Use of delta opioid receptor agonists in the field of cosmetics and dermocosmetics.

专利摘要:
The present invention relates to the use of an ROD ligand for the stimulation of pigmentation in a cosmetic composition and the use of rubiscoline 6 or its derivatives in a cosmetic composition.
公开号:CH706322B1
申请号:CH00651/13
申请日:2013-03-21
公开日:2017-08-31
发明作者:Auriol Daniel；Lefevre Fabrice；Schweikert Kuno；Redziniak Gérard
申请人:Induchem Holding Ag；
IPC主号:

专利说明:

Description
Field of the Invention [0001] The present invention relates to the field of cosmetics and dermocosmetics.
PRIOR ART [0002] The opioid receptors are part of the G protein-coupled receptor superfamily (GPCR) which comprises seven transmembrane domains. After activation by their respective ligands outside the cell, GPCRs release G proteins in activated form into the cytoplasm, which in turn activates several target proteins in the cell such as adenylate cyclase.
The most known opioid receptors are the mu (ROM) receptors, for which morphine is the ligand. Two other families of opioid receptors have been described in addition to mu receptors: delta and kappa receptors.
[0004] Opioid receptors are known to be involved in controlling the sensation of pain.
However, recent studies have shown that the deletion of mu and kappa opioid receptors in mice modifies epidermal hypertrophy, the density of peripheral nerve endings and the itching behavior (Bigliardi et al., 2007). Therefore, these receptors have been considered to be related not only to the pain and itch sensation, but also to the control of skin differentiation.
In the same approach, scientific studies have demonstrated that the deletion of ROD (delta opioid receptors) in mice leads to the formation of an abnormal thin epidermis. These results have suggested a key role of RODs in skin differentiation, proliferation and migration, factors that are important for healing (Bigliardi et al., 2006).
[0007] The skin and the brain share the same embryological origin during the development of the human embryo. Scientists have demonstrated that opioid receptors have been found on the surface of both neurons and skin cells (Bigliardi et al., 2009), showing that opioid receptors are not only localized in the nervous system but also in other organs like the skin. This discovery opened the door to explain why the deletion of opioid receptors could interact with a correct development of the skin.
Many chemical compounds are known to interact with opioid receptors: exogenous compounds such as opioids, or endogenous compounds such as enkephalins and endorphins. Some food-derived peptides have also been described as acting on opioid receptors. For example, small peptides from the digestion of the RubisCo protein, in particular rubiscolin 5 and rubiscolin 6 have been shown to be ROD ligands, but not ROMs (Yang et al., 2001; Yang et al. ., 2003). As these peptides are the result of digestive enzymes, it was considered that they could be involved in a neuro-calming action after digestion in our intestines. In addition, it has been shown that rubiscolin 6, when administered orally, enhances memory consolidation. However, because of their digestive origin, no one has imagined using such peptides for any kind of topical applications.
[0009] While opioid receptors appear to be interesting targets for regulating skin differentiation, so far no one has ever tried to act on these receptors with agonists or antagonists to control the evolution of the skin. or hair, such as the reversal of signs of aging or the modulation of pigmentation. The main reasons for this are as follows: • Opioid receptors are considered by scientists as pharmacological targets solely dedicated to pain control (for example for the screening and design of new pain-relieving molecules). As a result, individuals in the skin care industry will avoid acting on such a category of cellular targets for fear of reverse side effects. • The action on these receptors in the skin will only be considered as a means to control itching, pain sensations and neuroinflammation in therapeutic indications. • There is no clear link between delta opioid receptors and the process of pigmentation of the skin or hair: the use of delta opioids or opioid-like drugs has never been recognized as a way to change the color of the skin or hair. • There is no clear link between opioid receptors and the normalization of skin metabolism: although opioid receptor deletion leads to abnormal skin in mice, no one has ever demonstrated that opioid receptor action could reverse this phenotype. Especially since there is no evidence that the use of opioids such as morphine could reverse the signs of aging and erase wrinkles on human skin.
There is only one document, WO 2009/012 376, suggesting the use of delta opioid receptor agonists in a cosmetic composition, in particular as an anti-aging component for the skin. The experimental section consists of a test with deltorphine, an endogenous component that crosses the blood-brain barrier (BBB). Therefore, because of the endogenous nature of deltorphin and its ability to cross the BBB, the use of agonists may be associated with adverse side effects. SUMMARY OF THE INVENTION [0011] In a first aspect of the invention, the inventors have surprisingly discovered that delta opioid receptor agonists (ROD agonists) activate pigmentation. Therefore, the present invention relates to the cosmetic use of an ROD ligand, preferably an ROD agonist, for the stimulation of skin and hair pigmentation, in particular for the preparation of a cosmetic composition for an topical, intradermal, transdermal or subcutaneous administration, preferably for topical administration, for stimulating pigmentation of the skin of the hair. The present invention may also be used in a hair care product such as a shampoo or conditioner comprising a ROD ligand, preferably a ROD agonist. It further relates to an ROD ligand, preferably an ROD agonist for use in stimulating pigmentation of the skin or hair. Preferably, the ROD agonist is selective for RODs. Preferably, the ROD agonist is selected from the group consisting of BU-48, SNC-80, C-8813, DPI-287, DPI-221, TAN-67, BW373U86, SIOM, RWJ-394,674, rubiscoline 6. and its derivatives possessing δ opioid receptor agonist activity, deltorphin and its derivatives possessing opioid receptor agonist activity δ, DPDPE, DSLET, JOM-13, DSTBULET, BUBU, and BUBUC. More preferably, the ROD agonist is a peptide selected from rubiscolin 6 and its derivatives having δ opioid receptor agonist activity. Even more preferably, the opioid receptor agonist δ is a peptide which has or comprises the sequence of formula (I) YP-X1-D-X2-X3 (I) (SEQ ID No. 6) in which X1 represents a non-aromatic hydrophobic amino acid, preferably selected from the group consisting of L, I, Μ, V and A, more preferably selected from the group consisting of L, I, and M; Wherein X2 is a non-aromatic hydrophobic amino acid, preferably selected from the group consisting of L, I, and M, more preferably selected from the group consisting of L and I; and X3, present or absent, representing a hydrophobic amino acid, preferably selected from the group consisting of F, L, I, Μ, V and A, more preferably selected from the group consisting of F, I, and V, and in particular representing F or V.
In particular, the opioid receptor agonist δ is a peptide selected from the group consisting of or a peptide having an opioid receptor agonist activity δ and comprising a sequence selected from the group consisting of YPLDLF (SEQ ID No 1), YPIDLF (SEQ ID NO: 7), YPMDLF (SEQ ID NO: 8), YPLDIF (SEQ ID NO: 9), YPLDLL (SEQ ID NO: 10), YPLDLI (SEQ ID NO: 11), YPLDLM (SEQ ID NO: 12) , YPLDLV (SEQ ID NO: 13), YPLDLA (SEQ ID NO: 14), YPIDLV (SEQ ID NO: 15), YPMDLV (SEQ ID NO: 16), YPLDIV (SEQ ID NO: 17), YPIDIV (SEQ ID NO: 18), YPMDIV (SEQ ID NO: 19), YPIDLV (SEQ ID NO: 20), YPIDMV (SEQ ID NO: 21), YPIDII (SEQ ID NO: 22), YPMDII (SEQ ID NO: 23), YPMDL (SEQ ID NO: 24), YPIDL (SEQ ID NO. ID No. 25), and YPMDI (SEQ ID No. 26). Even more preferably, the peptide is YPLDLF.
In a second aspect, the invention may be used in a cosmetic composition for topical, intradermal, transdermal or subcutaneous administration, preferably for topical administration, comprising a peptide agonist ligand of opioid receptors δ selected from the group consisting of rubiscoline 6 and its derivatives and at least one cosmetic additive. It also relates to the use of rubiscolin 6 and its derivatives for the preparation of a cosmetic composition for topical, intradermal, transdermal or subcutaneous administration, preferably for topical administration. It further relates to a peptide selected from rubiscolin 6 and its derivatives for use in the preparation of a cosmetic composition for topical, intradermal, transdermal or subcutaneous administration, preferably for topical administration. It relates to a peptide selected from rubiscoline 6 and its derivatives for use as a cosmetic agent. Preferably, the cosmetic composition is intended for preventing and / or reversing the signs of aging of the skin and / or for filling wrinkles, for improving the smoothness of the skin, and / or for equalization of unbalanced markers of stressed skin, and / or normalization of disrupted gene expression in skin cells, and / or erasure of crow's feet wrinkles, and / or recovering the hydration of the skin, and / or preventing the trans-epidermal loss of water from the skin, and / or reactivating the differentiation of skin cells, and / or stimulating pigmentation of the skin or hair.
Preferably, the δ-opioid receptor peptide agonist ligand is a peptide which has or comprises the sequence of formula (I) YP-X1-D-X2-X3 (I) (SEQ ID No. 6) in which X1 represents a non-aromatic hydrophobic amino acid, preferably selected from the group consisting of L, I, Μ, V and A, more preferably selected from the group consisting of L, I, and M; Wherein X2 is a non-aromatic hydrophobic amino acid, preferably selected from the group consisting of L, I, and M, more preferably selected from the group consisting of L and I; and X3, present or absent, representing a hydrophobic amino acid, preferably selected from the group consisting of F, L, I, Μ, V and A, more preferably selected from the group consisting of F, I, and V, and in particular representing F or V.
More preferably, the peptide is a peptide selected from the group consisting of or a peptide having an opioid receptor agonist activity δ and comprising a sequence selected from the group consisting of YPLDLF (SEQ ID No. 1), YPIDLF (SEQ ID NO: 7), YPMDLF (SEQ ID NO: 8), YPLDIF (SEQ ID NO: 9), YPLDLL (SEQ ID NO: 10), YPLDLI (SEQ ID NO: 11), YPLDLM (SEQ ID NO: 12), YPLDLV ( SEQ ID No. 13), YPLDLA (SEQ ID No. 14), YPIDLV (SEQ ID No. 15), YPMDLV (SEQ ID No. 16), YPLDIV (SEQ ID No. 17), YPIDIV (SEQ ID No. 18), YPMDIV (SEQ ID No. 19), YPIDLV (SEQ ID NO: 20), YPIDMV (SEQ ID NO: 21), YPIDII (SEQ ID NO: 22), YPMDII (SEQ ID NO: 23), YPMDL (SEQ ID NO: 24), YPIDL (SEQ ID NO: 25). ), and YPMDI (SEQ ID No. 26). Even more preferably, the peptide is YPLDLF.
In a further aspect, the present invention may provide a device comprising an δ-opioid receptor peptide agonist ligand chosen from rubiscolin 6 and its derivatives, the device being capable of delivering said peptide via an intra injection. -epidermal and / or intradermal and / or subcutaneous.
Brief description of the drawings [0017]
Fig. 1: Agonist effect of the compound at the level of the Delta2 receptor (ROD). Fig. 1A with the DPDPE, EC50 = 5.9 10-1 ° M, A = 0.0, D = 95.8. Fig. 1B with protein fractions hydrolyzed with pepsin 02.01 PEPS, EC50 = 0.87% (v / v), A = 0.0, D = 100.0. Fig. 1C with YPLDLF, EC50 = 3.9 KT6M, A = -8.3, D = 100.0.
Fig. 2: Effect of cytokines on the level of expression of ROD in the epidermis. Fig. 2A: Normal human skin - epidermis and dermis; Fig. 2B: Normal human skin-dermis and sebaceous glands; Fig. 2C: reconstructed human epidermis (EHR); Fig. 2D: EHR treated with PMA at 2 μg; Fig. 2E: EHR treated with a mixture of cytokines (IL-17 + OSM + TNF-a).
Fig. 3: fig. 3A: Melanin formation in human skin explants irradiated with UVA or treated with the peptide for 6 days. Melanin: dark brown spots on the images. Fig. 3B: Quantification of melanin in basal layer keratinocytes from human skin explants irradiated with UVA or treated with peptide solutions for 6 days (* p <0.01 versus untreated control, Student's t test) , fig. 3C: Quantification of melanosomes in melanocytes from human skin explants irradiated with UVA or treated with peptide solutions for 6 days.
Fig. 4: fig. 4A: mean percent change as a function of TO obtained for the transepidermal water loss parameter; Fig. 4B: average percentage changes as a function of TO obtained for the skin hydration parameter; Fig. 4C: average of percentage changes as a function of TO obtained for the wrinkle depth parameter; Fig. 4D: average of the percentage changes as a function of TO obtained for the parameter Rz (importance of the wrinkles of the skin). In dark gray, PHN and light gray, PHG.
DETAILED DESCRIPTION OF THE INVENTION [0018] The inventors have surprisingly discovered that it is possible to act on the delta opioid receptors and reverse the aging process and have positive effects on the skin or the hair, such as a reversal of the signs. aging, recovery of the smoothness of the skin, activation of melanin production, filling of deep wrinkles, increase of the natural hydration of the skin. Even more surprisingly, they have discovered that peptides produced by the digestion of plant proteins have this ability to regulate the skin differentiation processes. In addition, they surprisingly discovered that one can act on the delta opioid receptors and stimulate the pigmentation of the skin and hair. 1. Peptides and hydrolysates of plants can act on delta opioid receptors.
The inventors have discovered for the first time the ability of several peptides and plant protein hydrolysates to act as agonists or antagonists of ROD (delta opioid receptors). A hexapeptide YPLDLF (SEQ ID No. 1) gave excellent results as an agonist with an EC50 = 3.9 μΜ. The inventors have demonstrated that either a pure peptide or a plant protein hydrolyzate can bind and activate the RODs. 2. Under conditions of simulated aging, opioid receptors are less expressed in the skin. ROD agonist peptides can reverse this phenomenon.
In the skin, the aging process is closely associated with an increase in the level of micro-inflammation in the skin (Giacomoni et al., 2005), due to an accumulation of external aggression (repeated mechanical stresses, rays). UV, pollutants), and the inability of skin cells to cope with these aggressions (lower detoxification activity, lower cell energy rate, lower cell regeneration). This so-called "inflamm-age" process generates retroactive responses that lead to visible signs of aging: wrinkles, loss of tone, dark circles, sagging, fine lines, and the like.
The inventors simulated aging conditions on reconstructed human epidermis (EHR) with a mixture of cytokines. They discovered that under these conditions of "aging", the level of expression of delta opioid receptors is reduced. As it is known from the literature that opioid receptors control skin differentiation processes and generate a thin skin phenotype, they discovered one of the causes of aging: the lower expression of opioid delta receptors due to cytokines lead to a weaker skin differentiation.
The inventors applied the peptide on the EHR at different doses and they discovered that the peptide YPLDLF can reactivate the expression of delta opioid receptors in the skin. As a result, they discovered that this peptide can penetrate the skin and reverse the aging process due to cytokines. 3. ROD agonist peptides can act on delta opioid receptors and lead to the regulation of several deregulated genetic factors in aged skin.
In order to better understand the effect of peptides on delta opioid receptors, the inventors measured the expression rate of 64 human genes on reconstructed human epidermis. These epidermals were treated either with nothing, or with a mixture of cytokines to simulate the aging process, or with the mixture of cytokines plus different amounts of peptides. The inventors have discovered that, in the presence of cytokines, the majority of the genes have been deregulated compared to the control condition: they have been either overexpressed or under-expressed. Under the conditions with the peptide, almost all the genes were brought back to a normal level of expression. Therefore, the inventors have discovered that ROD agonist peptides can act on delta opioid receptors and equalize the adverse effects of aging conditions. 4. ROD agonist peptides act on delta opioid receptors and lead to the regulation of several deregulated protein factors in aged skin. The inventors performed the same experiment as for the genes, but they measured the level of expression of key proteins, which are known to be involved in the differentiation of the skin. They found that, under cytokine-induced conditions, these proteins were deregulated (overexpressed or under-expressed). However, the epidermis treated with the peptides recovered a normal level of expression of these protein markers. The inventors have discovered that the ROD agonist peptides can balance and regulate the level of expression of differentiation markers in aged skin. 5. ROD agonists act on delta opioid receptors and lead to the activation of pigmentation by melanin.
Because the production of melanin is controlled by a G protein-coupled receptor (the MC1 receptor), the inventors had the idea to test the effect of ROD agonists previously tested on human skin explants to see what effect they could have on the pigmentation of the skin. After a few days of incubating these skin explants with the molecules, without any UV radiation, they discovered that the skin explants started to produce melanin and melanosomes in their melanocytes. The inventors have discovered that ROD agonists can stimulate the production of pigments in the skin. This result is very surprising because the μ (ROM) receptor is the receptor associated with pigmentation (Kauser et al., 2004). 6. ROD agonist peptides act on opioid receptors and lead to regeneration of the skin.
The inventors have tested a cream containing the ROD agonist peptide previously tested on human volunteers in a double blind clinical trial against a placebo. After several days of use, they found that the skin of volunteers was significantly improved in terms of hydration, reduction of transepidermal water loss, smoothness and reduction of wrinkle depth. The inventors have discovered that the use of ROD agonist peptides that act on opioid receptors can have clinical effects against placebo and can reverse the signs of aging on human skin.
Therefore, the present invention relates to the use of ROD agonists that act on delta opioid receptors in cosmetic and dermocosmetic applications to - prevent and reverse the signs of aging; and / or, - fill wrinkles (anti-aging products for normal or mature skin); and / or, - improve the smoothness of the skin (products for the body and the face); and / or, - equalize unbalanced markers in stressed skin; and / or, - normalize disrupted gene expression in skin cells; and / or, - erase wrinkles in the shape of crow's feet (products for the eye contour); and / or, - recover the hydration of the skin; and / or, - prevent the loss of trans-epidermal water in the skin and therefore prevent dehydration of the skin; and / or, - reactivate the differentiation of skin cells; and / or, - stimulate pigmentation (self-tanning, hair repigmentation, presolar products, hair care); and / or - act synergistically on the G-protein coupled pathways in the skin cells.
A first aspect of the present invention relates to the use of an ROD ligand to stimulate pigmentation of the skin and / or hair. It also relates to a cosmetic process for stimulating the pigmentation of the skin or hair, comprising the application to the human skin and / or the hair of a composition comprising an ROD ligand. In particular, the skin is the skin of the body and / or face. In a more specific aspect, the present invention relates to a hair care product comprising an ROD ligand. In this context, the ROD ligand is the active agent. In one particular aspect, he may be the only active agent. Alternatively, it can be combined with additional active agents. Non-exhaustive examples of such additional active agents include precursors for melanin synthesis, tyrosinase expression enhancers, and hair bulb strengthening active compounds. The ligand of the RODs may be an ROD agonist or an ROD antagonist. In a preferred embodiment, the ROD ligand is an ROD agonist.
In particular, the present invention relates to the use of an ROD agonist for the preparation of a cosmetic composition for self-tanning, pigmentation or repigmentation of hair, pre-solar or solar products, a hair care product such as a shampoo or a conditioner, or a cosmetic composition comprising an ROD agonist for self-tanning, hair pigmentation or repigmentation, pre-sun or sun products, a care product for hair like a shampoo or conditioner. The composition is for topical, intradermal, transdermal or subcutaneous application. More preferably, the composition is for topical administration, particularly to the skin or hair. The cosmetic composition may comprise at least one cosmetic additive. In one particular aspect, he may be the only active agent. Alternatively, it can be combined with additional active agents, for example as detailed above.
The ROD agonist may be a peptide or a non-peptide molecule. For example and non-exhaustively, it may be chosen from the group consisting of rubiscolin 6 and its derivatives, deltorphin and its derivatives, Leu-enkephalin, Met-enkephalin, DPDPE (D-Penicillamine (2.5 ) - enkephalin) and its derivatives, DSLET, labiphalin, JOM-13, DTLET, DSTBULET, BUBU, BUBUC and non-peptide agonists such as BU-48, BW373U86, C-8813, 7-spiroindanyloxymorphone (SIOM), N phenethyl-14-ethoxymetopone, ADL-5859, SNC-40, SNC-80, SNC-86, SNC-162, DPI-221, DPI-287, DPI 3290, TAN-67, RWJ-394,674, and norbuprenorphine.
In a preferred embodiment, the ROD agonist is selective for delta opioid receptors. Selectively, it is meant that the ROD agonist exhibits a lower IC50 for delta receptors than mu or kappa receptors. In particular, the ratio of IC50 for mu / kappa receptors by IC 50 for delta receptors is greater than 1, preferably greater than 10, even more preferably greater than 30. Selective ROD agonist can be a peptide agonist or a non-peptide agonist. For example, it may be selected from the group consisting of BU-48, SNC-80, C-8813, DPI-287, DPI-221, TAN-67, BW373U86, SIOM, RWJ-394,674, rubiscolin 6 and its derivatives. , deltorphin and its derivatives, DPDPE, DSLET, JOM-13, DSTBULET, BUBU, and BUBUC.
The peptide sequences defined in this document use the one-letter code as follows: A: Ala (alanine); R: Arg (arginine); N: Asn (asparagine); D: Asp (aspartic acid); C: Cys (cysteine); Q: Gin (glutamine); E: Glu (glutamic acid); G: Gly (glycine); H: His (histidine); I: Ile (isoleucine); L: Leu (leucine); K: Lily (lysine); M: Met (methionine); F: Phe (phenylalanine); P: Pro (proline); S: Ser (serine); T: Thr (threonine); W: Trp (tryptophan); Y: Tyr (tyrosine); V: Val (valine).
By "derivatives" is meant in this document a peptide with substitutions, deletions or additions of 1,2,3,4 or 5 amino acids and / or a peptide with modifications as detailed herein. below, but which retains the agonist activity of the RODs or which has an agonist activity of the RODs. Preferably, the substitutions are conservative, which means that the residue is substituted by an amino acid of the same physicochemical group. Physicochemical groups are generally defined as follows: non-polar or hydrophobic amino acids including A, V, I, L, RF, M, and W, but more narrowly, non-aromatic hydrophobic amino acids such as including A , V, I, L, P, and M; the unfilled polar group comprising G, S, T, C, Y, N and Q; the negatively charged polar group comprising E and D; and the positively charged polar group comprising R and K. Alternatively, the substitution may also be non-conservative. The derivative may also include naturally occurring non-naturally occurring amino acids such as azetidinecarboxylic acid, 2-aminoadipic acid, 3-aminoadipic acid, beta-alanine, aminopropionic acid, acid, and the like. 2-aminobutyric acid, A-aminobutyric acid, 6-aminocaproic acid, 2-aminoheptanoic acid, 2-aminoisobutyric acid, 3-aminoisobutyric acid, 2-aminopimelic acid, 2,4-diaminoisobutyric acid, desmosine, 2,2'-diaminopimelic acid, 2,3-diaminopropionic acid, N-ethylglycine, N-ethylasparagine, hydroxylysine, allo-hy-droxylysine , 3-hydroxyproline, 4-hydroxyproline, isodesmosine, allo-isoleucine, N-methylglycine, N-methyliso-leucine, N-methylvaline, norvaline, norleucine, ornithine, and pipecolic acid.
In a preferred embodiment, the peptide derivative does not comprise more than 10, 9,8, 7 or 6 amino acids, or comprises 5, 6, 7, 8, 9 or 10 amino acids.
The peptide bonds may be optionally modified to prevent proteolysis. For example, at least one peptide bond may be replaced by a bond selected from the group consisting of (-CH2-NH-), (-NH-CO-), (-CH2-0-), (-CH2-S- ), (-CH2-CH2-), (-CO-CH2-), (-CHOH-CH2-), (-N = N-), and (-CH = CH-). Optionally, all the peptide bonds are replaced.
The agonist peptides of the ROD may have enzymatic and / or chemical substitutions and modifications. In particular, the modifications may be substitutions of all or some of the L-amino acid residues to D-amino acid. In a very particular aspect, the peptides comprise only D-amino acids. The peptides can be acetylated, lipid-conjugated, esterified, glycosylated, amidated and / or cyclized.
In particular, the ROD agonist peptides may be conjugated to a lipid to facilitate penetration through the stratum corneum. In a particular embodiment, the peptides according to the invention may have one or more lipid radicals, attached covalently or non-covalently. The radical / lipid radicals can be any lipid having from C3 to C20 carbon atoms, preferably linked to the N- or C-terminal end. Preferably, the lipid is conjugated to the N-terminus of the peptide. Alternatively, the lipid is conjugated at its C-terminus. Non-exhaustive examples of lipids include, but are not limited to, acetic acid, butyric acid, capronic acid, caprylic acid, caprynic acid, lauric acid, myristic acid, acid palmitic acid, stearic acid, arachidic acid, behenic acid, lignocaine acid, palmitolic acid, oleic acid, linoleic acid, γ-linoleic acid, α-linoleic acid , eicosadinoic acid, eicosatrinoic acid, arachidonic acid, eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid. For example, the peptide may be palmitoylated. However, it can be noted that one advantage of rubiscolin 6 and its derivatives is their ability to penetrate the skin without any modification.
In a variant, the ROD agonist peptides may comprise a radical facilitating the cellular penetration of the ROD agonist peptides. For example, this radical is well known in the art (see for example, Vives et al., 2008).
The agonist peptides of ROD can be isolated from a natural source or they can be synthesized.
Deltorphin and its derivatives include deltorphin (Y-dM-FHLMD-NH2 (SEQ ID No. 2)) and derivatives such as the following peptides: Y-dA-FDVVG-NH2 (SEQ ID No. 3, deltorphin I) , Y-dA-FEVVG-NH2 (SEQ ID No. 4, deltorphin II), and Y-dL-FADVASTIGDFFHSI-NH2 (SEQ ID No. 5, Leu-deltorphin).
In the most preferred embodiment, the selective ROD agonist is rubiscoline 6 and its derivatives. Rubiscoline 6 has the sequence YPLDLF (SEQ ID No. 1).
Rubiscoline 6 and its derivatives include peptides which have or comprise the sequence of formula (I) YP-X1-D-X2-X3 (I) (SEQ ID No. 6) in which X1 represents a non-hydrophobic amino acid. aromatic, preferably selected from the group consisting of L, I, Μ, V and A, more preferably selected from the group consisting of L, I, and M; Wherein X2 is a non-aromatic hydrophobic amino acid, preferably selected from the group consisting of L, I, and M, more preferably selected from the group consisting of L and I; X3, present or absent, representing a hydrophobic amino acid, preferably selected from the group consisting of F, L, I, Μ, V and A, more preferably selected from the group consisting of F, I, and V, and in particular representing F or V.
[0042] Therefore, rubiscoline 6 and its derivatives may be a peptide selected from the group consisting of or a peptide comprising a sequence selected from the group consisting of YPLDLF (SEQ ID No. 1), YPIDLF (SEQ ID No. 7), YPLIF (SEQ ID NO: 9), YPLDIF (SEQ ID NO: 9), YPLDLL (SEQ ID NO: 10), YPLDLI (SEQ ID NO: 11), YPLDLM (SEQ ID NO: 12), YPLDLV (SEQ ID NO: 13), YPLDLA ( SEQ ID No. 14), YPIDLV (SEQ ID No. 15), YPMDLV (SEQ ID No. 16), YPLDIV (SEQ ID No. 17), YPIDIV (SEQ ID No. 18), YPMDIV (SEQ ID No. 19), YPIDLV (SEQ ID No. 20), YPIDMV (SEQ ID No. 21), YPIDII (SEQ ID No. 22), YPMDII (SEQ ID No. 23), YPMDL (SEQ ID No. 24), YPIDL (SEQ ID No. 25), and YPMDI (SEQ ID No. 26). In a preferred embodiment, rubiscolin 6 and its derivatives may be a peptide selected from the group consisting of YPLDLF (SEQ ID NO: 1), YPIDLF (SEQ ID NO: 7), YPMDLF (SEQ ID NO: 8), and YPMDL ( SEQ ID No. 24). In a very specific embodiment, the ROD agonist is a peptide YPLDLF (SEQ ID No. 1) or a peptide comprising the sequence YPLDLF (SEQ ID No. 1), optionally modified as described above.
In a second aspect, the present invention relates to a cosmetic composition for topical, intradermal, transdermal or subcutaneous administration, preferably a topical administration, comprising a peptide chosen from rubiscoline 6 and its derivatives and at least one additive. cosmetic. Rubiscoline 6 and its derivatives are as detailed above. It further relates to the use of a peptide selected from rubiscolin 6 and its derivatives for the preparation of a cosmetic composition for topical, intradermal, transdermal or subcutaneous administration, preferably topical administration. Preferably, the cosmetic composition is intended for preventing and / or reversing the signs of aging of the skin, and / or for filling wrinkles, for improving the smoothness of the skin, and / or for the equalization of imbalanced markers in stressed skin, and / or normalization of disturbed gene expression in skin cells, and / or erasure of croup-like wrinkles, and / or recovering the hydration of the skin, and / or preventing the loss of trans-epidermal water in the skin, and / or reactivating the differentiation of skin cells, and / or stimulating pigmentation. In particular, the skin is the skin of the body or face. It also relates to a cosmetic process for the prevention and / or reversal of the signs of aging of the skin, and / or the filling of wrinkles, the improvement of the smooth character of the skin, and / or the equalization of unbalanced markers. in stressed skin, and / or the normalization of disturbed gene expression in skin cells and / or the erasure of crow's feet wrinkles, and / or the recovery of skin hydration and / or prevention of transepidermal water loss in the skin, and / or reactivation of skin cell differentiation, and / or stimulation of pigmentation, including application to human skin and / or the hair of a composition comprising a peptide chosen from rubiscolin 6 and its derivatives. In this context, the ROD agonist peptide is the active agent. In one particular aspect, he may be the only active agent. Alternatively, it can be combined with additional active agents. In particular, such additional active agents may be anti-aging agents, photoprotective agents, antioxidant and anti-glycation agents.
Rubiscoline 6 and its derivatives can be used for the normalization of the cutaneous barrier, the restructuring of mature skin, the smoothing of the skin surface and / or the filling of deep wrinkles. Therefore, their applications may be eye care products, in particular for the eye contour, eye gel, the serum to be applied under the eyes, products for the treatment of expression lines, products anti-aging for the reduction of deep wrinkles, mature skin care products, neck care products, body restructuring products, and protection against daily aggressions. In the cosmetic composition of the present invention, the ROD agonist is added in a cosmetically effective amount. The amount may vary according to the condition to be treated, the age, the severity of the condition to be treated, the duration of treatment, and the like. In a particular embodiment, at the cosmetically effective amount, the ROD agonist has no therapeutic effect. Indeed, the uses contemplated in this document are non-therapeutic uses.
In general, when the ROD agonist is rubiscolin 6 and one of its derivatives, the composition may comprise between 0.000005 and 0.002% by weight of the peptide relative to the total weight of the composition, preferably between 0.00001% and 0.001%, even more preferably between 0.00003% and 0.0006%. When expressed in ppm, the composition generally comprises from 0.05 to 20 ppm of peptide, preferably from 0.1 to 10 ppm, more preferably from 0.3 to 6 ppm.
The cosmetic composition may be formulated in the form of a cream, a gel, a moisturizer, a lotion, a milk, an oil, an ointment, a wax, a mousse, a paste, a serum, an ointment, a hair care product, or a shampoo. It can optionally be applied in the form of an aerosol. It can also be in solid form, as in the form of a stick. It can be used as a care product and / or as a make-up product for the skin.
The cosmetic additives may be added to obtain a desired cosmetic result. The desired cosmetic results may be determined by one of ordinary skill in the art or the user of the disclosed compositions. Cosmetic additives may include, but are not limited to, carriers, excipients, carrier components, moisturizers, humectants, cosmetic salts, adjuvants, oils, emulsifiers, co-emulsifiers, gelling agents, absorbents solvents, photoprotective agents, and inert bases.
Compositions useful for topical application may contain additional components such as carrier components, excipients or vehicles such as, for example, water, acetone, ethanol, ethylene glycol, propylene glycol, butane-1,3-diol, isopropyl myristate, isopropyl palmitate, mineral oil, and mixtures thereof to form lotions, dyes, creams, emulsions, gels or ointments which are nontoxic and acceptable from a pharmaceutical or dermatological point of view. In addition, moisturizers or humectants may be added to the present compositions if desired. Examples of these additional components can be found in Remington's Pharmaceutical Sciences, Eighteenth Edition, A.Gennaro R., Ed., Mack Publishing Co., Easton, Pa., 1990.
This cosmetic composition may be in any form of presentation normally used in cosmetics, and it may be, for example, in the form of an optionally gelled aqueous solution, a lotion-type dispersion, optionally a two-part lotion. phases, of an emulsion obtained by the dispersion of a fatty phase in an aqueous phase (O / W emulsion) or conversely (W / O emulsion), of a triple emulsion (W / O / W or O / W emulsion) / H), nanoemulsions, in particular nanoemulsions O / W, in which the size of the drops is less than 100 nm; or a vesicular dispersion of ionic and / or nonionic type. These compositions are prepared according to the usual methods. In one embodiment, a composition in the form of an oil-in-water emulsion is used. In one aspect, the ROD agonist peptides may be prepared under specific conditions as incorporated into liposomes, niosomes, nanosomes, nanospheres or nanocapsules.
For topical application to the hair or the scalp, the cosmetic composition may be in the form of aqueous, alcoholic or aqueous-alcoholic solutions in the form of creams, gels, emulsions or foams; in the form of aerosol compositions also comprising a pressurized propellant.
When the composition is in aqueous form, especially in the form of a dispersion, an emulsion or an aqueous solution, it may comprise an aqueous phase, which may comprise water, a floral water and / or mineral water.
In a known manner, the cosmetic composition described in this document may also comprise at least one adjuvant chosen from adjuvants which are common in cosmetics, such as hydrophilic and lipophilic gelling agents, hydrophilic and lipophilic active agents, preservatives, antioxidants, solvents, fragrances, bulking agents, screening agents, pigments, odor absorbers and dyestuffs. The at least one adjuvant is present in an amount in the range of, for example, 0.01% to 20% by weight based on the total weight of the composition. Depending on its nature, the at least one adjuvant can be introduced into the fatty phase, into the aqueous phase, or into lipid vesicles. In any case, these adjuvants, and also their proportions, will be chosen so as not to alter the desired properties of the combination of anti-wrinkle active agents described herein.
When the cosmetic composition described in this document is an emulsion, the proportion of the fatty phase may be in the range of 5% to 80% by weight as 5% to 50% by weight relative to the total weight of the composition. The oils, emulsifiers and co-emulsifiers used in the cosmetic composition in emulsion form are chosen from those conventionally used in the field under consideration. The emulsifier and the co-emulsifier are present in the composition in an amount ranging from 0.3% to 30% by weight as from 0.5% to 20% by weight relative to the total weight of the composition.
As regards the oils which can be used in this description, mention may be made, for example, of mineral oils (liquid petroleum jelly or hydrogenated polyisobutene), vegetable oils ( avocado oil or soybean oil), animal oils (lanolin), silicone oils (cyclomethicone or dimethicone) and fluorinated oils (perfluoropolyethers). Fatty alcohols (cetyl alcohol), fatty acids and waxes (carnauba wax or ozokerite) can also be used as fatty substances.
As examples of emulsifiers and co-emulsifiers which may be used herein, mention may be made, for example, of polyethylene glycol fatty acid esters such as PEG-100 stearate, and esters. of glycerol fatty acids such as glyceryl stearate.
Hydrophilic gelling agents which may be incorporated are, for example, carboxyvinyl (carbomer) polymers, acrylic copolymers such as acrylate / alkyl acrylate copolymers, polyacrylamides, such as crosslinked polyacrylamido-sulphonic acid, polysaccharides, natural gums and clays, and lipophilic gelling agents which may be mentioned include, for example, modified clays, such as bentones, metal salts of fatty acids, hydrophobic silica and polyethylenes.
In one embodiment, the hydrophilic gelling agent for the composition described in this document is chosen from a crosslinked polyacrylamido-sulfonic acid as described in the documents EP 0850642, WO9800094 or Hos-tacerin AMPS marketed by Clariant.
In a further aspect, the present invention relates to a device comprising a δ-opioid receptor peptide agonist ligand chosen from rubiscolin 6 and its derivatives, the device being capable of delivering said omega-5 opioid receptor agonist ligand via an intra-epidermal and / or intradermal and / or subcutaneous injection. Said device may be, for example, a syringe with a needle or needleless injection device, such as those used in the care technique known as mesotherapy. A kit comprising a device may also be envisaged, said kit comprising a device, in particular a syringe or an injection device, and the ROD agonist, in particular rubiscoline 6 and its derivatives, as defined above. Said kit may also include a needle. Said device may also be in ready-to-use form, that is to say pre-filled, or it may be necessary to fill it. In the latter case, a composition or other device (such as a vial) comprises the ROD agonist, in particular rubiscolin 6 and its derivatives, as defined above, optionally in combination with at least one other active compound. Alternatively, the composition of the invention can be used in combination with a laser treatment which improves the penetration of the composition.
The composition of the invention may also be used in combination with other treatments such as light therapy or phototherapy, in particular low-intensity laser therapy or deep penetration light therapy. In addition, the topical application of the composition may be combined with the use of a facial massager.
Examples are provided solely to illustrate the present invention, which should not be interpreted as limiting the scope of the invention, as described in this document.
Examples
Example 1: Experiments 1. Protein and protein hydrolyzate assays on delta opioid receptors [0061] Frozen spinach leaves were thawed and broken into fine particles using a mixer. This juice was further sonicated to break the cells and the proteins were recovered by acid precipitation. These proteins were then digested by several enzymes, including pepsin and papain. The hydrolyzate was purified (ultrafiltration), fractionated and stored prior to analysis. At the same time, synthetic peptides were ordered from a manufacturer. Peptides and hydrolysates were tested on cells carrying the delta2 opioid receptor and cell impedance was measured to evaluate the binding activity of the test compounds (Law and Loh, 1993j.
The results were expressed as a percentage of the specific control agonist response (DPDPE (SEQ ID No. 27) was used for this purpose) ((measured specific response / specific control agonist response) x 100) obtained in presence of test compounds.
The EC50 values (concentration producing a semi-maximal specific response) and the IC 50 values (concentration causing a semi-maximal inhibition of the specific agonist response of the control) were determined by an analysis of the nonlinear regression of the concentration-response curves generated with replicate mean values using the curve fitting of the Hill equation (Y = D + [(AD) / (1 + (C / C50) nH)], where Y = specific response, D = minimal specific response, A = maximum specific response, C = concentration of compound, and C50 = EC50 or IC50, and nH = slope factor).
Table 1: determination of EC50 YP, YPL, YPLD (SEQ ID No. 29), YPLDL (SEQ ID No. 28), YPLDLF (SEQ ID No. 1): PEPS pure peptides: protein fractions hydrolyzed with pepsin PANE: hydrolysed protein fractions with papain.
N.C .: EC50 value not calculable. The concentration-response curve shows less than 25% effect at the highest concentration tested.
[0066]>: EC50 value higher than the highest tested concentration. The concentration-response curve shows less than 50% effect at the highest concentration tested.
This experiment (Table 1 and Fig. 1) revealed that a peptide was functionally active on ROD as ligand with EC50 = 3.9 μΜ. A protein hydrolyzate was also active on the RODs, showing that not only the pure peptides, but also the protein hydrolysates could be active as a ligand of the RODs. 2. Effect of cytokines on the level of expression of RODs in the epidermis The expression of opioid delta receptor (ROD) proteins was analyzed using a "tissue microarray" (TMA) composed of many skin-related cell models to identify the best models for other studies.
Paraffin Inclusion [0069] Formalin-fixed tissues were dehydrated in multiple baths with increasing concentration of ethanol and then included in paraffin "Paraplast X-tra". Cross sections were made using a microtome (5 μm thick) and stored at room temperature until staining.
Immunohistochemical Marking [0070] The sections were paraffin-free and the antigenic sites were recovered using specific buffers (pH 6 and pH 9). The sections were then washed and incubated with hydrogen peroxide. After an additional washing step, the sections were incubated with the primary antibody (anti-ROD). The labeling was then revealed using a secondary antibody conjugated to biotin. After the addition of peroxidase-conjugated streptavidin and the peroxidase substrate, the nuclei were counter-stained with a solution of hematoxylin. The slides were washed in ultrapure water and mounted in an aqueous medium.
Microscopic Observation [0071] The sections were observed using a NIKON E400 microscope. The images were captured with a NIKON DS-RM and processed with the NIS-Elements 3.10 software.
Fig. 2A: Normal human skin The expression of ROD proteins has been observed in the granular - epidermis and dermis layers of the epidermis. In addition, some dermal cells were slightly marbled in their cytoplasm.
Fig. 2B: Normal Human Skin Some areas of the sebaceous glands have expressed ROD proteins. - dermis and sebaceous glands
Fig. 2C: Human epidermis The ROD proteins were strongly expressed in the membranes of the reconstituted (EHR) cells of the granular layer of EHR. All living cells in the basal and suprabasal layers expressed the proteins in their cytoplasm.
Fig. 2D: EHR treated with PMA Compared to untreated EHR, the expression of the RODs was decreased after 2 μg treatment with phorbol myristate acetate (PMA) at 2 μg. It was observed at one mark in the thorny layer while the expression persisted strongly in the basal layer and slightly in the granular layer. Fig. Compared with untreated EHR, the expression was significantly decreased in cytokine mix EHR treated with the cytokine mixture: in granular and epi (IL-17 + OSM + TNF -a) neuse, the marking has completely disappeared. Only the expression in the dirty layer has been preserved.
Table 2: Analysis of the Expression of ROD in the Epidermis [0072] These results (Table 2 and Fig. 2) have shown that the ROD proteins have been expressed in human skin and in the 3D model of human epidermis. rebuilt. The expression was really important in the granular layer of both models. After inflammation treatments (cytokine mixture or PMA) simulating aging skin conditions, the expression of ROD proteins decreased or disappeared completely. This demonstrates that under aging conditions, opioid delta receptors are less expressed. 3. Anti-Cytokine Effect of an ROD Agonist Peptide on the ROD Expression Level in the Epidermis In the present study, the effects of a peptide (YPLDLF) on the expression of delta opioid receptors (ROD) were investigated on a reconstructed human epidermis (HRE) model under basal or stimulated conditions. More specifically, the EHRs were stimulated by a cytokine mixture (IL-17 + OSM + TNF-a) capable of inducing a strong inflammatory profile and a psoriatic phenotype in the keratinocytes.
A reconstructed human epidermis (EHR) of 11 days was prepared according to a derivative method described by Poumay et al. (2004). These EHRs were cultured at 37 ° C and 5% CO 2 in a specific holding medium.
EHR treated under basal conditions were placed in the medium of the test containing or not (non-stimulated control) peptide solutions and they were incubated for 54 hours. For inflammatory conditions, the EHRs were placed in the test medium containing or not (stimulated control) the peptide solutions or the reference (JAK I inhibitor at 10 μΜ) and they were preincubated for 6 hours. The EHRs were then stimulated with a mixture of cytokines (IL-17 + OSM + TNF-α at 3 ng / ml) and incubated for 48 hours. All the experimental conditions were realized in n = 3.
At the end of the incubation, the supernatants were collected and the EHRs were washed in phosphate buffer solution (PBS) for immunohistofluorescence analysis.
Paraffin Inclusion The formalin-fixed tissues were dehydrated in multiple baths with increasing concentration of ethanol and then they were embedded in paraffin. The cross sections were made using a microtome (thickness of 5 μιτι) and stored at room temperature until staining.
Immunohistochemical labeling The sections were stripped of paraffin and the antigenic sites were recovered using a specific buffer (pH 6). The sections were then washed and incubated with hydrogen peroxide. After an additional washing step, the sections were incubated with the primary antibody (anti-ROD). The labeling was then revealed using a secondary antibody conjugated to biotin. After the addition of peroxidase-conjugated streptavidin and the peroxidase substrate, the nuclei were counter-stained with a solution of hematoxylin. The slides were washed in ultrapure water and mounted in an aqueous medium.
Microscopic Observation [0079] The sections were observed using a NIKON E400 microscope. The images were captured using a NIKON DS-RM and processed with the NIS-Elements 3.10 software.
Table 3: Score of ROD1 expression in EHR under different conditions The ROD proteins were correctly detected in the reconstructed human epidermis by following in situ immunohistolabeling. ROD1 was strongly and almost exclusively expressed in the granular layer. After treatment with the cytokine mixture, the expression of ROD1 in the stimulated control was greatly decreased compared to the unstimulated control. The anti-inflammatory reference, the JAK I inhibitor, tested at 10 μΜ, reversed the inhibitory effect of the cytokine mixture on ROD1. The inhibitory effect of the cytokine mixture on the expression of ROD1 was also reversed after treatment with the peptide.
This experiment has demonstrated that an ROD agonist peptide, such as the YPLDLF peptide, can reverse the effect of a mixture of cytokines on the expression level of the RODs. 4. Effects of Peptide on Gene Expression in Reconstructive Human Epidermis The transcriptional effects of a peptide (YPLDLF) on gene expression were investigated on a reconstructed human epidermis model (EHR ) in inflammatory conditions. Inflammation of EHR was induced using a mixture of cytokines (IL-17 + OSM + TNF-a). The effects on gene expression were evaluated using RT-qPCR technology. The extracted mRNA was analyzed on a custom PCR chip designed by the study sponsor and containing 64 target genes (including 2 housekeeping genes) chosen for their role in keratinocyte differentiation, or their involvement in cell junctions. and lipid synthesis, or their relationship to opioid delta receptors (RODs).
The reconstructed human epidermis (EHR) of 11 days was prepared according to a derivative method described by Poumay et al. (2004). These EHRs were cultured at 37 ° C and 5% CO 2 in a specific holding medium.
The EHRs were cultured in a test medium containing or not (controls) the compounds to be tested or the reference (inhibitor of JAK I at 10 μΜ) and they were preincubated for 24 hours. The epidermis was then stimulated or not (unstimulated control) with a mixture of cytokines (IL-17 + OSM + TNF-a) at 3 ng / ml and the epidermis was incubated for 24 hours. All the experimental conditions were realized in n = 2.
At the end of the incubation, the supernatants were collected and the EHRs were washed in phosphate buffer solution (PBS) and immediately freeze dried at -80 ° C.
Differential Expression Analysis The expression of the markers was analyzed using the RT-qPCR method on the mRNA extracted from the EHRs for each treatment (before RNA extraction, the replicates were pooled ).
The analysis of the gene expression was performed in n = 2 using a custom PCR chip reserved for research and adapted to the "screening" format.
Inverse Transcription Total RNA was extracted from each sample using Reagenti® TriPure Isolation Reagent according to the suppliers instructions. The quantity and quality of the RNA were evaluated using a laboratory-on-chip bioanalyzer (Agitate technologies). RNA quality controls are presented in the appendix. Traces of potential contaminants of genomic DNA were removed using the DNAfree system (Ambion). Reverse transcription of the mRNA was conducted in the presence of oligo (dT) and Superscript II reverse transcriptase. Quantitation of the cDNA was performed using Nanovue (GE Healthcare) and cDNA adjustment at 10 ng / μl. Quantitative PCR [PCR] (Polymerase Chain Reactions) were performed using the "LightCycler®" system (Roche Molecular System Inc.) according to the supplier's instructions. This system allows fast and powerful PCR, after the determination of the analysis conditions of the primers to be tested.
The reaction mixture (10 μΙ in the final) was added as follows: - 2.5 μΙ of 10 ng / μΙ cDNA, - direct and reverse primers, - the reaction mixture containing the DNA polymerase taq , SYBR Green I and MgCI2.
Quantitative PCR Data Management [0091] The raw data was analyzed with Microsoft Excel® software.
Fluorescence incorporation into the amplified DNA was measured continuously during the PCR cycles. This resulted in a "fluorescence intensity" plot as a function of "PCR cycles" allowing the evaluation of a relative expression (RE) value for each marker. The value chosen for the ER calculations represents the "exit point" (Ct) of the fluorescence curve. For a marker considered, the number of cycles is high; the higher the amount of mRNA is low. The ER value was expressed in arbitrary units (AU) according to the formula: (1 / 2n ° decydes) ^ - | q6 Results [0093] The peptide, tested at 0.3 μg / ml, generally showed a modulation of the gene expression profile of EHR stimulated by the cytokine mixture.
This experiment has demonstrated that the ROD agonist peptides, such as the YPLDLF peptide, can reverse the deregulation effect of a mixture of cytokines on the level of expression of specific genes in the epidermis.
Relative Expression of Genes as a Function of Control Conditions With With (Non-stimulated EHR) Cytokine Cytokines and
peptide 0.3 PPM% of the control (mean H K)
Gene function Reference Name of proteins 100 100 of genes
Domestic RPS28 Ribosomal Protein S28 104 91 GAPDH Glyceraldehyde-3-phosphate 94 116 dehydrogenase
Associated Markers OPRD1 Opioid Receptor, delta 1 97 101 at opioid receptors delta 1 ADRB2 Adrenergic Receptor, 62 259 beta-2, surface CREB1 Protein 1 binding of sensitive elements at 120 109 cAMP GNAS Locus complex GNAS 121 130 MAPK1 Protein kinase 1 mitogen-activated 126 108 MAPK14 Mitogen-Activated Protein Kinase 14 117 PTGS2 Prostaglandin-Endoperoxide Synthase 2 42 119 (Prostaglandin G / H Synthase and Cyclooxygenase) STAT3 Signal Transducer and Activator 444 120 Transcription 3 (Response Factor in the acute phase) BIRC5 Survivin 25 88 ODC1 Ornithine decarboxylase 1 52 110 CASP3 Caspase 3, cysteine peptidase associated with apoptosis SLC1A3 117 104 Protein of the Carrier Solute 1 39 100 (high affinity glutamate glutamate transporter), EGFR member 3 Growth factor receptor for 138,141 epidermal cells (viral oncogene homologue of erythroblastic leukemia (v-erb-b), avian) [0095]
Differentiation of CALML5 Calmodulin-like 5 57 72 keratinocytes FLG Fiiaggrine 34 117 KRT1 Keratin 1 27 140 KRT10 Keratin 10 26 145 LOR Loricrin 60 121 SPRR1A Protein-rich protein 1A 181 142 SPRR1B Protein-rich protein 1B 251 127 (cornifine) SPRR2A Small proline-rich protein 2A 467 111 TGM1 Transglutaminase 1 (Epidermal 308-type I polypeptide, protein-glutamine-gamma-glutamyltransferase) CRNN Cornulin 55 71 IVL Involucrine 90 119 KRT19 Keratin 19 112 134 PADI1 Peptidyl-arginine deiminase, type I 19 105 SFN Stratified 173 143
Junctions GJA1 Interconnecting Junction Protein, 46 111 communicating alpha 1.43 kDa GJA5 Communicating Junction Protein, 100 90 alpha 5, 40 kDa GJB2 Interconnecting Junction Protein, 405 131 Beta 2 GJB3 Interconnecting Junction Protein, 73 111 Beta 3, 31 kDa GJB4 Communicating Junction Protein, 89 77 Beta 4, 30.3 kDa GJB5 Communicating Junction Protein, 78 122 Beta 5, 31.1 kDa GJB6 Communicating Junction Protein, 197 203 Beta 6, 30 kDa GJC1 Interconnecting Junction Protein, 96 126 gamma 1.45 kDa GJD3 communicating junction protein, 108 487 delta 3, 31.9 kDa PANX1 Pannexine 1 190 133
CLDN1 junctions Claudine 1 93 128 waterproof CLDN2 Claudine 2 72 121 OCLN Occludine 143 131 F11R Receptor F11 174 115 TJP1 Impervious junction protein 1,162,129 (zona occludens 1) TJAP1 Protein associated with junctions 87 81 impermeable 1 (peripheral)
Junctions CDFI1 Cadherin 1, type 1, E-cadherin 173 126 anchor (epithelial) CTNNA1 Catenin (cadherin-associated protein), 132 117 alpha 1, 102 kDa CTNNB1 Catenin (cadherin-associated protein), 93,134 beta 1,88 kDa PVRL1 Associated with poliovirus receptor 1140131 (mediator of herpesvirus C entry) DST Dystonin 38 93 CDSN Cornéodesmosine 115 161 DSG1 Desmoglein 1 75 98 DSP Desmoplakin 151 107 EPPK1 Epiplakine 1 99 82 EVPL Envoplakin 107 132 ITGAV Integral, alpha V (vitronectin 292 receptor, alpha polypeptide, CD51 antigen) ITGB3 Integrin, beta 3 (platelet glycoprotein Ilia, CD61 antigen) ITGA2 Integrin, alpha 2 (CD49B, 131 108 alpha 2 subunit of VLA-2 receptor)
Lipid synthesis ACSS2 Short-chain family of acyl-CoA 94 113 synthetases, member 2 GBA Glucosidase, beta; acid (includes 112 110 glucosylceramidase) SMPD1 Sphingomyelin phosphodiesterase 1, 88 87 lysosomal acid SPTLC1 Serine palmitoyltransferase, long chain base subunit 1 92 SULT2B1 Family of sulfotransferases, 92 173 cytosolic, 2B, member 1 UGCG UDP-glucose ceramide glucosyltransferase 119 117
Table 4: Analysis of Expression 5. Proteins In the present study, the effects of a peptide on the expression of 7 proteins were estimated on a reconstructed human epidermis model (EHR) stimulated or not with a mixture of cytokines (IL-17 + OSM + TNF-a).
More specifically, the effects of the compounds were evaluated on the expression of the proteins of the markers involved in: - the impermeable junctions (occludin), - the anchorage junctions (corneosdesmosin) - the differentiation of the keratinocytes (keratin 10, involucrin, calmodulin type 5), and lipid synthesis (acyl-CoA synthetase and sulfotransferase 2B).
The reconstructed human epidermis (EHR) of 11 days were prepared according to a derivative method described by Poumay et al. (2004). These EHRs were cultured at 37 ° C and 5% CO 2 in a specific holding medium.
The EHRs were treated with the test medium containing or not (control) the compounds to be tested and they were incubated for 72 hours with a renewal of treatment after 24 hours. All the experimental conditions were realized in n = 3.
At the end of the incubation, the supernatants were collected and the EHRs were washed in phosphate buffer solution (PBS) for in situ immunostaining.
The EHRs were treated with the test medium containing or not (control) the test compounds or the JAK I inhibitor at 10 μΜ and they were incubated for 24 hours. After preincubation, the test medium and treatments were renewed and the epidermises were stimulated with a mixture of cytokines (OSM + IL-17 + TNF-a *) at 3 ng / ml and were incubated for a further 48 hours. hours. All the experimental conditions were realized in n = 3.
At the end of the incubation, the supernatants were collected and the EHRs were washed in phosphate buffer solution (PBS) for in situ immunostaining.
Oncostatin M (OSM) + Interleukin 17 (IL-17) + tumor necrosis factor alpha (TNF-α) [0104] Immunofluorescent labeling of acetyl-coenzyme A synthetase, corneodesmosin, involucrine, keratin 10, and occludin.
After incubation, the EHRs were instantaneously frozen in liquid isopentane / N 2 and stored at -80 ° C. Cross sections were performed using a microtome (5 μm thick, one EHR plate, several sections per slide).
The sections were fixed with a mixture of acetone / methanol and dried. After saturation with 5% milk PBS, the sections were incubated with the specific primary antibody solutions. After washes, the binding sites were revealed using a suitable coupled secondary antibody and the cell nuclei were stained with a solution of propidium iodide. The sections were washed and then observed under epifluorescence microscopy.
Immunoperoxidase labeling of the calmodulin 5 protein and the cytosolic sulfotransferase 2b After the incubation, the EHRs were rinsed and fixed with a formalin solution. The fixed tissues were dehydrated in multiple baths with increasing concentration of ethanol and then they were included in paraffin. Cross sections were performed using a microtome (5 μm thick) and stored at room temperature.
The sections were freed of paraffin and the antigenic sites were recovered. The sections were washed and incubated with hydrogen peroxide. The sections, once washed, were incubated with the primary antibody (anti-calmodulin or anti-SULT2B1 protein). After washing, labeling was revealed using a secondary antibody conjugated to biotin. After the addition of peroxidase-conjugated streptavidin and peroxidase substrate, the nuclei were counterstained with a solution of hematoxylin. The sections were washed, mounted in an aqueous medium and observed under light transmission microscopy.
Microscopic Observation and Image Analysis [0110] The sections were observed using a NIKON E400 microscope. The images were captured with a NIKON DS-RM and processed with the NIS-Elements 3.10 software (3 images per replicate). Image analysis was performed by measuring the intensity of fluorescence using Image J software.
The results were expressed in% of the expression level of each protein label in untreated EHRs.
[0112]
Table 5: Protein Expression [0113] This experiment demonstrated that the ROD agonist peptides, such as the YPLDLF peptide, can normalize the effect of deregulation of a mixture of cytokines on the level of expression of specific proteins in the epidermis. Therefore, such compounds can reverse unbalanced situations as happens during aging. More significantly, these compounds regulate the expression of proteins involved in impermeable junctions (occludin), anchorage junctions (corneodesmosin) and differentiation of keratinocytes (keratin 10, involucrine, calmodulin-like protein 5) and synthesis. lipids (acetyl-coA synthetase and sulfotransferase 2B) in the skin. The ROD agonist peptides, such as the YPLDLF peptide, can therefore have major effects in the reorganization of a correct metabolism of the skin and they promote the restructuring of the skin. 6. Evaluation of the Proligmentation Properties of ROD Agonist Peptides on Skin Explants [0114] This study aims to explore the activity of pro-pigmentation of a component (YPLDLF peptide) on human skin explants maintained in vitro. survival. The activity of the product was evaluated by: - a histological expertise of the general morphology of the skin after Masson trichrome staining, - a visualization of melanin by silver impregnation, - an immunostaining of Melan-A.
Skin explants with a diameter of 10 mm were prepared from a skin sample from a plastic surgery performed on a woman aged 43 years. The explants were put into survival in a specific growth medium at 37 ° C in a humid atmosphere enriched with 5% CO 2.
The solutions of the peptide (at 0.3 PPM or 3 PPM) were applied topically for 2 hours every day using pre-soaked filter paper discs in 30 μl of each solution.
The control explants have not received any treatment except the renewal of the culture medium.
Some other control explants were irradiated daily with UV (+ 6 to 8% UVB) at a dose of 1.12 J / cm 2.
In OJ, a lot TO explants was taken and divided in two. One half was fixed in buffered formalin and the other half was frozen at -80 ° C. On day 6 and day 10, three explants from each lot were collected and treated in the same way.
Melanin was visualized by silver impregnation according to the Fontana variant of the Masson technique. The labeled melanin was evaluated by microscopic examination.
The expression of melanin in the basal layers was quantified by image analysis using the Cell-D software.
Melan-A was detected with an anti-Melan-A monoclonal antibody (Santa Cruz Company) for 1 h at room temperature with a Vectastain Universal Amplifier System VECTOR avidin / biotin RTU and revealed by FITC. The cell nuclei were stained with propidium iodide. The labeled Melan-A was evaluated by microscopic examination and Melan-A positive melanocyte counts and the results were expressed per centimeter of epidermis.
Table 6: Semi-quantitative physiological variations in melanocytes from human skin explants irradiated with UVA or treated with peptide solutions for 6 days.
This experiment has demonstrated, surprisingly, that a peptide that binds to opioid receptors can activate in a dose-dependent manner the production of pigment (melanin) in human skin in 6 days. The effectiveness of the stimulation of melanin production and the creation of melanosomes by this peptide is almost as good as the effect of UV rays on the skin. 7. Double-blind clinical evaluation controlled by a placebo of the effectiveness of an anti-wrinkle cosmetic product The purpose of this study was to evaluate the effectiveness of a cosmetic anti-wrinkle product in the attenuation of appearance of wrinkles, improving the surface of the skin and attenuating the signs of aging of the skin. In order to achieve this goal, a clinical study was conducted on 20 volunteers. The efficacy of the product was evaluated 15, 30 and 60 days after daily use of the product using an instrumental analysis technique as described here below. The analysis was then completed with both the clinical evaluation performed by the dermatologist and the self-evaluation of the subjects participating in the study.
The surface of the skin is estimated quantitatively by Primos 3D (GFMesstechnik GmbH). Primos 3D is a non-contact in vivo skin measurement device based on structured light projection. Together with a complete 3-D measurement and evaluation software, the detector can evaluate the properties of the skin's surface (ie, the depth of wrinkles, volume, roughness, etc. .). In this study, it is calculated the parameter Rz (ISO 4287, DIN 4768) and the depth of the wrinkles.
The measurement of the hydration of the skin is based on the CORNEOMETER® method recognized internationally (Courage + Khazaka, electronic GmbH). This measurement is based on the dielectric constant of water. The probe shows the capacitance variations according to the moisture content of the measuring object. An electric dispersion field penetrates into the very first layer of the skin and determines the dielectricity.
The trans-epidermal water loss is measured using the internationally recognized TEWAMETER® process. The instrument used is a Tewameter 300® (Courage + Khazaka, electronic GmbH).
Creams tested:
[0128] PHN (placebo): WATER, OCTYLDODECYL NEOPENTANOATE, OCTYLDODECANOL, MYRISTYL MYRISTATE, ACRYLATED CROSS POLYMER / C10 TO C30 ALKYL ACRYLATE, SODIUM HYDROXIDE, PHENOXYETHANOL, METHYL PARABENZOATE, ETHYL PARABENZOATE , BUTYL PARABENZOATE, PROPYL PARABENZOATE, ISOBUTYL PHOS PARABENZOATE (with 3 PPM of YPLDLF peptide): WATER, OCTYLDODECYL NEOPENTANOATE, OCTYLDODECANOL, MYRISTYL MYRISTATE, ACRYLATE CROSS POLYMER / C10 TO C30 ALKYL ACRYLATE , SODIUM HYDROXIDE, PHENOXYETHANOL, METHYL PARABENZOATE, ETHYL PARABENZOATE, BUTYL PARABENZOATE, PROPYL PARABENZOATE, ISOBUTYL PARABENZOATE, 1% PEPTIDE SOLUTION.
Clinical protocol [0129] Apply the two products (active and placebo) twice a day (morning and evening) to a perfectly cleansed face (following the half-face procedure, according to the randomization scheme described in the information form given to the subject) around the eye area, and gently massage until completely absorbed.
The data are submitted to Student's two-tailed "t-test" for matched data. Statistical meanings are reported as follows: n.s. not significant p> 0.05; * significant p <0.05. Results on Trans-epidermal Water Loss The diagram in FIG. 4A reports the average percent change based on TO obtained for the trans-epidermal water loss parameter.
This result demonstrates that ROD agonist peptides can significantly reduce the loss of trans-epidermal water in human skin. After 60 days, there was 82% reduction in water loss compared with placebo. Results on the hydration of the skin [0133] The diagram of FIG. 4B reports the average percent change based on TO obtained for the skin hydration parameter.
This result demonstrates that ROD agonist peptides can improve the natural hydration rate of human skin. Results on deep wrinkles [0135] The diagram of FIG. 4C reports the average of the percentages of variation as a function of TO obtained for the wrinkle depth parameter.
This result demonstrates that ROD agonist peptides can significantly reduce the depth of wrinkles in human skin. In particular, a significant 58% reduction in wrinkle depth was observed compared with placebo. Results on the Wrinkled Character of the Skin [0137] The diagram of FIG. 4D reports the average of the percentages of variation as a function of TO obtained for the parameter Rz (wrinkled character of the skin).
This result demonstrates that the ROD agonist peptides can improve the smoothness of human skin. Example 2 Examples of Skin Care Formulations Comprising YPLDLF Peptide
Regenerative Cream for Mature Skin [0139] A-Aqueous Phase
Glycerin 2.0%
Hexylene glycol 3.0%
0.5% xanthan gum
Conservatives q.s.
Carbomer 0.35%
Peptide at 300 PMM 1%
Water qs. 100% B-Oily phase
Squalane 15%
Cetyl alcohol 2%
Arachidyl Alcohol / Behenyl Alcohol / Arachidylglucoside 1%
Glycerol stearate 5%
1.5% water
0.35% NaOH
Preservative + perfume q.s.
Moisturizing and emollient lotion [0140] A-Oily phase Cétéareth-2 3,5% Cétéareth-21 2-4%
Wheat germ oil 3%
Cyclomethicone 7%
Octyl Palmitate 8% B-Phase aqueous
Water qs. 100%
Glycerin 7.0%
Hexylene glycol 3.0%
Peptide at 300 PPM 1%
Conservatives q.s.
C-Components added in the emulsion at a temperature below 40 ° C
0.1% sodium hyaluronate
Water 5%
Tocopherol 0.05%
0.1% vitamin A palmitate
Phospholipids 0.5% Ceramides 3 04%
Polyacrylamide &amp; C14_13 isoparaffin &amp; laureth-7 2-3.5%
Sun cream in the form of milk for sun-aged skins [0141] A-Oily phase
Glycerol monostearate 2%
PEG-100 Stearate 3%
C12 to C15 alkyl benzoate 10%
Dimethicone 5%
Tocopherol acetate 1%
Octyl triazone (Uvinul T150) 1.5%
Butyl-methoxy-dibenzoylmethane (Eusolex 9020) 2.0%
Cetostearyl alcohol 1% B-aqueous phase
Water qs. 100%
Conservatives 0.6%
Glycerin 7%
Hexylene glycol 3.0%
Carbomer 0.5% tetrasodium EDTA 0.2%
Peptide at 300 PPM 1%
0.1% sodium hyaluronate HPM
Water 5%
0.5% NaOH
Preservatives + perfume q.s.
Post-surgical wrinkle cream [0142] A-Oily phase
Squalane 5%
Cetyl alcohol 2%
Dimethicone 5%
Octyl Palmitate 5% B-Aqueous Phase
Butylene glycol 0.5-4%
Water qs. 100%
Peptide at 300 PPM 1%
Glycerin 2.0%
Hexylene glycol 3.0%
0.5% xanthan gum
Conservatives q.s.
C-Components added in the emulsion at a temperature below 40 ° C
0.1-1% tocopherol acetate
Pyridoxine 0.01-0.05%
Vitamin A palmitate 0.01-1% D-Panthenol 0.1-1%
0.1-0.5% citric acid
0.1-1% zinc gluconate
Trisodium citrate 1-2.5%
Water 5%
Cleansing lotion for mature skin [0143]
Polysorbate 20 1.0%
Caprylyl / capryl glucoside (Oramix CG110) 2.0%
Peptide at 300 PPM 0.1%
PEG-7 glyceryl cocoate 0.5%
Hexylene Glycol 4-5% D-Panthenol 0.1%
Mannitol 0.02%
Conservatives q.s.
Water qs. 100%
2 in 1 conditioner shampoo for hair repigmentation [0144]
Water q.s. 100%
Acrylate Crossed Polymer 4 9% PEG-7 Amodimethicone 1.5%
Ammonium laureth sulphate, ammonium laureth sulfate, lauryl glucoside and cocamide DEA 13%
Peptide at 300 PPM 1 to 2%
NaOH (18% solution) 0.84%
Cocamidopropyl betaine (active at 35%) 2%
Lauramide DEA 2%
Mica and titanium dioxide 0.02%
0.5% preservatives
Dye 0,15%
Perfume 0.5%
REFERENCES
Bigliardi et al., 2006, Differentiation, 74: 174-185.
Bigliardi et al., 2007, J Invest Dermatol., 127 (6): 1479-88 Bigliardi et al., 2009, Exp Dermafol .; 18 (5): 424-30 Giacomoni et al., 2005, EMBO reports, 6, S45-S48.
Kauser et al., 2004, J Invest Dermatol, 123: 184-195.
Law and Loh, 1993, Mol. Pharmacol., 43: 684-693.
Poumay et al., 2004, Arch Dermatol Res. 296 (5): 203-11 Vives et al., Biochemistry and Biophysica Acta, 2008, 1786, 126-138 Yang et al., 2001, FEBS Lett .; 509 (2): 213-7
Yang et al., 2003, Peptides, 24 (4): 503-8 [0146]
B1320EN SEQ LIST.ST25 SEQUENCE LISTING
<110> INDUCHEM HOLDING AG <120> Use of delta opioid receptor agonists in the field of cosmetics and dermocosmetics <130> B1320 <160> 29 <170> Patentin version 3.3
<210> 1 <211> 6 <212> PRT <213> Artificial sequence <220> <223> Rubiscolin-6 <400> 1
Tyr Pro Leu Asp Leu Phe 1 5 <210> 2 <211> 7 <212> PRT <213> artificial <220> <223> deltorphin <220> <221> MISC ^ FEATURE <222> (2) .. (2 ) <223> D-configuration <220> <221> MOD_RES <222> (7) .. (7)
<223> AMIDATION <400> 2
Tyr Met Phe Hi s Leu Met Asp 1 5 <210> 3 <211> 7 <212> PRT <213> artificial <220> <223> derived from deltorphin <220> <221> MISC_F EATU RE <222> (2) .. (2) <223> D-configuration <220>
<221> MOD_RES
Page 1 [0147] B1320EN SEQ LIST.ST25 <222> ¢ 7) .. (7)
<22 3> AMIDATION <400> 3
Tyr Ala Phe Asp val Val Gly 1 5 <210> 4 <211> 7 <212> PRT <213> artificial <220> <223> derived from deltorphin <220> <221> MISC_FEATURE <222> (2) .. ( 2) <223> D-configuration <220> <221> MOD_RES <222> ¢ 7) .. (7)
<223> AMIDATION <400> 4
Tyr Ala Phe Glu Val Val Gly 1 5 <210> 5 <211> 17 <212> PRT <213> artificial <220> <223> derivative of deltorphin <220>
<221> MISC_FEATURE <222> ¢ 2) .. (2) <223> D configuration <220> <221> MOD_RES <222> (17) .. (17)
<223> AMIDATION <400> 5
Tyr Leu Phe Ala Asp Val Ala Ser Thr Gly Asp Island Phe Phe His Ser 15 10 15
Isle
<210> 6 <211> 6 <212> PRT <213> artificial sequence
Page 2 [0148] B1320EN SEQ LIST.ST25 <220> <223> Formula (I) <220> <221> MISC_FEATURE <2 2 2> (3) .. CB)
Where X1 is a non-aromatic hydrophobic amino acid, preferably L, I, Μ, V or A, more preferably L, I, or M <220> <221> MISC_FEATURE <222> (5). 5) <223> X2 = being a non-aromatic hydrophobic amino acid, preferably L,
I, or M, more preferably L or I <220> <221> MISC_FEATURE <222> (6). (6) <223> X3, present or absent, being a hydrophobic amino acid, preferably F, L, I , Μ, V or A, more preferably F, I, or V, <400> 6
Tyr Pro xaa Asp Xaa xaa 1 5 <210> 7 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 7
Tyr Pro Ile Asp Leu Phe 1 5 <210> 8 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 8
Tyr Pro Met Asp Leu Phe 1 5 <210> 9 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 9
Tyr Pro Leu Asp Ile Phe 1 5
Page 3 [0149] B1320EN SEQ LIST.ST25 <210> 10 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 10
Tyr Pro Leu Asp Leu Leu 1 5 <210> 11 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 11
Tyr Pro Leu Asp Leu island 1 5 <210> 12 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 12
Tyr Pro Leu Asp Leu Met 1 5 <210> 13 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 13
Tyr Pro Leu Asp Leu Val 1 5 <210> 14 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 14
Page 4 [0150] B1320EN SEQ LIST.ST25
Tyr Pro Leu Asp Leu Ala 1 5 <210> 15 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 15
Tyr Pro Ile Asp Leu vai 1 5 <210> 16 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 16
Tyr Pro Met Asp Leu vai 1 5 <210> 17 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 17
Tyr Pro Leu Asp Ile Val 1 5 <210> 18 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 18
Tyr Pro Ile Asp Ile Val 1 5 <210> 19 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6
Page 5 [0151] B1320EN SEQ LIST.ST25 <400> 19
Tyr Pro Met Asp Ile Val 1 5 <210> 20 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 20
Tyr Pro Ile Asp Leu Val 1 5 <210> 21 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 21
Tyr Pro Asp Asp Met Val 1 5 <210> 22 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 22
Tyr Pro Ile Asp Ile Ile 1 5 <210> 23 <211> 6 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 23
Tyr Pro Met Asp island island 1 5 <210> 24 <211> 5 <212> PRT <213> artificial <220>
Page 6 [0152] B1320EN SEQ LIST.ST25 <223> derived from rubiscolin-6 <400> 24
Tyr Pro Met Asp Leu 1 5 <210> 25 <211> 5 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 25
Tyr Pro Ile Asp Leu 1 5 <210> 26 <211> 5 <212> PRT <213> artificial <220> <223> derived from rubiscolin-6 <400> 26
Tyr Pro Met Asp Island 1 5 <210> 27 <211> 5 <212> PRT <213> artificial <220> <22 3> DPDPE <400> 27
Asp Pro Asp Pro Glu 1 5 <210> 28 <211> 5 <212> PRT <213> artificial <220> <2 2 3> Rubiscolin-5 <400> 28
Tyr Pro Leu Asp Leu 1 5 <210> 29 <211> 4 <212> PRT <213> artificial
Page 7 [0153] B1320EN SEQ LIST.ST25 <220> <223> Rubi scoiin-4 <400> 29
Tyr pro Leu Asp 1

权利要求:
Claims (6)
[1]
claims
1. Cosmetic use of an opioid receptor agonist ligand δ for the stimulation of the pigmentation of the skin or hair.
[2]
The use according to claim 1, wherein the δ opioid receptor agonist is selective for delta opioid receptors, and preferably selected from the group consisting of BU-48, SNC-80, C-8813, DPI-287, DPI. -221, TAN-67, BW373U86, SIOM, RWJ-394,674, rubiscoline 6 and its derivatives possessing δ-opioid receptor agonist activity, deltorphin and its derivatives possessing δ-opioid receptor agonist activity, the DPDPE , the DSLET, JOM-13, DSTBULET, BUBU, and BUBUC.
[3]
3. Use according to claim 2, wherein the δ opioid receptor agonist is a peptide selected from rubiscolin 6 and its derivatives having δ opioid receptor agonist activity.
[4]
4. Use according to claim 3, wherein the δ opioid receptor agonist is a peptide which has or comprises the sequence of formula (I) YP-X1-D-X2-X3 (I) (SEQ ID No. 6) in which X1 represents a non-aromatic hydrophobic amino acid, preferably selected from the group consisting of L, I, Μ, V and A, more preferably selected from the group consisting of L, I, and M; Wherein X2 is a non-aromatic hydrophobic amino acid, preferably selected from the group consisting of L, I, and M, more preferably selected from the group consisting of L and I; and X3, present or absent, representing a hydrophobic amino acid, preferably selected from the group consisting of F, L, I, Μ, V and A, more preferably selected from the group consisting of F, I, and V, and in particular representing F or V.
[5]
5. Use according to claim 4, wherein the opioid receptor agonist δ is a peptide selected from the group consisting of a peptide having an opioid receptor agonist δ activity and comprising a sequence selected from the group consisting of YPLDLF (SEQ ID No 1), YPIDLF (SEQ ID No. 7), YPMDLF (SEQ ID No. 8), YPLDIF (SEQ ID No. 9), YPLDLL (SEQ ID No. 10), YPLDLI (SEQ ID No. 11), YPLDLM (SEQ ID No 12), YPLDLV (SEQ ID NO: 13), YPLDLA (SEQ ID NO: 14), YPLDLV (SEQ ID NO: 15), YPIDLV (SEQ ID NO: 16), YPMDLV (SEQ ID NO: 17), YPLDIV (SEQ ID NO: 18) , YPIDIV (SEQ ID NO: 19), YPMDIV (SEQ ID NO: 20), YPIDLV (SEQ ID NO: 21), YPIDIV (SEQ ID NO: 22), YPIDMV (SEQ ID NO: 23), YPIDII (SEQ ID NO: 24), YPMDII (SEQ ID No. 25), YPMDL (SEQ ID No. 26), YPIDL (SEQ ID No. 27), and YPMDI (SEQ ID No. 28).
[6]
6. Use according to claim 5, wherein the δ opioid receptor agonist is a YPLDLF peptide (SEQ ID No. 1).

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引用文献:

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公开号 | 申请日 | 公开日 | 申请人 | 专利标题

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FR2750325B1|1996-06-28|1998-07-31|Oreal|COSMETIC USE OF A POLY CROSSLINKED AND NEUTRALIZED AT LEAST 90% AND TOPICAL COMPOSITIONS CONTAINING THEM|

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FR2757767B1|1996-12-27|1999-02-05|Oreal|TOPICAL COMPOSITION CONTAINING AT LEAST ONE PLANT-BASED PROTEIN AND / OR ANIMAL-BASED PROTEIN AND A POLY CROSSLINKED|

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EP1595541A1|2004-05-12|2005-11-16|Alcasynn Pharmaceuticals Gmbh|Use of opioid receptor antagonist compounds for the prevention and/or treatment of diseases associated with the target calcineurin|

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US20100221200A1|2007-07-17|2010-09-02|The Ohio State University Research Foundation|Compositions and methods for skin care|

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法律状态:
2018-02-28| PCAR| Change of the address of the representative|Free format text: NEW ADDRESS: AVENUE DES MORGINES 12, 1213 PETIT-LANCY (CH) |

优先权:

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申请号 | 申请日 | 专利标题

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EP12305335.7A|EP2641588B1|2012-03-23|2012-03-23|Use of agonists of delta opioid receptor in cosmetic and dermocosmetic field|

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