p-Coumaric Acid Not Only Inhibits Human Tyrosinase Activity In Vitro but Also Melanogenesis in Cells Exposed to UVB

被引:125
作者
An, Sang Mi [1 ,2 ]
Koh, Jae-Sook [3 ]
Boo, Yong Chool [1 ,2 ]
机构
[1] Kyungpook Natl Univ, Dept Mol Med, Sch Med, Taegu 700422, South Korea
[2] Kyungpook Natl Univ, Cell & Matrix Res Inst, Sch Med, Med Educ Program Human Resources BK21, Taegu 700422, South Korea
[3] Deimapro Ltd, Seoul, South Korea
关键词
melanin; human tyrosinase; p-coumaric acid; human epidermal melanocytes; UVB; tyrosine; MELANOCYTE-STIMULATING HORMONE; MELANIN PIGMENTATION; SUICIDE INACTIVATION; CRYSTAL-STRUCTURE; SKIN; MECHANISM; SEQUENCE; BIOLOGY; AGENTS; DOPA;
D O I
10.1002/ptr.3095
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Tyrosinase (TYR) catalyzes rate-limiting steps of melanogenesis and thus its inhibitors are potentially useful as hypopigmenting agents. Recently. p-coumaric acid (p-CA) has been suggested to interfere with the pro-melanogenic actions of tyrosine due to its structural similarity with tyrosine (An SM et al., Br J Dermatol 2008. 159: 292). In this study, we compared the inhibitory effects of p-CA and two other well known TYR inhibitors used in cosmetics - arbutin and kojic acid - on the catalytic activities of mushroom, murine and human TYRs in vitro, using tyrosine and 3,4-dihydroxyphenylalanine (DOPA) as substrates. The results showed that p-CA is a weaker inhibitor of mushroom TYR but much stronger inhibitor or human or murine TYR in comparison with kojic acid and arbutin. In addition, p-CA inhibited human TYR at much lower concentrations than those required for the inhibition of murine or mushroom TYRs. Enzyme kinetics analysis indicated that p-CA is a mixed type (for tyrosine) or competitive inhibitor (for DOPA) of human TYR. Potent antimelanogenic effects of p-CA were observed in human epidermal melanocytes exposed to UVB. The present study demonstrated that p-CA is a potent and selective inhibitor of human TYR and is potentially useful as a hypopigmenting agent. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:1175 / 1180
页数:6
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