Inhibitory effect of Gastrodia elata Blume extract on alpha-melanocyte stimulating hormone-induced melanogenesis in murine B16F10 melanoma

被引:20
|
作者
Shim, Eugene [1 ]
Song, Eunju [2 ]
Choi, Kyoung Sook [3 ]
Choi, Hyuk-Joon [3 ]
Hwang, Jinah [2 ]
机构
[1] Soongeui Womens Coll, Dept Food & Nutr, Seoul 04628, South Korea
[2] Myongji Univ, Coll Nat Sci, Dept Food & Nutr, 116 Myongji Ro, Yongin 17058, Gyeonggi, South Korea
[3] BK Bio Co Ltd, Seongnam 13229, Gyeonggi, South Korea
基金
新加坡国家研究基金会;
关键词
Gastrodia elata; melanogenesis; tyrosinase; TYROSINASE; ERGOTHIONEINE; MUSHROOM; ALCOHOL; ACID;
D O I
10.4162/nrp.2017.11.3.173
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
BACKGROUND/OBJECTIVES: Gastrodia elata Blume (GEB), a traditional herbal medicine, has been used to treat a wide range of neurological disorders (e.g., paralysis and stroke) and skin problems (e.g., atopic dermatitis and eczema) in oriental medicine. This study was designed to investigate whether GEB extract inhibits melanogenesis activity in murine B16F10 melanoma. MATERIALS/METHOD: Murine B16F10 cells were treated with 0-5 mg/mL of GEB extract or 400 mu g/mL arbutin (a positive control) for 72 h after treatment with/without 200 nM alpha-melanocyte stimulating hormone (alpha-MSH) for 24 h. Melanin concentration, tyrosinase activity, mRNA levels, and protein expression of microphthalmia-associated transcription factor (MITF), tyrosinase, tyrosinase-related protein (Trp)1, and Trp2 were analyzed in alpha-MSH-untreated and alpha-MSH-treated B16F10 cells. RESULTS: Treatment with 200 nM alpha-MSH induced almost 2-fold melanin synthesis and tyrosinase activity along with increased mRNA levels and protein expression of MITF, tyrosinase, Trpl and Trp2. Irrespective of alpha-MSH stimulation, GEB extract at doses of 0.5-5 mg/mL inhibited all these markers for skin whitening in a dose-dependent manner. While lower doses (0.5-1 mg/mL) of GEB extract generally had a tendency to decrease melanogenesis, tyrosinase activity, and mRNA levels and protein expression of MITF, tyrosinase, Trp1, and Trp2, higher doses (2-5 mg/mL) significantly inhibited all these markers in alpha-MSH-treated B16F10 cells in a dose-dependent manner. These inhibitory effects of the GEB extract at higher concentrations were similar to those of 400 mu g/mL arbutin, a well-known depigmenting agent. CONCLUSIONS: These results suggest that GEB displays dose-dependent inhibition of melanin synthesis through the suppression of tyrosinase activity as well as molecular levels of MITF, tyrosinase, Trp1, and Trp2 in murine B16F10 melanoma. Therefore, GEB may be an effective and natural skin-whitening agent for application in the cosmetic industry.
引用
收藏
页码:173 / 179
页数:7
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