期刊文献+

阿托伐他汀对心肌梗死后大鼠基质金属蛋白酶-2及微小RNA-21的作用 被引量:3

Effects of atorvastatin on matrix metalloproteinase-2 and microRNA-21 in rats with myocardial infarction
原文传递
导出
摘要 目的 观察阿托伐他汀对心肌梗死后大鼠基质金属蛋白酶(MMP)-2、微小RNA(miRNA,miR)-21表达的影响.方法 选取140只Wistar大鼠建立急性心肌梗死模型,分为假手术组、对照组、阿托伐他汀低剂量组和高剂量组,进行左室重量指数、心肌胶原容积分数、miRNA-21及MMP-2 mRNA表达测定.结果 阿托伐他汀治疗组左室重量指数、心肌胶原容积分数、梗死周边区miR-21 、MMP-2 mRNA的表达均降低(P<0.05);各组梗死周边区miR-21表达量与MMP-2 mRNA水平呈正相关(r对照组=0.611,P<0.05;r阿托伐他汀低剂量组=0.502,P<0.05;r阿托伐他汀低剂量组=0.541,P<0.05).结论 阿托伐他汀能降低梗死周边区MMP-2和miR-21的表达,发挥减轻心室重构的作用. Objective To explore the effects of atorvastatin on the matrix metalloproteinase (MMP)-2 and microRNA (miRNA,miR)-21 expression in rats with myocardial infarction.Methods The models of acute myocardial infarction were established in 140 Wistar rats.All rats were divided into sham operation group,myocardial infarction control group,low atorvastatin group and high atorvastatin group.Left ventricular mass index (LVMI),collagen volume fraction (CVF),MMP-2 and miR-21 were detected after operation.Results LVMI,CVF,and the expression of miR-21 and MMP-2 mRNA were significantly decreased in atorvastatin groups (P 〈 0.05) ; The expression of miR-21 and MMP-2 mRNA in the surrounding infarct areas had a positive correlation (rcontrol group =0.611,P〈 0.05;r low atorvastatin group =0.502,P〈0.05; rhigh atorvastatin group =0.541,P〈0.05).Conclusion Atorvastatin could decrease the level of MMP-2 and the expression of miR-21 in rats with myocardial infarction,which could improve ventricular remodeling and heart function.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2015年第2期374-376,共3页 Chinese Journal of Experimental Surgery
关键词 阿托伐他汀 心肌梗死 基质金属蛋白酶-2 微小RNA-21 Atorvastatin Myocardial infarction Matrix metalloproteinase - 2 MicroRNA - 21
  • 相关文献

参考文献5

二级参考文献36

  • 1尹倪,陈胜喜,罗万俊,蒋海河,龚伟.冠状动脉前降支结扎法制作大鼠急性心肌梗死模型[J].中国医师杂志,2006,8(9):1193-1195. 被引量:28
  • 2Degabriele N M,Griesenbach U,Sato K,et al.Critical appraisal of the mouse model of myocardial infarction.[J].Exp Physiol,2004,89(4):497-505. 被引量:1
  • 3Takagawa J,Zhang Y,Wong M L,et al.Myocardial infarct size measurement in the mouse chronic infarction model:comparison of area-and length-based approaches[J].Appl Physiol,2007,102(6):2104-2111. 被引量:1
  • 4Bhind R,Witting P K,Mcmahon A C,et al.Rat models of myocardial infarction.Pathogenetic insights and clinical relevance[J].Thromb Haemost,2006,96(5):602-610. 被引量:1
  • 5Copaja Soto M,Valenzuela R,Salda A,et al.Early expression of monocyte chemoattractant protein-1 correlates with the onset of isoproterenol-induced cardiac fibrosis in rats with distinct angiotensin-converting enzyme polymorphism[J].J Renin Angiotensin Aldosterone Syst,2008,9(3):154-162. 被引量:1
  • 6Davidoff A W,Boyden P A,Schwartz K,et al.Congestive heart failure after myocardial infarction in the rat:cardiac force and spontaneous sarcomere activity[J].Ann NY Acad Sci,2004,10(15):84-95. 被引量:1
  • 7Supinski G S,Callahan L A.Diaphragmatic free radical generation increases in an animal model of heart failure[J].J Appl Physiol,2005,99(3):1078-1084. 被引量:1
  • 8Zhou R,Xu Q,Zheng P,et al.Cardioprotective effect of fluvastatin on isoproterenol-induced myocardial infarction in rat[J].Eur J Pharmacol,2008,586(1-3):244-250. 被引量:1
  • 9Yang BF, Lin HX, Xiao J N, et al. The muscle-specific mi croRNA miR-1 regulates cardiac arrhythmogenic potential by targeting GJA1 and KCNJ2[J]. Nature Med, 2007,13 (4) :486-491. 被引量:1
  • 10Tang Y, Zheng J, Sun J, et al. MieroRNA-1 regulates car- diomyocyte apoptosis by targeting Bcl-2[J]. Int Heart J, 2009,50(3) :377-387. 被引量:1

共引文献33

同被引文献37

引证文献3

二级引证文献14

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