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山东大学学报(医学版) ›› 2010, Vol. 48 ›› Issue (11): 1-.

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二甲双胍对内皮细胞血管紧张素II受体1表达的影响

张栩1,于文2,王孝勇1,管庆波1,赵家军1   

  1. 1. 山东大学附属省立医院内分泌科,济南 250021; 2.滨州市人民医院内分泌科,山东  滨州 256606
  • 收稿日期:2010-09-16 出版日期:2010-11-16 发布日期:2010-11-16
  • 通讯作者: 赵家军(1961- ),男,主任医师,教授,博士生导师,主要从事内分泌与代谢病的相关研究。 E-mail:jjzhao@medmail.com.cn
  • 作者简介:张栩(1969- ),男,副主任医师,博士,主要从事糖尿病及其慢性并发症的研究。 E-mail:zhangxu@medmail.com.cn
  • 基金资助:

    山东省优秀中青年科学家奖励基金资助项目(2006BS03012);山东省医药卫生科技发展计划资助项目(2009HW058);2008山东省人事厅留学人员科技活动项目择优经费资助项目。

Effect of metformin on type 1 angiotensin II receptor expression in endothelial cells

ZHANG Xu1, YU Wen2, WANG Xiao-yong1, GUAN Qing-bo1, ZHAO Jia-Jun1   

  1. 1. Department of Endocrinology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China;
    2. Department of Endocrinology, Binzhou People′s Hospital, Binzhou 256606, Shandong, China
  • Received:2010-09-16 Online:2010-11-16 Published:2010-11-16

摘要:

目的    观察二甲双胍对内皮细胞1型血管紧张素II受体(AT1R)表达的影响并探讨其机制。方法   应用western-blot检测内皮细胞AT1R、腺苷酸活化蛋白激酶α亚基(AMPKα)、核转录因子κB抑制蛋白(I-κB)的表达,应用激光共聚焦观察核转录因子κB(NF-κB )P65 在细胞核内变化,比色法测定各组内皮细胞培养液乳酸脱氢酶(LDH)活性。同时应用RNA干扰技术,进一步观察I-κB 、AMPKα的作用。结果    二甲双胍显著减少肿瘤坏死因子α(TNFα)诱导的内皮细胞AT1R的蛋白表达(P<0.01),显著降低IκB的磷酸化(P<0.01),同时二甲双胍显著降低内皮细胞培养液LDH活性(P<0.01),而AMPKαSiRNA干预后,二甲双胍对内皮细胞AT1R的影响作用显著减弱(P<0.01)。结论   二甲双胍通过促使AMPKα磷酸化,激活AMPKα信号通路,抑制NF-κB活化和内皮细胞AT1R的表达,减轻内皮细胞损伤,保护内皮细胞功能,从而发挥其对心血管的有益作用。

关键词: 二甲双胍;内皮细胞;血管紧张素II受体1;腺苷酸活化蛋白激酶α;核转录因子κB

Abstract:

Objective   To observe the effect of metformin on type 1 angiotensin II receptor (AT1R)expression in endothelial cells and investigate its mechanism. Methods     AT1R, inhibitor protein κB (I-κB)and AMP-activated protein kinase α(AMPKα ) protein expressions in endothelial cells were determined by Western blot, and nuclear factor-κB (NF-κB) activation in endothelial cells was observed by con-focal laser scanning microscopy. The lactate dehydrogenase (LDH) activation in the culture medium was detected by colorimetric assay. Also, the roles of NFκB and AMPKα in the effect of metformin on AT1R were determined by RNA interference technology. Results    I-κB phosphorylation and AT1R protein expression induced by tumor necrosis factor α (TNFα) in endothelial cells were significantly reduced by metformin, and  LDH activity in the endothelial cell culture medium was significantly decreased (P<0.01). The inhibitory effect of metformin on AT1R expression in endothelial cells was significantly reversed by AMPKαSiRNA (P<0.01). Conclusion    NF-κB activation and AT1R expression can be inhibited by the intervention of metformin, and activation of the AMPKα pathway plays an important role in the beneficial effect of metformin on cardiovascular endothelial cells.

Key words: Metformin;Endothelial cells;  Type 1 angiotensin II receptor; AMP-activated protein kinase α; Nuclear factor-κB

中图分类号: 

  • R364.5
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