CA2314569A1 - Methods for treating skin pigmentation - Google Patents

Abstract

This invention relates to methods and compositions for bringing about changes in skin pigmentation. More particularly, this invention relates to compounds which affect melanogenesis and can be used as depigmenting agents or as agents for darkening skin utilizing the PAR-2 pathway.

Description

,.
w METHODS FOR TREATING SKIN PIGMENTATION
Background This is a continuation-in-part application of U.S. Patent Application Serial No. 09/ 110,409 (Attorney Docket No. JBP 430), which is hereby incorporated herein by reference.
1. Field of the Invention 1 o This invention is related to methods and compositions for bringing about skin pigmentation and/or for causing skin depigmentation. More particularly, this invention relates to compounds which affect melanogenesis and can be used as depigmenting agents or as agents for darkening skin.
i 5 2. Background of the Imrention Skin coloring has been of concern to human beings for marry years. In particular, the ability to remove hyperpigmentation, such as found in age spots, freckles or aging skin generally, is of interest to individuals desiring a uniform complexion. In certain areas of the a o world, general body whitening is desirable. There are also hypopigmentation and hyperpig~nentation disorders that are desirable to treat. Likewise, the ability to generate a tanned appearance without incurring photodamage due to solar radiation is important to many individuals. There have been many methods proposed to accomplish depigmentation, as well as to accomplish darkening of the skin. For example, kojic acid, hydivquinone, retinoids and 25 Other chemical compounds have been used for depigmentation.
Dihydroxyacetone and like chemical compounds have Been utilized for their ability to "tan" the skin without exposure to the sun.
Marry of these previous solutions have not been found acceptable. There is often a distinct line of demarcation between the areas of skin to which such previous compositions 3 o have been applied. Therefore, precise application of all these compounds is necessary in order JBF~-465 l to achieve the desired result. Many of these compounds have been found to be quite irntating to the skin and therefore undesirable for use.
The understanding of the chemical and enzymatic basis of melanogenesis is heavily documented. Melanocytes :migrate from the embryonal neural crest into the skin to produce secretory granules, melanosomes, which produce melanin. Melanogenesis occurs within the melanosome, and the melanin is later distributed to keratinocytes via the melanocyte dendrites.
The key enzyme izi melanogenesis is tyrosinase, which initiates a cascade of reactions which convert tyrosine to the biopolymer melanin. Two tyrosinase-related proteins (TRl''s) are known, TRP-1 and TRP-2. These proteins share with tyrosinase about 40%
homology and i o have catalytic activities as well as regulatory roles in melanogenesis.
TRP-1 is the most abundant glycoprot:ein in m~lanocytes.
In spite of the fact that the chemical and enzymatic basis of melanogenesis is well-documented, its regulation at the cellular level is only partially understood.
Tyrosinase and the TRP's share structural and biological properties with the lysosomal-associatxd membrane protein (I AMP) gene family, therefore their targeting to the melanosomal membrane might induce their activation. A phosphoryiation/dephosphorylation reaction at the cytoplasmic tails of these proteins could be involved in the regulation of melanogenesis. The beta isoform of the Protein Kinase C ~'PKC) fam~y has been shown to regulate human melonogenesis through tyrosinase activation. Gene expression of tyrosinase, TRP-1 and TRP-2 is coordinated All 2 o three eare expressed in human epidermis. In melanocytes co-cultured with keratinocytes, these transcripts are expressed at a ratio of 45:45:10, respectively. In melanocytes cultured alone, only TRP-1 transcripts are present, indicating that a keratinocyte-derived signal is involved in the coordinate expression of these genes. The regulation of keratinocyte-melanocyte interactions and the mechanism of melanosome transfer into keratinocytes are not 2 5 yet underSCOOd.
The Protease-activated receptor-2 (PAR-2) is a seven transmetnbrane Gpmtein-coupled receptor, that is related to, but distinct from the thrombin receptors (TR, also named PAR-1, and PAR-3) in its sequence. Both receptors are activated proteolytically by an arginine-serine cleavage at the extracellular domain. The newly created N-termini then activate these JBF'-465 ' CA 02314569 2000-07-26 receptors as tethered ligands. Both receptors could be activated by trypsin, but only the TRs aie activated by thrombin. Only PAR-2 is activated by mast cell tryptase. Both receptors could also be activated by the peptides that correspond to their new N-termini, independent of receptor cleavage. SLIGRL, the mouse PAR-2 activating peptide, is equipotent in the activation of the human receptor. While the function of the TR is well documented, the biology of the PAR-2 has not yet been fully identified. A role for PAR-2 activation in the inhibition of kerarinocyte gxowth and differentiation has been recently described (Derian et al., "Differential Regulation of Human Keratinocyte Growth and Differentiation by a Novel Family of Protease-activate Receptors", Cell Graph fs Ditia~aorz, Vol. 8, pp. 743-749, July 1997).
to Summary of the Icn~ention In accordance with this invention, we have found a method for affecting changes in rnarnmalian skin pigmentation comprising topically applying to the skin of a mammal a compound which affects the PAR-2 pathway. The compositions of this invention may contain i s one or more compounds that act as tzypsin, as tryptase, as serine protease or as PAR-2 agonists, for increase in pigmentation. Alternatively, they may contain one or more compounds that act as serine protease inhibitors, trypsin inhibitors, thrombin inhibitors, tryptase inhibitors, as PAR-2 pathway inhibitors or as a PAR-2 antagonist for decrease in pigmentation, or "depigmentation".
a o As used herein, "marntnal" means any member "of the higher vertebrate animals comprising the class "Marnmalia", as defined in Webster's Medical Desk Dictionary 407 (1986), and includes but is not limited to humans. As used herein, "receptor" shall include both intracellullar and extracellular receptors and shall mean those molecules capable of receiving and transducing a signal. The term PAR-2 refers to the protease-activated receptor-2 or a related 2 5 protease activated receptor. The Protease-activated receptor-2 (hereinafter, "PAR-2") is a serine-protease activated receptor that is expressed in numerous tissues, including keratinocytes and fibroblasts. The thrombin receptor (also named PAR-1, ha~inafter, "TR") is a serine-protease activated receptor that is expressed in numerous tissues, including keratinocytes. The biological roles of PAR-2 and TR in skin are not entirely known. However, we have found that JBF'-4 65 interactions between keratinocytes and melanocytes, via the PAR-2 pathway, affect melanogenesis. V~'e have found that thrombin inhibitors, and/or tryptase inhibitors, and/or trypsin inhibitors and PAR-;2 antagonists can be used as depigmenting agents without irntation of the skin. PAR-2 agonists and serine proteases such as trypsin and tryptase can be used as darkening agents. :Furthermore, PAR-2 could be useful as a target for whitening and darkening agents.
We have further discovered that BBI, a Bowman-Birk type inhibitor, may also be used as an active depigmenting agent. Soybean-derived extracts and mixtures that were suggested in. U.S. Patent Application Serial No. 09/ 110,409 as depigmenting 1 o agents contain both STI and BBI. We have now found that BBI alone is effective to depigment skin. BBI may be used in all the formulations and compositions set forth in the parent application in the same range of concentration as STI.
Brief Description of the Drawings Figure 1 shows epidermal equivalents containing melanocytes of an African-American donor. Treatment with BBI reduces pigment deposition in these equivalents, as demonstrated by top view of the equivalents, with no staining.
2 o Figure 2 shows epidermal equivalents containing melanocytes of an African-American donor. Treatment with BBI reduces pigment deposition in these equivalents, as demonstrated by Fontana-Mason staining of histolog~cal sections of these equivalents.
Figure 3 shows epidermal equivalents containing melanocytes of an African-American 2 s donor. Treatment with increasing concentrations of BBI reduces pigment deposition in these equivalents in a dose-dependent fashion, as demonstrated by Fontana-Mason staining of histological sections of these equivalents.
JBF'-465 - S -Figure 4 is a graph quantifying the percent of inhibition of pigment deposition following BBI treatment.
Figure ~ shows F&M stained histological sections from swine skin treated with BBI and s STI. Melanin deposition in the swine skin is dramatically reduced following BBI or STI
treatment.
Figure 6 is a graph of computerized image analvsis of pigment deposition in skin sections such as those demonstrated in Figure 3. The graph quantifies the percent of i o inhibition of pigment deposition in the swine skin following BBI or STI
treatment.
Detailed Description of the Preferred Embodiments We have discovered that trypsin, tryptase and PAR-2 agonists can be used to increase pigmentation and that trvpsin inhibitors, and/or tryptase inhibitors, and/or thrombin inhibitors 1 s and PAR-2 antagonists act to decrease pigmentation in marnrnalian skin. In our opinion, some of the compounds described in U.S. Patent No. 5,23,308, which is hereby incorporated herein by reference, and behave as thrombin and/or trypsin and/or tryptase inhibitors, will be useful in methods of this invention. Some of these compounds are also described in Costanzo, et al., "Potent Thrombin Inhibitors That Probe the S,' Subsite: Tripeptide Transition State 2 o Analogues Based on a I-ieterocvcle-Activated Carborryl Group", J. Med.
Chem., 1996, old. 39, pp. 3039-3043 and have the following structural formula:
z5 A~/~ /E
(B)p 3 o wherein:
A is selected from the group consisting of C,.galkyl, carboxyC,~alkyl, C,.,alkoxycarbonylC,~alkyl, ;phenylC,.,alkyl, substituted phenylC,~alkyl (where the pherryl substituents are independently selected from one or more of, C,,~
alliyl, perfluoroC,.~allryl, ~:,,~alkoxy, hydroxy, halo, amido, vitro amino, C,~,alkylamino, C,~dialkylamino, carboxy or C,~ alkoxycarbonyl), formyl, C,~alkoxycarbonyl, C,_~all~ylcarbonyl, phenylC,~alkoxycarbonyl, C3-7cycloakylcarbotryl, pherrylcarbonyl, substituted phenylcarbonyl (where the phenyl substituents are independently selected from one or more of, C,.,alkyl, perfluoroC,.~alkyl, C,.,alkoxy, hydroxy, halo, amido, vitro, amino, C,.~alkylamino" C,~dialkylamino, carboxy or C,., alkoxycarborryl), C,_ 4alkylsulforryl, C,~alkoxysulfonyl, perffuoroC,.~alkyl-sulforryl, phenylsulfonyl, substituted 1 o phenylsulfonyl (where the phenyl substituents are independently selected from one or more of, C,~all~l, pertluoroC,.,alltyl, C,~alkoxy, hydroxy, halo, amido, vitro, amino, C,_ ,alkylamino, C,.,dialkylamino, carboxy or C,., alkoxycarbonyl), 10-camphorsulforryl, phenylC,.,a)lkysulfonyl, substituted phenylC,-,alkysulfonyl, C,~alliylsulfmyl, pertluroC,_ 4alkylsulfinyl, phenylsulfinyl, substituted phenylsulfinyl (where the phenyl substituents 15 are independently selected from one or more of, C,.~alkyl, perffuoroC,.,alkyl, C,.,alkoxy, hydroxy, halo, amido, vitro, amino, C,.,alliylamino, C,.,diallsylamino, carboxy or C,_ 4alkoxycarbonyl), phenylC,.,alkylsulfinyl, substituted pehrrylC,~alkylsulfirryl, 1-naphthylsulforryl, 2-~naphthyl.sulfonyl or substituted naphthylsulfonyi (where the naphthyl substituents are independently selected from one or more of, C,_ a o 4alkyi,perfluoroC,,~alkyi, C,.,alkoxy, hydroxy, halo, amido, vitro, amino, carboxy or C,_ ,alkoxyy-carbonyl), 1-naphthyisulfirryl, 2-naphthylsulfirryl or substituted naphthyli~ulfinyl (where the naphthyl substituents are independently selected from one or more of, C,_ ,alkyl, perffuoroC,.,alkyl, C,~alkoxy, hydroxy, halo, amido, vitro, amino, C,~alkylamino, C,~dialkylamino, carboxy or C,.~alkoxycarborryl);
a5 a D or L amino acid which is coupled as its carboxy terminus to the nitrogen depicted in formula I and is selected from the group consisting of alanine, asparagine, azetidinecarboxylic acid, glycine, N-C,$alltyg~ycine, proline, 1-amino-1-cycloC~
8alkyicarboxylic acid, thiazzolidine-4-carbo~cyfic acid, 5,5-dimethylthiazolidine-4-carboxylic acid, oxadolidine-4-carboxylic acid, pipecolinic acid, valine, methionine, _ 7 _ cysteine, serine, threonine, norleucine, leucine, tent-leucine, isoleucine, phecrylalanine, 1-naphthalanine, 2-naphthalatnine, 2-thie~lalanine, 3-thienylalanine, [1,2,3,4]-tetrahydroisoquinoline- 1-carboxylic acid and 1,2,3,4,]-tetrahydroisoquinoline-caroboxylic acid where the amino terminus of said amino acid is connected to a member selected form the group consisting of C,~,alkyl,tetrazol-5yl-Cl_Zalliyi, carboxytC,~alkyl, C,_ ,alkoxycarbony1C14alkyl, phenylC,.~alkyl, substituted phenyl Cl~ alkyl {where the pherryl substituents are independently selected from one or more of, C,~alkyl, perfluoroC,_ 4alkyl, C,.,alkoxy, hydroxy, halo, amido, vitro, amino, C,,,alkylamino, C,.~dialkylamino, to carboy or Cl~alkoxycarbo~l), 1,1-diphetrylC,~alliyl, 3-phenyl-2-hydroxypropiorryl, 2,2-diphenyl- 1-hydroxyethylcarbonyl, [1,2,3,4]-tetrahydroisoquinoline- 1-carbonyl, [1,2,3,4]-tetrahydroisoquinoline-3,carbonyl, 1-methylamino=1-cyclohexanecarborryl, 1-hydroxy-1-cyclohexanecarbanyl, l-hydroxy-1-pheny-lacetyl, 1-cyclohexyl-1-hydroxyacetyl, 3-phenyl-2-hydroxypropionyl, 3,3-diphe~l-2-hydroxypropionyl, 3-15 cyclohexyl-2-hydroxypropionyl, formyl, C,~,alkoxycarbonyl, C,_,zalkylcarbonyl, perfluoroC,~,alkyl, C,~alkylcarbonyl, phenylCl_ ~alltylcarbonl, substituted phenylC"allrylcarbonyl (where the phenyl substituents are independently selected from. one or more of, Cl.~alkyl, perfluoroCl.,alkyl, Cl.,alkoxy, hydroxy, halo amido, vitro amino, C,.,alkylamino, C,.,diallrylamino, carboxy or C,_ 2 0 4alkoxycarbonyl) l, a-diphenylC,~alkyicarbonyl, substituted 1,1-diphenylC,_ 4allrylcarbonyl (whe.re the phenyl substituents are independently selected from one or more of, C,.~alkyl, pertluoro C,,~alkyl, C,~alkoxy, hydroxy, halo, amido, vitro, amino, C,_ 4alkylamino, Cmdialkylarmna, carboxy or C,~ alkoxy-carbonyl), pertluoroC,_ 4alkysulfonyl, C,.,alkysulfonyl, C,.~alkoxysulfonyl, phenysulfonyl, substituted 25 phenylsulforryl (where the phenyl substituents are independently selected from one or more of, C-lalkyl, perfluoro C,~alkylamino, C,~dialkylarnino, carboxy or C,_ ,alkoxycarbonyl), 10-cxamphorsulfonyl, phenylC,.,alkylsulfonyl, substituted pherrylC,_ ,alkylsufonyl, pertluroC,.~alkysulfinyl, C-l4alkysulfinyl, phenyisulfinyl substituted phenysulfi~l (where the phenyl substituents are independently selected from one or _ g _ more of, C,.~allryl, perffuoro C,.,allryl, C,.~ alkoxy, hydroxy, halo, amido, vitro, amino, C,~ alkylamino, Cl., dialkylamino, carboxy or C,~ alkoxycarbonyl), 1-naphthysulfonl, 2-naphthylsulfonyl, substituted naphthylsulfonyl (where the naphthyl substituents are independently selected from one or more of, C,.,alkyl, perfluroC,.,alkyl, C,.,alkoxy, hydroxy, halo, amido, vitro, amino, C,.~alkylamino, C,.~dialliyiamino, carboy or C,_ 4alkoxycarbonyi),1-naphthysulfinyi, 2-naphthysulfuryl, and substituted naphthylsulfinyl (where the naphthyi substituents are independently selected from one or more of, C,_ 4allcyl, perfluoroC,~alkyl, C,,,alkoxy, hydroxy, halo amido, nia-o, amino, C,.,allcylamino, C104dialliylamono, carboxy or C-l4alkoxycarborryl):
or a poly peptide comprised of two amino acids, where the first amuio acid is a D or L amino acid, bound via its carboxy terminus tot he nitrogen depicted in Formula I and is selected from the group consisting of glycine, N-Cl~alkylglycine, alanine, 2-azetidinecarboxylic acid, proline, thiazolidine-4-carboxylic acid, 5.5-dimethylthiazolidine-4-carboxylic acid, oxazolidine-4-carboxylic acid, 1-amino-1-cycloC~.B alkylcarboxylic acid, 3-hydroxypropoline, 4-hydroxyproline, 3-(Cl_ 4alkoxy)proline, 4(C;,-,alkoxy)proline, 3,4-dehydroprline, 2,2-dimethyl-4-thiazolidine carboxylic acid, 2.2-dimethyl-4-oxadolidine carboxylic acid, pipecolinic acid, valine, methionine, cysteine, asparagine, serine, threonine, leucine, tert-leucine, isoleucine, phenylalanine, 1-naphthalanine, 2-naphthalanine, 2-thienylalanine, 3-thienylalnine, ao [1,2,3,4]-tetrahydroisoquinoline- 2-carboxylic acid, aspartic acid-4-C,.,alkyl ester and glutamic acid 5-C,-,alkyl ester and the second D or L amino acid, is bound to the amino terminus of said first amino acid, and is selected from the group consisting of pherrylalanine, 4-benzolypherrylalanine, 4-carboxypheirylalanine, 4-(Carboxy Cl-2alkyl)phe~lalanine, as substituted phenylalanine (where the phenyl substituents are independently selected from one or more of C,.~alkyl, perfluoroC,.~allryl, C,~alkoxy, hydroxy, halo, amido, vitro, amino, Cl.,alkylamino, C,~dialkylamino, carboxy or C,.,alkoxycarbonyl), benzothierrylalanine, 4-biphenylalanine, homophenylalanine, octahydroindole-2-_ g _ carboxylic acid, 2-pyridylalanine, 3-pyridyialanine, 4-thiazolyalanine, 2-thie~lalanie, 3-(3-benzothienyl)alanine, 3-thierrylalanine, tryptophan, tyrosine, asparagine, 3-tri-C,~alkyisilylalanine, cyclohexylglycine, dipherrylglycine, phenylglycine, methionine sulfoxide, methionine sulfone, 2,2-dicyclohexylalanine, 2-(1-naphthylalanine), 2-(2-naphthylalanine), phenyl substituted phenylalanine (where the substituents are selected from C,~alkyl, perfluoroC,~,alkyl, C,.~ alkoxy, hydroxy, halo, amido, vitro, amino, C,_ 4alkylammo, C,~,dialylamino, carboxy or C,~, alkoxycarborryl), aspartic acid, aspartic acid-4C,.~alkyi, perfluoroc,.,allryl, C,.~alkoxy, hydroxy, halo, amido, vitro, amino, C,_ 4alkylamino, C,.,dialkylamino, carboxy or C,.~alkoxycarbony), aspartic acid, aspartic 1 o acid-4-C,.~alkyl ester glutamic acid, glutamic acid-5-C,.~ alkyl ester, cycloC3-salkylaalanine, substituted cycloC~alkyialanine (where the ring substituents are carboxy, C,~ alkyl ester, cyclaC3-sallryialanine, substituted cycloC~alliylalanine (where the ring substituents are carboxy, C,~,alkylcarboxy, C,~alkoxycarbonyl or aminocarbonyl), 2,2-diphenylalanine and all alpha-C,_Salkyl of all amino acid derivatives thereof, 15 where the amino terminus of said second amino acid is unsubstituted or monosubstituted with a member of the group consisting of fornryl, Cl-12 alkyl, tetrazol-5-ylCl-2alkyl, carboxyCl-8 alkyl, carboalkoxyC,.~alkyl, pherryl C,.,alkyl, substituted phenylC;,~alkyl (where the phenyl substituents or independently selected from one or more of, C,.,alkyl, perffuoroC,.~alltyl, C,~alkoxy, hydroxy, halo, amido, 2 o vitro, amino, C,.,alkylamino, C,.,diallrylamino, carboxy or C,~alkoxycarbonyl), 1,1-dipehnylC,.~alkyl, C1-6alkoxycarbonyl, phenylCl-6alkoxycarborryl, Cl-2alkylcarbonyl, perfluoroC,.~alkylG~r4alkylcarbonyl, pherryC,~alkylcarborryl, substituted pherryC,_ 4alkylcarborryl(where the phenyl substituents are independently selected from one or more of C,.,alkyi, pertluoro C,~alkyl, C,., alkoxy, hydroxy, halo, amido, vitro, amino, C,_ 2 5 ,alltylarnino, C,-,dialkylamina, carboxy or C,~alkoxycarbonyl), 1,1-diphenylC,.,alkyl, perffuoroC,.,alkyl, C;,~alkoxycarbonyl), 10-camphorsulfonyl, pheirylC,.~alkysulfonyl, substituted phenylC;,~alliyisulfonyl, C,~,alltysulfinyl, perffuoro C,~allrylsulfinyl, phenylsulfinyl, substituted phenylsulfinyl (where the pherryl substituents are independently selected from one or more of, C,~,alkyl, perfluoroC,~allryi, C,~alkoxy, hydroxy, halo, amido, vitro, amino, C,.,alkylamono, C,-,dialliylamono, carboxy orC,.
,alkoxvcarbonyl), phenyC,~alkylsulfinyl, substituted phenylC,.,alkylsulfinyl 1-naphthylsulfonyl, 2-naphthylsulfonyl, substituted naphthylsulfonyi (where the naphthyl substituent is selected from C,_,alky-1, perfluoroC,.,alkyl, C,~alkoxy, hydroxy, halo amido, vitro, amino, C,_,alkyiamino, C,.,dialkylamino, carboxv or C,~alkoxycarbonyl), 1-haphthyl-sulfinyl, 2-haphthylsulfim~i and substituted naphthyl-sulfinyl (where the naphthyl substituer~t is selected from C,.,alkyl, perfluoroC,~alkyl, C,~alkoxy, hydmxy, halo, amido, niuo, .amino, C'.,.,alkvlamino, C-l4dialkylamino, carboxy or C,.
,alkoivcarbonyl); R., is selecred from the group consisting of hydrogen and alkyl;
to R: is selected from the group consisting of aminoC2-salkyll, guanidinoC_.salkyl, C, adlkylb .lIUdIIlOC=.5~~1Cyl,dlC,~alkVl~llaI11d1110C_.5alky~l, amldlIlOC,.ca11Sy1, Cl,~alkV_ IamidinoC,_Salkyl, diC"alley-lamidinoC= salkyl, C,.,alkoay,C,.Salkyl, phenyl, substituted phenyl (where the substituents are independently selected from one or more of amino, amidino, guanidino, C,.,allcy~iamino, C,~,dialkylamino, halogen, perfluoro C,~alkyl, C,_ 15 ,alkyl, C,., alkoxy or nivo), benryl, phenyl substituted benryl (where the substituents are independently selected from one or more of, amino, amidino, guanidino, C,_ ,allcylamino, C, ~dia(ky-lamino, halogen, perfluoro C,alkyl, C1-04a1ky1, C,..alkoxy or vitro), hydroxyC_.Salkl, C',.SalkylaminoC,.~alkyl, C, SdialkylaminoC,.Salkyl, aminocyclohe.~rylC~=alkyl and C,.salky-1;
2o pis0orl;
B is (Cli~n where n is C)-3, R, is :H or C1-Salkyl and the carbonyl moiety of B is bound to E;

E is a heterocycle selected from the group consisting of oxazolin-2-yl, oxazol-2-yl, thiazol-2-yl, thiazol-5-yl, thiazol-4-yl, thiazolin-2-yl, imidazol-2-yl, 4-oxo-2-quinoxalin-2y1, 2-pyridyl, 3-pyridyl, benxo[b}thiophen-2-yl, triazol-4-yl triazol-6-yl, pyrazol-2-yl, 4,5,6,7-tetrahydrobenzothiazol-2y1, naphtho[2,1-d]thiazol-2-yl, naphtho[1-2-d]thiazol-2-yl quinoxalin- 2-yl, isoquinolin-1-yl, isoquinolin-3-yl, benzo [b]furan-2-yl, [pyrazin-2-yl, quinazolin-2-yl, isothiazol-5-yl, isothiazol-3-yl, purin-8yu1 and a substituted heterocycle where the substituents are selected from C,~, from C-l4alky, perfluoro C,.,a$iyl,Cl, 4alkOxy, hydrOXy, halo, amldo, nlir0, am1110, Cl~all~ylam1110, C~~yd1a11tylamlll0, CarbOxy, Cl.,alkoxycarbonyl, hydroxy or pheirylC" alkylaminocarbotryl;
i o or pharmaceutically acceptable salts thereof.
More particularly, in our opinion, some of the compounds of the foregoing formula containing a d-phenylalanine-proline-arginine motif should be effective in inhibiting the PAR 2 pathway and causing depigrnentation. One particularly preferred compound which acts as a thrombin and trypsin inhibitor and is active in depigmenting mammalian shin is (S)-N-Methyl-D-pherrylalanyl-N-{4-[(aminoiminomethyl)amino]-1-(2-benzothiazolyicarborryl)butyl]-L-prolinamide (Chemical Abstracts name) (hereinafter referred to as "Compound I"). We suggest that other compounds which are analogs or function similarly to Compound I and are set forth in U.S. Patent No. 5,,523,308 may be active in the methods and compositions of this invention.
Other compounds that inhibit trypsin, such as serine protease inhibitors, and in a o particular, soybean trypsin uihibitor (ST'I) will also be useful in methods of this invention.
Soybean, limabean and blackbean extracts, and other natural products made from these beans, such as, but not limited to, bean milk, bean paste, miso and the like, also serve to reduce pigmentation by this mechanism Additional sources of serine protease inhibitors may be e~ca~acted from the species 2 5 belonging to the following plant families: Solanaceae (e.g., potato, tomato, tomatilla, and the like); Gramineae (e.g., rice, buckwheat, sorghum, wheat, barley, oats and the like); Cua~rbitaceae (e.g., cucumbers, squash, gourd, luffa and the li'ke); and, preferably, Leguminosae (e.g., beans, peas, lentils, peanuts,, and the :like).

Wh~e not w~ling to be bound by the following theory, we theorize that the compounds capable of affecting the pigmentation of the skin do so by interacting directly or indirectly with the keratinocyte P.AR-2 or with its activating protease, and thereby affect melanogenesis, directly or indirectly. Possibly, the compounds of this invention induce, in the case of increased pigmentation or reduce, in the case of decreased pigmentation, the signal to transport melanosomes by melanocytes, or to receive melanosomes by keratinocytes in the skin.
Recently we have identified that the Bowman-Birk Inhibitor ("BBI"), a different group of legume-derived proteins, are also depigmenting agents.
While STI is a 21 KD protein with primarily trypsin inhibitory activity, the 1 o soybean-derived BBI is a smaller, 8 KD protein, which inhibits chymotrypsin and trypsin.
Unl~e STI, BBI does not have a Kunitz type domain, su~esting different interactions with serine proteases. BBI i,4 known for its ability to prevent carcinogenesis in nurr~erous in ~ and »z vitro models. In some animal carcinogenesis models BBI was found to have strong anti-inflammatory effects. BBI is more resistant than STI to heat-denaturation.
1 s For a review on BBI see Kennedy AR, Chemopreventive agents: protease inhibitors, Phannacol Ther 78: 3,167-209, Jun,1998.
The compounds which are active in the compositions and methods of this invention may be delivered topically by arty means known to those of skill in the art.
If the delivery parameters of the topically active pharmaceutical or cosmetic agent so require, the topically a o active composition of this invention may preferably be further composed of a phaemaceutically or cosmetically acceptable vehicle capable of functioning as a delivery system to enable the penetration of the topically active agent into the skin.
One acceptable vehicle for topical delivery of some of the compositions of this invention, particularly proteins such as trypsin and STI, may contain liposomes. The 25 liposomes are more preferably non-ionic and contain a) glycerol d~aurate (preferably in an amount of between about 5W° and about 70% by weight); b) compounds having the steroid backbone found in cholesterol (preferably in an amount of between about 5°~ and about 45% by weight); and c) one or more fatty acid ethers having from about 12 to about 18 carbon atoms (preferably in an amount of between about 5% and about 70%
byweight collectively), wherein the constituent compounds of the liposomes are preferably in a ratio of about 37.5:12.5:33.:3:16.7. Liposomes comprised of glycerol dilaurate /
cholesterol/
polyoxyethylene -10-stearyl ether/polyoxyethylene-9-lauryl ether (GDL
liposomes) are most preferred. Preferably the liposomes are present in an amount, based upon the total volume of the composition, of from about 10 mg/mL to about 100 mg/mL, and more preferably from about 20 mg/mL to about 50 mg/mL. A ratio of about 37.5:12.5:33.3:16.7 is most preferred. Suitable liposomes may preferably be prepared in accordance with the protocol set forth in Example 1, though other methods commonly used in the art are also acceptable.
The above described composition may be prepared by combining the desired 1 o components in a suitable container and mixing them under ambient conditions in arty conventional high shear mixing means well known in the art for non-ionic liposomes preparations, such as those disclosed in Niemiec et al., "Influence of Nonionic Liposomal Composition On Topical Delivery of Peptide Drugs Into Pilosebacious Units: An In Vivo Study Using the Hamster Ear Model," 12 Pharm. Res. 1184-88 (1995) ("Niemiec"), which is i5 incorporated by reference herein in its entirety. We have found that the presence of these liposomes in the compositions of this invention may enhance the depigmenting capabilities of some of the compositions of this invention.
Other preferable forrtu~lations may contain, for example, soybean milk or other liquid formulations derived directly from legumes or other suitable plant. For example, such a a o formulation may contain a large proportion of soybean milk, an emulsifier that maintains the physical stability of the soybean milk, and, optionally a chelating agent, preservatives, emollients, hucnectants and/or thickeners or gelling agents.
Oil-in water emulsions, water-in-oil emulsions, solvent-based formulations and aqueous gels known to those of skill in the art may also be utilized as vehicles for the delivery of the a 5 compositions of this invention.
Tl~e source of active compound to be formulated w~l generally depend upon the particular form of the compound. Small organic molecules and peptidyl fragments can be chemically synthesized and provided in a pure form suitable for pharrnaceutical/cosmetic usage.
JBF?-465 Products of natural extracts can be purified according to techniques known in the art.
Recombinant source's of compounds are also available to those of ordinary skill in the art.
In alternative embodiments, the topically active pharmaceutical or cosmetic composition may be optionally combined with other ingredients such as moisturizers, s cosmetic adjuvants, anti-oxidants, bleaching agents, tyrosinase inhibitors and other known depigrnentation agents, surfactants, foaming agents, conditioners, humectants, fragrances, viscosifiers, buffering agents, preservatives, sunscreens and the like. The compositions of this invention may ;also contain active amounts of retinoids (i.e., compounds that bind to any members of the family of retinoid receptors), including, for example, tretinoin, retinol, esters of tretinoin and/or retinol and the like.
The topically active pharmaceutical or cosmetic composition should be applied in an amount effective to affect changes in the pigmentation of mam~r~alian skin. As used herein "amount effective" shall mean an amount sufficient to cover the region of skin surface where a change in pigmentation is desired. Preferably, the composition is liberally applied to 1 s the skin surface such that, based upon a square cm of skin surface, from about 2 pl /cm2 to about 200 E.~.1 /cm2 of topically active agent is present when a change in pigmentation is desired. When using a thrombin and trypsin inhibitor such as Compound I or its analogs, whether synthetically- or naturally-derived in a formulation, such an active compound should be present in the amount of from about 0.0001% to about 15% byweight/volume of the a o composition. More preferably, it should be present in an amount from about 0.0005% to about 5% of the composition; most preferably, it should be present in an amount of from about 0.001 to about 1% of the composition. Of course, these ranges are suggested for the foregoing components. The lower set of ranges is intended to be efficacious for PAR-2 pathway agonists/antagonists and/or inhibitors having high therapeutic indices and which 25 do not require significantlylarger concentrations or doses to be effective in the methods of this invention. Such compounds may be synthetically or naturally-derived.
Liquid derivatives and natural extracts made directly from plants or botanical sources may be employed in the compositions of this invention in a concentration (w/v) from about 1 to about 99%. Fractions of natural ezctracts and naturally-derived protease inhibitors such as STI may have a different preferred range, from about 0.01% to about 20%
and, more preferably, from about 1% to about 10% of the composition. Of course, mixtures of the active agents of this invention may be combined and used together in the same formulation, or in serial applications of different formulations.
We have unexpectedly found that when topically active agents, such as PAR-2 agonists and/or inhibitors and trypsin and/or thrombin and/or tryptase and/or their inhibitors, are topically applied to an animal's skin, a significant change in pigmentation was achieved. Preferably, depigmenting agents (as well as other pigmentation-affecting agents of 1 o this invention) are applied to the skin of a mammal at a relatively high concentration and dose (from about 0.005% to about 1% for compounds having high therapeutic indices such as Compound I and related compounds; from about 20% to about 99% for liquid derivatives and extracts of batanical materials; and from about 1% to about 20% for fractions of natural extracts and naturally-derived protease inhibitors such as STI or mixtures i 5 thereof) between one and two times daily for a period of time until the skin evidences a change in pigmentation. This may be for from about four to about ten weeks or more.
Thereafter, once the change in pigmentation has been achieved, a lower concentration and dose (from about 0.,00001% to about 0.005% for compounds having high therapeutic indices such as Compound I and related compounds; from about 10% to about 90%
for 20 liquid derivatives and extracta of botanical materials; and from about 0.01% to about 5% for fractions of natural extracts and naturally-derived protease inhibitors such as STI or mixtures thereof), of active ingredient may be applied on a less frequent time schedule, e.g., about once per day to abaut twice ;per week. The effects of the active agents of this invention are reversible, therefore, in order to maintain these effects, continuous application or 2 5 administration should be performed. The invention illustratively disclosed herein suitably may be practiced in the absence of any component, ingredient, or step which is not specifically disclosed herein.
The invention illustratively disclosed herein suitably may be practiced in the absence of arty component, ingredient, ar step which is not specifically disclosed herein. Several examples are set forth below to further illustrate the nature of the invention and the manner of carrying it out, but do not serve to limit the scope of the methods and compositions of this invention.
Example 1: BBI Affects Pigmentation In order to study the possible roles of BBI in pigmentation, an in zido epidermal s equivalent system containing melanocytes was used. The epidermal equivalent system used in this study is the MelanoDerm mel-300 system, available commercially from MatTek Co. of Ashland, MA. This system contains human normal melanocytes, together with normal, human-derived epidermal keratinorytes, derived from African-American foreskin. These cells have been cultured to form a mufti-layered, highly differentiated model of the human epidermis. In to the following examples, equivalents were treated with BBI (0.1%) for three days and samples were harvested on the fourth day after beginning of treatment. The harvested equivalents were first compared for their color without staining, following by histolog~cal examination with Fontana-Mason (F8~ staining, a stain known to those of skill in the art. F&M
staining is a silver staining technique that clearly and cleanly marks mdanins which have higf r silver nitrate 1 s reducing activity. Images of the stained sections were also captured for image analysis. At least three sections per equivalent, three equivalents per experiment were processed. Empire Irnages database 1.1 was used on a Gateway 2000 P5-100 computer (Media Cybernetics, Silver Springs, MD) for capturing images. Image Pro Plus version 3.0 was used for image analysis. Parameters measured were the surface area of silver deposits within melanocytes and the density luminosity a o of each pixel. A "pigmentation factor" was defined as the surface area of silver deposits divided by the total epidernaal surface area. A value of one (100%) was assigned to untreated controls, and values of treatment groups were norn>alized to their relevant controls.
As shown in Figure 1, unueated mel-300 equivalents are visibly dark without any 2 s staining. BBI treated equivalents were lighter than these controls, demonstrating the ability of BBI to visually reduce pigmentation. Figure 2 shows the histological sections of these equivalents, following F&M staining. In this Figure, black areas represent melanin deposits within both melanocytes and keratinocytes. As shown in Figure 2, BBI treatment results in reduced melanin deposition both in the rrrelanocytes and in the kerxtinocytes of the treated equivalents. Image analysis revealed that BBI treated equivalents have only 50.6% melanin deposits relative to controls.
Example 2: The depigmenting effect of BBI is dose-responsive.
Epidermal .equivalents containing melanocytes as described in example 1 were treated with increasing concentrations of BBI, from 0.001% to 0.1%. Following the same experimental procedure described in example 1, the depigmenting effect of BBI
was found to be dose-dependent. Figure 3 shows F&M stained sections of the treated equivalents, demonstrating the dose-response and the depigmenting effect of as low as l0 0.001% BBI. Computerizxd image analysis, shown in figure 4, quantifies this effect and further demonstrates its dose-responsive nature.
Example 3: In vivo demonstration of the depigmenting effect of BBI
A dark skin Yucatan microswine was treated with BBI, or STI, 1%, in PBS, with 1 s 20/mg/ml liposomes. Non-ionic liposomes preparations, such as those disclosed in Nianiec et al., "Influence of Nonionic Liposomal Composition Crn Topical Delivery of Peptide Drugs Into Pilosebacious Units: An In Vivo Study Using the Hamster Ear Model," 12 Phann. Res.
1184-88 (1995) ("Niemiec")" which is incorporated by reference herein in its entirety, are well known in the art, and are described in JBP-430. We have found that the presence of these a o liposomes in the compositions of this invention may enhance the depigmenting capabilities of some of the compositions of this invention. GDL liposomes were prepared as set forth in Niemiec, et al., above, with she exception of the following changes: the non-ionic liposomal formulation contained glycerol dilaurate (Emulsynt GDL, ISP Van Dyk)/cholesterol (Croda)/polyoxyethylene-10-stearyi ether (Brij76, ICI)/polyoxyethylene-9-laurylether, as at 25 ratio of 37.5:12.5:3:f.3:16.7. Hepes buffer, 0.05M, pH 7.4 (Gibco-BRL of Gaithersburg, MD) was used as the aqueous phase in the preparation of the liposomes.
JHF~-465 The BBI, STI and liposome vehicle preparations were applied each onto two sites of the swine's flank, twice daily, five days per week, for eigk~t weeks. After eight weeks of treatment, the appli<:ation of either BBI or STI resulted in a visible lightening effect.
I-hstological analysis of F&M stained skin sections from untreated and treated sites confirmed this observation. Figure 5 shows the F&M stained skin sections of the treated swine, demonstrating a dramatic reduction in pigment deposition in sites ueated with BBI
or STI. Computerized image analysis, shown in figure 6, quantifies this effect and further demonstrates the depigmenting effect of BBI.
JBl?-465

Claims (27)

1. A method of effecting changes in mammalian skin pigmentation comprising administering to a matrunal a pigmentation-changing effective amount of a Bowman-Birk Inhibitor or of a natural extract containing a Bowman-Birk Inhibitor.

2. A method of depigmenting mammalian skin pigmentation comprising administering to a mammal a pigmentation-lightening effective amount of a Bowman-Birk Inhibitor or of a natural extract containing a Bowman-Birk Inhibitor.

3. A method according to claim 2 wherein said Bowman-Birk Inhibitor is derived from one or more of the botanical families leguminosae, solanaceae, gramineae and cucurbitaceae.

4. A method according to claim 3 wherein said compound is derived from legumes.

5. A method according to claim 4 wherein said compound is derived from undenatured soybean extract:

6. A method according to claim 5 wherein said compound is derived from fractions of undenatured soybean extract.

7. A composition for affecting changes in mammalian skin pigmentation comprising a pigmentation-changing effective amount of a Bowman-Birk Inhibitor or of a natural extract containing a Bowman-Birk Inhibitor.

8. A composition for depigmenting mammalian skin pigmentation comprising administering to a mammal a pigmentation-lightening effective amount of a Bowman-Birk Inhibitor or of a natural extract containing a Bowman-Birk Inhibitor.

9. A composition according to claim 8 wherein said Bowman-Birk Inhibitor is derived from one or more of the botanical families leguminosae, solanaceae, grunineae and cucurbitaceae.

10. A composition according to claim 9 wherein said compound is derived from legumes.

11. A composition according to claim 10 wherein said compound is derived from undenatured soybean extract.

12. A composition according to claim 11 wherein said compound is derived from fractions of undenatured soybean extract.

13. A composition according to claim 7 wherein said Bowman-Birk Inhibitor is present in an amount of from about 0.0001% to about 20% by weight/volume of said composition.

14. A composition according to claim 13 wherein said compound is present in an amount from about 0.001 to about 15% of said composition.

15. A composition according to claim 14 wherein said compound is present in an amount from about 0.005 to about 1% of said composition.

16. A method according to claim 1 wherein said composition is applied at least once daily for at least eight weeks.

17. A method according to claim 16 wherein said composition is applied at a relatively high dosage for at least about four to about ten weeks and then applied at a relatively lower dosage on a continuous basis to maintain skin lightening effect.

18. A method according to claim 1 wherein said composition is administered orally.

19. A method according to claim 1 wherein said composition is administered parenterally.

20. A cosmetic composition according to claim 7 comprising said pigmentation-affecting compound and a cosmetically-acceptable vehicle.

21. A composition according to claim 20 wherein said composition further comprises additional depigmenting agents.

22. A composition according to claim 21 wherein said composition further comprises tyrosinase inhibitors.

23. A composition according to claim 20 wherein said composition further comprises liposomes.

24. A composition according to claim 23 wherein said composition comprises glycerol dilaurate, cholesterol, polyoxyethylene-10-stearyl ether and polyoxyethylene-9-lauryl ether.

25. A composition according to claim 20 wherein said composition further comprises anti-oxidants.

26. A composition according to claim 20 wherein said composition further comprises a sunscreen.

27. A composition according to claim 20 wherein said composition further comprises a compound selected from the group consisting of anti-oxidants, sunscreens, moisturizers, bleaching agents, depigmentation agents, surfactants, foaming agents, conditioners, humectants, fragrances, viscosifiers, buffering agents, preservatives and a mixture thereof.