated under vacuum, together or separately, until one or more dry extracts are obtained. An assay of ot2-receptor antagonist activity performed on an aliquot of each of the extracts makes it possible to evaluate their activity and to check the reproducibility of the process. The dry extract thus obtained may be taken up in various solvents usually used in cosmetology. The uptake concentration is chosen to allow complete dissolution of the extract and to be compatible with the subsequent use. In order to eliminate all trace of residual bioxnass and to ensure its microbiological stability, the extract is filtered on a 0.2 p filter and divided aseptically into sterile flasks. The a2-antagonist activity of the extracts was evaluated using the technique described by Chapleo CB et al., J. Med. Chem., 1983, 26, 823-831, on the in vitro displacement, in rat cortex, of the o2-receptor antagon¬ist reference ligandt tritiated idazoxan. The a2 -antagonist extract, containing 30% dry extract, is introduced into a 50/50 propylene glycol/water mixture and makes a preferred dilution according to the invention. Dilutions for aseptic preparation of these solutions, which makes it possible to avoid the addition of preserving agent, may also be used. In the preparation of the compositions according to the present invention, the extracts thus made up with Qf2-receptor antagonist activity are mixed with aqueous or non-aqueous solvents and with conventional diluents which are compatible with a topical use, as well as with the active components of the composition itself. Suitable solvents and/or diluents will be chosen according to their capacity to transport the active component from the extract of the invention into the subcutaneous adipose layer. These compositions generally contain excipients or additives chosen from the ingredients usually used in compositions intended for a local application, according to the need for the specific formulations envisaged. They may contain, for example, thickeners, softeners, emollients, stabilizers, preserving agents, anti-foaming agents, surfactants, antioxidants, dyes and/or pigments, and fragrances. They may also contain other active components having either an effect of the same type, for example products which contribute towards regulating lipolysis/lipogenesis, or products which are useful in this standard type of composition, such as collagen synthesis stimulators, collagenase or elastase inhibitors, or vasoprotectors. The a2-antagonist extracts of the invention moreover proved to be completely devoid of genotoxicity in the Ames test and the test of PNA repair. Their stability is compatible with their use in cosmetic compositions. The cosmetic compositions of the present inven¬tion contain the NPY antagonist in percentages of between 0.00001% to 5% relative to the total weight of the composition, mixed with the excipients commonly used to prepare cosmetic formulations to be applied to the skin. The said percentages may vary within the range indicated above as a function, of the intrinsic activity of the NPY-antagoniet component included in the composi¬tion. Preferably, the said NPY-antagonist component is present in percentages of from 0.0001% to 2%. The NPY-antagonist component is advantageously chosen from the products included in classes A, B and C above, those of class C being particularly advantageous. The components belonging to groups XV, XVI and XVII are preferred. In the preparation of the compositions according to the present invention, the NPY-antagonist component is mixed with aqueous or non-aqueous solvents and with conventional diluents which are compatible with use on the skin, as well as with other components of the compo¬sition itself. Suitable solvents and/or diluents will be chosen according to their capacity to deposit the NPY-antagonist active component of the invention onto the skin. These compositions generally contain excipients or additives selectedfrom the ingredients usually used in compositions intended for a local application according to the need for the specific formulations envisaged. They may contain, for example, thickeners, softeners, emollients, stabilizers, preserving agents, anti-foaming agents, surfactants, antioxidants, dyes and/or pigments, and fragrances. When the NPY-antagonist component is an extract of cells or tissues of animal or plant origin or a product, in particular an extract, obtained by fermenta¬tion of a microorganism, for example a bacterium or a fungus, the amount of NPY-antagonist component is always from 0.00001% to 5%, preferably from 0.0001 to 2%, relative to the total weight of the composition, the said amount being calculated relative to the weight of the dry extract. The compositions according to the present inven¬tion comprise, according to a preferred aspect, an extract obtained by fermentation of the novel strain SEBR 2794 in proportions, on a weight/weight percentage basis, which depend on the degree of NPY receptor antagonist activity of the extract used and therefore on the concen¬tration of dry substance and on the specific activity of this substance. The higher the antagonist activity of the extract used towards the NPY receptors, the lower is the weight amount required to obtain the desired lipolytic effect, and vice versa. In order to obtain the cosmetic compositions according to the invention, the crude extracts (supernat-ants filtered through a 0.2 p filter) obtained directly from the fermentation may conveniently be used without any purification step, in proportions of between 0.00001 and 5%, advantageously from 0.0001 to 2%, better still from 0.01 to 2% by weight and preferably from 0.1 to 2% by weight. These weight percentages are, naturally, calculated on the basis of the weight of extract pre¬pared. When the compositions of the present invention also contain, in addition to the NPY-antagonist component, an a2-antagonist component, the latter is present in a percentage of from 0.00001 to 5%, advantage¬ously from 0.0001 to 2%, better still from 0.001 to 1% and preferably from 0.01 to 0.5%, relative to the total weight of the composition. The said percentages may vary within the ranges indicated above as a function of the intrinsic activity of the «2-antagonist component included in the composi¬tion. The a2-antagonist component is advantageously chosen from the products included in classes D and E above, those of class E being particularly advantageous. The compounds belonging to group XXVII are preferred. When the t2 -antagonist component is an extract of cells or tissues of animal or plant origin or a product obtained by fermentation of a microorganism, for example a bacterium or a fungus, the amount of a2-antagonist component is that indicated above, the said amount being calculated on the basis of the weight of the dry extract. jiccgroing co an advantageous aspect of the present invention, the cosmetic composition contains both an NPY-antagonist component and an c2 -antagonist compo¬nent, the NPY-antagonist component being selected from those of classes A, B and C above and the a2-antagonist component being selected from those of classes D and E above. According to a particularly advantageous aspect, the cosmetic composition of the present invention, con¬tains an NPY-antagonist component selected from those belonging to class C, in particular to groups XV, XVI and XVII and an a2-antagonist component selected from those belonging to class E, in particular to group XXVII. According to a preferred aspect, the present invention relates to a cosmetic composition containing an NPY-antagonist component consisting of an extract selected from those of group XVII above and an a2-antagonist component consisting of an extract selected from those of group XXVII above. More particularly, the composition according to this preferred aspect of the present invention contains an NPY-antagonist component which may be obtained by fermentation of the strain Streptomyces sp. SEBR 2794 deposited at the CNCM of the Pasteur Institute under the number I 1132, or productive mutants thereof, and an a2-antagonist component which can be obtained by fermentation of the strain Bacillus licheniformis SEBR 2464 filed at the CNCM of the Pasteur Institute under the number 1-1778, with excipients normally used for formulations of this type, such as those mentioned above. The form of the compositions according to the present invention may be an emulsion in which the consti¬tuent or the mixture of constituents, with an optional stabilizer, is combined with excipients which are com¬monly used in cosmetic compositions and which are compat¬ible with the said constituents, such as lanolin or plant/ mineral or synthetic oils. The compositions of the invention may also be in the form of a gel in suitable excipients, such as cellulose esters or other gelling agenta such aa acrylic derivatives and may contain the active principle in dissolved form or suspended as microgranulea. The compositions according to the invention may also take the form of a lotion or a solution in which the mixture of constituents is dissolved or microdispersed. The form of the compositions according to the invention may thus be a microdispersion in a liquid containing water as well as one or more compatible surfactants. The disparsions have microemulsion prop¬erties and have virtually the appearance of true solutions. They may also be prepared at the time of use. An advantageous form of the compositions accord¬ing to the invention is a fluid applied topically via an adhesive support, referred to hereinbelow as a "patch", this patch allowing controlled diffusion of the active components, this diffusion possibly being activated by physical phenomena such as electrical microcurrents. The cosmetic compositions of the present inven¬tion may also contain other active components having either an effect of the same type as that of the NPY antagonists, for example products which contribute towards controlling lipolysis/lipogenesis, or collagen synthesis stimulators, collagenase or elastase inhibitors, or vasoprotectors. The compositions of the present invention are of good stability and may be stored for the time required for use at temperatures of between 0C and 60°C without any sedimentation of the constituents or separation of the phases talcing place, and also without their being any decrease in activity which might compromise the use of these compositions. These compositions are very well tolerated, they have no phototoxicity and their application to the skin for prolonged periods involves no side effects. The compositions of the present invention, in their various forms of presentation, may be used as lipolysis/lipogenesis regulators in the skin. More particularly, they can be used as cosmetic products for slimming or seborrhoeia-regulating use or as adjuvants in the treatment of acne. The cosmetic compositions of the present inven¬tion may be placed in contact with the epidermis or the , hair or pilous system so as to modify the appearance thereof and afford protection thereto. For example, when these compositions are placed in contact with the epidermis, the latter takes on a "healthy" appearance as if it had been exposed to the air and/or the sun, without, however, tanning, if this is not desired. More particularly, the cosmetic compositions of the present invention make the skin lose its "fatty1 appearance with the result of slimming that part of the body with which the said composition is placed in contact and of keeping it in good condition. Prom the first applications and onwards, the skin relief is smooth and the skin becomes firmer with better tonus. After applica¬tion for one month, the slimming effect appears, the "orange peel" appearance is visibly attenuated and the figure becomes shaplier. when the compositions of the present invention are placed in contact with the hair or pilous system, for example after a specific anti-seborrhoeia treatment, the said system is maintained in good condition. Similarly, the compositions of the present invention kaep the facial skin is good condition, also making the formation of comedones more difficult. A slimming fluid obtained according to Example 12 below was tested on 50 female volunteers who used the said fluid applied twice a day onto the thighs, with very good results. The slimming fluid described in Example 13 below was tested in a study including 150 female volunteers, carried out under double-blind conditions against placebo. The analysis and comparison of the results obtained with this slimming fluid and with its placebo under the experimental conditions adopted, which are similar to the normal conditions of use for repeated applications over 60 consecutive days on both thighs and the abdomen from the waist to the knees, made it possible to demonstrate a clear and statistically significant slimming effect in favour of the slimming fluid according to the invention relative to the placebo. The efficacy and tolerance of a slimming fluid as described in Example 14 was tested on more than 1000 women. These tests showed a decrease in the thickness of the adipose tissue, a tonifying and firming action and a slimming effect demonstrated by centimetric echographic measurement and by biphotonic absorptiometry. One object of the invention is also a cosmetic treatment method, wherein an amount of an NPY antagonist with a cosmetic effect and optionally an amount of an a2-antagonist with a cosmetic effect in a vehicle for cosmetic use is applied to the epidermis and/or the hair or pilous system. Lastly, the subject of the present invention is the use of an NPY antagonist for the preparation of cosmetic compositions intended to control lipolysis/lipogenesis in the skin, in particular for slimming and seborrhoeia-regulating purposes and as an adjuvant in or after the treatment of acne. More particularly, the invention relates to the use of an NPY antagonist for the manufacture of cosmetic compositions intended to maintain the facial skin in good condition by making the formation of comedones difficult. The invention also relates to the use of an NPY antagonist for the manufacture of cosmetic compositions intended for placing in contact with the hair or pilous system. In particular, the invention relates to the use of an NPY antagonist for the manufacture of cosmetic compositions intended to control lipolysis/lipogenesis of the skin, the said compositions also containing an a.2-antagonist component. The examples which follow illustrate the inven¬tion without, however, limiting it. EXAMPLE 1 Preparation of an extract obtained from the € strain Streptomyces sp SEBR 2794 1.1 Fermentation The strain Streptomyces sp SEBR 2794 was fer¬mented in six different culture media. 1.1.2. (a) A suspension of spores from the strain SEBR 2794 is prepared according to the method indicated in 1.1.1. (a) and (b) 3 ml of this suspension is used to seed 100 ml of culture having the following composition: to maintain a dissolved oxygen pressure of close to 20%. The pH is not regulated and changes freely between 7.2 and 6.3. 1.2. Extraction 1.2.1. The extraction is carried out on 1.5 litre of broth obtained according to Example 1.1.1. The fermentation broth is centrifuged at 13,000 revolutions/minute (27,500 g) for 20 minutes and is filtered in the presence of 15 g of filtering adjuvant on a filter press. The filtrate obtained is lyophilised directly and the dry residue thus obtained (16.3 g) is redissolved in 80 ml of water (final pH = 8.4). The 50% inhibitory dilution of this fraction (ID50) is 1/4500. 1.2.2. The extraction is performed on 10 1 of culture broth obtained by working according to Example 1.1.5. and are frozen beforehand. The broth is centrifuged in 500 ml buckets at 8000 rpm (11,000 g) for 20 min. 9 1 of completely clear supernatant are obtained. An aliquot sample is concentrated five times by a Centripep concentrator. The 50% inhibitory dilution of this fraction is , equal to 1/10,000. 1.2.3. The extraction is performed on 10 1 of prefrozen culture broth obtained under the same conditions as in Example 1.1.5. The separation is performed on a Sharpies-type continuous centrifuge. The 9 1 of supernatant obtained are filtered through a 0.2 /a filter in order to remove all trace of residual biomass. 8.5 1 of filtrate are obtained. An aliquot sample is concentrated five times by a Centripep concentrator. The 50% inhibitory dilution of this fraction is 1/16,000 1.3. Concentration by ultrafiltration 1.3.1. Concentration on a 5 kD membrane The process is performed by ultrafiltration of the solution of Example 1.2.1. using an Ami con 5000 membrane in a stirring cell in 25 mH phosphate buffer pH = 7.5 containing 150 mM NaCl and an active retentate and a totally inactive permeate are obtained. 1.3.2. Concentration on a 10 kD membrane A 10 kD Ami con membrane is used to concentrate the 9 litres of supernatant obtained in Example 2.2. By concentrating by a factor of 5, 1.8 1 of concentrate five times more active (ID5fl ■ 1/10,000) and a totally inac¬tive permeate are obtained. 1.3.3. Concentration on a 30 kD membrane A 30 kD Ami con membrane is used to concentrate the 8.5 1 of filtrate obtained in Example 2.3. By concen¬trating by a factor of 5, 1.7 1 of concentrate which is up to five times more active (ID50 > 1/10,000} and a permeate containing very weak activity {20% inhibition at 1/250) are obtained. 1.4. Purification 1.4.1. Gel permeation chromatography The samples of the solution from 1.2.1. are subjected to gel permeation chromatographies using various gels: Sephadex G 25, G 50, G 75 and G 100 and the results indicated below are obtained: the activity is eluted at the exclusion volume on Sephadex G 25 and G 50 and very close to the exclusion volume of G 75. On Sephadex G 100 gel, the activity may be separated from the products of higher molecular weight (> 100 KD). On a Superose 12 analytical column (1 KD to 100 KD fractionation domain), the active molecule showed a retention time of between that of ovalbumin (44 KD) and that of cytochrome (14.4 KD). 1.4.2. Ultrafiltration on a membrane with a cut-off threshold of 5000 daltons 100 ml of a culture supernatant (ID50 - 1/3600) are dialysed in 5 volumes of 20 mH phosphate buffer pH 7.4, 150 mH HaCl, in a magnetically-stirred cell equipped with an Amicon 5000 membrane, and pressurized with compressed air to a pressure of 1 x 10s Pa (1 bar). 100 ml of retentate (ID50 1/2500) freed of mol¬ecules of low molecular weight and 500 ml of an ultra- filtrate of negligible activity are recovered. 1.4.3. Ultrafiltration on a membrane with a cut-off threshold of 10,000 daltons 100 ml of a culture supernatant (ID50 1/3600) are dialysed in 7 volumes of 20 mH phosphate buffer pH 7.4, 150 mM NaCl in a magnetically-stirred cell pressurized to 1 x 10s Pa (1 bar) with compressed air and fitted with a Filtron 10K membrane. 100 ml of retentate having an ID50 activity 1/1500 in terms of inhibition of binding to the NPY receptor are recovered* The ultrafiltrate (700 ml) is reconcentrated in a cell of the same type fitted with an Ami con 1000 . membrane. 100 ml of solution having an ID50 value of 1/500 are obtained. 1.4.4. Removal of the hydrophobic impurities 1500 ml of a culture supernatant are treated for 2 hours, with stirring, with 180 g of polystyrene- divinylbenzene resin (XAD2). The resin is then filtered and washed with twice 300 ml of methanol and then with 300 ml of acetone. The combined methanol and acetone solutions are evaporated under vacuum. The residue taken up in 40 ml of methanol gives a solution which has no activity. The aqueous solution freed of the hydrophobic products is lyophilized. The residue taken up in 80 ml of water gives a solution having an ID50 value of 1/4500 in terms of inhibition of binding to the NFY receptor. 1.4.5. Extraction of the active molecule by cation exchange. 1500 ml of a culture supernatant are adjusted to pH 5 with 1 N acetic acid and are then treated with 120 g of cation exchange resin (Dowex 50 WX-4, ACO form). After stirring for one hour, the resin is filtered and then de a orbed with 300 ml of IN aqueous ammonia for half an hour. This solution is then lyophilized. The residue obtained taken up in 40 ml of water gives a solution which, when measured in terms of inhibition of binding to the NPY receptor, has an ID50 value of 1/3S00. Solutions with NPY receptor antagonist activity may also be obtained by extracting the culture broths of Examples 1.1.2, 1.1.3, 1.1.4 and 1.1.6 according to the extraction examples described in 1.2.1 to 1.2.3. EXAMPLE 2 Preparation of an extract obtained from the strain Bacillus licheniformis SEBR 2464 (cf. XXVII above) 2.1 Fermentation The strain Bacillus licheniformis SEBR 2464 was fermented in 4 different culture media. The solution of trace elements has the same composition as in Example 2.1.2. 2.2. Extraction 2.2.1. Tha extraction is performed on 12 1 of culture broth of 2.1.1. The broth is centrifuged at 13,000 revolu¬tions/minute (27,500 g) for 10 min and 11 1 of supernatant are obtained. 2.1 kg of Amberlite XAD2 resin preconditioned with methanol and acetone are added to these 11 1 of supernatant. The supernatant/resin mixture is placed together overnight at room temperature. The resin is then filtered off and the products bound thereto are successively eluted with twice 5 litres of methanol and with 5 litres of acetone. The organic phases are combined after filtration and evaporated to dryness under vacuum. The evaporation residue (46 g) constitutes the dry extract; it is redissolved in 100 ml of propylene glycol/water mixture (50/50). The fraction thus obtained has an ID50 value = 1/3000. 2.2.2. The extraction is performed on 3.5 1 of culture broth of Example 2.1.3. The same procedure as in Example 2.2.1. is followed but the amounts of resin and of solvent are adapted to the volume of supernatant treated. 11 g of dry extract are obtained/ which are taken up in 27 ml of the propylene glycol/water mixture (50/50). The solution thus obtained has an IDS0 value -1/4000. 2.2.3. The extraction is performed on 50 1 of culture broth of Example 2.1.4. A tangential microfiltration system (0.2 ftm) is used to separate the biomass. 46 1 of permeate are obtained, which are placed in contact with 9 kg of preconditioned Amberlite XAD2 resin overnight at room temperature. The loaded resin is then filtered off and the products bound thereto are eluted with twice 23 1 of methanol and once 23 1 of acetone. Between each elution, the organic phase and the resin are separated by filtra¬tion. The organic phases are then combined and evapor¬ated to dryness under vacuum. 285 g of dry extract are obtained, which are taken up with 620 g of the propylene glycol/water mixture (50/50). The solution obtained is filtered through a U.J nm filter and has an ID50 value * 1/8200. A solution with a2-receptor antagonist activity may also be obtained by extracting the culture broth of Example 2.1.2. according to Example 2.2.3. EXAMPLES 14 to 25 A slimming microemulaion having the composition of Example 6 above is prepared, in which the dry extract of Exmaple 1.4.3. is replaced by: 1- (2- [(N- (2-naphthylsulphamoyl) -5-methoxy-2-indol-yDcarboxamido] -3- (4- (N- [4- (dimethylaminomethyl) -trans-cyclohexylmethylj amidino) phenyl) propionyl) pyr¬rolidine, class A, group I (Example 14); 3-(4-methoxyphenyl) -4- [4-(2-pyrrolidin-l-ylethoxy) -benzoyl]-1,2-dihydronaphthalene hydrochloride, class A, group Ha (Examle 15); 2-{4-hydroxyphenyl)-3-[4-(2-pyrrolidin-l-ylethoxy)-benzoyl] benzothiophene hydrochloride, class A, group lib (Example 16); PD 160170, class A, group III (Example 17); SC 3117, class A, group IV (Example 18); D-myoinositol 1,2,6-triphosphate, class A, group Va (Example 19); inositol monophosphate, zinc salt, class A, group Vb (Example 20); 1- (3-methoxyphenyl) -1- (4-phenylpiperazin-l-yl)cyclo- hexane dihydrochlorida, class A, group VI (Example 21); BIBP 3226, class A, group VII (Example 22); He 90481, class A, group VIII (Example 23); dimethyl l,4-dihydro-4-[3-[[[{3-[spiro WE CLAIM: 1. A composition for the treatment of celluilte by topical application characterized in that it comprises an NPY- (neuropeptide Y) antagonist component consisting of a product of fermentation of the strain Streptomyces sp SEBR 2794, deposited with the CNCM of the Institut Pasteur under the number 1-1332, and an a 2-antagonist component consisting of a product of fermentation of the strain Bacillus licheniformis SEBR 2464, deposited with the CNCM of the Institut Pasteur under the number 1-1778, in combination with a cosmetically acceptable excipient, wherein the NPY-antagonist is selected from those of classes A, B and C and the a 2-antagonist component is selected from those of classes D & E as described herein. 2. The composition as claimed in claim 1, wherein it comprises from 0 % to 5% by weight of the NPY-antagonist component and from 0.00001% to 5% by weight of an a2- antagonist component. 3. The composition as claimed in claim 1, wherein it also contains a collagen synthesis stimulator, a collagenase or elastase inhibitor or a vasoprotector. 4. A method of cosmetic treatment for producing a slimming effect, wherein it comprises the topical application of a composition as claimed in claim 1, 2 or 3, to selected parts of the human body. 5. The method as claimed in claim 4, wherein the composition as claimed in claims 1, 2 or 3 is applied to the thighs, 6. The method as claimed in claim 5, wherein the composition as claimed in claims 1, 2 or 3 is applied to the thighs and abdomen from the waist to the knees. 7. The method of cosmetic treatment intended to lessen the fatty, "orange peel" appearance of the skin, wherein it comprises the application to the skin of a composition as claimed in any one of Claims 1, 2 or 3.

Full Text

The present invention relates to a cosmetic composition containing a neuropeptide Y receptor antagon¬ist. Neuropeptide Y, referred to hereinbelow as "NFY" for short, is a neuromediator which is involved in a certain number of physiological processes and for which an involvement in regulating lipolysis has been demonstrated (P. Valet and M. J. Clin. Invest. 1990, 85, 291-295). NPY receptor antagonists, hereinafter referred to as "NPY antagonists", have been described as medicines, but their efficacy in the treatment of any disease has not been proven to date.
It has now been found that NPY antagonists can be used for the preparation of cosmetic compositions.
More particularly, it has been found that cos¬metic compositions containing an NPY-antagonist component can be used as lypolysis/lypogenesis regulators in the skin without, however, interferring with the skin's natural functions.
It has also been found, that cosmetic compositions containing an NPY-antagonist component and an ^-antagon¬ist component are particularly advantageous.
Thus, according to one of its aspects, the present invention relates to a cosmetic composition containing at least one NPY-antagonist component mixed with a cosmetic excipient. The NPY antagonist contained in the cosmetic composition may be a non-pep tide com¬pound, a peptide, a cell or tissue extract of animal or plant origin or a product obtained by fermentation of a microorganism, for example a bacterium or a fungus.
NPY antagonists which are advantageous in the cosmetic compositions of the present invention are those of groups A, B and C below.
A. Synthetic products selected from groups (I) to (VIII) below are advantageous NPY-antagonist components. t. Compounds of formula (I)

in which
Ar2 represents naphthyl, phenyl, quinolyl or isoquinolyl, optionally substituted with CI, F, (C1-C4) alkyl, (Cj^C1alkoxy, hydroxyl or (Cj^C1dialkylamino;
- Ar2 represents phenyl or thienyl, optionally substi¬tuted with CI, F, (Cx-C4) alkyl, {C1-C4}alJcoxy or hydroxyl;
- Rx, R2 and R'2 represent, independently of each other, hydrogen, (C1-C4)alkyl or alternatively Rx represents nothing and N is attached to Ar2 and, optionally, R2 and R'2 form a double bond,
or alternatively Rx or R2 is attached to Ar2 and repre¬sents (CJ^-CJ) alkylene;
- R3 and R4, which are identical or different, represent hydrogen, (C1-C4) alkyl or form, with the nitrogen atom to which they are attached, a saturated C5-C7 heterocycle selectedfrom pyrrolidine, piperidine and hexahydroazepine;
- zx represents (C1C1) alkylene interrupted or substi¬tuted optionally with {C5-C7)cycloalkyl or phenyl;
- Q1 represents methyl, amino, {C1-C4)alkoxycarbonylamino, (C1C1) alkylamino, di (C1-C4) alkylamino, pyrrolidinyl,
piperidino, morpholino, piperazinyl, (C1-C4)alkyl-4-piperazinyl, amidino, (C1-C4)alkylamidino, guanidino, (C1-C4)alkylguanidino, pyridyl, imidazolyl, pyrimidinyl, indolyl, hydroxyl, {C1-C4)alkoxy, (C2-Ca)alkoxycarbonyl, N- [amino {C1C1) alkyl] -N- [ (C1-C4) alkyl] amino, carbamoyl or phenyl optionally substituted with CI, F, (C1-C4)alkyl, (C1-C4)alkoxy or hydroxyl;
- Q2 represents hydrogen or (C1-C4) alkyl;
- Q-$ represents hydrogen or {CI-C4)alkyl or Qx and Q3 are linked to form a heterocycle and together represent (C2-C3) alkylene whereas Zx represents nothing, in the form of

pure enantiomers or mixtures thereof in any proportions, as well as the addition salts thereof with acids; which can be prepared according to EP 614,911.
II - Raloxifen analogues, in particular

in which R*4 and R*5 are, independently, a (C1-C6)alkyl or constitute, with the nitrogen atom to which they are attached, a heterocyclic group selected from hexamethylene-iminyl, piperazino, heptamethyleneiminyl, 4-methyl-piperidyl, imidazolinyl, piperidyl, pyrrolidinyl or morpholinyl;
- R° is a hydroxy 1, a halogen, a hydrogen, a (C3-
C8)cycloalkyl, a (C2-C7) alkanoyloxy, a (C1-Cg) alkoxy or a
phenyl, the said phenyl optionally being substituted with
one, two or three substitutents selected, from groups
consisting of (C1-C1 alkyl, (Cj-C1) alkoxy, nitro, chloro,
fluoro, trif luoromethyl, -0S02- (Ci-Cj^) alkyl or
-0-C(0) -NH-R°3;
- RL is hydroxyl, halogen, hydrogen, (C3-C3)cycloalkyl,
(C2-C7) alkanoyloxy, (C1-Cg) alkoxy or phenyl, it being
possible for the said phenyl optionally to be substituted

with one, two or three substituents selected from the group consisting of (C1-C1) alJcyl, (C1-C4) alkoxy, nitro, chloro, fluoro, trifluoromethyl, -0S02- (Cj-C1J alkyl or -0-C(0)-NH-R°3;
in which each R°3 represents, independently, (C1-Cg) alkyl, (C3-C8)cycloalkyl, unsubstituted or substituted phenyl in which the substitutant is halogen, {Cj_-C6) alkyl or {C1-Cs)alkoxy;
with the limitation that when X° is a bond and A* is -S-, then R° and R8^ are not both selected from the group consisting of hydroxyl, methoxy and (C2-C7)alkanoyloxy; as well as the salts or solvates thereof, which can be prepared according to WO 96/12489, in particular a compound selected from:
• 3- (4-methoxyphenyl)-4-[4-(2-pyrrolidin-l-ylethoxy)-benzoyl]-1,2-dihydronaphthalene,
• 3-phenyl-4-[4- (2-pyrrolidin-1-ylethoxy)benzoyl] -7-methoxy-1,2-dihydronaphthalene,
• 3- (4-methoxyphenyl) -4- [4- [2- (piperid-1-yl)ethoxy]benzo¬yl] -1,2-dihydronaphthalene,
■ 3- (4-hydroxyphenyl) -4- [4- [2- (pyrrolidin-1-yl) ethoxy] -
benzoyl]-1,2-dihydronaphthalene,
• 3-(4-methoxyphenyl)-4-[4-[2-(hexamethyleneimin-1-
yl)ethoxy]benzoyl]-1,2-dihydronaphthalene,
■ 3- (4-methoxyphenyl) -4- [4- [2- (piperid-l-yl)ethoxy]benzo-
yl]-1,2-dihydronaphthalene,
• 3- (4-methoxyphenyl) -4- [4- [2- (piperid-l-yl)ethoxy]benzo-
yl]-7-methoxy-1,2-dihydronaphthalene,
- 3- (4-methoxyphenyl) -4- [4- [2- (N-methyl-1-pyrrolidinium) -ethoxy]benzoyl] -1,2-dihydronaphthalene,
• 3- (4-methoxyphenyl)-4-[4-(2-dimethylaminoethoxy)benzo¬yl] -1,2-dihydronaphthalene,
• 3-(4-methoxyphenyl)-4-(4-diethylaminoethoxybenzoyl)-1,2-dihydronaphthalene,
• 3- (4-methoxyphenyl) -4- (4-diisopropylaminoethoxybenzo-yl)-1,2-dihydronaphthalene,
• 2-(4-hydroxyphenyl)-3-[4-[2-(hexamethyleneimin-1-yl)ethoxy]benzoyl]-6-hydroxybenzofuran,
• 2- (4-hydroxyphenyl) -3- [4- [2- (piperid-1-yl)ethoxy]ben-

zoyl]-6-hydroxybenzofuran,
• 2- (4-hydroxyphenyl) -3- [4- [2 -pyrrolidin-1-yl) ethoxy] -benzoyl]-6-hydroxybenzofuran,
• 2- (4-hydroxyphenyl)-3-[4-[2-(N,N-diethylamino)ethoxy]-benzoyl]-6-hydroxybenzofuran,
• 2- (4-hydroxyphenyl) -3- [4- [2- (N,N-diisopropylamino) -ethoxy]benzoyl]-6-hydroxybenzofuran,
■ 2- (4-hydroxyphenyl) -3- [4- [2- (N,N-dimethylamino) ethoxyj -
benzoyl]-6-hydroxybenzofuran,
• l-ethyl-2- (4-methoxyphenyl) -3- [4- [2- (piperid-1-yl) -ethoxy]benzoyl]-6-hydroxyindole,
• 2- (4-methoxyphenyl)-3-[4-[2-(hexamethyleneimin-1-yl)ethoxy]benzoyl]-6-methoxybenzofuran,
• 2- (4-methoxyphenyl)-3-[4-[2-(piperid-1-yl)ethoxy]-benzoyl]-6-methoxybenzofuran,
• 2- (4-methoxypbenyl) -3- [4- [2- (pyrrolidin-1-yl] ethoxy] -benzoyl]-6-methoxybenzofuran,
• 2- (4-methoxyphenyl)-3-[4-[2-(N,N-dieChylamino>ethoxy]-benzoyl]-6-methoxybenzofuran,
• 2- (4-methoxypbenyl) -3- [4- [2- (N,N-diisopropylamino) -ethoxy]benzoyl]-6-methoxybenzofuran,
• 2- {4-methoxyphenyl) -3- [4- [2- (N,N-dimethylam±no)ethoxy] -benzoyl]-6-methoxybenzofuran,
• l-ethyl-2-(4-methoxyphenyl)-3-[4-[2-(piperid-1-yl)ethoxy]benzoyl]-6-methoxyindole,
• 2-(4-methoxyphenyl)-3-[4-[3-(hexamethyleneimin-1-yl)propoxy]benzoyl]benzo[b]thiophene,
• 2- (4-methoxyphenyl)-3-[4-[2-(hexamethyleneimin-1-yl) ethoxy] benzoyl] benzo [b] thiophene,
• 2- (4-methoxyphenyl) -3-[4-[3-(piperid-1-yl)propoxy]-benzoyl] benzo [b] thiophene,
■ 2- (4-methoxyphenyl) -3- [4- [2- (pyrrolidin-1-yl) ethoxy] -
benzoyl] benzo [t>] thiophene,
- 2- (4-methoxyphenyl) -3- [4- [2-(N,N-diethylamino) ethoxy] -benzoyl] benzo [b] thiophene,
• 2- (4-methoxyphenyl) -3- [4- [2- (N,N-diisopropylamino) -ethoxy] benzoyl] benzo [b] thiophene,
• 2- (4-methoxyphanyl) -3- [4- [2- (N,H-dimethylamino) ethoxy] -benzoyl]benzo[b]thiophene,

• 2-(4-chlorophenyl)-3-[4-[2-(hexamethyleneimin-1-yl)-ethoxy]benzoyl]-6-hydroxybenzo Eb]thiophene,
• 2- (4-hydroxyphenyl) -3- [4- [2- (piperid-1-yl) ethoxy] benzo¬yl] benzo[b]thiophene,
• 2-(4-hydroxyphenyl)-3- [4- [2-(pyrrolidin-1-yl)ethoxy] -benzoyl]benzo[b]thiophene,
■ 2- (4-hydroxyphenyl) -3- [4- [2- • 2- (4-hydroxyphenyl) -3- [4- [2- (N,N-diisopropylamino) -ethoxy]benzoyl]benzo[b]thiophene,
• 2- (4-hydroxyphenyl) -3- [4- [2- (N,N-dimethylamino)ethoxy] -benzoyl]benzo[b]thiophene,
• 2-(4-chlorophenyl)-3-[4-[2-(pyxrolidin-1-yl)ethoxy]-benzoyl]benzo[b]thiophene 1-oxide,
• 2- (4-chlorophenyl)-3-[4-[2-(piperid-1-yl)ethoxy]benzo¬yl] benzo [b] thiophene 1-oxide,

- [S- (n-butylsulphonyl) -2- [4- (n-butylsulphonyl)phenyl] -benzo[b]thien-3-yl][4-[2-(1-piperidyl)ethoxy]phenyl-methanone,
- [6- (n-pentylsulphonyl) -2- [4- (n-pentylsulphonyl)phenyl] -benzo [b] thien-3-yl] [4-[2-(1-piperidyl)ethoxy]phenyl]-methanone,

• [6- (n-hexylsulphonyl) -2- [4- (n-hexylsulphonyl)phenyl] -benzo[b]thien-3-yl] [4-[2-(1-piperidyl)ethoxy]phenyl]-methanone,
• [6- (n-butylsulphonyl) -2- [4- (n-butylsulphonyl)phenyl] -benzo[b]thien-3-yl][4-[3-(1-piperidyl)propyloxy]-phenyl]methanone,
- [6- (n-butylsulphonyl) -2- [4- (n-butylsulphonyl) phenyl] -
benzo[b]thien-3-yl]- [4- [2-(1-pyrrolidinyl)ethoxy]-
phenyl]methanone,
• [6-hydroxy-2- [4- (n-butylsulphonyl)phenyl]benzo[b] thien-3-yl]-[4-[2-(1-piperidyl)ethoxy]phenyl]methanone,
• [6-n-butylsulphonyl-2- [4-hydroxyphenyl]benzo tbl thien-3-yl]-[4-[2-(1-piperidyl)ethoxy]phenyl]methanone,

• [6- [N- (4-chlorophenyl)carbamoyl! -2- [4- [N- (4-chlorophen¬yl) carbamoyl]phenyl] benzo[b]thien-3-yl] [4- [2- (1-piperidyl)ethoxy]phenyl]methanone,
• [6- (N-(n-butyl)carbamoyl] -2- [4- [N- (n-butyl) -

carbamoyl]phenyl]benzo £b]thien-3-yl] [4- [2-(1-piperid¬yl) ethoxy]phenyl]methanone, ■ [S- (N-methylcarbamoyl) -2- [4- (N-methylcarbamoyl)phenyl] -benzo[b]thien-3-yl] [4-[2-(1-piperidyl)ethoxy]phenyl]-methanone,
• [6- (N-ethylcarbamoyl) -2- [4- (N-ethylcarbamoyl)phenyl] -
benzo[b]thien-3-yl] [4-[2-(1-piperidyl)ethoxy]phenyl]-
methanone,
• [6-(N-isopropylcarbamoyl)-2-[4-(N-isopropylcarbamoyl)-phenyl] benzo [b] thien-3-yl] [4- [2-(1-piperidyl)ethoxy]-phenyl]methanone,
• [6- (N-cyclohexylcarbamoyl) -2- [4- (N-cyclohexylcarbamo-yl) phenyl] benzo [b] thienyl-3-yl] [4- [2- (1-piperidinyl) -ethoxy] phenyl] methanone
and the salts and solvates thereof.

in which R0 and R30 represent, independently, H, CH3, -C0-(Cj^-CgJalkyl or optionally substituted phenyl and R20 represents pyrrolidino, piperidino, hexamethyleneimino or the pharmaceutically acceptable salts or solvates thereof, NPY antagonists described in US 5,504,094, in particular the compound of formula (III) in which R0 and R30 are both hydrogen and R20 is pyrrolidino, as well as the salts and solvates thereof.
Ill - Phenylsulphonylguinolines of formula (IV):

in which R3y ia as defined above, - R2y is -HN2, -OH or -SH
and salts thereof, described in US 5,552,411, in particular 8-amino-6-(2-isopropylphenylsulphonyl)-5-nitroquinoline known under the code PD-160170 and 8-amino-6-(4-aminophenylsulphonyl)-5-nitroquinoline, known under the coda PD-9262, which are described in Bioorganic and Medicinal Chemistry Letters, 1996, 6, 15, 1809-1814.
IV - Benextramine and analogues thereof described in
J. Med. Cham. 1993, 36, 272-279, in Eur. J. Pharmacology 1994, 37, 2242-2248 and in Current Pharmaceutical Design, 1995, I, 295-304, in particular SC3117, SC3199, CC217 and CC2137.
V - Inositol phosphate derivatives, in particular:
a) specific isomers of inositol triphosphate, in par¬ticular D-myoinositol 1,2,6-triphosphate.

myoinositol 1,2,3-triphosphate and L-myoinositol 1,3,4-triphosphate, which are described as NPY antagonists in WO 92/00079 and US 5,128,332.
b) Inositol monophosphate in acidic form and salts thereof, in particular the sodium, potassium, calcium or zinc salts, which are described as NPY antagonists in WO 92/00744.
VI - Compounds of formula

in which:
- Ar' is phenyl, 2-, 3- or 4-pyridyl, 2- or 3-thienyl, 4-or 5-pyrimidinyl, each optionally being mono- or disub¬stituted with a halogen, a hydroxyl or a linear or branched lower alkyl chain having from 1 to 6 carbon atoms;
- A', W*, X', Y* and T' are identical or different and represent a hydrogen, a halogen, a hydroxyl, a linear or branched lower alkoxy chain having 1 to 6 carbon atoms;
- R'i and R'2 are identical or different and represent a hydrogen, a linear or branched lower alkyl chain having 1 to 6 carbon atoms;
- R'3 and R'4 are identical or different and represent a hydrogen or a linear or branched lower alkyl chain having 1 to 6 carbon atoms; and
- R'g represents a hydrogen, a linear or branched lower alkyl chain having 1 to 6 carbon atoms or a phenyl;
and salts thereof, which can be prepared as described in
WO 96/14307, in particular
• 1-cyano-l-(4-phenylpiperazin-l-yl)cyclohexane,

• 1-phenyl-l-(4-phenylpiperazin-l-yl)cyclohexane,
• 1-(3-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)cyclo-hexane,
• 1-{3-methoxyphanyl)-1-[4-(2-pyrimidinyl)piperazin-l-yl]cyclohexane,
• 1- (3-methoxyphenyl)-1-[4-(2-pyridyl)piperazin-1-yl]cyclohexane,
• 1- (3-methoxyphenyl) -1- [4- (2-fluorophenyl)piperazin-l-yl]cyclohexane,
• 1- (3-methoxyphenyl) -1- [4- (4-£luorophenyl)piperazin-l-yl]cyclohexane,
• 1-(3-hydroxypheayl)-1-(4-phenylpiperazin-l-yl)cyclo¬hexane ,
• 1 - (3 , 5-dimethoxyphenyl)-1-(4-phenylpiperazin-l-yl) cyclohexane,
• 1- (3-ethoxyphenyl) -1- (4-phenylpiperazin-l-yl) cyclo¬hexane ,
• 1- (3-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-phenylcyclohexane,
• 1- (3-n-butoxyphenyl) -1- (4-phenylpiperazin-l-yl)cyclo¬hexane,
• 1-(3-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-methylcyclohexane dihydrochloride cis isomer and trans isomer,
• 1-(4-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)cyclo¬hexane,
• 1-(2-methoxyphenyl)-1-{4-phenylpiperazin-l-yl)cyclo¬hexane ,
• 1-(3,4-methylenedioxyphenyl)-1-(4-phenylpiperazin-l-yl) cyclohexane,
• 1- (3-ethoxyphenyl) -1- (4-phenylpiperazin-l-yl) -4-methyl-cyclohexane cis isomer and trans isomer,
• 1- (3-ethoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-ethyl-cyclohexane cis isomer and trans isomer,
• 1-(3-isopropoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-methylcyclohexane cis isomer and trans isomer,
• 1-(3-methoxyphenyl)-1-(4-phenylpiperazin-l-yl)-3-methylcyclohexane cis isomer and trans isomer,
• 1- (3-benzyloxyphenyl)-1-(4-phenylpiperazin-l-yl)cyclo-

hexane,
• 4- (3-ethoxyphenyl) -4- (4-phenylpiperazin-l-yl) tetra-hydropyran,
• 4- (3-ethoxyphenyl)-4- (4-phenylpiperazin-l-yl)tetra-hydro thiopyran,
• 1- (3-methoxymethoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-methylcyclohexane cis isomer and trans isomer/
• 1- (3-ethoxymethoxyphenyl) -1- (4-phenylpiperazin-l-yl) -4-methylcyclohexane cis isomer and trans isomer,
• 1- (3-ethoxyphenyl)-1-(4-phenylpiperazin-l-yl)-4-methoxycyclohexana cis isomer and trans isomer.
VII - Compounds of formula
Ta-Za-NR1a- in which
- na represents 0, 1, 2, 3, 4 or 5;
- Ra represents a hydrogen atom or a phenyl or naphthyl group optionally mono- or disubstituted with identical or different substituents selected from a fluorine, chlorine, bromine or iodine atom, a cyano, alkyl, phenyl, hydroxyl, alkoxy, dialkylaminoalkoxy, hydroxyphenyl, phenylalkoxy, alkylcarbonyl, amino, alkylamino, dialkylamino, alkylsulphonylamino, alkylcarbonylamino, alkoxycarbonylamino, alkoxycarbonyloxy, carboxyl, alkoxycarbony1, aminocarbonyl, alkylaminocarbony1, dialkylaminocarbonyl, alkylcarbonyloxy, alkylsulphonyloxy, hydroxymethyl, hydroxyethyl, hydroxypropyl, hydroxybutyl, trifluoromathyl, trifluoromethoxy, trifluoromethylthio, aminoalkyl, alkylaminoalkyl, aminocarbonylaminoalkyl, benzoylamino, alkanoylaminoalkyl, a1koxycarbonylaminoalkyl, benzyloxycarbonylaminoalkyl, aminosulphonyl, alkylamino-sulphonyl, dialkylaminosulphonyl, aminosulphonylamino, alkylaminosulphonylamino,
dialkylaminosulphonylamino, cyanamino, aminocarbonyl-amino, alkylaminocarbonylamino, dialkylaminocarbonyl-amino, aminosulphonylaminoalkyl, alky1aminosulphonyl-

aminoalkyl, carboxyalkyl, alkoxycarbonylalkyl, amino-carbonylalkyl, alkylaminocarbonylalkyl, aminosulphonyl-alkyl, alkylaminosulphonylalkyl, alkylsulphonyl, amino-sulphonyloxy, alkylaminosulphonyloxy, dialkylamino-sulphonyloxy or cyanoguanidi.no group/
an aminophenyl or aminonaphthyl group disubstituted with
a chlorine or bromine atom, wherein the
substituents rfay be identical or different, or
a hydroxyphenyl or hydroxynaphthyl group disubstituted
with a chlorine or bromine atom or with alkyl or alkoxy
groups, wherein the substituents may' be
identical or different,
a diphenylmethyl group, an aminocarbonylalkyl group substituted on the alkyl part with a hydroxyphenylalkyl , group or with a (2,2-diphenylethyl)amlnocarbonylamino-phenyl group,
a 5-membered heteroaryl group attached via a carbon or nitrogen atom, the said heteroaryl comprising an imino group optionally substituted with a (Cj-Cg) alkyl group or a phenyl group and an oxygen, sulphur or nitrogen atom, or a 6-membered heteroaryl group attached via a carbon atom, the said heteroaryl comprising one or two nitrogen atoms,
as well as the 5 - or 6 -membered heteroaromatic rings defined above which constitute a heteroaromatic bicyclic system with two neighbouring carbon atoms of the hetero¬aromatic ring and a 1,4-butadienylene group, and, furthermore, all the mono- or bicyclic heteroaryl groups mentioned above may be monosubstituted on the carbon skeleton with a fluorine, chlorine or bomine atom, with an alkyl, alkoxy, hydroxy1, phenyl, nitro, cyano, carbonyl, alkoxycarbonyl, aminocarbonyl, alkylamino-carbonyl, dialkylaminocarbonyl, fluoromethyl, difluoro-methyl, trifluoromethyl, alkanoyl, aminosulphonyl, alkylaminosulphonyl or dialkylaminosulphonyl group, or disubstituted with a fluorine, bromine or chlorine atom, with methyl, methoxy or hydroxyl groups, wherein
the substituents nay, be identical or different.

a phenyl group substituted with a (1,5-dihydro-2,4-dioxo-3ff-l,2,4-triazol-4-yl]alkyl residue, in which the imidazole or triazole part is substituted with l or 2 phenyl groups,
a eycloalkyl group having from 4 to 8 carbon atoms
optionally substituted with a hydroxy1, amino, alkylamino
or dialkylamino group, therein the substituents described above
are not attached to position 1 of the eycloalkyl
residue when Y represents an oxygen atom, a 1-[[[5,ll-dihydro-6 or a hydroxy 1 group, when Y, is an oxygen atom or a group -NR4a- and na represents a figure between 2 and 5,
- R3 is a hydrogen atom, a linear or branched {Cr~
C10)alkyl group, a eycloalkyl group having from 3 to 7
carbon atoms, a phenyl group optionally substituted with
a hydroxy1 or hydroxyalkyl group, or a phenylmethyl group
optionally substituted on the phenyl part with a hydroxyl
or hydroxyalkyl group,
- R23 is an unbranched (C1-C5)alkyl substituted in the u
position with an amino or alky1amino group which is
protected, by an amine-protecting group, with a dialkyl¬
amino, N-alkylbenzylamino, aminocarbonyl, aminocarbonyl-
amino, aminoethylimine, aminoiminomethy1,
amino(hydroxyimino)methyl, amino(alkoxyimino)methyl,
guanidino, hydrazinoiminomethyl, amino(nitroimino)methyl,
[amino(nitroimino)methyl]amino, amino(cyanimino)methyl,
[amino (cyan imino) methyl] amino, [ (alky 1 amino) iminome thyl] -
amino, [{alkylamino)(alkylimino)methyl]amino,
[amino (alkylimino)methyl] amino, 2-aminoimidazol-l-yl,
triazol-3-yl)methylamino, {3 -amino-1,2,4-oxadiazol-5 -
yDamino or (5-amino-l,2,4-oxadiazol-3-yl)amino group or
with an imidazol-4-yl, imidazol-2-yl, l-methylimidazol-2-
yl, imidazol-2-ylamino, imidazol-2-ylmethylamino or (4,5-

dihydro-lH-imidazol-2-yl)amino group, optionally substi¬tuted on the carbon with one or two methyl groups, or a phenyl or phenylmethyl group optionally substituted on the aromatic rings with a cyano, iminomethylamino, cyaniminometbylamino, (methylamino)methylideneamino, aminoiminomathy1, amino(hydroxyimino)methyl, amino(alkoxyimino)methyl, hydrazineiminomathy1, amino (cyanimino) methyl or guanidino group or with an imidazol-2-yl, 1-methylimidazol-2-yl or 4,5 -dihydro- 1H-imidazol-2-yl group, optionally substituted on the carbon atoms with one or two methyl groups,
in which, in the aminoiminomethyl, amino(hydroxyimino)methyl and guanidino groups mentioned in the definition of R2a above, one or more hydrogen-, atoms connected to the nitrogen atom, independent of each other, may be replaced by alkyl groups, or in which two hydrogen atoms connected to different nitrogen atoms may be replaced by an alkyl bridge having from 2 to 4 carbon atoms and for which the hydrogen atom of an HN ♦ R15a is a (Cj-C1) alkyl group, a (C3-C7) cycloalkyl group, a phenyl group or a phenylalky1 group in which the alkyl is C1-Cj,
♦ R1* and R17 , which are identical or different, represent a hydrogen atom, a (C1-Cg) alkyl group or alternatively one of the residues Risa and R17a represents a (C3-C7) cycloalkyl group or a phenyl group,
♦ R18a and R19a, which are identical or different, represent a hydrogen atom, (^-C,,) alkyl groups, benzyl or phenyl groups,

- R3a is a hydrogen atom, a (C1-C7)alkyl group or a (C4-C7) cycloalkyl group,
- Ta is a hydrogen atom, a phenyl group or a 5-membered

heteroaryl group attached via a carbon or nitrogen atom and comprising a nitrogen, oxygen or sulphur atom option¬ally substituted with an alkyl group, or comprising a nitrogen atom optionally substituted with an alkyl group as well as an additional sulphur, oxygen or nitrogen atom, or alternatively, when Za represents a bond, Ta is a protecting group for an amino group or the residues (T^T^U,) - (CH2)m- or T3,0-, in which
♦ T2a to T3a, which are identical or different, are phenyl or 6-membered heteroaryl groups attached via carbon atoms, which, depending on the case, comprise one or two nitrogen atoms,
5-membered heteroaryl groups attached via carbon or nitrogen atoms, comprising a nitrogen atom . optionally substituted with an alkyl group, sulphur or oxygen, or comprising a nitrogen atom optionally substituted with an alkyl group as well as an addi¬tional nitrogen, sulphur or oxygen atom, in which a 1,4-butadienylene bridge may be made between two neighbouring carbon atoms of the 5- or 6-membered heteroaryl groups mentioned above in the definition of the Ta residues; the bicyclic aromatic or heteroaromatic rings thus constituted may also be attached to a carbon atom of the 1,4-butadienylene group and, moreover, not only the phenyl groups and the 5- or 6-membered heteroaryl groups but also the bicyclic aromatic or heteroaromatic rings may be mono- or disubstituted on the carbon skeleton with fluorine, chlorine, bromine or iodine atoms or with cyano, hyroxyl, amino, dimethylamino, diethylamino, N-ethylmethylamino, trifluoromethyl, trifluoro-methoxy, trifluoromethylthio, acetylamino, propionylamino, methanesulphonylamino, methane-sulphonyloxy, phenyl, phenylmathoxy, 2-phenylethoxy, alkyl or alkoxy groups or trisubstituted with an amino or hydroxyl group and two chlorine or bromine atoms or with a hydroxyl group and two alkyl or alkoxy groups, the substituents being identical or different, and the alkvl and alkoxv Darts mentioned

above comprising from 1 to 4 carbon atoms, hydrogen atoms, (C1-C1alkyl groups, cycloalkyl groups having from 3 to 10 carbon atoms, bicyclo-alkyl or tricycloalkyl groups having from 6 to 12 carbon atoms or
♦ Txa and T2a together represent a linear-chain (C3-C7)alkylene group,
♦ XJa is the group >CH in which the hydrogen atom may be replaced by an alkyl, phenyl, hydroxyl, alkoxy, alkanoyloxy, alkoxycarbonyl or alkanoylamino group, in which the alkyls or alkoxys mentioned above may comprise, depending on the case, from 1 to 3 carbon atoms and the alkanoyls mentioned above may comprise
' 2 or 3 carbon atoms, or alternatively the ?CHCH2- , group or a nitrogen atom,
♦ m represents 0, 1, 2 or 3
♦ or alternatively Ta is a group (T^T^UJ - (CH2)M in which
♦ T1a, T2a, Ua and ma are as defined above, except that the mono- or bicyclic aromatic or betero-aromatic rings mentioned above for Txa and T2a are connected together by a bond or by a -CH2 -, -C{CH3)2-, -CH2CH2-, -CH»CH- or -NHCO- bridge,

- Ya is an oxygen atom or a group -NR*a in which R4a makes the definition mentioned above form R1a, it being pos¬sible for the residues of Rxa and of R4a to be identical or different, and
- Za is a single bond defined by a -CO-, -CH2-, -SO- or -S02- group,
and, except where otherwise mentioned, the alkyl and alkoxy parts mentioned above may comprise from 1 to 3 carbon atoms,
and the tautomers, diastereomers, enantiomers, mixtures and salts described in WO 94/17035.
Among these compounds,
• (R) -N2-(diphenylacetyl)-N-(phenylmethyl)argininamide,
• (R) -N2-(diphenylacetyl) -N- [
argininamide,
• (R)-N-[2- • N- [ (4-aminocarbonylaminophenyl)methyl] -N2- (diphenyl-acetyl)argininamide,
• (R)-N-[{4-hydroxyphenyl)methyl]-N2-[[5-(2-phanyl-ethoxy)-lff-indol-2-yl]carbonyl]argininamide,
• (R) -N2- (diphenylacetyl) -N- [ (4-fluorophenyl)methyl] -argininamide,
■ (R)-N-[(4-bromophenyl)methyl-N2-(diphenylacetyl)argin¬
inamide/
• the optically active diastereoisomers of N2-(a-cyclo-
pentylphenylacetyl) -N- [ (4-hydroxyphenyl)methyl] -D-argin- .
inamide,
• N-[[4-(dimethylamino)phenyl]methyl]-N2-(diphenyl¬
acetyl) argininamide,
■ (R) -N2- (diphenylacetyl) -N- [ [4- (hydroxymethyl)phenyl] -
methyl]argininamide,
• (R) -N2-(diphenylacetyl)-N-[[4-(1-oxoethyl)phenyl]meth¬yl] argininamide,
• • (R) -N2- (diphenylacetyl) -N- [ [4- [ (mathylaminocarbonyl) -
amino] phenyl] methyl] argininamide,
. (R)-N-[(4-amino-3,5-dichlorophenyl)methyl]-N2-(diphenylacetyl)argininamide,
• (R)-N- [(4-amino-3,5-dichlorophenyl)methyl]-N2-(3,3-dipheny1-1-oxopropyl)argininamide,
• • N2-(diphenylacetyl)-N-[3-[1-[2-[5,ll-dihydro-6(6H)oxo-pyrido[2,3-b][l,4]benzodiazepin-5-yl]-2-oxoethyl]-4-piperidyl] propyl] argininamide,

■ N2- (diphenylacetyl) -N- [ (4-hydroxy-3-methoxyphenyl)meth-yl]argininamide,
■ H2- (diphenylacetyl) -N- [(3-hydroxy-4-methoxyphenyl)meth-yl] argininamide,
• (R,S)-N-[(4-amino-3,5-dibromophenyl)methyl]-Ns-

(aminoiminomethyl) -N2- (diphenylacetyl) lysinamide,
■ N-[(3,5-dimethyl-4-hydroxyphanyl)methyl]-N2-(diphenyl¬
acetyl) argininamide,
• N- [(lff-benzimidazol-5-yl)methyl]-N2-(diphenyl¬acetyl) argininamide,
• N2-(diphenylacetyl)-N-[(4-hydroxy-3-methylphenyl)meth-yl]argininamide,
• N-[[4-(aminocarbonyl)phenyl]methyl]-N2-(diphenyl¬acetyl )argininamide,
• • (R) -N- [ ■ N2- (diphenylacetyl) -N- [ (lff-indol-5-yl)methyl] arginin- .
amide,
• (R) -N- [ [4- (aminosulphonyl)phenyl]methyl] -N2- (diphenyl¬acetyl) argininamide,
• (R) -N2-(diphenylacetyl)-N-[[4-methoxycarbonyl)phenyl)-methyl]argininamide,
• (R)-N2- (diphenylacetyl) -N- [ (4 -pyridyl) methyl] arginin¬amide ,
• (R)-N- [(4-amino-3,5-dibromophenyl)methyl]-N2- (diphenyl¬acetyl) argininamide,
• (R)-H2-(diphenylacetyl)-N-[(2-thienyl)methyl]-N2- (2-
naphthoyl)argininamide,
• (R)-N-[(4-amino-3,5-dichlorophenyl)methyl]-N2-(2-naphthoyl)argininamide,
• (R,S) -N5- (4, 5-dihydro-lJr-imidazol-2-yl) -N2- (diphenyl¬acetyl) -N-[(4-hydroxyphenyl)methyl]ornithinamide,
• (R,S) -N2-(diphenylacetyl)-N-[(4-hydroxyphenyl)methyl] -N5-(lff-imidazol-2-yl)ornithinamide,
• (R)-N- [[3- [(l,2-dihydro-3,5(4H)dioxo-l,2-diphenyl-3ff-l,2,4-triazol-4-yl)methyllphenyl]-N2-diphenylacetyl)-argininamide,
• N2- (diphenylacetyl) -N- [ (3-hydroxyphenyl)methyl]arginin-amide,
■ (R)-N- [[3-[(4,5-dihydro-2,4 imidazol-3-yDmethyl] phenyllmethyl] -N2- (diphenyl¬
acetyl) argininamide.

• (R)-N2-(diphenylacetyl)-N-[(4-hydroxyphenyl)methyl]-
argininamide, known under the code BIBP3226,
■ ^-(diphenylacetyl) -N- [2- (4-hydroxyphenyl) ethyl] argin¬
inamide,
• N2-(diphenylacetyl)-[(4'-hydroxy-[1,1'-biphenyl]-4-y1)me thy1]argininamide,
• N- [[4- t(l,2-dihydro-3,5(4tf)dioxo-l,2-diphenyl-3if-l,2,4-triazol-4-yl)methyl]phenyl]methyl]-N2-(diphenyl¬acetyl) argininamide,
• N2- (diphenylacetyl) -N- E (4-methoxyphenyl)methyl] arginin¬amide,
■ N2-(diphenylacetyl)-K-[2-(4-methoxyphenyl)ethyl]arg¬
ininamide,
• N2-(diphenylacetyl)-N-[2-(3-methoxyphenyl)ethyl]arg¬
ininamide,
- N2- (diphenylacetyl) -N- [(3-methoxyphenyl)methyl] arginin¬amide,
■ (R,S) -3- [4- (aminoiminomethyl) phenyl] -N2- (diphenyl¬
acetyl) -N- [ (4-hydroxyphenyl)methyl] alaninamide,
• (R,S)-3-[3- (amino iminomethyl) phenyl] -N2- (diphenyl¬acetyl) -N- [ (4-methoxyphenyl)methyl] alaninamide,
• (R,S)-3-[3- (aminoiminomethyl) phenyl] -N2- (diphenyl¬acetyl) -N- [ (4-hydroxyphanyl)methyl] alaninamide,
• (R) -N2-[bis(4-bromophenyl)acetyl]-N-[(4-hydroxy¬phenyl) methyl] argininamide,
• (R) -N2-(diphenylacetyl)-N-[(4-ethoxyphenyl)methyl]-argininamide,
• (R) -N2-(diphenylacetyl)-N-[(4-hydroxyphenyl)methyl]-N-metnylargininamide,
■ (R,S)-N-[(4-amino-3,5-dibromophenyl)methyl]-3-[3-
(aminoiminomethyl)phenyl] -N2- (diphenylacetyl) alanin¬
amide,
• (R) -N- [ (4-hydroxyphenyl)mathyl] -N2- (2-naphthoyl)argin¬inamide,
• (R) -N- [ (4-hydroxyphenyl)methyl] -N2- (2-naphthoyl) argin¬inamide ,
• (R)-N2-(2,2-diphenyl-2-hydroxyacetyl)-N-[(4-hydroxy¬
phenyl) methyl] argininamide,
■ (R,S)-M2-(diphenylacetyl)-N5-(lH-imidazol-2-yl)-M-[(4-

methoxyphenyDmethyl] ornithinamide,
• methyl) amino] carbonyl] -N- [(4-hydroxyphenyl)methyl]alan-
inamide,
• (R,S) -N2- (diphenylacetyl) -N5- (lff-imidazol-2 -yl) -K-
(phenylmethyl)ornithinamine,
■ (R,S)-N-[(4-amino-3,5-dichlorophenyl)methyl]-N2-
(diphenylacetyl) -N5- {lff-imidazol-2-yl)omithinamide,
• (R,S) -N-[(4-hydroxyphenyl)methyl]-N5-{lH-imidazol-2-
yl) -N2- (2-naphthoyl)ornithinamide,
■ (R,S) -N2-[ [(diphenylmathyl)amino]carbonyl]-N-[(4-hy-
droxyphenyDmethyl] -N5- (LH-imidazol-2-yl)ornithinamide,
• (R,S)-N- [(4-hydroxyphenyl)methyl] -N5- (li*-imidazol-2-yl)-N2-[(2-naphthyl)acetyl]ornithinamide,
• (R,S)-N-[(4-hydroxyphenyl)methyl]-N5-(lff-imidazol-2-yl)-N2-[[(2-naphthyl)amino]carbonyl]ornithinamide,
• (R,S)-N-[(4-hydroxyphenyl)methyl]-N5-(ltf-imidazol-2-yl) -N2- [ (1,2,3,4-tetrahydroquinolin-3-yl)carbonyl]-orni thinamide,
• (R,S)-N-[(4-hydroxyphenyl)methyl]-N5-(lH-imidazol-2-yl) -N2-[(1,2,3, 4-tetrahydroquinolin-2-yl)carbonyl]-ornithinamide,
• (R) -N- [ (4-aminosulphonylaminophenyl)methyl] -N2- (diphen¬ylacetyl) argininamide,
■ (R) -H- [ (4-aminophenyl)methyl] -N2- (diphenylacetyl) argin¬
inamide/
- (R)-N-[(6-quinolinyl)methyl]-N2-(diphenylacetyl)argin¬inamide,
• (R)-N2-[(3,4-dichlorophenyl)acetyl]-N-[(4-hydroxy-phenyl )me thyl]argininamide,
• (R)-N2-(diphenylacetyl)-N-[[4-(2-hydroxyethyl)phenyl]-methyl]argininamide,

■ (R,S) -Ns- (3-amino-l,2,4-oxadiazol-5-yl) -N2- (diphenyl¬acetyl) -N-[(4-hydroxyphenyl)methyl]ornithinamide,
■ (R)-N2-[(9-fluorenyl)carbonyl]-N-[(4-hydroxyphenyl)-methyl] argininamide,

• (R,S) -6-(aminoiminomethyl) -H2- (diphenylacetyl) -N- [(4-hydroxyphenyl)methyl]norleucinamide,
• (R,S)-3-[4-
(diphenylacetyl) -N- [ (4 -hydroxyphenyl) methyl] alanin-amide,
• (R,S)-3 - [3 - (aminoiminomethyl)phenyl] -N2- (diphenyl-acetyl)-N-[ (4-ethoxycarbonyloxyphenyl)methyl]alanin-amide,
• ■ (R,S)-H2-(diphanylacetyl)-N-[(4-hydroxyphenyl)methyl]-2-methylarglninamlde,
• (R,S)-N2-(diphanylacetyl)-H-[ [4-(3-hydroxypropyl)-phenyl] methyl] argininamide,
• (R)-N- [ [4- [(4,5-dihydro-5,5-dimethyl-2,4(3H)dioxo-lH-imidazol-3-yl)methyl]phenyl]methyl]-N2-(diphenyl-acetyl)argininamide,
are advantageous, BIBP 3226 being preferred,

in which R'^ represents a phenyl group unsubstituted or substituted with one or two halogen atoms, a (C1-Cjjalkyl group or a pyridyl group unsubstitutad or substituted with one or two halogen atoms, a (Cj-Cjialkyl group or a (ci-c3) alkoxy group,
- R'2 represents a hydrogen atom, a (C1-C3)alkyl group, a phenyl group optionally substituted with one or two halogen atoms or with a (C1-Cj) alkyl group or with a (C1-C3)alkoxy group, a benzyl or heteroaryl group uneubstitu¬ted or substituted with one or two halogen atoms or a (C1-C3)alkyl or (C1-Cj)alkoxy group.

- n' represents 1, 2, 3 or 4
or in which R' is defined by the formula:

in which R'3 represents a pyridyl ring unsubstituted or substituted with one or two halogen atoms, with a (C1-C3)alkyl or (Cj^-Cjjalkoxy group, R"4 represents a hydro¬gen atom or a phenyl group optionally substituted with one or two halogen atoms or with a (C1-C3)alkyl group or with a (C1-C3)allcoxy group, R' 's represents a hydrogen , atom or a methyl or hyroxyl group and Z' ' represents a single bond, an oxygen atom or a sulphur atom and p' represents 1, 2 or 3, mf' represents 1, 2 or 3 and R'0 represents a hydrogen atom or a methyl group, as well as the pharmaceutically acceptable salts thereof, the NPY-antagonist effect of which is described in EP 448,765.
Among these compounds, those of formula (VII) in which m" is 3, R"0 is hydrogen and R" is 2- (3-pyridyl-methylthio) ethyl, 3,3-diphenylpropyl, 2- (2-pyridylamino) -ethyl, 2 -(5-bromo-3-methyl-2-pyridylamino)ethyl, 2-(diphenylmethoxy)ethyl, 3-(3,5-difluorophenyl)-3-(2-pyridyl)propyl, 2-[N-{5-bromo-3-methyl-2-pyridyl)-H-benzylamino]ethyl or 2-(5-bromo-3-methyl-2-pyridyl)ethyl and the salts thereof are particularly advantageous, 1- [3- (3, 5-difluorophenyl) -3-(2-pyridyl)]propyl-3- [4- (Iff) -imidazolyl]guanidine trihydrochloride (Be 90481) being preferred.
IX - Dihydropyridines of formula:

the solid or dotted lines representing a single or double bond, as well as the additional salts or solvates thereof

described in US 5,554,621.
B. Other NPY antagonists which are advantageous in the cosmetic compositions of the present invention are peptides chosen from those of groups IX to XII below.
X - Compounds of formula
Tyr-Pro-Ser-Lys-Pro-Asp-D-Cya-NH- (CH2) BC0-Xxx2 (IX) -Arg-Cys-Tyr-Xxx3-Ala-Leu-Arg-His-Tyr-Xxx4 -Asn-Leu-Xxxs-Thr-Arg-Ile-Arg-Tyr-Tc in which
- Xxx2 and Xxx3 are Ser or Ala, Xxx4 and Xxxs are Leu, lie. Met, Nle (norleucine) or Val
- Tc is OH, 0(C1-C4)«lfcyl, NH2 or NHK^-C1 alkyl,
- s is an integer from 1 to 11, and the salts thereof, described in EP 355,794.
Among these compounds, that of formula (IX), in which s is 7, Xxx2 is Ala, Xxx3 is Ser, Xxx4 and Xxx5 are both lie and Tc is NH2, and the salts thereof, are advantageous.
XI - Compounds of formula
8b-*ia-Bka-B»k3-l>fc4-«kB-»M-0fc7-DP-Tlir-BP'-01u (X)
-BP'-K-NH2 in which klr k2, k3, k4, k5, k6 and k7 represent zero or 1, their sum being at least 1, A is Phe or Tyr; B is Pro, Ser, Ala, Gly, Abu, Cys, Pro-Ser, Cys-Sar, Ala-Ser, Gly-Ser, Abu-Ser or Pro-Ala, Abu being 2-aminobutyrie acid; BP, BP' and BP' are amino acids with a basic side chain; D is Pro or Cys; E is NH- Among these compounds, those of Formula (X) in which BP is Lys or Arg; E is MH-(CH2) t-CO, with t = 1-7;

tr is
where t' is 0, 1 or 2, and the salts thereof, are advan¬tageous , the compound of formula
H-Tyr-Abu-Ser-Lys-Aoc-Abu-Ile-Asn-Leu-Ile- (X') Thr-Arg-Gln-Arg-Tyr-NH2 where Aoc represents 8-aminooctanoic acid being particu¬larly preferred.
XII - Cyclic or linear compounds of formula
(Xxxa-Xxxb-Xxxc-Xxxd-Xxx,-Xxxf-Xxxg-Xxxh-Xxx1-Xxxj)n (XI) in which Xxxa, Xxxb, Xxxc and XxXj either do not exist, or alternatively Xxxa is Px or Cys; Xxxj, is Cys, Px or one or two amino acids; Xxxc is P1# Cys, Ser, Thr, Ala or Gly; Xxxd is Rx, Cys, Ser, Thr, Ala or Gly; Xxxm is Leu, lie, Val or Nle; Xxx is Arg, Lye or His; Hxx is Arg, Lys, His, Val, Leu, lie or Nle; Xxxb is Tyr, Pha, Trp, His, Lys or Arg; Xxx^ represents an NH2 group or an ester group or alternatively one or two amino acids; XXXJ is Cys or P2; 2X is hydrogen or a group P-CO where P is hydrogen, a glycosyl, nucleosyl or lipolyl radical or a (C1CjoJalkyl group, optionally containing double bonds and substituents selected from halogens and the H02, NH2, OH, sulpho, phospho, carboxy1 and alkyl groups; P2 is a group NP12P13 or OP14 in which P12 and P13 represent hydrogen or an alkyl, cycloalkyl, N-glycosyl, N-lipolyl, aralkyl or aryl group, optionally substituted with a halogen or with an H02, NH2, OH, sulpho, phospho, carboxyl or alkyl group; and P14 represents hydrogen or an alkyl, cycloalkyl, aralkyl, -O-glycosyl, -O-lipolyl, aralkyl or aryl group, optionally subsitituted with a halogen or wi tb an N02, NH2, OH, sulpho, phospho, carboxyl or alkyl group, with the limitation that

- when Xxxb does not exist or represents Cys or Px, then Xxxa is nonexistent,
- when Xxxd is Cya or Px, then Xxxc is nonexistent,
- when Xxxi is NH2 or an ester, then XxXj is nonexistent.
These compounds are described in WO 93/12139.
Among these, the peptide of formula:
Ser-Ala-Leu-Arg-His-Tyr-NH2 (XI')
known under the code number BRC 672, is particularly advantageous.
XXII - Compounds of formula
H-Tyr-Pro-Ser-Lys-Pro-Asp-Asn-Pro-Gly-Glu- (XII) Asp-Ala-Pro-Ala-Glu-Asp-Xxxs-Ala-Arg-Tyr-Tyr-Ser-Ala-Leu-Arg-His-Tyr-He-Asn-Leu-Ile-Thr-Arg-Xxx7-Xxx8-Ll-(CH2)B-P3 in which z is 0, 1 or 2, Xxx6 is Mat or Leu; Xxx7 is Glu, (R)-Glu, Pro or (R)-Pro; Xxx8 is Arg, (R)-Arg or -Arg; h1 is O or NP', P' being H or alkyl; and P3 is
a phenyl or naphthyl group which is unsubstituted or substituted with one or two P, CI, Br, alkyl, phenyl, OH, (phenyl)alkoxy, alkylcarbonyl, NH2 (optionally substituted with one or two alkyls), alkylsulphonyl, alkyl- or alkoxycarbonylamino, COOH, alkoxycarbonyl, NH2C0 (optionally substituted with one or two alkyls), alkylcarbonyloxy, alkylsul-phonyloxy, CH2OH, 1 - or 2-hydroxyethyl, (alkyl)-aminosulphonyl, cyanamino, aminocarbonylamino (optionally substituted with one or two alkyls) or NH2C(-N.CN)NH;
a S-membered aromatic heterecycle containing oxygen, sulphur or nitrogen, an imino group or an imino group containing oxygen, sulphur or nitrogen; a 6-membered aromatic heterocycle with one or two nitrogen atoms; it being possible for the said heterocycles to be C-substituted with (C1-C6)alkyl or with phenylalkyl and optionally fused with ben¬zene and optionally also substituted either with an F, CI, Br, (Cj-Cg) alkyl, alkoxy, OH, phenyl, N02, NH2 (optionally substituted with one or two alkyls or

with an allcanoyl) , CN, COOH, alkoxycarbonyl, NH2CO (optionally substituted with one or two alkyls), CH2F, CHF2, CF3, alkanoyl or NH2S02 (optionally substituted with one or two alkyls), or with two F, CI, Br, methyl, methoxy or OH;
a phenyl group substituted with a [1,5-dihydro-2,4 (3ff)dioxoimidazol-3-yl] alkyl group or with a [dihydro-3,5 These compounds are illustrated in DE 4,311,756.

C. NPY-antagonist products, in particular extracts with NFY-antagonist activity, which can be obtained by extrac¬tion of cells or tissues of animal or plant origin or by fermentation of microorganisms, in particular bacteria and fungi, for example yeasts, are advantageous NPY-antagonist components in the cosmetic compositions of the present invention.
Particularly advantageous and even preferred products of this class are the products of groups XV, XVI and XVII illustrated below.

XV - Extracts with NPY-antagonist activity obtained by
extraction of a sponge, Orina. sp. Gray (or Gelliua sp.),
in particular the indole compounds described in J. Nat.
Products, 1994, 57, 1294-1299 and ibid. 1995, 58, 8,
1254-1260, or mixtures thereof, more particularly
gelliusine A, gelliusine B, 2-[5-hydroxy-3-(2-amino-
ethyl)]indol-2-yl-6-bromo-3- indolethanamine and
2-[S-bromo-3-(2-aminoethyl]indol-2-yl-6-bromo-3-indol-
ethanamine, and the salts and mixtures thereof.
XVI - Extracts from fermentation of Aspergillus strains,
for example of Aspergillus niger with NPY-antagonist
activity, in particular the compound known under the code
name BMS-192548, which can be prepared by extraction of
the culture medium of Aspergillus niger WB 2346, as
described in J. Antibiotics, 1995, 48, 10, 1055-1059,
having the formula (XV)

XVII - Products, in particular extracts obtained by
fermentation of Actinomycetaceae strains, having NPY-
antagonist activity. More particularly, extracts obtained
from a novel strain of actinomycetes having a parti¬
cularly advantageous activity as NPY-receptor antagonists
are particularly preferred NPY-antagonist components.
Fractions with NPY receptor antagonist activity are obtained from the fermentation broths of this strain, by filtration of the supernatant, optionally followed by steps of concentration, purification and/or lyophilization, these fractions being devoid of genotoxi¬city and having a stability which is sufficient to allow them to be formulated in the cosmetic compositions of the present invention.
The supernatant of the fermentation broth can also be used as it is.

These novel extracts constitute a subsequent and particularly advantageous aspect of the present inven¬tion.
The organism producing the extracts with NPY receptor antagonist activity according to this specific aspect of the present invention is an actinomycetes strain which has been isolated from a sample of grassland taken from the Haute Garonne (France) , which has been assigned the in-house number SEBR 2794. A sample of this microorganism was deposited on 13 July 1993 at the CNCM of the Pasteur Institute where it was registered under the reference I 1332.
The biochemical characteristics of this micro¬organism were determined on API 50 CH (specific for sugars) , API 50 AO (specific for organic acids) and API 50 AA (specific for amino acids) kits, (marketed by BioMerieux for API 50 CH and by the API Research Labora¬tory for the others) . It was thus determined that this microorganism belongs to the family of Sfcreptomycefcaceae, genua Streptomycaa.
This is a polymorphous, filamentous micro¬organism. It grows well at 28°C on an ISP2 culture medium (agar yeast malt extract), the colour of its vegetative mycelium being pinkish-grey.
This organism, which has properties that did not allow it to be identified as a species already described, must be considered as a novel species and it has been designated as Stxaptomycea ap SEBR 2794.
The strain Streptomyces ap SEBR 2794, deposited at the CNCM of the Pasteur Institute under the number I 1332, and productive mutants thereof, also constitute a subject of the present invention.
This noval strain was isolated according to the usual method, which consists in placing a small amount of soil in suspension in distilled water, in diluting the suspension to different concentrations and in plating out a small volume of each dilution on the surface of a Petri dish containing » nutrient agar medium. After incubating for a few days at 28°C, which allows the microorganisms

to grow, the various colonies are taken separately and subcultured on nutrient agar so as to obtain more abundant cultures therefrom. After culturing on nutrient agar medium and subculturing several times successively, which makes it possible to obtain an abundant and pure culture of the strain of interest, a batch 0 for storage of the parent strain is manufactured, followed by primary and secondary inoculation batches.
For this, a suspension of spores is prepared from a culture on nutrient agar medium in a Petri dish and from maintenance medium; this medium contains a cryo-protective agent making it possible to ensure good viability of the spores during conservation by freezing.
The suspension of spores obtained is divided into cryotubes which will be stored at - 80 °C; these tubes constitute the batch 0.
Following the same procedure, but starting with a tube from batch 0, a primary inoculation batch is prepared.
Next, still according to the same procedure, a secondary inoculation batch is prepared from a cryotube of the primary inoculation batch.
The manufacture of the inoculation batches 0, 1 and 2 ensures long-lasting accessibility of the strain and thus of the desired activity.
The process for preparing the extracts with NPY receptor antagonist activity consists essentially in cultivating the novel strain SEBR 2794, or productive mutants thereof, on a suitable medium and under suitable culture conditions and in then extracting from the fermentation broth the active fraction produced during the culturing; this active fraction is found in the supernatant.
Streptomycma ap SEBR 2794 can be cultured by any aerobic culture method. For this purpose, the various types of apparatus which are in common use in the fermen¬tation industry are used. It is possible, in particular, to adopt the following approach for carrying out the operations.

Starting with a tube of the secondary inoculation batch, Petri dishes are seeded and, after incubating for five days, these provided a suspension of spores.
This suspension of spores is used to seed stirred conical flasks containing a suitable medium. The stirred flask can also be seeded directly with a tube of the inoculation batch. The culturing in stirred flasks can last for two to seven days but a duration of three to five days is preferred.
The production of activity is observed in the supernatant, from the first stage and onwards of cultur¬ing in flasks, but it may be advantageous to perform two successive culturing stages: a first stage for propagat¬ing the biomass, a second for production. In the latter case, a duration of one or two days is sufficient for the first stage.
The antagonist activity contained in the flask culture supernatants is expressed as ID50 (50% inhibitory dilution, namely the dilution which inhibits binding of the ligand to its receptors by 50%); the ID50 is generally between 1/200 and 1/1000.
The NPY receptor antagonist activity is obtained in the supernatant of the flask cultures, but it appears to be advantageous, in order to obtain a higher activity, to perform culturing in a fermenter and then to extract the supernatant therefrom. The fermenter is seeded with a one- or two-day-old stirred flask culture. In the fermenter, depending on the culture medium used, the antagonist activity may be observed in the supernatant from the first day onwards, but it is advantageous to prolong the culturing beyond three days in order to obtain an optimal production.
Culturing SEBR 2794 in a fermenter makes it possible to control better the culture conditions which are described below, such as, for example, the pH or the aeration.
The antagonist activity obtained in the fermenter supernatants, before concentrating, may vary, according to the culture conditions applied, between an ID50 of

1/500 and an ID50 of 1/10000.
The culture medium used in the fermentation process must contain at least one assimilable carbon source, an assimilable nitrogen source and mineral elements. Assimilable carbon sources which may be used are carbohydrates such as glucose, mannose, maltose, dextrine, glycerol, amino acids and proteins. Assimilable carbon sources which may also be used are acetic? acid, suberic acid, citric acid, propionic acid, succinic acid and 2-ketoglutaric acid or certain animal or plant oils.
Proteins, peptones and amino acids are among the best sources of assimilable nitrogen. These sources comprise, for example, casein, lactalbumin, gluten and hydrolysates thereof, fish meal, yeast extracts and peptones.
The production of biomass may be increased by the addition, during culturing, of one and/or the other of these two main substrates.
Potassium, sodium, iron, magnesium, calcium and manganese salts are among the mineral elements added to the culture medium to ensure growth of the microorganism and to optimize the assimilation of the carbon and nitrogen sources by the cells of the microorganism, as well as phosphorus compounds such as phosphates and trace elements.
To grow the SEBR 2794 source on a medium contain¬ing these components, the process of culturing under aeration and with stirring, in which a liquid medium is used, is advantageous, although culturing on an agar medium can also be used.
The temperature, the duration of incubation, the aeration and the pH of the medium must be such that they give rise to maximum growth of the microorganism used and a maximum yield of extracts with NPY receptor antagonist activity; a culture stirred for about 2 to 7 days is usually advantageous.
The pH of the culture medium is preferably maintained at a more or less neutral or very weakly basic value and the optimum incubation temperature is between

about 23°C and 35°C, the preferred range being 25°C to 33°C.
The culture conditions, such as the composition and pH of the medium/ the incubation temperature, the stirring speed and the aeration of the fermentation may vary within a wide range and should obviously be chosen so as to obtain the best possible results.
In order to obtain extracts of the NPY receptor antagonists produced during the culturing, the supernatant is separated from the mycelium after the fermentation broth has or has not been frozen. For this separation, centrifugation, filter-press filtration or clarifying filtration, that is to say filtration in the presence of a filtering adjuvant, or any other technique usually used to extract an extracellular product from a fermentation broth can be used.
The active extract for cosmetic use is prepared from the culture supernatant obtained.
The supernatant may be concentrated by a membrane technique or by any other concentration method so as to facilitate the packaging or the use of the active solution.
It is thus possible to obtain activities with ID50 values ranging from 1/250 to 1/50000.
Whether it has been concentrated or not, the supernatant may be diluted in various solvents which are compatible with cosmetological use.
The extract thus obtained according to this specific aspect of the present invention is filtered through a 0.2 pm filter in order to remove all trace of residual biomass and to ensure microbiological cleanliness: it is then packaged asaptically in sterile bottles and the active solution which can be used in cosmetology is obtained.
Fluids containing the NFY-antagonist extracts of the present invention in a glycol, preferably in propylene glycol, constitute another very advantageous aspect of the present invention. If it is desired to obtain a powder instead of an active solution, the

filtrate can simply be lyophilized.
An assay of NPY receptor antagonist activity carried out on an aliquot makes it possible to evaluate the activity of the active solution and to check the reproducibility of the process.
On the supernatant or the lyophilizate, the extract of the invention may be purified in a more or less thorough manner according to the conventional techniques for purifying "biomolecules", polymers, protein substances or the like, such as, for example, gel permeation chromatography, ultrafiltration, adsorption chromatography, countercurrent chromatography or electro-focalization.
The extracts obtained from this novel strain have a very advantageous NPY receptor antagonist activity. Their strong affinity for these receptors, both for the Yl and Y2 subtypes, has been demonstrated in dog adipo¬cytes, this model displaying great homology with human adipocyte. More particularly, the adipocyte membranes were obtained from omental adipose tissue taken from dogs, essentially used in the technique described by Taouis et al., J. Pharmacol. Exp. Ther {1987), 242, 1041-1049. The binding studies were performed according to the known conventional techniques. In particular, the adipocyte membranes (200 jj.g/ml) are incubated for 60 minutes at 30°C in a buffered binding medium (20 mM Krebs-Ringer Hepes solution, pH-7.4, 1% bovine serum albumin, 0.25 mg/ml bacitracin) with 0.08 nM of [125I] -NPY labelled with the Bolton-Hunter reagent (Amersham IM 170.2000 Ci/mmol) in the presence or absence of 0.3 /iM pig NPY. The incubation is stopped by filtration using Whatman GF/C filters and the radioactivity retained by the filter is evaluated with a gamma counter.
The non-specific binding, measured in the presence of 0.3 /xH unlabel led NPY, represents 25% of the total binding. The dog adipocyte membrane preparation carries Y1 and Y2 receptors which may be distinguished on the basis of the selective affinity of the NPY fragment (13-36) for the Y2 receptors.

The extracts according to the present invention demonstrated good affinity for the NPY receptors of this tissue, by displacing the [125I] -NPY bound to the adipocyte membranes in a dose-dependent manner with IC50 values (that is to say concentrations which inhibit the specific binding of [125I] -NPY by 50%) which depend on the degree of purification of the extracts and which, in the case of the crude extracts obtained directly from the fermentation supernatanta by lyophilization, are at least about 10"2 mg/ml.
The NPY-antagonist nature of the extracts accord¬ing to this specific aspect of the present invention was demonstrated by studies on isolated organs and more particularly in the model of rat "vas deferens", The . extracts showed antagonist properties towards the effects of NPY in Y2 models of rat vas deferens and were studied according to the procedure described in Regulatory Peptides 1986, 13, 307-318.
This activity was confirmed on human adipocytes isolated from subcutaneous adipose tissue, by assaying the release of fatty acids into the culture medium and comparing it with the control (incubation without product).
50% (w/w) solutions of these extracts in propylene glycol are particularly preferred.
The aseptic preparation of these solutions makes It possible to avoid the addition of preserving agent.
In the preparation of the compositions according to the present invention, the extracts with NPY receptor antagonist activity are mixed with aqueous or non-aqueous solvents and with conventional diluents which are compatible with topical use, as well as with the active components of the composition itself. Suitable solvents and/or diluents will be chosen according to their capac¬ity to transport the active component from the extfact of the invention into the subcutaneous adipose layer.
These compositions generally contain excipients or additives chosen from the ingredients usually used in compositions intended for local application according to

the need for the specific formulations envisaged.
They may contain, for example, thickeners, softeners, emollients, stabilizers, preserving agents, anti-foaming agents, surfactants, antioxidants, dyes and/or pigments, and fragrances.
They may also contain other active components having either an effect of the same type, for example products which contribute towards controlling lipolysis/ lipogenesis or products which are useful in this type of composition, such as collagen synthesis stimulators, collagenase or elastase inhibitors, and vasoprotectors.
The preferred cosmetic compositions according to the present invention contain, besides the NPY antagonist, an ct2-antagonist which may itself also be a . non-peptide synthetic compound, a peptide or a product obtained by fermentation of a microorganism, for example a bacterium or a fungus, or by extraction of cells or tissues of plant or animal origin.
a2-Antagonists which are advantageous to use as additional components, along with the NPY antagonist, are those of classes D and E below.
D. Synthetic products chosen from those of groups XVIII to XXV below.
XVIII - The compounds described in BE 840,363, in par¬
ticular mirtazapine.
XIX - The compounds described in DE 2,603,407, in par¬ticular eetiptiline and structural analogues thereof.
XX - The compounds described in ITS 4,337,260, in particular mosapramine
XXI - The compounds described in US 2,979,511, in par¬ticular idazoxan.
XXII - The compounds described in WO 92/13856, in par¬
ticular 5-thiazolyl-N,N-dimethyltryptaminea including
CP 93393.

t
XXIII - The compounds described in US 4,229,449, in
particular reboxetine.
XXIV - The compounds described in GB 2,157,631, in
particular fluparoxan.
XXV - The compounds described in GB 2,167,408, in par¬
ticular altipamezole.
E. e*2 -Antagonist products obtained by extraction of cells or tissues of animal or plant origin or by fermentation of microorganisms, in particular bacteria and fungi, for example yeasts. Examples of products of this class, also including semisynthetic products, are the products of . groups XXVI and XXVII below.
XXVI - Extracts of ergot, components and semisynthetic
compounds thereof, having an c*2-antagonist action, in
particular nicegoline.
XXVII - Products, in particular extracts obtained from
the fermentation of strains of Bacillus lichenifonnis,
with antagonist activity towards the a2 receptor, in
particular from the strain SEBR 2464.
These products, in particular the extracts belonging to this group, represent another specific aspect of the present invention.
The productive organism according to this speci¬fic aspect of the present invention is a strain of Bacillus lichenlformla which has been isolated and has been given the code number SEBR 2464. A sample of this microorganism was deposited on 22 October 1996 at the CNCM of the Pasteur Institute, where it was registered under the reference 1-1778.
The characteristics of this microorganism were determined on API 20B, API 50 CHB, 50 CH, 50 AA, 50AO and 20E API kits.
This is a bacterium in uniformly shaped mobile rod form, from 2 to 10 (no. in length and from 0.5 to 1 /JM

in width, individually or in short chains.
As with most Bacilli, this bacterium is gram+, facultative anaerobic, catalase positive, oxidase nega¬tive and has the characteristic of sporulating under certain conditions.
It grows well at pH 5 to 7, at temperatures between 15 and 55°C and for salinities (MaCl) of up to 7%.
This strain was isolated as a contaminant, during experiments using columns of sand, according to the conventional microbiological techniques known to those skilled in the art.
This particular strain, along with productive mutants thereof, therefore constitutes a further subject of the present invention.
After culturing on nutrient agar medium and subculturing several times successively, which make it possible to obtain an abundant and pure culture of the strain of interest, a batch 0 is manufactured for storage of the parent strain, followed by primary and secondary inoculation batches.
For this, a suspension of spores is prepared from a culture on nutrient agar medium in a Petri dish and from a maintenance medium; this medium contains a cryo-protective agent making it possible to ensure good viability of the spores during storage by freezing.
The suspension of spores obtained is divided into cryotubes which will be stored at -80°C: these tubes constitute batch 0.
Following the same procedure, but starting with a tube from batch 0, a primary inoculation batch is prepared.
Next, still according to the same procedure, a secondary inoculation batch is prepared from a cryotube of the primary inoculation batch.
The manufacture of the inoculation batches 0, 1 and 2 ensures long-lasting accessibility of the strain and thus of the desired activity.
The process for preparing the extracts with

or2-receptor antagonist activity consists essentially in growing the novel strain SEBR 2464, or productive mutants thereof, on a suitable medium and under suitable culture conditions and in then extracting the active fraction from in the culture supernatant.
This supernatant may be concentrated until a dry extract is obtained.
The Bacillus lichenlformiB SEBR 2464 can be cultured by any aerobic culture method and in various types of apparatus usually used in the fermentation industry. It is possible, in particular, to adopt the following approach for carrying out the operations.
Starting with a tube of the secondary inoculation batch, Petri dishes are seeded and, after incubating for . two days, these allow stirred conical flasks containing a suitable medium to be inoculated.
A stirred flask can also be seeded directly with a tube of the inoculation batch. In this case, the duration of culturing will be longer for the same medium.
The antagonist activity is obtained in the flask cultures within 10 hours to 48 hours depending on the culture conditions used.
The a2-receptor antagonist activity is extracted from the culture supernatants. The activity of the extracts is expressed as ID50 (50% inhibitory dilution); one litre of culture makes it possible to obtain 10 ml of extract having an ID50 value of between 1/2500 and 1/10,000.
The a2-receptor antagonist activity may be obtained by extracting the supernatant of the flask cultures, but it appears to be advantageous, in order to obtain a higher activity, to perform culturing in a fermenter and then to extract the supernatant therefrom.
The fermenter is seeded with a 1- to 2-day-old culture in a stirred flask; it is preferable for the culture not to have begun to sporulate.
In the fermenter, according to the culture conditions used, the antagonist activity may be observed from the first hours of culturing and onwards, but it is

advantageous to wait until the stationary growth phase has been reached before extracting.
Culturing SEBR 2464 in a fermenter allows better control of the culture conditions which are described below, for example the pH and the aeration.
The a2-receptor antagonist activity obtained in the fermenter may vary, depending on the culuture condi¬tions applied.
One litre of culture makes it possible to obtain from the supernatant, after extraction, 10 ml of extract having an ID50 of between 1/3000 and 1/15,000.
The characteristics of the medium are identical to those described above for the strain SEBR 2794.
In order to grow the strain SEBR 2464 on a medium containing these components, the process of culturing under aeration and with stirring, in which a liquid medium is used, is advantageous, although culturing on an agar medium can also be used.
The temperature, the duration of incubation, the aeration and the pH of the medium must be such that they give rise to a maximum growth of the microorganism used and a maximum yield of extract with a2-receptor antagon¬ist activity.
A culture stirred and aerated for about 10 hours to 48 hours is usually advantageous.
The pH of the culture medium is preferably maintained at a more or less neutral or very weakly acidic value and the optimum incubation temperature is between 25°C and 50°C.
The culture conditions, such as the composition and pH of the medium, the incubation temperature, the stirring speed and the aeration of the fermentation, may vary within a wide range and should obviously be chosen so as to obtain the best possible results.
The production of an extract having a high a2-receptor antagonist activity requires several extraction steps.
A first step consists in eliminating the biomass. For this, centrifugation, tangential microfiltration,

clarifying filtration, that is to say a filtration in the presence of a filtering adjuvant, or any other method usually used to extract an extracellular product from a fermentation broth may be used. The supernatant is then placed in contact overnight with a hydrophobic resin preferably made of polystyrene-divinylbenzene, for example such as Amberlite XAD2 resin (Rohm & Haas) or CHP20P resin (Mitsubishi).
The loaded resin is then separated by frontal filtration and the filtrate is removed.
The resin undergoes several successive extrac¬tions with different solvents, allowing molecules of a hydrophobic nature to be extracted. After each extrac¬tion, the resin is separated from the organic phase by filtration.
The various organic phases are then evaporated under vacuum, together or separately, until one or more dry extracts are obtained.
An assay of ot2-receptor antagonist activity performed on an aliquot of each of the extracts makes it possible to evaluate their activity and to check the reproducibility of the process.
The dry extract thus obtained may be taken up in various solvents usually used in cosmetology.
The uptake concentration is chosen to allow complete dissolution of the extract and to be compatible with the subsequent use. In order to eliminate all trace of residual bioxnass and to ensure its microbiological stability, the extract is filtered on a 0.2 p filter and divided aseptically into sterile flasks.
The a2-antagonist activity of the extracts was evaluated using the technique described by Chapleo CB et al., J. Med. Chem., 1983, 26, 823-831, on the in vitro displacement, in rat cortex, of the o2-receptor antagon¬ist reference ligandt tritiated idazoxan.
The a2 -antagonist extract, containing 30% dry extract, is introduced into a 50/50 propylene glycol/water mixture and makes a preferred dilution according to the invention.

Dilutions for aseptic preparation of these solutions, which makes it possible to avoid the addition of preserving agent, may also be used.
In the preparation of the compositions according to the present invention, the extracts thus made up with Qf2-receptor antagonist activity are mixed with aqueous or non-aqueous solvents and with conventional diluents which are compatible with a topical use, as well as with the active components of the composition itself. Suitable solvents and/or diluents will be chosen according to their capacity to transport the active component from the extract of the invention into the subcutaneous adipose layer.
These compositions generally contain excipients or additives chosen from the ingredients usually used in compositions intended for a local application, according to the need for the specific formulations envisaged.
They may contain, for example, thickeners, softeners, emollients, stabilizers, preserving agents, anti-foaming agents, surfactants, antioxidants, dyes and/or pigments, and fragrances.
They may also contain other active components having either an effect of the same type, for example products which contribute towards regulating lipolysis/lipogenesis, or products which are useful in this standard type of composition, such as collagen synthesis stimulators, collagenase or elastase inhibitors, or vasoprotectors.
The a2-antagonist extracts of the invention moreover proved to be completely devoid of genotoxicity in the Ames test and the test of PNA repair. Their stability is compatible with their use in cosmetic compositions.
The cosmetic compositions of the present inven¬tion contain the NPY antagonist in percentages of between 0.00001% to 5% relative to the total weight of the composition, mixed with the excipients commonly used to prepare cosmetic formulations to be applied to the skin.
The said percentages may vary within the range

indicated above as a function, of the intrinsic activity of the NPY-antagoniet component included in the composi¬tion. Preferably, the said NPY-antagonist component is present in percentages of from 0.0001% to 2%.
The NPY-antagonist component is advantageously chosen from the products included in classes A, B and C above, those of class C being particularly advantageous. The components belonging to groups XV, XVI and XVII are preferred.
In the preparation of the compositions according to the present invention, the NPY-antagonist component is mixed with aqueous or non-aqueous solvents and with conventional diluents which are compatible with use on the skin, as well as with other components of the compo¬sition itself. Suitable solvents and/or diluents will be chosen according to their capacity to deposit the NPY-antagonist active component of the invention onto the skin.
These compositions generally contain excipients or additives selectedfrom the ingredients usually used in compositions intended for a local application according to the need for the specific formulations envisaged.
They may contain, for example, thickeners, softeners, emollients, stabilizers, preserving agents, anti-foaming agents, surfactants, antioxidants, dyes and/or pigments, and fragrances.
When the NPY-antagonist component is an extract of cells or tissues of animal or plant origin or a product, in particular an extract, obtained by fermenta¬tion of a microorganism, for example a bacterium or a fungus, the amount of NPY-antagonist component is always from 0.00001% to 5%, preferably from 0.0001 to 2%, relative to the total weight of the composition, the said amount being calculated relative to the weight of the dry extract.
The compositions according to the present inven¬tion comprise, according to a preferred aspect, an extract obtained by fermentation of the novel strain SEBR 2794 in proportions, on a weight/weight percentage basis,

which depend on the degree of NPY receptor antagonist activity of the extract used and therefore on the concen¬tration of dry substance and on the specific activity of this substance.
The higher the antagonist activity of the extract used towards the NPY receptors, the lower is the weight amount required to obtain the desired lipolytic effect, and vice versa.
In order to obtain the cosmetic compositions according to the invention, the crude extracts (supernat-ants filtered through a 0.2 p filter) obtained directly from the fermentation may conveniently be used without any purification step, in proportions of between 0.00001 and 5%, advantageously from 0.0001 to 2%, better still from 0.01 to 2% by weight and preferably from 0.1 to 2% by weight. These weight percentages are, naturally, calculated on the basis of the weight of extract pre¬pared.
When the compositions of the present invention also contain, in addition to the NPY-antagonist component, an a2-antagonist component, the latter is present in a percentage of from 0.00001 to 5%, advantage¬ously from 0.0001 to 2%, better still from 0.001 to 1% and preferably from 0.01 to 0.5%, relative to the total weight of the composition.
The said percentages may vary within the ranges indicated above as a function of the intrinsic activity of the «2-antagonist component included in the composi¬tion.
The a2-antagonist component is advantageously chosen from the products included in classes D and E above, those of class E being particularly advantageous. The compounds belonging to group XXVII are preferred.
When the t*2 -antagonist component is an extract of cells or tissues of animal or plant origin or a product obtained by fermentation of a microorganism, for example a bacterium or a fungus, the amount of a2-antagonist component is that indicated above, the said amount being calculated on the basis of the weight of the dry extract.

jiccgroing co an advantageous aspect of the present invention, the cosmetic composition contains both an NPY-antagonist component and an c*2 -antagonist compo¬nent, the NPY-antagonist component being selected from those of classes A, B and C above and the a2-antagonist component being selected from those of classes D and E above.
According to a particularly advantageous aspect, the cosmetic composition of the present invention, con¬tains an NPY-antagonist component selected from those belonging to class C, in particular to groups XV, XVI and XVII and an a2-antagonist component selected from those belonging to class E, in particular to group XXVII.
According to a preferred aspect, the present invention relates to a cosmetic composition containing an NPY-antagonist component consisting of an extract selected from those of group XVII above and an a2-antagonist component consisting of an extract selected from those of group XXVII above.
More particularly, the composition according to this preferred aspect of the present invention contains an NPY-antagonist component which may be obtained by fermentation of the strain Streptomyces sp. SEBR 2794 deposited at the CNCM of the Pasteur Institute under the number I 1132, or productive mutants thereof, and an a2-antagonist component which can be obtained by fermentation of the strain Bacillus licheniformis SEBR 2464 filed at the CNCM of the Pasteur Institute under the number 1-1778, with excipients normally used for formulations of this type, such as those mentioned above.
The form of the compositions according to the present invention may be an emulsion in which the consti¬tuent or the mixture of constituents, with an optional stabilizer, is combined with excipients which are com¬monly used in cosmetic compositions and which are compat¬ible with the said constituents, such as lanolin or plant/ mineral or synthetic oils.
The compositions of the invention may also be in the form of a gel in suitable excipients, such as

cellulose esters or other gelling agenta such aa acrylic derivatives and may contain the active principle in dissolved form or suspended as microgranulea.
The compositions according to the invention may also take the form of a lotion or a solution in which the mixture of constituents is dissolved or microdispersed.
The form of the compositions according to the invention may thus be a microdispersion in a liquid containing water as well as one or more compatible surfactants. The disparsions have microemulsion prop¬erties and have virtually the appearance of true solutions. They may also be prepared at the time of use.
An advantageous form of the compositions accord¬ing to the invention is a fluid applied topically via an adhesive support, referred to hereinbelow as a "patch", this patch allowing controlled diffusion of the active components, this diffusion possibly being activated by physical phenomena such as electrical microcurrents.
The cosmetic compositions of the present inven¬tion may also contain other active components having either an effect of the same type as that of the NPY antagonists, for example products which contribute towards controlling lipolysis/lipogenesis, or collagen synthesis stimulators, collagenase or elastase inhibitors, or vasoprotectors.
The compositions of the present invention are of good stability and may be stored for the time required for use at temperatures of between 0*C and 60°C without any sedimentation of the constituents or separation of the phases talcing place, and also without their being any decrease in activity which might compromise the use of these compositions.
These compositions are very well tolerated, they have no phototoxicity and their application to the skin for prolonged periods involves no side effects.
The compositions of the present invention, in their various forms of presentation, may be used as lipolysis/lipogenesis regulators in the skin. More particularly, they can be used as cosmetic products for

slimming or seborrhoeia-regulating use or as adjuvants in the treatment of acne.
The cosmetic compositions of the present inven¬tion may be placed in contact with the epidermis or the , hair or pilous system so as to modify the appearance thereof and afford protection thereto.
For example, when these compositions are placed in contact with the epidermis, the latter takes on a "healthy" appearance as if it had been exposed to the air and/or the sun, without, however, tanning, if this is not desired. More particularly, the cosmetic compositions of the present invention make the skin lose its "fatty*1 appearance with the result of slimming that part of the body with which the said composition is placed in contact and of keeping it in good condition. Prom the first applications and onwards, the skin relief is smooth and the skin becomes firmer with better tonus. After applica¬tion for one month, the slimming effect appears, the "orange peel" appearance is visibly attenuated and the figure becomes shaplier.
when the compositions of the present invention are placed in contact with the hair or pilous system, for example after a specific anti-seborrhoeia treatment, the said system is maintained in good condition.
Similarly, the compositions of the present invention kaep the facial skin is good condition, also making the formation of comedones more difficult.
A slimming fluid obtained according to Example 12 below was tested on 50 female volunteers who used the said fluid applied twice a day onto the thighs, with very good results.
The slimming fluid described in Example 13 below was tested in a study including 150 female volunteers, carried out under double-blind conditions against placebo. The analysis and comparison of the results obtained with this slimming fluid and with its placebo under the experimental conditions adopted, which are similar to the normal conditions of use for repeated applications over 60 consecutive days on both thighs and

the abdomen from the waist to the knees, made it possible to demonstrate a clear and statistically significant slimming effect in favour of the slimming fluid according to the invention relative to the placebo.
The efficacy and tolerance of a slimming fluid as described in Example 14 was tested on more than 1000 women. These tests showed a decrease in the thickness of the adipose tissue, a tonifying and firming action and a slimming effect demonstrated by centimetric echographic measurement and by biphotonic absorptiometry.
One object of the invention is also a cosmetic
treatment method, wherein an amount of an
NPY antagonist with a cosmetic effect and optionally an amount of an a2-antagonist with a cosmetic effect in a vehicle for cosmetic use is applied to the epidermis and/or the hair or pilous system.
Lastly, the subject of the present invention is the use of an NPY antagonist for the preparation of cosmetic compositions intended to control lipolysis/lipogenesis in the skin, in particular for slimming and seborrhoeia-regulating purposes and as an adjuvant in or after the treatment of acne.
More particularly, the invention relates to the use of an NPY antagonist for the manufacture of cosmetic compositions intended to maintain the facial skin in good condition by making the formation of comedones difficult.
The invention also relates to the use of an NPY antagonist for the manufacture of cosmetic compositions intended for placing in contact with the hair or pilous system. In particular, the invention relates to the use of an NPY antagonist for the manufacture of cosmetic compositions intended to control lipolysis/lipogenesis of the skin, the said compositions also containing an a.2-antagonist component.
The examples which follow illustrate the inven¬tion without, however, limiting it.
EXAMPLE 1
Preparation of an extract obtained from the

€
strain Streptomyces sp SEBR 2794 1.1 Fermentation
The strain Streptomyces sp SEBR 2794 was fer¬mented in six different culture media.

1.1.2.
(a) A suspension of spores from the strain SEBR 2794 is
prepared according to the method indicated in 1.1.1. (a)
and
(b) 3 ml of this suspension is used to seed 100 ml of
culture having the following composition:

to maintain a dissolved oxygen pressure of close to 20%. The pH is not regulated and changes freely between 7.2 and 6.3.

1.2. Extraction
1.2.1. The extraction is carried out on 1.5 litre of broth obtained according to Example 1.1.1.
The fermentation broth is centrifuged at 13,000 revolutions/minute (27,500 g) for 20 minutes and is filtered in the presence of 15 g of filtering adjuvant on a filter press. The filtrate obtained is lyophilised

directly and the dry residue thus obtained (16.3 g) is redissolved in 80 ml of water (final pH = 8.4).
The 50% inhibitory dilution of this fraction (ID50) is 1/4500.
1.2.2. The extraction is performed on 10 1 of culture
broth obtained by working according to Example 1.1.5. and
are frozen beforehand.
The broth is centrifuged in 500 ml buckets at 8000 rpm (11,000 g) for 20 min. 9 1 of completely clear supernatant are obtained.
An aliquot sample is concentrated five times by a Centripep concentrator.
The 50% inhibitory dilution of this fraction is , equal to 1/10,000.
1.2.3. The extraction is performed on 10 1 of prefrozen
culture broth obtained under the same conditions as in
Example 1.1.5.
The separation is performed on a Sharpies-type continuous centrifuge.
The 9 1 of supernatant obtained are filtered through a 0.2 /a filter in order to remove all trace of residual biomass.
8.5 1 of filtrate are obtained. An aliquot sample is concentrated five times by a Centripep concentrator. The 50% inhibitory dilution of this fraction is 1/16,000
1.3. Concentration by ultrafiltration
1.3.1. Concentration on a 5 kD membrane
The process is performed by ultrafiltration of the solution of Example 1.2.1. using an Ami con 5000 membrane in a stirring cell in 25 mH phosphate buffer pH = 7.5 containing 150 mM NaCl and an active retentate and a totally inactive permeate are obtained.
1.3.2. Concentration on a 10 kD membrane
A 10 kD Ami con membrane is used to concentrate the 9 litres of supernatant obtained in Example 2.2. By

concentrating by a factor of 5, 1.8 1 of concentrate five times more active (ID5fl ■ 1/10,000) and a totally inac¬tive permeate are obtained.
1.3.3. Concentration on a 30 kD membrane
A 30 kD Ami con membrane is used to concentrate the 8.5 1 of filtrate obtained in Example 2.3. By concen¬trating by a factor of 5, 1.7 1 of concentrate which is up to five times more active (ID50 > 1/10,000} and a permeate containing very weak activity {20% inhibition at 1/250) are obtained.
1.4. Purification
1.4.1. Gel permeation chromatography
The samples of the solution from 1.2.1. are subjected to gel permeation chromatographies using various gels: Sephadex G 25, G 50, G 75 and G 100 and the results indicated below are obtained:
the activity is eluted at the exclusion volume on Sephadex G 25 and G 50 and very close to the exclusion volume of G 75.
On Sephadex G 100 gel, the activity may be separated from the products of higher molecular weight (> 100 KD).
On a Superose 12 analytical column (1 KD to 100 KD fractionation domain), the active molecule showed a retention time of between that of ovalbumin (44 KD) and that of cytochrome (14.4 KD).
1.4.2. Ultrafiltration on a membrane with a cut-off
threshold of 5000 daltons
100 ml of a culture supernatant (ID50 - 1/3600) are dialysed in 5 volumes of 20 mH phosphate buffer pH 7.4, 150 mH HaCl, in a magnetically-stirred cell equipped with an Amicon 5000 membrane, and pressurized with compressed air to a pressure of 1 x 10s Pa (1 bar).
100 ml of retentate (ID50 1/2500) freed of mol¬ecules of low molecular weight and 500 ml of an ultra-

filtrate of negligible activity are recovered.
1.4.3. Ultrafiltration on a membrane with a cut-off
threshold of 10,000 daltons
100 ml of a culture supernatant (ID50 1/3600) are dialysed in 7 volumes of 20 mH phosphate buffer pH 7.4, 150 mM NaCl in a magnetically-stirred cell pressurized to
1 x 10s Pa (1 bar) with compressed air and fitted with a
Filtron 10K membrane.
100 ml of retentate having an ID50 activity * 1/1500 in terms of inhibition of binding to the NPY receptor are recovered*
The ultrafiltrate (700 ml) is reconcentrated in a cell of the same type fitted with an Ami con 1000 . membrane.
100 ml of solution having an ID50 value of 1/500 are obtained.
1.4.4. Removal of the hydrophobic impurities
1500 ml of a culture supernatant are treated for
2 hours, with stirring, with 180 g of polystyrene-
divinylbenzene resin (XAD2). The resin is then filtered
and washed with twice 300 ml of methanol and then with
300 ml of acetone. The combined methanol and acetone
solutions are evaporated under vacuum. The residue taken
up in 40 ml of methanol gives a solution which has no
activity.
The aqueous solution freed of the hydrophobic products is lyophilized.
The residue taken up in 80 ml of water gives a solution having an ID50 value of 1/4500 in terms of inhibition of binding to the NFY receptor.
1.4.5. Extraction of the active molecule by cation
exchange.
1500 ml of a culture supernatant are adjusted to pH 5 with 1 N acetic acid and are then treated with 120 g of cation exchange resin (Dowex 50 WX-4, ACO form).
After stirring for one hour, the resin is

filtered and then de a orbed with 300 ml of IN aqueous ammonia for half an hour. This solution is then lyophilized. The residue obtained taken up in 40 ml of water gives a solution which, when measured in terms of inhibition of binding to the NPY receptor, has an ID50 value of 1/3S00.
Solutions with NPY receptor antagonist activity may also be obtained by extracting the culture broths of Examples 1.1.2, 1.1.3, 1.1.4 and 1.1.6 according to the extraction examples described in 1.2.1 to 1.2.3.
EXAMPLE 2
Preparation of an extract obtained from the strain
Bacillus licheniformis SEBR 2464 (cf. XXVII above)
2.1 Fermentation
The strain Bacillus licheniformis SEBR 2464 was fermented in 4 different culture media.

The solution of trace elements has the same composition as in Example 2.1.2.

2.2. Extraction
2.2.1. Tha extraction is performed on 12 1 of culture broth of 2.1.1.
The broth is centrifuged at 13,000 revolu¬tions/minute (27,500 g) for 10 min and 11 1 of supernatant are obtained. 2.1 kg of Amberlite XAD2 resin preconditioned with methanol and acetone are added to these 11 1 of supernatant.
The supernatant/resin mixture is placed together overnight at room temperature.
The resin is then filtered off and the products

bound thereto are successively eluted with twice 5 litres of methanol and with 5 litres of acetone.
The organic phases are combined after filtration and evaporated to dryness under vacuum.
The evaporation residue (46 g) constitutes the dry extract; it is redissolved in 100 ml of propylene glycol/water mixture (50/50).
The fraction thus obtained has an ID50 value = 1/3000.
2.2.2. The extraction is performed on 3.5 1 of culture
broth of Example 2.1.3.
The same procedure as in Example 2.2.1. is followed but the amounts of resin and of solvent are adapted to the volume of supernatant treated.
11 g of dry extract are obtained/ which are taken up in 27 ml of the propylene glycol/water mixture (50/50).
The solution thus obtained has an IDS0 value -1/4000.
2.2.3. The extraction is performed on 50 1 of culture
broth of Example 2.1.4.
A tangential microfiltration system (0.2 ftm) is used to separate the biomass. 46 1 of permeate are obtained, which are placed in contact with 9 kg of preconditioned Amberlite XAD2 resin overnight at room temperature.
The loaded resin is then filtered off and the products bound thereto are eluted with twice 23 1 of methanol and once 23 1 of acetone. Between each elution, the organic phase and the resin are separated by filtra¬tion.
The organic phases are then combined and evapor¬ated to dryness under vacuum.
285 g of dry extract are obtained, which are taken up with 620 g of the propylene glycol/water mixture (50/50).
The solution obtained is filtered through a

U.J nm filter and has an ID50 value * 1/8200.
A solution with a2-receptor antagonist activity may also be obtained by extracting the culture broth of Example 2.1.2. according to Example 2.2.3.

EXAMPLES 14 to 25
A slimming microemulaion having the composition
of Example 6 above is prepared, in which the dry extract
of Exmaple 1.4.3. is replaced by:
1- (2- [(N- (2-naphthylsulphamoyl) -5-methoxy-2-indol-yDcarboxamido] -3- (4- (N- [4- (dimethylaminomethyl) -trans-cyclohexylmethylj amidino) phenyl) propionyl) pyr¬rolidine, class A, group I (Example 14); 3-(4-methoxyphenyl) -4- [4-(2-pyrrolidin-l-ylethoxy) -benzoyl]-1,2-dihydronaphthalene hydrochloride, class A, group Ha (Examle 15);
2-{4-hydroxyphenyl)-3-[4-(2-pyrrolidin-l-ylethoxy)-benzoyl] benzothiophene hydrochloride, class A, group lib (Example 16);
PD 160170, class A, group III (Example 17); SC 3117, class A, group IV (Example 18); D-myoinositol 1,2,6-triphosphate, class A, group Va (Example 19);
inositol monophosphate, zinc salt, class A, group Vb (Example 20); 1- (3-methoxyphenyl) -1- (4-phenylpiperazin-l-yl)cyclo-

hexane dihydrochlorida, class A, group VI (Example 21);
BIBP 3226, class A, group VII (Example 22); He 90481, class A, group VIII (Example 23); dimethyl l,4-dihydro-4-[3-[[[{3-[spiro

WE CLAIM:
1. A composition for the treatment of celluilte by topical application characterized in that it comprises an NPY- (neuropeptide Y) antagonist component consisting of a product of fermentation of the strain Streptomyces sp SEBR 2794, deposited with the CNCM of the Institut Pasteur under the number 1-1332, and an a 2-antagonist component consisting of a product of fermentation of the strain Bacillus licheniformis SEBR 2464, deposited with the CNCM of the Institut Pasteur under the number 1-1778, in combination with a cosmetically acceptable excipient, wherein the NPY-antagonist is selected from those of classes A, B and C and the a 2-antagonist component is selected from those of classes D & E as described herein.
2. The composition as claimed in claim 1, wherein it comprises from 0 % to 5% by weight of the NPY-antagonist component and from 0.00001% to 5% by weight of an a2- antagonist component.
3. The composition as claimed in claim 1, wherein it also contains a collagen synthesis stimulator, a collagenase or elastase inhibitor or a vasoprotector.
4. A method of cosmetic treatment for producing a slimming effect, wherein it comprises the topical application of a composition as claimed in claim 1, 2 or 3, to selected parts of the human body.
5. The method as claimed in claim 4, wherein the composition as claimed in claims 1, 2 or 3 is applied to the thighs,

6. The method as claimed in claim 5, wherein the composition as claimed in
claims 1, 2 or 3 is applied to the thighs and abdomen from the waist to the knees.
7. The method of cosmetic treatment intended to lessen the fatty, "orange peel"
appearance of the skin, wherein it comprises the application to the skin of a
composition as claimed in any one of Claims 1, 2 or 3.

Documents:

159-mas-1997 abstract-duplicate.pdf

159-mas-1997 abstract.pdf

159-mas-1997 claims-duplicate.pdf

159-mas-1997 claims.pdf

159-mas-1997 correspondence-others.pdf

159-mas-1997 correspondence-po.pdf

159-mas-1997 description (complete)-duplicate.pdf

159-mas-1997 description (complete).pdf

159-mas-1997 form-1.pdf

159-mas-1997 form-13.pdf

159-mas-1997 form-19.pdf

159-mas-1997 form-2.pdf

159-mas-1997 form-26.pdf

159-mas-1997 form-4.pdf

159-mas-1997 form-6.pdf

159-mas-1997 petition.pdf

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Patent Number

226996

Indian Patent Application Number

159/MAS/1997

PG Journal Number

07/2009

Publication Date

13-Feb-2009

Grant Date

31-Dec-2008

Date of Filing

28-Jan-1997

Name of Patentee

SANOFI-SYNTHELABO

Applicant Address

174 AVENUE DE FRANCE, 75013 PARIS,

Inventors:

#	Inventor's Name	Inventor's Address
1	BLANC-FERRAS ELISABETH	CHEMIN DE 1'ORFEVRE, 31450, DONNEVILLE,
2	BONO FRANCOISE	21 RUE PHILADELPHE DE GERDE 31300 TOULOUSE,
3	BREDA BERNARD	30 RUE DA LA MARE, 78380 BOUGIVAL,
4	COURREGELONGUE JEAN	3 RUE G.CLEMENCEAU, 31120 PORTET SUR GARONNE,
5	DUCASSE CATHERINE	9 RUE MARTIAL ROBERT, 78800 HOUILLES,
6	MOUNIER REMY	17 ALLEE DES FONTIGNEUX, 78126 AULNAY-SUR-MAULDRE,
7	PAUL RAYMOND	75 RUE DES CHANTERELLES, 34980 SAINT VELY DU FESC,
8	PEREILLO JEAN-MARIE	9 RUE DES MIMOSAS, 31120 PORTET SUR GARONNE,
9	SABADIE MICHEL	RUE DE LA FONTAINE SAINT, GERMAIN 27300 BERNAY,
10	SERRADEIL-LE-GAL CLAUDINE	45, AVENUE DES TROUBADOURS, 31750 ESCALDENS,
11	VILAIN POL	LOTISSEMENT LES VIOLETTES, N 21, 34570 SAUSSAN,

PCT International Classification Number

A61K35/74

PCT International Application Number

N/A

PCT International Filing date

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	9612916	1996-10-23	France