中华皮肤科杂志 ›› 2009, Vol. 42 ›› Issue (2): 108-111.

• 论著 • 上一篇    下一篇

内皮素拮抗剂对鼠黑素瘤细胞黑素生成影响的研究

吴品茹 陈向东 徐慧 刘健航   

  1. 上海市第九人民医院 上海第二医科大学附属第九人民医院皮肤科 上海第二医学院第九人民医院皮肤科
  • 收稿日期:2008-03-03 修回日期:2008-05-15 出版日期:2009-02-15 发布日期:2009-02-15
  • 通讯作者: 吴品茹 E-mail:synthia_2000@sina.com;smlwzm@hotmail.com

Effects of endothelin antagonist on melanogenesis of cultured B16 murine melanoma cells

  • Received:2008-03-03 Revised:2008-05-15 Online:2009-02-15 Published:2009-02-15

摘要:

目的 研究天然提取的内皮素拮抗剂对体外培养的B16鼠黑素瘤细胞的生物学作用。方法比较观察了内皮素拮抗剂和甘草黄酮对体外培养的B16鼠黑素瘤细胞酪氨酸酶活性、黑素含量和细胞增殖率的影响,以及内皮素拮抗剂对内皮素(ET-1)引起的B16细胞酪氨酸酶活性变化的作用。结果 在实验浓度下,甘草黄酮具有浓度依赖性黑素合成抑制作用,内皮素拮抗剂对培养的B16黑素瘤细胞黑素生成没有直接的抑制作用,但能特异性抑制内皮素对黑素瘤细胞分化和酪氨酸酶的激活作用,200 μg/mL该拮抗剂即可显著拮抗0.5 μg/mL ET-1对黑素瘤细胞的刺激增殖作用,与甘草黄酮相比,细胞毒性较小。结论 内皮素拮抗剂是一种安全的皮肤美白物质,在UVB照射后内皮素增加引起的皮肤色素沉着中,具有广泛的应用前景。

关键词: 甘草黄酮;内皮素拮抗剂;酪氨酸酶抑制剂

Abstract:

Objective To evaluate the biological effect of endothelin (ET) antagonist on cultured B16 murine melanoma cells. Methods B16 murine melanoma cells were cultured in the presence of various concentrations (31.25, 62.5, 125, 250, 500 μg/mL) of ET antagonist or licoflavone. Then, melanoma cells were harvested for the detection of tyrosinase activity and melanin content. The proliferation rate of melanoma cells was measured with MTT method. The effect of ET antagonist was compared with that of licoflavone. Results Licoflavone had a concentration-dependent inhibition on melanogenesis. The ET antagonist selectively suppressed the ET-induced stimulation of tyrosinase and cell differentiation of B16 cells, but had no direct inhibitory effect on melanogenesis in culture, and little influence on melanocyte viability. The addition of ET antagonist at 200 μg/mL could significantly inhibit ET (0.5 μg/mL) -induced melanogenesis in B16 cells. The cytotoxity of the antagonist was relatively lower than that of licoflavone. Conclusions The results suggest that the ET antagonist is a safe skin-whitening ingredient,and may have a wide application perspective in the prevention of endothelin-induced skin pigmentation after UVB irradiation.

Key words: Glabridin;ET antagonist;Tyrosinase Inhibitor