Inhibitory effects of esculetin on melanin biosynthesis

被引:49
作者
Masamoto, Y
Murata, Y
Baba, K
Shimoishi, Y
Tada, M
Takahata, K
机构
[1] Okayama Univ, Fac Agr, Okayama 7008530, Japan
[2] Okayama Univ, Grad Sch Nat Sci & Technol, Okayama 7008530, Japan
[3] Osaka Univ Pharmaceut Sci, Fac Pharmacognosy, Osaka 5691195, Japan
关键词
esculetin; tyrosinase activity; melanogenesis; 3,4-dihydroxyphenylalanine (DOPA) reaction; coumarin;
D O I
10.1248/bpb.27.422
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To investigate the structure-activity relationship of coumarins for the inhibitory activity on mushroom tyrosinase, the 50% inhibitory concentration (IC50 values) of 18 coumarins and four cinnamic acid derivatives were measured. Among these compounds, esculetin had the strongest inhibitory activity (IC50 = 43 muM) on mushroom tyrosinase. Introduction of a hydroxy group to the C6 and C7 positions of the coumarin ring and no substitution on the lactone ring played an important role in the expression of the strong inhibitory activity of esculetin. We performed further studies to estimate the in vitro inhibitory effects of esculetin on melanogenesis. Esculetin 5 muM significantly suppressed melanin production in murine B16 melanoma cells without affecting cell growth. Furthermore, the number of 3,4-dihydroxyphenylalanine (DOPA)-positive melanocytes in the split-epidermal sheets treated with 0.05% or 0.1% esculetin was significantly lower than that in the control. From these results, it is suggested that esculetin has inhibitory effects on tyrosinase activity in vitro. However, further detailed studies are necessary to understand the inhibitory mechanism of esculetin.
引用
收藏
页码:422 / 425
页数:4
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