期刊文献+

补肾活血方对动脉粥样硬化新西兰兔miRNA-217/Sirt1/FoxO1信号通路的影响 被引量:6

The Influence of Bushen Huoxue Recipe on miRNA-217/Sirt1/FoxO1 Signaling Pathway in New Zealand Rabbits with Atherosclerosis
下载PDF
导出
摘要 目的观察补肾活血方对动脉粥样硬化新西兰兔MicroRNA-217(miRNA-217)/沉默信号调节器1(Sirt1)/叉头转录因子(FoxO1)信号通路的影响。方法将新西兰兔44只随机分为对照组、模型组、补肾活血方组和阿托伐他汀钙组,除对照组外,其余3组高脂饲料喂养16周,灌胃8周后实时荧光定量PCR检测miRNA-217基因表达水平,免疫印迹实验检测Sirt1、FoxO1蛋白表达水平。结果与模型组相比,补肾活血方组和阿托伐他汀钙组miRNA-217表达降低(P <0.01),Sirt1、FoxO1表达增高(P <0.01)。补肾活血方组miRNA-217水平低于阿托伐他汀钙组(P <0.05),Sirt1蛋白水平高于阿托伐他汀钙组(P <0.05)。结论补肾活血方可能通过调控miRNA-217/Sirt1/FoxO1信号通路延缓内皮细胞衰老从而起到抗动脉粥样硬化作用。 Objective To observe the effect of Bushen Huoxue recipe(BHR)on the miRNA-217/silencing signal regulator 1(Sirt1)/fork-head transcription factor(FoxO1)signaling pathway in atherosclerosis of New Zealand rabbits.Methods Forty-four New Zealand rabbitswere randomly divided into control group,model group,BHR group,and atorvastatin group.Except the control group,the rabbits were fedwith high-fat diet for 16 weeks.The expression of miRNA-217 gene was detected by Realtime-PCR after 8 weeks of intragastric adminis-tration.The expression of Sirt1 and FoxO1 protein was detected by western blot.Results Compared with the model group,the expressionof miRNA-217 in BHR group and atorvastatin group decreased(P <0.05),while the expression of Sirt1 and FoxO1 increased(P <0.05).Among them,the levels of miRNA-217 in BHR group were lower than those in atorvastatin group(P <0.05),and the levels of Sirt1 pro-tein were higher than those in atorvastatin group(P <0.05).Conclusion BHR may play an anti-atherosclerotic role by delaying endothe-lial cell senescence through regulating the miRNA-217/Sirt1/FoxO1 signaling pathway.
作者 楼丹飞 闫国良 汪海慧 李越华 王馨璐 Lou Danfei;Yan Guoliang;Wang Haihui;Li Yuehua;Wang Xinlu(Shanghai Municipal Hospital of Traditional Chinese Medicine,Shanghai 200071,China)
出处 《中西医结合心脑血管病杂志》 2018年第24期3608-3610,共3页 Chinese Journal of Integrative Medicine on Cardio-Cerebrovascular Disease
基金 上海市卫生和计划生育委员会科研课题(No.201640039) 上海中医药大学高峰高原学科(临床人才专项)(No.171319) 上海中医药大学后备业务专家培养计划 上海市"杏林新星"计划(No.ZY3-RCPY-2-2016)
关键词 动脉粥样硬化 补肾活血方 阿托伐他汀钙 内皮细胞衰老 miRNA-217 沉默信号调节器1 叉头转录因子 atherosclerosis Bushen Huoxue recipe atorvastatin endothelial cell senescence miRNA-217 silencing signal regulator 1 forkhead transcription factor
  • 相关文献

参考文献9

二级参考文献190

  • 1罗萍,许钟镐,孙广东,张冬梅,苗里宁,李才.ERK1/2对高糖刺激肾小球系膜细胞葡萄糖转运蛋白1和p27^(Kip1)表达的作用[J].中华肾脏病杂志,2006,22(9):569-571. 被引量:7
  • 2Orimo M, Minamino T, Miyauchi H, et al. Protective role of SIRTI in diabetic vascular dysfunction. Arterioscler Thromb Vasc Biol, 2009, 29: 889-894.
  • 3Sharma S, Anjaneyulu M, Kulkami SK, et al. Resveratrol, a polyphenolic phytoalexin, attenuates diabetic nephropathy in rats. Pharmacology, 2006, 76: 69-75.
  • 4Nakae J, Cao Y, Daitoku H, et al. The LXXLL motif of murine forkhead transcription factor FoxO1 mediates Sirt1- dependent transcriptional activity. J Clin Invest, 2006, 116: 2473-2483.
  • 5Wild S, Roglic G, Green A, et al. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care, 2004, 27:1047-1053.
  • 6Fox C S, Coady S, Sorlie P D, et al. Trends in cardiovascular complications of diabetes. JAMA, 2004, 292:2495-2499.
  • 7Libby P, Ridker P M, Hansson G K. Progress and challenges in translating the biology of atherosclerosis. Nature, 2011,473:317-325.
  • 8de Haan J B, Cooper M E. Targeted antioxidant therapies in hyperglycemia-mediated endothelial dysfunction. Front Biosci(Schol Ed), 2011, 3:709-729.
  • 9Sitia S, Tomasoni L, Atzeni F, et al. From endothelial dysfunction to atherosclerosis. Autoimmun Rev, 2010, 9:830-834.
  • 10Minamino T, Miyauchi H, Yoshida T, et al. Endothelial cell senescence in human atherosclerosis: role of telomere in endothelial dysfunction. Circulation, 2002, 105:1541-1544.

共引文献56

同被引文献119

引证文献6

二级引证文献24

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部