Pharmaceutical composition for preventing or treating autoimmune diseases comprising cedrol or derivatives thereof, or pharmaceutically acceptable salts thereof

Abstract

The present invention relates to a pharmaceutical composition for preventing or treating autoimmune diseases having cedrol or a pharmaceutically acceptable salt thereof as an active ingredient. Particularly, the cedrol or the derivative thereof of the present invention inhibits the expression of IL-17A, and in particular, cedrol, cedryl acetate, and cedrene exhibit the effect of delaying the outbreak of psoriasis and treating thereof in a psoriasis animal model. Therefore, these compounds can be used for the treatment of autoimmune diseases mediated by IL-17.

Claims

1. A method of treating autoimmune diseases in a subject, consisting of orally administering to the subject an effective amount of one or more compounds selected from the group consisting of the compounds represented by the following formulas 23 or a pharmaceutically acceptable salt thereof as the only active ingredient, wherein the autoimmune disease is psoriasis: ##STR00009##

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The application of the preferred embodiments of the present invention is best understood with reference to the accompanying drawings, wherein:

(2) FIG. 1 is a graph illustrating the inhibitory effect of cedrol, cedryl acetate, alpha-cedrene, methyl cedryl ketone, methyl cedryl ether, and cedrene epoxide on the expression of IL-17A (Con: the control group not-treated with any of those compounds).

(3) FIG. 2A is a set of photographs illustrating the therapeutic effect of distilled water (IMQ), cedrol (C), cedryl acetate (CA), or alpha-cedrene (CE) on psoriasis induced by imiquimod in the ear and the back of a mouse, observed before (D0) or one day after (D1) the application of imiquimod while the compound was orally administered to the mouse.

(4) FIG. 2B is a set of photographs illustrating the therapeutic effect of distilled water (IMQ), cedrol (C), cedryl acetate (CA), or alpha-cedrene (CE) on psoriasis induced by imiquimod in the ear and the back of a mouse, observed two days after (D2) or three days after (D3) the application of imiquimod while the compound was orally administered to the mouse.

(5) FIG. 2C is a set of photographs illustrating the therapeutic effect of distilled water (IMQ), cedrol (C), cedryl acetate (CA), or alpha-cedrene (CE) on psoriasis induced by imiquimod in the ear and the back of a mouse, observed four days after (D4) or five days after (D5) the application of imiquimod while the compound was orally administered to the mouse.

(6) FIG. 2D is a set of photographs illustrating the therapeutic effect of distilled water (IMQ), cedrol (C), cedryl acetate (CA), or alpha-cedrene (CE) on psoriasis induced by imiquimod in the ear and the back of a mouse, observed six days after (D6) or seven days after (D7) the application of imiquimod while the compound was orally administered to the mouse.

(7) FIG. 3 is a graph illustrating the weight changes of the psoriasis induced mice orally administered with distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod and the non-treated control group (CONT).

(8) FIG. 4 is a graph illustrating the comparison of the reduction effect on the ear thickness of the psoriasis induced mice according to the oral administration of distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod.

(9) FIG. 5 is a graph illustrating the comparison of the reduction effect on keratosis of the psoriasis induced mice according to the oral administration of distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod.

(10) FIG. 6 is a graph illustrating the comparison of the reduction effect on skin flair of the psoriasis induced mice according to the oral administration of distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod.

(11) FIG. 7 is a graph illustrating the changes of the psoriasis area severity index (PASI) reflecting the ear thickness, keratosis, and skin flair in the psoriasis induced mice according to the oral administration of distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod.

(12) FIG. 8 is a graph illustrating the comparison of the reduction effect on skin pain of the psoriasis induced mice according to the oral administration of distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod.

(13) FIG. 9 is a graph illustrating the comparison of the reduction effect on skin hemorrhage spots of the psoriasis induced mice according to the oral administration of distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod.

(14) FIG. 10 is a graph illustrating the comparison of the reduction effect on skin wrinkles of the psoriasis induced mice according to the oral administration of distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod.

(15) FIG. 11 is a graph illustrating the inhibitory effect on the expression of IL-17A in the spleen of the psoriasis induced mice orally administered with distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod and the non-treated control group (Control).

(16) FIG. 12A is a set of photographs illustrating the skin thickness of the psoriasis induced mice orally administered with distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod and the non-treated control group (Control).

(17) FIG. 12B is a graph illustrating the skin thickness of the psoriasis induced mice orally administered with distilled water (IMQ), cedrol (IMQ+C), cedryl acetate (IMQ+CA), or alpha-cedrene (IMQ+CE) after the application of imiquimod and the non-treated control group (Control).

(18) FIG. 13A is a set of photographs illustrating the therapeutic effect of distilled water (IMQ), cedrol (C), cedryl acetate (CA), or alpha-cedrene (CE) on psoriasis induced by imiquimod in the ear and the back of a mouse, observed a day after the termination of imiquimod application (D8) or two days after the termination of imiquimod application (D9) while the compound was orally administered to the mouse.

(19) FIG. 13B is a set of photographs illustrating the therapeutic effect of distilled water (IMQ), cedrol (C), cedryl acetate (CA), or alpha-cedrene (CE) on psoriasis induced by imiquimod in the ear and the back of a mouse, observed three days after the termination of imiquimod application (D10) or four days after the termination of imiquimod application (D11) while the compound was orally administered to the mouse.

(20) FIG. 13C is a set of photographs illustrating the therapeutic effect of distilled water (IMQ), cedrol (C), cedryl acetate (CA), or alpha-cedrene (CE) on psoriasis induced by imiquimod in the ear and the back of a mouse, observed five days after the termination of imiquimod application (D12) or six days after the termination of imiquimod application (D13) while the compound was orally administered to the mouse.

(21) FIG. 13D is a set of photographs illustrating the therapeutic effect of distilled water (IMQ), cedrol (C), cedryl acetate (CA), or alpha-cedrene (CE) on psoriasis induced by imiquimod in the ear and the back of a mouse, observed seven days after the termination of imiquimod application (D14) or eight days after the termination of imiquimod application (D15) while the compound was orally administered to the mouse.

(22) FIG. 14 is a graph illustrating the comparison of the recovery effect on ear thickness of the psoriasis induced mice according to the oral administration of distilled water (IMQ(1-7)), cedrol (IMQ(1-7)+C), cedryl acetate (IMQ(1-7)+CA), or alpha-cedrene (IMQ(1-7)+CE) after the termination of imiquimod application.

(23) FIG. 15 is a graph illustrating the comparison of the recovery effect on keratosis in the psoriasis induced mice according to the oral administration of distilled water (IMQ(1-7)), cedrol (IMQ(1-7)+C), cedryl acetate (IMQ(1-7)+CA), or alpha-cedrene (IMQ(1-7)+CE) after the termination of imiquimod application.

(24) FIG. 16 is a graph illustrating the comparison of the recovery effect on skin flair in the psoriasis induced mice according to the oral administration of distilled water (IMQ(1-7)), cedrol (IMQ(1-7)+C), cedryl acetate (IMQ(1-7)+CA), or alpha-cedrene (IMQ(1-7)+CE) after the termination of imiquimod application.

(25) FIG. 17 is a graph illustrating the changes of the psoriasis area severity index (PASI) reflecting the ear thickness, keratosis, and skin flair in the psoriasis induced mice according to the oral administration of distilled water (IMQ(1-7)), cedrol (IMQ(1-7)+C), cedryl acetate (IMQ(1-7)+CA), or alpha-cedrene (IMQ(1-7)+CE) after the termination of imiquimod application.

(26) FIG. 18 is a graph illustrating the comparison of the recovery effect on skin hemorrhage spots in the psoriasis induced mice according to the oral administration of distilled water (IMQ(1-7)), cedrol (IMQ(1-7)+C), cedryl acetate (IMQ(1-7)+CA), or alpha-cedrene (IMQ(1-7)+CE) after the termination of imiquimod application.

(27) FIG. 19 is a graph illustrating the comparison of the recovery effect on skin wrinkles in the psoriasis induced mice according to the oral administration of distilled water (IMQ(1-7)), cedrol (IMQ(1-7)+C), cedryl acetate (IMQ(1-7)+CA), or alpha-cedrene (IMQ(1-7)+CE) after the termination of imiquimod application.

(28) FIG. 20 is a graph illustrating the comparison of the accelerating effect on hair regrowth in the psoriasis induced mice according to the oral administration of distilled water (IMQ(1-7)), cedrol (IMQ(1-7)+C), cedryl acetate (IMQ(1-7)+CA), or alpha-cedrene (IMQ(1-7)+CE) after the termination of imiquimod application.

DETAILED DESCRIPTION OF THE INVENTION

(29) Hereinafter, the present invention is described in detail.

(30) The present invention provides a pharmaceutical composition for preventing or treating autoimmune diseases comprising one or more compounds selected from the group consisting of the compounds represented by formulas 16 or a pharmaceutically acceptable salt thereof as an active ingredient.

(31) TABLE-US-00001 TABLE 1 Formula Compound Chemical structure 1 Cedrol 2 Cedryl acetate 3 Alpha-cedrene 4 Methyl cedryl ketone 5 Methyl cedryl ether 6 Cedrene epoxide

(32) The compounds represented by formulas 16 of the present invention can be used as the form of a pharmaceutically acceptable salt, in which the salt is preferably acid addition salt formed by pharmaceutically acceptable free acids. The acid addition salt can be obtained from inorganic acids such as hydrochloric acid, nitric acid, phosphoric acid, sulfuric acid, hydrobromic acid, hydroiodic acid, nitrous acid and phosphorous acid, or non-toxic organic acids such as aliphatic mono/dicarboxylate, phenyl-substituted alkanoate, hydroxy alkanoate, alkandioate, aromatic acids and aliphatic/aromatic sulfonic acids. The pharmaceutically non-toxic salts are exemplified by sulfate, pyrosulfate, bisulfate, sulphite, bisulphite, nitrate, phosphate, monohydrogen phosphate, dihydrogen phosphate, metaphosphate, pyrophosphate, chloride, bromide, iodide, fluoride, acetate, propionate, decanoate, caprylate, acrylate, formate, isobutylate, caprate, heptanoate, propiolate, oxalate, malonate, succinate, suberate, cabacate, fumarate, maliate, butyne-1,4-dioate, hexane-1,6-dioate, benzoate, chlorobenzoate, methylbenzoate, dinitrobenzoate, hydroxybenzoate, methoxybenzoate, phthalate, terephthalate, benzenesulfonate, toluenesulfonate, chlorobenzenesulfonate, xylenesulfonate, phenylacetate, phenylpropionate, phenylbutylate, citrate, lactate, hydroxybutylate, glycolate, malate, tartrate, methanesulfonate, propanesulfonate, naphthalene-1-sulfonate, naphthalene-2-sulfonate and mandelate.

(33) The acid addition salt in this invention can be prepared by the conventional method known to those in the art. For example, the compounds of formulas 16 are dissolved in an organic solvent such as methanol, ethanol, acetone, methylenechloride, or acetonitrile, to which organic acid or inorganic acid is added to induce precipitation. Then, the precipitate is filtered and dried to give the salt. Or the solvent and the excessive acid are distillated under reduced pressure, and dried to give the salt. Or the precipitate is crystallized in the organic solvent to give the same.

(34) A pharmaceutically acceptable metal salt can be prepared by using a base. Alkali metal or alkali earth metal salt is obtained by the following processes: dissolving the compound in excessive alkali metal hydroxide or alkali earth metal hydroxide solution; filtering non-soluble compound salt; evaporating the remaining solution and drying thereof. At this time, the metal salt is preferably prepared in the pharmaceutically suitable form of sodium, potassium, or calcium salt. And the corresponding silver salt is prepared by the reaction of alkali metal or alkali earth metal salt with proper silver salt (ex; silver nitrate).

(35) The compounds represented by formulas 16 above have a non-symmetrical structure, so that they exist in the form of different enantiomers. So, all the compounds represented by formulas 16 can include all the optical isomers, (R) or (S) type stereoisomers, or the mixtures thereof. The compound represented by formula 1 can contain the racemic body thereof, one or more enantiomers, one or more diasteromers, or the mixtures thereof. The optical isomer according to the present invention can be obtained by the separation method or the preparation method well known to those in the art.

(36) The autoimmune disease herein can be mediated by interleukin-17. Particularly, the autoimmune disease above can be selected from the group consisting of psoriasis, eczema, scleroderma, vitiligo, Crohn's disease, inflammatory bowel disease, type 1 diabetes, asthma, osteoarthritis, rheumatoid arthritis, polymyalgia rheumatica, ankylosing spondylitis, psoriatic arthritis, multiple sclerosis, IL-17-induced dementia, peripheral neuropathy, autism, uveitis, dry eye disease, allograft rejection, gastric cancer, pancreatic cancer, breast tumor, ovarian cancer, colorectal cancer, and lung cancer.

(37) In a preferred embodiment of the present invention, the present inventors confirmed that the cedrol or the derivatives thereof inhibited the expression of IL-17A using cedrol, cedryl acetate, alpha-cedrene, methyl cedryl ketone, methyl cedryl ether, and cedrene epoxide (see FIG. 1).

(38) The present inventors observed the ear thickness (see FIG. 4), keratosis (see FIG. 5), skin flair (see FIG. 6), skin pain (see FIG. 8), skin hemorrhage spots (see FIG. 9), and skin wrinkles (see FIG. 10) in the psoriasis induced mice according to the oral administration of cedrol, cedryl acetate, and alpha-cedrene. As a result, the present inventors confirmed that those compounds were effective in reducing the ear thickness, keratosis, skin flair, skin pain, skin hemorrhage spots, and skin wrinkles and also efficient in inhibiting the expression of IL-17A in the spleen (see FIG. 11). It was also confirmed that the thickness of the epidermal layer was thinner than that of the control group (see FIG. 12).

(39) In addition, the present inventors confirmed that the oral administration of cedrol, cedryl acetate, and alpha-cedrene to the psoriasis induced mice was efficient not only in the recovery of the ear thickness (see FIG. 14), keratosis (see FIG. 15), skin flair (see FIG. 16), skin hemorrhage spots (see FIG. 18), and skin wrinkles (see FIG. 19) but also in accelerating hair regrowth (see FIG. 20).

(40) Therefore, the compounds represented by formulas 16 of the present invention can be effectively used for the treatment of autoimmune diseases since they inhibit the expression of IL-17A, and have the effect of delaying the outbreak of psoriasis, the disease mediated by IL-17A, and treating thereof.

(41) The pharmaceutical composition can include the compounds represented by formulas 16 or the pharmaceutically acceptable salt thereof by 10 to 95 weight % by the total weight of the composition. The pharmaceutical composition of the present invention can additionally contain one or more active ingredients having the same or similar functions to the compounds.

(42) The pharmaceutical composition of the present invention can include any generally used carrier, diluent, excipient, or a combination of at least two of those. The pharmaceutically acceptable carrier can be any carrier that is able to deliver the composition of the present invention in a living body without limitation, which is exemplified by saline, sterilized water, Ringer's solution, buffered saline, dextrose solution, maltodextrin solution, glycerol, ethanol, liposome and a mixture comprising one or more of those components. If necessary, a general additive such as antioxidant, buffer, and bacteriostatic agent can be additionally added.

(43) The composition of the present invention can be prepared by mixing with generally used diluents or excipients such as fillers, extenders, binders, wetting agents, disintegrating agents and surfactant.

(44) The composition of the present invention can be prepared for oral or parenteral administration. Solid formulations for oral administration are tablets, pills, powders, granules, capsules, and troches. These solid formulations are prepared by mixing with one or more suitable excipients such as starch, calcium carbonate, sucrose or lactose, gelatin, etc. Except for the simple excipients, lubricants, for example magnesium stearate, talc, etc, can be added. Liquid formulations for oral administrations are suspensions, solutions, emulsions and syrups, and the above-mentioned formulations can contain various excipients such as wetting agents, sweeteners, aromatics and preservatives.

(45) Formulations for parenteral administration can include injections such as sterilized aqueous solutions, water-insoluble excipients, suspensions, and emulsions.

(46) Water-insoluble excipients and suspensions can contain propylene glycol, polyethylene glycol, vegetable oil like olive oil, injectable ester like ethylolate, etc.

(47) The composition of the present invention can be administered orally or parenterally according to the desired method. The parenteral administration can be selected from the group consisting of external administration, intraperitoneal injection, intra-rectal injection, subcutaneous injection, intravenous injection, intramuscular injection or intra-thoracic injection.

(48) The composition of the present invention is administered in a pharmaceutically effective dose. The effective dose can be determined according to the type and the severity of a disease, drug activity, drug sensitivity, administration time, administration pathway, excretion rate, treatment period, and other medicines applied together.

(49) The composition of the present invention can be administered alone or in combination with other therapeutic agents. When coadministered, the administration can be performed sequentially or simultaneously.

(50) For a desired effect, the effective dose of the active ingredient contained in the pharmaceutical composition of the present invention can be 0.001 to 10,000 mg/kg, particularly 0.1 to 5 g/kg. The administration frequency can be once a day or a few times a day.

(51) The present invention also provides a health functional food for improving autoimmune diseases comprising one or more compounds selected from the group consisting of the compounds represented by formulas 16 or a pharmaceutically acceptable salt thereof as an active ingredient.

(52) According to an example of the present invention, the compound above can be cedrol represented by formula 1, cedryl acetate represented by formula 2, alpha-cedrene represented by formula 3, methyl cedryl ketone represented by formula 4, methyl cedryl ether represented by formula 5, or cedrene epoxide represented by formula 6.

(53) The said compound can have the characteristics described hereinbefore. The autoimmune disease herein can be mediated by interleukin-17. Particularly, the autoimmune disease above can be selected from the group consisting of psoriasis, eczema, scleroderma, vitiligo, Crohn's disease, inflammatory bowel disease, type 1 diabetes, asthma, osteoarthritis, rheumatoid arthritis, polymyalgia rheumatica, ankylosing spondylitis, psoriatic arthritis, multiple sclerosis, IL-17-induced dementia, peripheral neuropathy, autism, uveitis, dry eye disease, allograft rejection, gastric cancer, pancreatic cancer, breast tumor, ovarian cancer, colorectal cancer, and lung cancer.

(54) In a preferred embodiment of the present invention, the present inventors confirmed that cedrol, cedryl acetate, alpha-cedrene, methyl cedryl ketone, methyl cedryl ether, and cedrene epoxide could suppress the expression of IL-17A (see FIG. 1) and in particular cedrol, cedryl acetate, and alpha-cedrene could delay the development of psoriasis (see FIGS. 2a12) and further treat the disease (see FIGS. 13a19) in the psoriasis induced animal model.

(55) Therefore, the compounds represented by formulas 16 can be effectively used for the improvement of autoimmune diseases mediated by IL-17A.

(56) The compounds represented by formulas 16 of the present invention or a pharmaceutically acceptable salt thereof can be used as a food additive. In that case, the compounds represented by formulas 16 of the present invention or a pharmaceutically acceptable salt thereof can be added as it is or as mixed with other food components according to the conventional method. The mixing ratio of active ingredients can be regulated according to the purpose of use. In general, to produce a health functional food, the compounds represented by formulas 16 of the present invention or a pharmaceutically acceptable salt thereof is added preferably by 0.0190 weight part to the total food weight.

(57) The form and kind of the health functional food is not limited. The health functional food can be tablets, capsules, powders, granules, liquids, and pills.

(58) The health functional food of the present invention can additionally include various flavors or natural carbohydrates, etc, like other health foods. The natural carbohydrates above can be one of monosaccharides such as glucose and fructose, disaccharides such as maltose and sucrose, polysaccharides such as dextrin and cyclodextrin, and glucose alcohols such as xilytole, sorbitol and erythritol. Besides, natural sweetening agents such as thaumatin and Stevia extract, and synthetic sweetening agents such as saccharin and aspartame can be included as a sweetening agent.

(59) In addition to the ingredients mentioned above, the health functional food of the present invention can include in variety of nutrients, vitamins, minerals, flavors, coloring agents, pectic acid and its salts, alginic acid and its salts, organic acid, protective colloidal viscosifiers, pH regulators, stabilizers, antiseptics, glycerin, alcohols, etc. All the mentioned ingredients can be added singly or together. The mixing ratio of those ingredients does not matter in fact, but in general, each can be added by 0010.1 weight part per 100 weight part of the composition of the present invention.

(60) The present invention also provides a cosmetic composition for alleviating skin irritation comprising one or more compounds selected from the group consisting of the compounds represented by formulas 16 or a pharmaceutically acceptable salt thereof as an active ingredient.

(61) According to an example of the present invention, the compound above can be cedrol represented by formula 1, cedryl acetate represented by formula 2, alpha-cedrene represented by formula 3, methyl cedryl ketone represented by formula 4, methyl cedryl ether represented by formula 5, or cedrene epoxide represented by formula 6.

(62) The said compound can have the characteristics described hereinbefore. The autoimmune disease herein can be mediated by interleukin-17. Particularly, the autoimmune disease above can be selected from the group consisting of psoriasis, eczema, scleroderma, vitiligo, Crohn's disease, inflammatory bowel disease, type 1 diabetes, asthma, osteoarthritis, rheumatoid arthritis, polymyalgia rheumatica, ankylosing spondylitis, psoriatic arthritis, multiple sclerosis, IL-17-induced dementia, peripheral neuropathy, autism, uveitis, dry eye disease, allograft rejection, gastric cancer, pancreatic cancer, breast tumor, ovarian cancer, colorectal cancer, and lung cancer.

(63) In a preferred embodiment of the present invention, the present inventors confirmed that cedrol, cedryl acetate, alpha-cedrene, methyl cedryl ketone, methyl cedryl ether, and cedrene epoxide could suppress the expression of IL-17A (see FIG. 1) and in particular cedrol, cedryl acetate, and alpha-cedrene could delay the development of psoriasis (see FIGS. 2a12) and further treat the disease (see FIGS. 13a19) in the psoriasis induced animal model.

(64) Therefore, the compounds represented by formulas 16 can be effectively used for the alleviation of autoimmune diseases mediated by IL-17A.

(65) The compounds represented by formulas 16 of the present invention or a pharmaceutically acceptable salt thereof can be included in the cosmetic composition by 0.1 to 50 weight %, particularly 1 to 10 weight % to the total weight of the cosmetic composition. However, the ratio above can be changed according to the form of cosmetics, the specific application site (face or hand) or the application volume.

(66) The cosmetic composition of the present invention can include, in addition to the compounds represented by formulas 16 of the present invention or a pharmaceutically acceptable salt thereof, any conventional ingredients generally used in cosmetics, for example such additives and carriers as stabilizers, solubilizers, vitamins, pigments and flavors, but not always limited thereto.

(67) The cosmetic composition of the present invention can be formulated in any form that can be accepted in the art, which is exemplified by pastes, creams, gels, powders, sprays, solutions, emulsions, suspensions (anhydrous and aqueous), surfactant containing cleansings, anhydrous products (oils and glycols), masks, packs, powders, lotions, soaps, oils, powder foundations, emulsion foundations, and wax foundations, etc. Particularly, the cosmetic composition of the present invention can be prepared in the form of soft lotion (skin), nutritional lotion (milk lotion), nutritional cream, massage cream, essence, eye cream, cleansing cream, cleansing foam, cleansing water, pack, spray, or powder.

(68) In the case that the cosmetic composition is formulated as paste, cream or gel, the proper carrier can be selected from the group consisting of animal oil, vegetable oil, wax, paraffin, starch, tracanth, cellulose derivative, polyethylene glycol, silicon, bentonite, silica, talk and zinc oxide.

(69) In the case that the cosmetic composition is formulated as powder or spray, the proper carrier can be selected from the group consisting of lactose, talc, silica, aluminum hydroxide, calcium silicate and polyamide powder, and in particular if the composition of the present invention is formulated as spray, a propellant such as chlorofluorohydrocarbon, propane/butane or dimethyl ether can be additionally included.

(70) In the case that the cosmetic composition is formulated as liquid or emulsion, the proper carrier can be selected from the group consisting of solvent, solubilizer and emulsifier, which is exemplified by water, ethanol, isopropanol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butyl glycol oil, glycerol aliphatic ester, polyethylene glycol and fatty acid ester of sorbitan.

(71) In the case that the cosmetic composition is formulated as suspension, the proper carrier can be selected from the group consisting of liquid diluent such as water, ethanol or propylene glycol, suspending agent such as ethoxylated isostearyl alcohol, polyoxyethylene sorbitol ester and polyoxyethylene sorbitan ester, microcrystalline cellulose, aluminum methahydroxide, bentonite, agar, and tragacanth.

(72) In the case that the cosmetic composition is formulated as surfactant-containing cleansing, the proper carrier can be selected from the group consisting of aliphatic alcohol sulfate, aliphatic alcohol ether sulfate, sulfosuccinic monoester, isethionate, imidazolinum derivative, methyltaurate, sarcosinate, fatty acid amide ether sulfate, alkyl amidobetain, aliphatic alcohol, fatty acid glyceride, fatty acid diethanolamide, vegetable oil, lanolin derivative and ethoxylated glycerol fatty acid ester.

(73) In addition, the present invention provides a hair tonic composition comprising one or more compounds selected from the group consisting of the compounds represented by formulas 16 or a pharmaceutically acceptable salt thereof as an active ingredient.

(74) According to an example of the present invention, the compound above can be cedrol represented by formula 1, cedryl acetate represented by formula 2, alpha-cedrene represented by formula 3, methyl cedryl ketone represented by formula 4, methyl cedryl ether represented by formula 5, or cedrene epoxide represented by formula 6.

(75) In a preferred embodiment of the present invention, the present inventors confirmed that cedrol, cedryl acetate, and alpha-cedrene exhibited the effect of promoting hair regrowth (see FIGS. 13a13d and FIG. 20).

(76) Therefore, the compounds represented by formulas 16 can be effectively used as a hair tonic composition.

(77) The hair tonic composition of the present invention can contain the compounds represented by formulas 16 of the invention at the concentration of 0.00199.99 weight % by the total weight of the hair tonic composition, and preferably at the concentration of 0.150 weight %. However, the concentration ratio above can be changed according to the severity of hair loss or the purpose of use as long as the concentration does not cause toxicity in a human body.

(78) The hair tonic composition of the present invention can include, in addition to the compounds represented by formulas 16, any conventional ingredients generally used as pharmaceuticals or cosmetics raw materials, for example such additives as purified water, mineral water, ethanol, glycerin, squalane, 1,3-propylene glycol, 1,3-butylene glycol, castor oil, tsubaki oil, liquid petrolatum, surfactants, emulsifiers, thickeners, preservatives, antioxidants, fragrances, or carriers.

(79) In addition to the ingredients mentioned above, the composition of the present invention can contain any ingredient that can supply nutrients to hair follicles or a hair growth promoting auxiliary component, which is exemplified by vitamins, amino acids, vegetable and animal oils, or sodium chloride. At this time, the vitamins herein can be exemplified by vitamin A, vitamin B1, vitamin B2, niacin (nicotinic acid), vitamin C, vitamin E, sodium pantothenate, potassium pantothenate, or biotin H (vitamin H). The amino acid herein can be dopa. The vegetable and animal oils herein can be exemplified by hempseed oil, egg oil, olive oil, Camellia oil, rapeseed oil, sesame oil, or germ oil. Such auxiliary component can be added to the composition of the present invention at the concentration of 0.000110 weight %, preferably 0.011 weight % by the total weight of the composition.

(80) The composition of the present invention can be directly applied or dispersed on hair or scalp. So, the composition can be prepared in the form of hair tonic, hair lotion, hair cream, hair spray, hair mousse, hair gel, hair conditioner, hair shampoo, hair rinse, hair pack, hair treatment, eyebrow hair growth agent, eyelash hair growth agent or eyelash nutrient, pet shampoo or pet rinse.

(81) The composition of the present invention can be formulated in any form that can be conventionally prepared in this field, which is exemplified by cream, lotion, tonic, spray, aerosol, oil, solution, suspension, gel, ointment, emulsion, or paste.

(82) In the case that the composition of the present invention is formulated as paste, cream or gel, the proper carrier can be selected from the group consisting of animal oil, vegetable oil, paraffin, starch, tracanth, cellulose derivative, polyethylene glycol, silicon, bentonite, silica, talk and zinc oxide.

(83) In the case that the composition of the present invention is formulated as spray, the proper carrier can be selected from the group consisting of lactose, talc, silica, aluminum hydroxide, calcium silicate and polyamide powder, and in particular if the composition of the present invention is formulated as spray, a propellant such as chlorofluorohydrocarbon, propane/butane or dimethyl ether can be additionally included.

(84) In the case that the composition of the present invention is formulated as liquid, the proper carrier can be selected from the group consisting of solvent, solubilizer and emulsifier, which is exemplified by water, ethanol, isopropanol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butyl glycol oil, glycerol aliphatic ester, polyethylene glycol and fatty acid ester of sorbitan.

(85) In the case that the composition of the present invention is formulated as suspension, the proper carrier can be selected from the group consisting of liquid diluent such as water, ethanol or propylene glycol; suspending agent such as ethoxylated isostearyl alcohol, polyoxyethylene sorbitol ester and polyoxyethylene sorbitan ester, microcrystalline cellulose, aluminum methahydroxide, bentonite, agar, and tragacanth.

(86) Practical and presently preferred embodiments of the present invention are illustrative as shown in the following Examples.

(87) However, it will be appreciated that those skilled in the art, on consideration of this disclosure, may make modifications and improvements within the spirit and scope of the present invention.

Example 1: Inhibition of IL-17A Expression by Cedrol and its Derivatives

(88) <1-1> Investigation of IL-17A Down-Regulation by Cedrol and its Derivatives

(89) To investigate the inhibitory effect of cedrol and its derivatives on the expression of IL-17A, IL-17 luciferase-(LUCPorter) stable reporter cell line (IMGENEX, USA, Cat No. IML-301)] was treated with cedrol (Sigma-Aldrich, USA, Cat No. 22135), cedryl acetate (Sigma-Aldrich, USA, Cat No. 45885), alpha-cedrene (Sigma-Aldrich, USA, Cat No. 22133), methyl cedryl ketone (Sigma-Aldrich, USA, Cat No. W522805), methyl cedryl ether (Sigma-Aldrich, USA, Cat No. W525405), and cedrene epoxide (Sigma-Aldrich, USA, Cat No. S528188), followed by performing IL-17A inhibition assay. The IL-17 luciferase-(LUCPorter) stable reporter cell line is the cell line that secretes IL-17, which is prepared by inserting pLightSwitch promoter vector HEK 293, the human embryonic kidney cell line, and inserting Renilla luciferase in the human IL-17A target gene as a reporter gene.

(90) Particularly, the IL-17 luciferase-(LUCPorter) stable reporter cell line was cultured in DMEM (GIBCO, USA) comprising 4.5 g/, of glucose, 4 mM L-glutamine, 1 mM sodium pyruvate, 10% FBS, 100 g/ of streptomycin, 100 units/ of penicillin, and 3 g/ of puromycin. The prepared cells were distributed in a 96-well plate at the density of 510.sup.4 cells/well, followed by culture in a 37 C. 5% CO.sub.2 incubator for 16 hours. The cultured cells were treated with 6 kinds of the compounds of the present invention at the concentration of 10, 100, or 1,000 g/, followed by further culture in a 37 C. 5% CO.sub.2 incubator for 6 hours. Then, LightSwitch luciferase assay solution (CAT Number LS010, Switchgear Genomics, USA) included in LightSwitch assay kit (SwitchGear Genomics, USA) was loaded to the plate (50 /well), followed by reaction in a dark room for 30 minutes. Then, fluorescence was measured by using the multimode Reader LB-942 (Berthold, USA) and ICE program. The results obtained from the three repeated experiments were made as meanstandard deviation, which are presented as a graph.

(91) TABLE-US-00002 TABLE 2 Inhibition of IL-17A expression (%) Average Conc. Experi- Experi- Experi- Inhibition Compound (g/ml) ment -1 ment -2 ment -3 (%) cedrol 0 0 0 0 0 10 24 0 33 19.0 100 21 14 43 26.0 1000 76 59 72 69.0 alpha- 0 0 0 0 0 cedrene 10 6 3 21 10.0 100 21 11 32 21.3 1000 36 23 35 31.3 cedryl 0 0 0 0 0 acetate 10 Experi- 15 23 19.0 ment X 100 Experi- 27 36 31.5 ment X 1000 Experi- 74 90 82.0 ment X methyl 0 0 0 0 0 cedryl 10 0 1 13 4.7 ketone 100 12 15 25 17.3 1000 78 58 66 67.3 methyl 0 0 0 0 0 cedryl 10 6 4 4 0.7 ether 100 5 5 8 2.7 1000 48 18 26 30.7 cedrene 0 0 0 0 0 epoxide 10 11 4 0 5.0 100 14 16 12 14.0 1000 60 56 46 54.0

(92) As a result, as shown in FIG. 1 and Table 2, the expression of IL-17A in the control group was 2,582 units. When those 6 compounds were treated at the concentration of 10, 100, or 1,000 g/ to experimental groups, the expression of IL-17A in the group treated with cedrol was 1,718174 units (67% by the control), 1,460124 units (57% by the control), and 71545 units (28% by the control). The expression of IL-17A in the group treated with alpha-cedrene was 2,042114 units (79% by the control), 1,757310 units (68% by the control), and 1,68864 units (65% by the control). The expression of IL-17A in the group treated with cedryl acetate was 1,994304 units (77% by the control), 1,648138 units (64% by the control), and 2576 units (10% by the control). The expression of IL-17A in the group treated with methyl cedryl ketone was 2,248194 units (87% by the control), 1,930111 units (75% by the control), and 866106 units (34% by the control). The expression of IL-17A in the group treated with methyl cedryl ether was 2,479136 units (96% by the control), 2,379206 units (92% by the control), and 1,921239 units (74% by the control). The expression of IL-17A in the group treated with cedrene epoxide was 2,591458 units (100% by the control), 2,267806 units (88% by the control), and 1,38287 units (54% by the control). In particular, cedrol, cedryl acetate, and alpha-cedrene suppressed the expression of IL-17A dose-dependently.

(93) Based on the results above, cedrol, cedryl acetate, and alpha-cedrene were selected as the compounds to be used in the following experiments.

(94) <1-2> Investigation of IC.sub.50 Values of Cedrol and its Derivatives to IL-17A Expression

(95) To investigate IC.sub.50 values of cedrol, cedryl acetate, alpha-cedrene, methyl cedryl ketone, methyl cedryl ether, and cedrene epoxide, the average IL-17A expression inhibition rate of each compound was calculated by applying the values obtained in Example <1-1> to the following mathematical formula 1.

(96) IC.sub.50 of each compound to inhibit the IL-17A expression by 50% was obtained by using the calculated values. The average IL-17A expression inhibition rate of each compound is shown in Table 2 above.
Inhibition rate (%)=100(measured value of controlmeasured value of experimental group)/measured value of control[Mathematical Formula 1]

(97) TABLE-US-00003 TABLE 3 Compound IC.sub.50(g/ml) cedrol 726 alpha-cedrene 1,507 cedryl acetate 608 methyl cedryl ketone 841 methyl cedryl ether 1,130 cedrene epoxide 942

(98) As a result, as shown in Table 3, cedryl acetate displayed the strongest IL-17A expression inhibition activity and cedrolmethyl cedryl ketonecedrene epoxidemethyl cedryl etheralpha-cedrene followed in that order (Table 3).

Example 2: Delayed Effect of Cedrol, Cedryl Acetate, and Alpha-Cedrene on Psoriasis Development

(99) <2-1> Preparation of Psoriasis Induced Mice

(100) To investigate the delayed effect of cedrol, cedryl acetate, and alpha-cedrene on the development of psoriasis, total 5 groups of mice were prepared (8 mice/group). First, the hair of the entire back of the 8-week-old male Balb/c mouse whose immune system was weakened was removed by using a hair clipper (Kimlaube Hair pen 325,327, Rikei, Korea). In the middle of the shaved back of the mouse, 2 mg of imiquimod (3M Health Care Limited, England) was applied in the area of 2 cm1.5 cm and also 1,125 mg of imiquimod was applied on the right ear of the mouse every day once a day to induce psoriasis.

(101) The mice prepared above were divided into the distilled water treated group (IMQ), the cedrol treated group (C), the cedryl acetate treated group (CA), and the alpha-cedrene treated group (CE). At this time, the mice were orally treated with distilled water at the concentration of 200 /mouse and cedrol or its derivatives at the concentration of 200/mouse (100 mg/kg). The day when distilled water or the compound administration started was recorded as day 0 and the administration was performed once a day for a week, during which photo-recording was performed every day (FIGS. 2A2D). In the meantime, instead of applying imiquimod, 40 mg of vaseline was applied on the back of the control group (CONT) and 22.5 mg of vaseline was applied on the right ear of the control group. And the control group was orally administered with distilled water (200 /mouse).

(102) <2-2> Weight Changes in the Psoriasis Induced Mice According to the Oral Administration of Cedrol, Cedryl Acetate, and Alpha-Cedrene

(103) To compare the weight changes in the psoriasis induced mice according to the oral administration of cedrol, cedryl acetate, and alpha-cedrene of Example <2-1>, the weight of each mouse was measured at the same time every day for a week.

(104) As a result, as shown in FIG. 3, the weight of the control mouse (CONT) was gradually increased and increased by 1.13 g, seven days later. However, in the group treated with imiquimod (IMQ), the weight was reduced for 2 days from day 0 but reversely the weight was increased from day 3 to day 5 and once again the weight was decreased after day 5. In the group treated with IMQ alone, the weight was reduced by 0.48 g for 7 days, while the weight of the group treated with cedrol during the application of IMQ was increased by 0.025 g for 7 days (FIG. 3).

(105) <2-3> Investigation of Ear Thickness Reduction Effect in the Psoriasis Induced Mice According to the Oral Administration of Cedrol, Cedryl Acetate, and Alpha-Cedrene

(106) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <2-1> was observed with the naked eye. Then, the psoriasis area severity index (PASI) was calculated with the range of 14 to confirm the reduction effect of the compounds on the ear thickness.

(107) As a result, as shown in FIGS. 2A2D and FIG. 4, the ear thickness of the group treated with IMQ alone was increased the most. Precisely, the mean point was 0.83 on day 1, which continuously increased to 3.5 on day 7. In the group treated with cedrol after the application of IMQ, the mean ear thickness point was 2.6 on day 7. In the group treated with cedrol acetate after the application of IMQ, the mean ear thickness point was 2.3 on day 7. In the group treated with alpha-cedrene after the application of IMQ, the mean ear thickness point was 2.6 on day 7. The ear thickness reduction effect was observed in the group treated with the compounds of the present invention, among which cedryl acetate showed the strongest reduction effect, followed by alpha-cedrene and cedrol in that order (FIGS. 2A2D and FIG. 4).

(108) <2-4> Investigation of Keratosis Reduction Effect in the Psoriasis Induced Mice According to the Oral Administration of Cedrol, Cedryl Acetate, and Alpha-Cedrene

(109) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <2-1> was observed with the naked eye. Then, the psoriasis area severity index (PASI) was calculated to confirm the reduction effect of the compounds on keratosis. Keratosis is a symptom of psoriasis. The application of IMQ can induce keratosis.

(110) As a result, as shown in FIGS. 2A2D and FIG. 5, keratosis was strongly induced in the group treated with IMQ alone and the mean point was 3.8 on day 7. The mean point of the group treated with cedrol after the application of IMQ was 3.00 on day 7, while the mean point of the group treated with cedryl acetate after the application of IMQ was 3.08 on day 7. The mean point of the group treated with alpha-cedrene after the application of IMQ was 2.66 on day 7. Therefore, the keratosis reduction effect was observed in those groups treated with the compounds of the invention, among which alpha-cedrene showed the strongest reduction effect, followed by cedryl acetate and cedrol in that order (FIGS. 2A2D and FIG. 5).

(111) <2-5> Investigation of Skin Flair Reduction Effect in the Psoriasis Induced Mice According to the Oral Administration of Cedrol, Cedryl Acetate, and Alpha-Cedrene

(112) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <2-1> was observed with the naked eye. Then, the psoriasis area severity index (PASI) was calculated to confirm the reduction effect of the compounds on skin flair. Skin flair is a symptom of psoriasis. The application of IMQ can induce skin flair.

(113) As a result, as shown in FIGS. 2A2D and FIG. 6, skin flair was strongly induced in the group treated with IMQ alone and the mean point was 4.00 on day 7. The mean point of the group treated with cedrol after the application of IMQ was 3.33 on day 7, while the mean point of the group treated with cedryl acetate after the application of IMQ was 3.16 on day 7. The mean point of the group treated with alpha-cedrene after the application of IMQ was 3.33 on day 7. Therefore, the skin flair reduction effect was observed in those groups treated with the compounds of the invention, among which alpha-cedrene showed the strongest reduction effect, followed by cedrol and cedryl acetate in that order (FIGS. 2A2D and FIG. 6).

(114) <2-6> Comparison of Cumulative Score of Psoriasis Area Severity Index for Ear Thickness, Keratosis, and Skin Flair of the Psoriasis Induced Mice Orally Administered with Cedrol, Cedryl Acetate, and Alpha-Cedrene

(115) The psoriasis area severity index obtained in Examples <2-3> and <2-5> was accumulated to compare the psoriasis area severity index for ear thickness, keratosis and skin flair of the mouse groups respectively treated with cedrol, cedryl acetate, and alpha-cedrene via oral-administration.

(116) As a result, as shown in FIG. 7, alpha-cedrene and cedryl acetate exhibited the strongest reduction effect at a similar level (FIG. 7).

(117) <2-7> Investigation of Skin Pain Reduction Effect in the Psoriasis Induced Mice According to the Oral Administration of Cedrol, Cedryl Acetate, and Alpha-Cedrene

(118) When the back of the psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <2-1> was pinched, those mice who sound painfully with strong rejection were counted. Skin pain is a symptom of psoriasis, and when IMQ is applied, skin pain becomes stronger as time goes by.

(119) As a result, as shown in FIG. 8, the mice in all groups showed pain from 3 days after the administration. In the group treated with IMQ alone, 5 mice were confirmed to have pain on day 7. However, in the group treated with cedrol after the application of IMQ, only one mouse showed pain on day 4 and no mice were confirmed to have pain on day 5. In the group treated with cedryl acetate after the application of IMQ, only one mouse showed pain on day 6 and no mice were confirmed to have pain on day 7. In the group treated with alpha-cedrene after the application of IMQ, no mice showed pain during the 7 day observation period. Therefore, the skin pain reduction effect was observed in those groups treated with the compounds of the invention, among which alpha-cedrene showed the strongest reduction effect, followed by cedrol and cedryl acetate in that order (FIG. 8).

(120) <2-8> Investigation of Skin Hemorrhage Spot Reduction Effect in the Psoriasis Induced Mice According to the Oral Administration of Cedrol, Cedryl Acetate, and Alpha-Cedrene

(121) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <2-1> were observed by the naked eye, and the number of mice showing hemorrhage spots was counted. Hemorrhage spot is a symptom of psoriasis, and when IMQ is applied, the number of skin hemorrhage spots increases as time goes by.

(122) As a result, as shown in FIGS. 2A2D and FIG. 9, only one mouse in the group treated with IMQ alone showed hemorrhage spots on day 3 and 5 mice showed hemorrhage spots on day 7. In the group treated with cedrol after the application of IMQ, one mouse showed hemorrhage spots on day 4 and 3 mice showed hemorrhage spots on day 7. In the meantime, in the group treated with cedryl acetate after the application of IMQ, one mouse showed hemorrhage spots on day 5 and one mouse showed hemorrhage spots on day 7. In the group treated with alpha-cedrene after the application of IMQ, two mice showed hemorrhage spots on day 5 and only one mouse showed hemorrhage spots on day 7. Therefore, the skin hemorrhage spot reduction effect was observed in those groups treated with the compounds of the invention, among which cedryl acetate showed the strongest reduction effect, followed by alpha-cedrene and cedrol in that order (FIGS. 2A2D and FIG. 9).

(123) <2-9> Investigation of Skin Wrinkle Reduction Effect in the Psoriasis Induced Mice According to the Oral Administration of Cedrol, Cedryl Acetate, and Alpha-Cedrene

(124) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <2-1> were observed by the naked eye, and the number of mice showing skin wrinkles was counted. Skin wrinkle is a symptom of psoriasis, and when IMQ is applied, skin keratinization increases and accordingly skin wrinkles are formed as time goes by.

(125) As a result, as shown in FIGS. 2A2D and FIG. 10, only one mouse in the group treated with IMQ alone showed skin wrinkles on day 6 and 3 mice showed skin wrinkles on day 7. In the group treated with cedrol after the application of IMQ, one mouse showed skin wrinkles on day 5 and 2 mice showed skin wrinkles on day 7. In the meantime, in the group treated with cedryl acetate after the application of IMQ, one mouse showed skin wrinkles on day 5 and one mouse showed skin wrinkles on day 7. In the group treated with alpha-cedrene after the application of IMQ, one mouse showed skin wrinkles on day 6 and only one mouse showed skin wrinkles on day 7. Therefore, the skin wrinkle reduction effect was observed in those groups treated with the compounds of the invention, among which alpha-cedrene showed the strongest reduction effect, followed by cedryl acetate and cedrol in that order (FIGS. 2A2D and FIG. 10).

(126) <2-10> Inhibition of IL-17A Expression in the Spleen of the Psoriasis Induced Mice According to the Oral Administration of Cedrol, Cedryl Acetate, and Alpha-Cedrene

(127) The inhibition of IL-17A expression in the spleen of the psoriasis Induced mice according to the oral administration of cedrol, cedryl acetate, and alpha-cedrene was investigated by real-time PCR (polymerase chain reaction).

(128) Particularly, the spleen was extracted from the psoriasis Induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <2-1>. Total RNA was extracted from the spleen by the conventional method. To synthesize cDNA, 2 g of RNA was loaded in 9 of DEPC (RNase free water), indicating the dilution of the concentration. 1 of oligo dT was added thereto, followed by reaction at 70 C. for 10 minutes. The sample was treated on ice for 5 minutes, to which 2 of 10 reaction buffer, 2 of dNTP (10 mM each), 1 of M-MLV reverse transcriptase, and 5 of DNase free water were added to make the total volume of the reaction mixture 20 . The mixture was reacted at 42 C. for 1 hour to synthesize cDNA. The reaction mixture was heated at 72 C. for 10 minutes to remove the reverse transcriptase activity. Then, the reaction mixture was stored at 20 C. Real-time PCR was performed by using AMPIGENE qPCR 1-Step Green Kit (Enzo Life Sciences Inc, USA).

(129) Before performing real-time PCR, each well of a 96-well plate was added with 10 l of 2 Ampigene qPCR Green Mix Lo-Rox, 1 l of forward primer [IL-17A forward primer (SEQ ID NO:1): 5-TCTCCTCTGAATGGGGTGAA-3], and 1 l of reverse primer [IL-17A reverse primer (SEQ ID NO:2): 5-CAGAGTAGGGAGCTAAATTATCCA-3], 2 l of the cDNA template synthesized above, and 6 l of distilled water (20 l total). PCR was performed with the sample as follows; predenaturation at 95 C. for 2 minutes (polymerase activation), denaturation at 95 C. for 5 seconds, annealing/extension at 65 C. for 30 seconds, 40 cycles from denaturation to extension.

(130) As a result, as shown in FIG. 11, when the IL-17A expression of the non-treated control group was regarded as value 1, the value of the IL-17A expression of the group treated with IMQ alone was 54.95.5. The IL-17A expression value of the group treated with cedrol, cedryl acetate, or alpha-cedrene after the application of IMQ was 1.10.1, 7.40.7, and 31.03.1, respectively. Therefore, the expression of IL-17A was inhibited in those groups treated with the compounds of the invention, among which alpha-cedrene showed the strongest inhibition effect, followed by cedryl acetate and cedrol in that order (FIG. 11).

(131) <2-11> Comparison of Skin Thickness of the Psoriasis Induced Mice Orally Administered with Cedrol, Cedryl Acetate, and Alpha-Cedrene

(132) The skin of the psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <2-1> was stained with hematoxyline and eosine in order to compare the skin thickness.

(133) Particularly, the psoriasis induced mice of Example <2-1> were sacrificed with CO.sub.2, from which 1 cm1 cm portions of the back surface were obtained and placed in PBS. The tissues washed with PBS were loaded in 10% formalin, followed by fixing at room temperature for a day. The fixed tissues were washed with PBS once, followed by dehydration with 25% methanol, 50% methanol, 75% methanol, and 100% methanol for 30 minutes each. Further dehydration of those tissues was additionally performed with 100% ethanol twice for 30 minutes each; with the mixed solution comprising ethanol and xylene (1:1) for 30 minutes, and with 100% xylene twice for 30 minutes each. 4 hours before washing, the modular tissue embedding center (LEICA EG 1150H, Leica, Germany) was turned on and paraplast plus (Sigma Aldrich, Korea) was melted at 60 C., followed by washing the paraffin. The tissues were loaded in a bottle, to which the melted paraffin was poured in, followed by washing in a 60 C. warm chamber twice for one hour each. The xylene-free tissues were placed in the paraffin solution, followed by reaction in the warm chamber for a day. The tissue sections were then placed on a Peel-A-Way embedding mold (Polysciences, Taiwan) and the paraffin solution was filled to half of the mold. The tissue sections were placed on top of the Peel-A-Way embedding mold, followed by fixing. An embedding ring (Thomas Scientific, USA) was placed on the mold, which was treated with the paraffin solution to solidify the mold and the ring at 4 C. for 3 hours, followed by reaction at 4 C. for a day. The embedded tissues can be semipermanently stored at 4 C. The embedded tissues were cut by using a semi-motorized rotary microtome (LEICA RM2145 Microtome, Leica, Germany), which were suspended in a 37 C. water bath to spread the paraffin wrinkles. The straightened wrinkles were collected by using a micro silane coating slide (Muto Pure Chemicals, Japan), which were dried at 37 C. for a day. When the tissues were completely dried, they were treated with xylene twice for 5 minutes each in order to eliminate the paraffin remaining in the tissues. The tissues were further washed with the mixed solution comprising ethanol and xylene (1:1), 100% ethanol, 100% methanol, 75% methanol, and 50% methanol for 2 minutes each to stain the tissues easily. The tissues were treated with a Mayer hematoxylin solution (MHS 1-100ML, Sigma Aldrich, Korea) at room temperature for 30 minutes, followed by washing with PBS for 10 minutes. Then, an eosin Y solution (Daejung, Korea) was treated thereto at room temperature for 1 minute to stain the tissues. Upon completion of the staining, the tissues were dehydrated with 75% methanol, 100% methanol, 100% ethanol, and the mixed solution comprising ethanol and xylene (1:1) for 10 seconds each to preserve the tissues permanently. At last, the stained tissues were treated with xylene for 2 minutes for fixing. Then, the skin thickness was measured by using NIS-Elements F (Nikon software, DS-F12-U3, Nikon, USA) program on Nikon eclipse Ti microscope (Nikon Instruments, USA) plan fluor 40.13.

(134) As a result, as shown in FIGS. 12A and 12B, the skin thickness of the non-treated control group and the group treated with IMQ alone was respectively 1,045 m and 1,181 m on day 7. The skin thickness of the group treated with cedrol, cedryl acetate, or alpha-cedrene after the application of IMQ was respectively 954 m (19.2% inhibition), 999 m (15.3% inhibition), and 954 m (19.2% inhibition) on day 7. The skin thickness reduction effect was observed in the groups treated with the compounds of the invention and the effects of cedrol and alpha-cedrene were similar (FIGS. 12A and 12B).

Example 3: Confirmation of Therapeutic Effect of Cedrol, Cedryl Acetate, and Alpha-Cedrene on Psoriasis

(135) <3-1> Preparation of Psoriasis Induced Mice

(136) Imiquimod was applied to the psoriasis induced mice which had developed psoriasis for a week in Example <2-1>. The application was stopped 8 days after the application began. The groups CON and IMQ were treated with distilled water, the group C was treated with cedrol, the group CA was treated with cedryl acetate, the group CE was treated with alpha-cedrene alone at the concentration of 100 mg/kg in 200 , every day via oral-administration. Day 8 was the day the imiquimod application was stopped, since then the compounds were administered for 1 week once a day, during which photo-recording was performed (FIGS. 13A13D).

(137) <3-2> Recovery Effect of Cedrol, Cedryl Acetate, and Alpha-Cedrene on Ear Thickness of the Psoriasis Induced Mice

(138) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene in Example <3-1> were observed with the naked eye. The psoriasis area severity index (Psoriasis Area Severity Index, PASI) was given from the point 1 to point 4, based on which the recovery effect on the ear thickness was evaluated.

(139) As a result, as shown in FIGS. 13A13D, and FIG. 14, PASI reflecting the ear thickness of the group orally administered with distilled water alone was 4.01.0 on day 4, and the point was maintained at average 2.00 from day 14 and did not decrease from that point any further. PASI reflecting the ear thickness of the group orally administered with cedrol was 4.00.6 on day 8, and the point was reduced to 0.70.6 on day 16. PASI reflecting the ear thickness of the group orally administered with cedryl acetate was 4.00.6 on day 8, and all 8 mice were recovered to normal from day 15. PASI reflecting the ear thickness of the group orally administered with alpha-cedrene was 4.00.0 on day 8, and the point was reduced to 0.70.6 on day 15. So, it was confirmed that the ear thickness was recovered in the groups treated with the compounds of the invention, among which cedryl acetate showed the strongest recovery effect, followed by cedrol and alpha-cedrene in that order (FIGS. 13A13D, and FIG. 14).

(140) <3-3> Recovery Effect of Cedrol, Cedryl Acetate, and Alpha-Cedrene on Keratosis of the Psoriasis Induced Mice

(141) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene in Example <3-1> were observed with the naked eye. Then, the psoriasis area severity index (Psoriasis Area Severity Index, PASI) was calculated, based on which the recovery effect on keratosis was evaluated.

(142) As a result, as shown in FIGS. 13A13D, and FIG. 15, PASI reflecting keratosis of the group orally administered with distilled water alone was 4.01.0 on day 8, and the point was 0.70.6 on day 16. PASI reflecting keratosis of the group orally administered with cedrol was 3.00.6 on day 8, and all 8 mice were recovered to normal on day 15. PASI reflecting keratosis of the group orally administered with cedryl acetate was 4.00.6 on day 8, and the point was 1.00.0 on day 14. PASI reflecting keratosis of the group orally administered with alpha-cedrene was 4.00.6 on day 8, and the point was reduced to 0.30.6 on day 15. So, it was confirmed that keratosis was recovered in the groups treated with the compounds of the invention, among which cedrol showed the strongest recovery effect, followed by cedryl acetate and alpha-cedrene in that order (FIGS. 13A13D, and FIG. 15).

(143) <3-4> Recovery Effect of Cedrol, Cedryl Acetate, and Alpha-Cedrene on Skin Flair of the Psoriasis Induced Mice

(144) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene in Example <3-1> were observed with the naked eye. Then, the psoriasis area severity index (Psoriasis Area Severity Index, PASI) was calculated, based on which the recovery effect on keratosis was evaluated.

(145) As a result, as shown in FIGS. 13A13D, and FIG. 16, PASI reflecting skin flair of the group orally administered with distilled water alone was 4.00.0 on day 8, and the point was 0.70.6 on day 16. PASI reflecting skin flair of the group orally administered with cedrol was 3.00.6 on day 8, and skin flair of all mice disappeared on day 16. PASI reflecting skin flair of the group orally administered with cedryl acetate was 4.00.0 on day 8. PASI reflecting skin flair of the group orally administered with alpha-cedrene was 4.01.0 on day 8, and skin flair of all mice disappeared on day 16. So, it was confirmed that skin flair was recovered in the groups treated with the compounds of the invention, among which cedrol showed the strongest recovery effect, followed by cedryl acetate and alpha-cedrene in that order (FIGS. 13A13D, and FIG. 16).

(146) <3-5> Comparison of Cumulative Score of Psoriasis Area Severity Index for Ear Thickness, Keratosis, and Skin Flair of the Psoriasis Induced Mice Orally Administered with Cedrol, Cedryl Acetate, and Alpha-Cedrene

(147) The psoriasis area severity index obtained in Examples <3-2> and <3-4> was accumulated to compare the psoriasis area severity index for ear thickness, keratosis and skin flair of the mouse groups respectively treated with cedrol, cedryl acetate, and alpha-cedrene via oral-administration.

(148) As a result, as shown in FIG. 17, cedrol showed the strongest recovery effect, followed by cedryl acetate and alpha-cedrene in that order (FIG. 17).

(149) <3-6> Recovery Effect of Cedrol, Cedryl Acetate, and Alpha-Cedrene on Hemorrhage Spots of the Psoriasis Induced Mice

(150) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <3-1> were observed by the naked eye, and the number of mice showing the recovery of hemorrhage spots was counted.

(151) As a result, as shown in FIGS. 13A13D and FIG. 18, all 8 mice of the group orally administered with distilled water alone showed hemorrhage spots on day 8 but on day 16 when the experiment was terminated only 1 mouse showed hemorrhage spots. In the group treated with cedrol, 6 mice showed hemorrhage spots on day 8 but no mouse showed hemorrhage spots on day 12. In the group treated with cedryl acetate, 6 mice showed hemorrhage spots on day 8 but no mouse showed hemorrhage spots on day 16. In the group treated with alpha-cedrene, 4 mice showed hemorrhage spots on day 8 but no mouse showed hemorrhage spots on day 16. So, it was confirmed that the recovery effect on hemorrhage spots was confirmed in the groups treated with the compounds of the invention, among which cedrol showed the strongest recovery effect, followed by cedryl acetate and alpha-cedrene in that order (FIGS. 13A13D and FIG. 18).

(152) <3-7> Recovery Effect of Cedrol, Cedryl Acetate, and Alpha-Cedrene on Skin Wrinkles of the Psoriasis Induced Mice

(153) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <3-1> were observed by the naked eye, and the number of mice showing the recovery of skin wrinkles was counted.

(154) As a result, as shown in FIGS. 13A13D and FIG. 19, 5 mice in the group orally treated with distilled water alone without being treated with the compounds of the invention showed skin wrinkles but only one mouse showed skin wrinkles on day 16 when the experiment was terminated. In the group treated with cedrol, 5 mice showed skin wrinkles on day 8 but no mouse showed skin wrinkles after day 15. In the group treated with cedryl acetate, 3 mice showed skin wrinkles on day 8 but no mouse showed skin wrinkles on day 16. In the group treated with alpha-cedrene, 3 mice showed skin wrinkles on day 8 but no mouse showed skin wrinkles on day 16. So, it was confirmed that the recovery effect on skin wrinkles was confirmed in the groups treated with the compounds of the invention, among which cedrol showed the strongest recovery effect, followed by alpha-cedrene and cedryl acetate in that order (FIGS. 13A13D and FIG. 19).

(155) <3-8> Accelerating Effect of Cedrol, Cedryl Acetate, and Alpha-Cedrene on Hair Regrowth of the Psoriasis Induced Mice

(156) The psoriasis induced mice orally administered with cedrol, cedryl acetate, and alpha-cedrene of Example <3-1> were observed by the naked eye, and the number of mice showing hair regrowth was counted.

(157) As a result, as shown in FIGS. 13A13D and FIG. 20, one mouse of the group orally treated with distilled water alone without being treated with the compounds of the invention showed hair regrowth on day 14 but 5 mice showed hair regrowth on day 16 when the experiment was terminated. In the group treated with cedrol, 2 mice showed hair regrowth on day 13 but no mouse showed skin wrinkles after day 15. In the group treated with cedrol, 2 mice showed hair regrowth on day 13 and all the mice in that group showed hair growth on day 16. In the group treated with cedryl acetate, one mouse showed hair regrowth on day 14 and 7 mice showed hair regrowth on day 16. In the group treated with alpha-cedrene, one mouse showed hair regrowth on day 13 and all the mice showed hair regrowth on day 16. So, it was confirmed that the accelerating effect on hair regrowth was confirmed in the groups treated with the compounds of the invention, among which cedrol showed the strongest accelerating effect, followed by alpha-cedrene and cedryl acetate in that order (FIGS. 13A13D and FIG. 20).