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中国临床药理学与治疗学 ›› 2018, Vol. 23 ›› Issue (4): 377-382.doi: 10.12092/j.issn.1009-2501.2018.04.003

• 基础研究 • 上一篇    下一篇

黄芩苷对H2O2氧化损伤人黑素细胞的保护机制研究

祝逸平,金 嵘,林福全,周妙妮,王遂泉,许爱娥   

  1. 浙江中医药大学附属杭州市第三人民医院皮肤科,杭州 310009,浙江
  • 收稿日期:2017-12-27 修回日期:2018-02-22 出版日期:2018-04-26 发布日期:2018-04-13
  • 通讯作者: 许爱娥,女,本科,主任医师,教授,博士生导师,研究方向:中西医结合防治色素性皮肤病。 Tel: 0571-87827535 E-mail: xuaiehz@man.com
  • 作者简介:祝逸平,女,博士,主治医师,研究方向:中西医结合防治皮肤病。 Tel: 0571-87827535 E-mail: juyeapy@126.com
  • 基金资助:

    浙江省自然科学基金(LQ16H290001,LY18H110001);国家自然科学基金(81472887,81773335);浙江省基础公益研究计划项目(LGF18H110002);国家临床重点专科建设项目

Protective effects of Baicalin to the human melanocyte cocultured with H2O2

ZHU Yiping, JIN Rong, LIN Fuquan, ZHOU Miaoni, WANG Suiquan, XU Aie   

  1. The Third People's Hospital in Hangzhou Affiliated to Zhejiang Chinese Medicine University, Hangzhou 310009, Zhejiang, China
  • Received:2017-12-27 Revised:2018-02-22 Online:2018-04-26 Published:2018-04-13

摘要:

目的:探讨黄芩苷对H2O2氧化损伤正常人黑素细胞的保护作用及其机制研究。方法:构建H2O2氧化损伤黑素细胞模型,通过观察不同浓度的黄芩苷处理H2O2氧化损伤正常人黑素细胞,采用倒置显微镜观察黄芩苷对黑素细胞形态的影响;cell counting kit-8(CCK-8)法检测黄芩苷对黑素细胞增殖活力作用;乳酸脱氢酶(lactate dehydrogenase,LDH)法检测黄芩苷对黑素细胞LDH表达的影响, 并通过流式细胞仪检测活性氧(ROS)水平,荧光实时定量RT-PCR检测过氧化氢酶(catalase,CAT)、谷胱甘肽过氧化物酶1(peroxidase 1,GPX1)mRNA表达情况,通过ELISA试剂盒检测黄芩苷和H2O2处理黑素细胞后分泌的热休克蛋白70(heat shock protein 70,HSP70)。结果:镜下观察黄芩苷给药后细胞较对照组形态明显改变,细胞数增多;黄芩苷作用黑素细胞后增殖率较对照组升高(P<0.05);黄芩苷明显抑制黑素细胞中LDH表达,呈剂量-效应关系(P<0.05)。黄芩苷能显著促进CAT和GPX1 mRNA表达,且明显抑制HSP70分泌。结论:黄芩苷对H2O2氧化损伤的正常人黑素细胞具有明显保护作用,可为临床白癜风的治疗提供参考。

关键词: 黄芩苷, 黑素细胞, 氧化应激, 白癜风

Abstract:

 AIM: To study the mechanism of anti-oxidant and melanocyte protection by Baicalin.  METHODS: Different concentration of Baicalin and H2O2 were cocultured with normal human melanocyte. Cell proliferation was detected by cell counting kit-8 assay, morphology of the human melanocyte was observed by ordinary inverted microscope, and LDH assay was used to detect cell viability. For mechanism research, DCFH-DA ROS level was assayed by flow cytometry. Induced HSP70 from melanocyte was detected using HSP70 high sensitivity ELISA kit. By RT-PCR, mRNA levels of CAT and GPX1 were dectected. RESULTS: Baicalin has obvious protective effects on melanocytes damage caused by H2O2. Compared with control group,in Baicalin groups, cell shape was changed and increased. In 12.5, 25, 50 μmol/L Baicalin groups, the effects of on melanocyte proliferation rate were higher than the control group (P<0.05). Baicalin inhibited the expression of LDH in black pigment cells in a dose-dependent manner, there was statistically significant difference (P<0.05). After H2O2 oxidative damage of melanocytes, Baicalin could significantly promote the expression of CAT and GPX1 mRNA, and the secretion of HSP70 was significantly increased. CONCLUSION: Baicalin protects human melanocytes from oxidative damage by inhibiting H2O2-induced apoptosis. It is referential for the treatment of vitiligo.

Key words: Baicalin, melanocyte, oxidative damage, vitiligo

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