期刊文献+

辛伐他汀干预急性心肌梗死后gp130表达与左室重塑的关系 被引量:1

Effect of simvastatin on gp130 expression and ventricular remolding after acute myocardial infarction in rats
原文传递
导出
摘要 目的:研究辛伐他汀干预急性心肌梗死(AMI)后左室非梗死区(LVNIZ)糖蛋白链细胞因子受体亚单位(gp)130(gp130)表达及其与左室重塑(LVRM)的关系。方法:40只SD雄性大鼠平分为4组:心肌梗死组、心肌梗死+辛伐他汀组(辛伐他汀40 mg·kg-1·d-1灌胃)、假手术组和正常组。4周后用RT-PCR测定LVNIZ gp130mRNA基因表达和用Western Blot法测定LVNIZ蛋白合成水平,同时测定左室非梗死区肌细胞横截面积,和心肌胶原容积分数。结果:4周后心肌梗死组LVNIZ gp130mRNA表达和蛋白合成水平于明显高于正常组和假手术组(P<0.05)。心肌梗死+辛伐他汀组LVNIZ gp130mRNA表达和蛋白合成水平明显低于心肌梗死组(P<0.05)。同时与正常组及假手术组比较心肌梗死组心肌细胞横截面积(CA),I,III胶原容积分数(CVFI,CVFIII)均明显增加(P<0.05)。随着辛伐他汀的干预与心肌梗死组比较,心肌梗死+辛伐他汀组心肌细胞横截面积(CA),I,III胶原容积分数(CVFI,CVFIII),均明显改善(P<0.05)。结论:大鼠AMI后LVNIZ gp130mRNA和蛋白的过度表达与AMI后LVRM的发生有联系,辛伐他汀可改善LVRM,其机制可能与抑制gp130基因过度表达与蛋白合成有关。 Objective :To determine the effect of simvastatin on gpl30 expression in left ventricular non infarct zone (LVNIZ) and related left ventricular remodeling (LVRM) after acute myocardial infarction (AMI). Methods : Male SD rats (n = 40) were divided into four groups : AMI, AMI + simvastatin, sham-operated, and normal groups. Four weeks after AMI, gp130 mRNA and protein expression in LVNIZ were determined by RT-PCR and Western blot. Moreover, the cross-sectional area of cardiocytes and the collagen volume fraction (CVF) were determined. Results: Compared with normal and sham-operated rats, the expression of gp130 mRNA and protein in LVNIZ significantly increased 4 weeks after AMI (P 〈 0. 05). Compared with AMI control, simvastatin decreased gp130 mRNA and protein expression. Moreover, cardiocyte cross-sectional area (CA) and CVF in LVNIZ were significantly increased ( P 〈 0. 05 ) after AMI ; the increased CA and CVF were alleviated by simvastatin (P 〈 0.05 ). Conclusion: Gp130 mRNA and protein are overexpressed in LVNIZ after AMI. Simvastatin prevents LVRM which may be partly through depressing gp130 mRNA and protein expression.
出处 《中国新药杂志》 CAS CSCD 北大核心 2015年第6期687-690,共4页 Chinese Journal of New Drugs
基金 重庆市自然科学基金[渝发科技字(2004)54号文]
关键词 心肌梗死 心室重塑 糖蛋白 辛伐他汀 myocardial infarction ventricular remodeling glycoprotein simvastatin
  • 相关文献

参考文献3

二级参考文献29

  • 1颜素娟,李菊香,陈静,罗伟,苏海,程晓曙.心肌营养素-1在高静水压刺激心肌成纤维细胞增殖中的作用[J].江西医学院学报,2005,45(6):54-56. 被引量:4
  • 2张冬颖,覃数,唐显军,杨辉.辛伐他汀对大鼠心肌梗死后心室重塑影响的实验研究[J].中国药理学通报,2006,22(7):814-818. 被引量:15
  • 3Pennica D, King K I, Shaw K J, et al. Expression cloning of cardiotrophin-1, a cytokine that induces cardiac myocyte hypertrophy [J]. Proc Natl Acad Sci USA,1995,92(4) :1142.
  • 4Aoyama T,Takimoto Y, Pennica D, et al. Augmented expression of cardiotrophin-1 and its receptor component, gp130, in both left and right ventricles after myocardial infarction in the rat[ J]. J Mol Cell Cardio1,2000,32 (10) : 1821 - 30.
  • 5Indolfi C, Di Lorenzo E, Perrino C, et al. Hydroxymethylglutaryl coenzyme A reductase inhibitor simvastatin prevents cardiac hypertrophy induced by pressure overload and inhibits p21ras activation [ J ]. Circulation,2002,106 (16) :2118 - 24.
  • 6Tsuruda T, Jougasaki M, Boerrigter G, et al. Cardiotrophin-1 stimulation of cardiac fibroblast growth: roles for glycoprotein 130/ leukemia inhibitory factor receptor and the endothelin type A receptor [ J ] Circ Res ,2002 ,90 ( 2 ) : 128 - 34.
  • 7Dechend R, Fiebeler A,Park J K, et al. Amelioration of angiotensin Ⅱ-induced cardiac injury by a 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibitor[ J ]. Circulation, 2001,104 ( 5 ) : 576 -81.
  • 8Sano M, Fukuda K, Kodama H, et al. Interleukin-6 family of cytokines mediate angiotensin Ⅱ-induced cardiac hypertrophy in rodent cardiomyoCytes[ J]. J Biol Chem,2000,275 (38) :29717 - 23.
  • 9Hishinuma S,Funamoto M, Fujio Y, et al. Hypoxic stress induces cardiotrophin-1 expression in cardiac myocytes [ J ]. Biochem Biophys Res Commun, 1999,264 ( 2 ) :436 - 40.
  • 10Liu J, Shen Q, Wu Y. Simvastatin prevents cardiac hypertrophy in vitro and in vivo via JAK/STAT pathway[ J]. Life Sci,2008,82 (19-20) :991 -6.

共引文献5

同被引文献12

引证文献1

二级引证文献1

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