Inhibitory effect of magnesium L-ascorbyl-2-phosphate (VC-PMG) on melanogenesis in vitro and in vivo

被引:190
作者
Kameyama, K
Sakai, C
Kondoh, S
Yonemoto, K
Nishiyama, S
Tagawa, M
Murata, T
Ohnuma, T
Quigley, J
Dorsky, A
Bucks, D
Sagamihara, KB
机构
[1] KITASATO UNIV, SCH MED, DEPT DERMATOL, SAGAMIHARA, KANAGAWA 228, JAPAN
[2] NIKKO CHEM CO LTD, TOKYO, JAPAN
[3] PENEDERM INC, FOSTER CITY, CA USA
关键词
MURINE MELANOMA-CELLS; L-ASCORBIC-ACID; DOPACHROME TAUTOMERASE; MAMMALIAN TYROSINASE; CLONE; INTERFERON; EXPRESSION; INVITRO;
D O I
10.1016/S0190-9622(96)90830-0
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Background: An inhibitory effect of ascorbic acid (AsA) on melanogenesis has been described. However, AsA is quickly oxidized and decomposed in aqueous solution and thus is not generally useful as a depigmenting agent. Objective: Our purpose was to examine the effect on pigmentation of magnesium-L-ascorbyl-2-phosphate (VC-PMG), a stable derivative of AsA. Methods: Percutaneous absorption of VC-PMG was examined in dermatomed human skin, and its effect on melanin production by mammalian tyrosinase and human melanoma cells in culture was also measured. A 10% VC-PMG cream was applied to the patients. Results: VC-PMG suppressed melanin formation by tyrosinase and melanoma cells. In situ experiments demonstrated that VC-PMG cream was absorbed into the epidermis and that 1.6% remained 48 hours after application. The lightening effect was significant in 19 of 34 patients with chloasma or senile freckles and in 3 of 25 patients with normal skin. Conclusion: VC-PMG is effective in reducing skin hyperpigmentation in some patients.
引用
收藏
页码:29 / 33
页数:5
相关论文
共 33 条
[1]
BARTON D E, 1988, Genomics, V3, P17, DOI 10.1016/0888-7543(88)90153-X
[2]
SOME PROPERTIES OF ASCORBATE FREE-RADICAL [J].
BIELSKI, BHJ ;
RICHTER, HW ;
CHAN, PC .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1975, 258 (SEP30) :231-237
[3]
METHODS FOR INVITRO PERCUTANEOUS-ABSORPTION STUDIES .4. THE FLOW-THROUGH DIFFUSION CELL [J].
BRONAUGH, RL ;
STEWART, RF .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1985, 74 (01) :64-67
[4]
DAHL H, 1976, ACTA PATH MICRO IM B, V84, P280
[5]
ENZYMATIC CONTROL OF PIGMENTATION IN MAMMALS [J].
HEARING, VJ ;
TSUKAMOTO, K .
FASEB JOURNAL, 1991, 5 (14) :2902-2909
[6]
HEARING VJ, 1987, METHOD ENZYMOL, V142, P154
[7]
JIMENEZ M, 1989, J BIOL CHEM, V264, P3397
[8]
JIMENEZ M, 1991, J BIOL CHEM, V266, P1147
[9]
JIMENEZCERVANTES C, 1994, J BIOL CHEM, V269, P17993
[10]
HLA-DR AND MELANOMA-ASSOCIATED ANTIGEN (P97) EXPRESSION DURING THE CELL-CYCLE IN HUMAN-MELANOMA CELL-LINES, AND THE EFFECTS OF RECOMBINANT GAMMA-INTERFERON - 2-COLOR FLOW CYTOMETRIC ANALYSIS [J].
KAMEYAMA, K ;
TAKEZAKI, S ;
KANZAKI, T ;
NISHIYAMA, S .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1986, 87 (03) :313-318