Berberine regulates melanin synthesis by activating PI3K/AKT, ERK and GSK3β in B16F10 melanoma cells

被引:30
|
作者
Song, Young Chan [1 ,3 ]
Lee, Yonghee [2 ]
Kim, Hyeong Mi [2 ]
Hyun, Moo Yeol [2 ,3 ]
Lim, Yun Young [2 ]
Song, Kye Yong [1 ,3 ]
Kim, Beom Joon [2 ,3 ]
机构
[1] Chung Ang Univ, Coll Med, Dept Pathol, Seoul 137701, South Korea
[2] Chung Ang Univ, Coll Med, Dept Dermatol, Seoul 137701, South Korea
[3] Chung Ang Univ, Grad Sch, Dept Med, Seoul 137701, South Korea
关键词
B16F10 melanoma cells; melanin synthesis; tyrosinase; microphthalmia-associated transcription factor; phosphotidyl inositol 3-kinase/AKT; extracellular signal-regulated kinases; glycogen synthase kinase 3 beta; KOJIC ACID; INHIBITORY-ACTIVITY; MELANOGENESIS; INVOLVEMENT; MECHANISM; KINASE; PIGMENTATION; MELANOCYTES; PLANT;
D O I
10.3892/ijmm.2015.2113
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Berberine, an isoquinoline alkaloid, has a wide range of beneficial properties, including anti-bacterial, antiinflam-matory, anti-cancer, and cholesterol-lowering effects. Recently findings suggest that berberine improves glucose and lipid metabolism disorders. In the present study, we examined the mechanism underlying the inhibitory effect of berberine on a-melanocyte-stimulating hormone (alpha-MSH) -stimulated B16F10 melanoma cells. The results showed that berberine attenuated a-MSH induction of the microphthalmia-associated transcription factor (MITF) and tyrosinase in a dose-dependent manner. To elucidate the mechanism underlying the inhibitory effect of berberine, we examined the effect of alpha-MSH-stimulated phosphorylation of PI3K/AKT, ERK, and GSK3 beta. The results showed that treatment with berberine resulted in a reduction in the phosphorylation of PI3K/AKT, ERK, and GSK3 beta. Taken together, the results suggested that berberine inhibits melanin synthesis and tyrosinase activity by downregulating the expression of MITF and tyrosinase. Thus, these findings may contribute to the potential application of berberine in the prevention and treatment of skin pigmentation disorders.
引用
收藏
页码:1011 / 1016
页数:6
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