Skin collagen production-promoting agent

Abstract

A problem of the present invention is to provide a skin collagen production-promoting agent without safety problems. Another problem of the present invention is to provide a skin collagen production-promoting food or drink product and a skin collagen production-promoting cosmetic product containing such a substance. TGF-β and/or a TGF-β degradation product, which is acquired by degrading TGF-β with a protease such as pepsin, pancreatin, etc., are used as a skin collagen production-promoting agent or the active ingredient of a skin collagen production-promoting food or drink product and a skin collagen production-promoting cosmetic product. The aforementioned TGF-β and/or TGF-β degradation product have an effect of increasing the collagen content of the skin.

Claims

1. A method of increasing the collagen content in the skin of a subject comprising orally administering a TGF-β degradation product to a subject in recognized need thereof in an amount effective to increase the collagen content in the skin of the subject, wherein the TGF-β degradation product is acquired by degrading TGF-β with pancreatin, and wherein the TGF-β degradation product has an average molecular weight of 500 or more and 8,000 or less.

2. A method of increasing the collagen content in the skin of a subject comprising orally administering 10 μg per day or more of a TGF-β degradation product to a subject in recognized need thereof to increase the collagen content in the skin of the subject, wherein the TGF-β degradation product is acquired by degrading TGF-β with pancreatin, and wherein the TGF-β degradation product has an average molecular weight of 500 or more and 8,000 or less.

3. The method according to claim 1, which comprises orally administering said TGF-β degradation product in combination with vitamin C.

4. The method according to claim 2, which comprises orally administering said TGF-β degradation product in combination with vitamin C.

5. The method according to claim 1, wherein the TGF-β degradation product has an average molecular weight of 1500 or more and 6500 or less.

6. The method according to claim 2, wherein the TGF-β degradation product has an average molecular weight of 1500 or more and 6500 or less.

Description

DESCRIPTION OF EMBODIMENTS

(1) A feature of the skin collagen production-promoting agent of the present invention is that TGF-β and/or a TGF-β degradation product acquired by degrading TGF-β with a protease is contained as an active ingredient. TGF-β of any origin is usable in the present invention. For example, human- and bovine-derived TGF-βs have gene sequences already revealed and can be produced with gene recombination, and TGF-β produced with a genetic engineering technique is usable in the present invention. TGF-β is contained in a relatively large amount in bovine colostrum and may be collected from the milk. TGF-β is also collectable from the medium of cell culture and such cell-derived TGF-β is also usable. For example, milk-derived TGF-β is producible in accordance with a known method (see, e.g., J. Protein Chem., Vol. 10, pp. 565-575, 1991), and TGF-β can be acquired from raw milk, powdered milk, skim milk, reconstituted milk, or other processed milk by heat treatment, salting treatment, ethanol treatment, various chromatographic processes such as ion exchange chromatography and gel filtration chromatography, and an ultrafiltration process in a combined manner as needed.

(2) For the TGF-β degradation product, a peptide mixture is usable that is acquired by limited proteolysis of TGF-β with a protease such as trypsin, pancreatin, chymotrypsin, pepsin, papain, kallikrein, cathepsin, thermolysin, and V8 protease to an average molecular weight of 8,000 or less. Meanwhile, the lower limit of the average molecular weight is preferably equal to or greater than 500. For example, the average molecular weight of the TGF-β degradation product is 500 or more and 8000 or less, 1500 or more and 8000 or less, 2500 or more and 8000 or less, 3500 or more and 8000 or less, 4500 or more and 8000 or less, 5500 or more and 8000 or less, 6500 or more and 8000 or less, 7500 or more and 8000 or less, 500 or more and 7500 or less, 1500 or more and 7500 or less, 2500 or more and 7500 or less, 3500 or more and 7500 or less, 4500 or more and 7500 or less, 5500 or more and 7500 or less, 6500 or more and 7500 or less, 500 or more and 6500 or less, 1500 or more and 6500 or less, 2500 or more and 6500 or less, 3500 or more and 6500 or less, 4500 or more and 6500 or less, 5500 or more and 6500 or less, 500 or more and 5500 or less, 1500 or more and 5500 or less, 2500 or more and 5500 or less, 3500 or more and 5500 or less, 4500 or more and 5500 or less, 500 or more and 4500 or less, 1500 or more and 4500 or less, 2500 or more and 4500 or less, 3500 or more and 4500 or less, 500 or more and 3500 or less, 1500 or more and 3500 or less, 2500 or more and 3500 or less, 500 or more and 2500 or less, 1500 or more and 2500 or less, or 500 or more and 1500 or less.

(3) The skin collagen production-promoting agent of the present invention is orally administered or applied to produce the skin collagen production-promoting effect. When the skin collagen production-promoting agent of the present invention is orally administered, the active ingredient, i.e., TGF-β or a TGF-β degradation product may directly be used or may be formulated in a usual manner and used as an oral agent such as powders, granules, tablets, capsules, and drinkable preparations. In the present invention, for example, oral agents such as powders, granules, tablets, and capsules are formulated in a usual manner by using excipients such as starch, lactose, sucrose, mannitol, carboxymethylcellulose, corn starch, and inorganic salts. This kind of formulation can be achieved by using the excipients as well as pharmaceutical additives such as binders, disintegrating agents, surfactants, lubricants, fluidity promoters, coloring agents, and flavors as needed. More specifically, binding agents include, for example, starch, dextrin, gum arabic, gelatin, hydroxypropyl starch, sodium carboxymethyl cellulose, methylcellulose, crystalline cellulose, ethyl cellulose, and polyvinyl pyrrolidone. Disintegrating agents include, for example, starch, hydroxypropyl starch, carboxymethyl cellulose, sodium carboxymethyl cellulose, cross-linked sodium carboxymethyl cellulose, and crystalline cellulose. Surfactants include soybean lecithin, sucrose fatty acid ester, etc.; lubricants include talc, wax, sucrose fatty acid ester, hydrogenated vegetable oil, etc.; and fluidity promoters include anhydrous silicic acid, dried aluminum hydroxide, magnesium silicate, etc.

(4) TGF-β or a TGF-β degradation product may be combined with nutrients, food or drink etc., directly or after formulated into preparations. If TGF-β or a TGF-β degradation product is contained together with a component conventionally considered to be effective in collagen production, such as vitamin C, a further skin collagen production-promoting effect can be expected. Since TGF-β or a TGF-β degradation product is relatively stable to heat, raw materials containing TGF-β or a TGF-β degradation product can be heat-sterilized under the normally used conditions.

(5) When the skin collagen production-promoting agent of the present invention is applied, the skin collagen production-promoting agent can be combined with known normally used components depending on the purpose of use and prepared as various dosage forms such as liquid formulation, solid formulation, and semisolid formulation and preferable compositions include ointment, gel, cream, spray, patches, lotion, powder, etc. For example, the skin collagen production-promoting agent of the present invention can be mixed with hydrocarbons such as vaseline, stearyl alcohol, higher fatty acid lower alkyl ester such as isopropyl myristate, animal oil and fat such as lanolin, polyhydric alcohol such as glycerin, glycerin fatty acid ester, mono-stearic acid, surfactants such as polyethylene glycol, inorganic salt, wax, resin, water, and, if needed, preservatives such as methyl parahydroxybenzoate and butyl parahydroxybenzoate, so as to produce skin collagen production-promoting cosmetics and pharmaceutical agents.

(6) Although an effective oral administration dose of the skin collagen production-promoting agent of the present invention is not constant and is prescribed as needed depending on the drug formulation, the administration method, the purpose of use, and the age, body weight, and disease condition of the patient to which the promoter is administered, it was found as a result of animal experiments using rats that the skin collagen production-promoting effect can be expected to be produced by ingesting 10 μg per one kilogram of rat body weight or more of TGF-β and/or a TGF-β degradation product. Therefore, according to the extrapolation method, the effect can be expected by ingesting 10 μg per adult human or more of TGF-β and/or a TGF-β degradation product daily and, thus, TGF-β and/or a TGF-β degradation product may be combined with food or drink or administered as a medical drug so that this required amount can be ensured. The administration can be performed several times per day in a divided manner as needed.

(7) Although an effective application dose of the skin collagen production-promoting agent of the present invention varies depending on the dosage form, TGF-β and/or a TGF-β degradation product may preferably be contained to be 0.001 to 2 wt % based on the total dosage of the composition to be applied. However, if the composition is diluted upon use as in the case of bath additives, the contained amount may further be increased.

EXAMPLES

(8) The present invention will hereinafter be described in detail with reference to examples and test examples; however, these examples only exemplarily illustrate embodiments of the present invention and the present invention is not limited by these examples.

Example 1

(9) After a column packed with 3,000 gram of S-Sepharose was sufficiently washed with deionized water and 10,000 liter of skim milk was allowed to flow therethrough, the column was sufficiently washed with deionized water before elution with a linear concentration gradient of 0.1 to 1.0 M sodium chloride. An elution fraction containing TGF-β was fractionated again with phenyl-S Sepharose hydrophobic column chromatography. This fraction was further sequentially processed by C4 and C8 reverse phase chromatography and gel filtration chromatography in an HPLC system to acquire 412 mg of TGF-β (fraction A). TGF-β acquired in this manner is directly usable as the skin collagen production-promoting agent.

Example 2

(10) After 25 mg of the fraction A acquired in Example 1 was suspended in 100 ml of water, pancreatin was added at the final concentration of 1% to perform enzyme treatment at 37° C. for 5 minutes to 6 hours. After heat treatment was performed at 90° C. for 5 minutes to inactivate the enzyme, 24 mg of TGF-β degradation products (fractions B, C, and D) was acquired by lyophilization. The average molecular weights of the TGF-β degradation products B, C, and D acquired in this manner were about 8,000, about 500, and about 300, respectively. The fractions B and C are directly usable as the skin collagen production-promoting agent.

Test Example 1

(11) The collagen production-promoting effects of the fraction A acquired in Example 1 and the fractions B to D acquired in Example 2 were examined by animal experiments using rats. Seven-week-old Wistar male rats were divided into nine test groups (n=6) consisting of a group administered saline (control group), a group administered 10 μg per one kilogram of rat body weight of the fraction A acquired in Example 1 (A-1 group), a group administered 100 μg per one kilogram of rat body weight of the fraction A acquired in Example 1 (A-2 group), groups administered 10 μg per one kilogram of rat body weight of the fractions B to D acquired in Example 2 (B-1 to D-1 groups), and groups administered 100 μg per one kilogram of rat body weight of the fractions B to D acquired in Example 2 (B-2 to D-2 groups), and each of the rats received oral administration once a day with a probe and was fed for 10 days. With regard to the collagen content in the skin, after treating the dermis of the rats in accordance with the method of Nimni et al., (see Arch. Biochem. Biophys., p. 292, 1967), hydroxyproline content in the soluble fraction was measured. Since hydroxyproline is a specific amino acid contained only in collagen and accounts for about 10% of the total amino acid constituting collagen, collagen content can be estimated (see Ryuji Asano et al., Bio Industry, p. 12, 2001). The results are shown in Table 1.

(12) TABLE-US-00001 TABLE 1 Hydroxyproline content (μg/ml) Control group 0.3 ± 0.1  A-1 group 0.7 ± 0.1* A-2 group 1.1 ± 0.2  B-1 group 0.6 ± 0.1* C-1 group 0.7 ± 0.2* D-1 group 0.5 ± 0.1* B-2 group 1.0 ± 0.3* C-2 group 1.1 ± 0.2* D-2 group 0.6 ± 0.2* Each numerical value is a mean ± standard deviation (n = 6). *A significant difference exists as compared to the control group (p < 0.05).

(13) As a result, the hydroxyproline content in the soluble fraction after 10 weeks indicated significantly higher values in all the test groups as compared to the control group. Therefore, it was clarified that TGF-β and a TGF-β degradation product having an average molecular weight of 500 or more and 8,000 or less have the skin collagen production-promoting effect and are useful as a skin collagen production-promoting agent. It was also clarified that the skin collagen production-promoting effect is observed when TGF-β and a TGF-β degradation product are administered in an amount of at least 10 μg per one kilogram of rat body weight.

Test Example 2

(14) The collagen production-promoting effects of the fraction A acquired in Example 1 and the fraction B acquired in Example 2 were examined by experiments using a human fibroblast cell line [CCD45SK (ATCCRL 1506) collected from the skin of Caucasian women]. The normal human fibroblast cell line was seeded onto a 24-well plate at 4×10.sup.4 cells/well/0.4 ml by using a modified Eagle's medium (MEM, 10-101, Dainippon Pharmaceutical Co., Ltd.) containing 10 vol % fetal bovine serum (hereinafter abbreviated as FBS), cultured with 5% carbon dioxide under saturated water vapor at 37° C. for 24 hours, and then replaced to a 0.6 vol % FBS-containing MEM medium. The fraction A acquired in Example 1 and the fraction B acquired in Example 2 were added to each well (0.1 vol % final) (n=6) and cultured for 24 hours, and β-aminopropionitrile and tritium-L-proline were then added (50 μg/ml and 1 μCi/ml final, respectively), to acquire culture medium after further culturing for 24 hours. From the culture medium acquired in this manner, collagen fractions were fractionated in accordance with the method of Webster et al., (see, Analytical Biochemistry, p. 220, 1979) to measure radioactivity incorporated into the collagen fractions. The same test was conducted as a control without adding TGF-β and the TGF-β degradation product. The results are shown in Table 2.

(15) TABLE-US-00002 TABLE 2 Collagen production (%) Control 100 ± 3  Fraction A 204 ± 11* Fraction B 215 ± 9*  Each numerical value is a mean ± standard deviation (n = 6). *A significant difference exists as compared to the control group (p < 0.05).

(16) The results indicate that all the groups with TGF-β and the TGF-β degradation product added exhibited a collagen production-promoting ability twice or more greater than the group without the addition of TGF-β and the TGF-β degradation product (control). Therefore, it was clarified that TGF-β and a TGF-β degradation product have an effect on the skin fibroblast cells to promote collagen production and are useful as a skin collagen production-promoting agent.

Example 3

(17) Skin collagen production-promoting drink having composition shown in Table 3 was manufactured in a usual manner. Flavor of the manufactured drink was favorable and did not deteriorate after storage for one year at room temperature, and there was no problem such as precipitation.

(18) TABLE-US-00003 TABLE 3 Mixed isomerized sugar 15.0 (wt %) Fruit juice 10.0 Citric acid 0.5 Fraction A (product of Example 1) 0.1 Flavors 0.1 Mineral mixture 0.1 Water Added to a total amount of 100.0

Example 4

(19) Dough having composition shown in Table 4 was prepared, shaped, and baked in a usual manner to manufacture skin collagen production-promoting biscuits.

(20) TABLE-US-00004 TABLE 4 Flour 50.0 (wt %) Sugar 20.0 Salt 0.5 Margarine 12.5 Egg 12.5 Water 3.5 Mineral mixture 0.8 Fraction C (product of Example 2) 0.2

Example 5

(21) Skin collagen production-promoting agent having composition shown in Table 5 was manufactured in a usual manner.

(22) TABLE-US-00005 TABLE 5 Dextrose monohydrate 90.5 (wt %) Mineral mixture 5.0 Fraction A (product of Example 1) 3.0 Sugar ester 1.0 Flavors 0.5

Example 6

(23) Skin lotion having composition shown in Table 6 was manufactured in a usual manner.

(24) TABLE-US-00006 TABLE 6 Glycerin 3.0 (wt %) 1,3-butylene glycol 3.0 Polyoxyethylene sorbitan 0.5 monooleate (20 E.O.) Methyl parahydroxybenzoate 0.15 Citric acid 0.1 Sodium citrate 1.0 Flavors 0.05 Fraction B (product of Example 2) 0.05 Purified water Added to a total amount of 100.0

Example 7

(25) Cream having composition shown in Table 7 was manufactured in a usual manner.

(26) TABLE-US-00007 TABLE 7 Liquid paraffin 5.0 (wt %) White beeswax 4.0 Cetanol 3.0 Squalane 10.0 Lanolin 2.0 Stearic acid 1.0 Polyoxyethylene sorbitan 1.5 monooleate (20 E.O.) Glyceryl monostearate 3.0 1,3-butylene glycol 6.0 Methyl parahydroxybenzoate 1.5 Flavors 0.1 Fraction A (product of Example 1) 0.5 Purified water Added to a total amount of 100.0

Test Example 3

(27) The skin lotion acquired in Example 6 and the cream acquired in Example 7 were used for a practical use test. Comparison products were used that had the same compositions as Examples 6 and 7 except that TGF-β and the TGF-β degradation product were removed. Twenty adult women having dry skin with sagging and fine wrinkles recognized on the facial surfaces were randomly divided into two groups of 10 each (groups E and F) and twenty women with roughening of skin recognized on the hands were randomly divided into two groups of 10 each (groups G and H) to apply 2 g of the skin lotion of the preset invention to the facial surfaces of the group E, 2 g of the skin lotion of the comparison product to the facial surfaces of the group F, 2 g of the cream of the preset invention to the fingers of the group and 2 g of the cream of the comparison product to the fingers of the group H, twice a day in a similar manner to the normal usage condition for 10 days. The results are shown in Table 8.

(28) TABLE-US-00008 TABLE 8 Feeling of Roughening dryness of the skin Wrinkles Sagging Group E ++ ++ ++ + Group F ± ± ± ± Group G ++ + ND ND Group H ± ± ND ND ++: A prominent improvement effect was observed after application for 10 days. +: An improvement effect was observed after application for 10 days. ±: No improvement effect was observed after application for 10 days (no change occurred from 10 days ago). ND: Not determined

(29) From Table 8, it was clarified that prominent improvement effects were exhibited especially for feeling of dryness and roughening of the skin in the groups E and G using the skin lotion of the product of Example 6 and the cream of the product of Example 7, as compared to the groups F and H using the skin lotion and the cream of the comparison products.