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氟伐他汀对大鼠心肌梗死后左室功能、肌球蛋白重链基因表达及胶原重建的影响
引用本文:刘宇宏,曾秋棠,陈斌.氟伐他汀对大鼠心肌梗死后左室功能、肌球蛋白重链基因表达及胶原重建的影响[J].中国病理生理杂志,2005,21(12):2341-2345.
作者姓名:刘宇宏  曾秋棠  陈斌
作者单位:华中科技大学同济医学院附属1协和医院心内科,2同济医院超声影像科, 湖北 武汉 430022
摘    要:目的:观察羟甲基戊二酰辅酶A还原酶抑制剂氟伐他汀对大鼠急性心肌梗死(AMI)后左室功能、肌球蛋白重链(α、β MHC)基因转录mRNA表达及胶原重建的影响。 方法: 雌性SD大鼠AMI术后6 h随机分为:①AMI对照组;②氟伐他汀组;③假手术组。 直接灌胃给药8周后行高频多普勒超声、血流动力学、左室心肌α、β MHC的mRNA、非梗死区胶原容积分数(CVF)及Ⅰ/Ⅲ胶原的免疫组化测定。 结果: AMI组E峰、E峰减速度、E/A、左室舒张末压(LVEDP)、β MHC mRNA、非梗死区CVF及Ⅰ/Ⅲ胶原比值明显高于假手术组,左室短轴速短率(FS)、射血分数(EF)、平均动脉压(MAP)和α MHC mRNA 显著低于假手术组。氟伐他汀组的E峰、E峰减速度、E/A、LVEDP、β MHC mRNA、非梗死区CVF及I/Ⅲ胶原比值明显低于AMI组,FS、EF、MAP和α MHC mRNA显著高于AMI组。 结论: 氟伐他汀对心梗后左室功能、肌球蛋白链基因mRNA表达及胶原重建可产生有益的影响。

关 键 词:氟伐他汀  心肌梗死  肌球蛋白重链  胶原  
文章编号:1000-4718(2005)12-2341-05
收稿时间:2004-04-10
修稿时间:2004-04-102004-06-18

Effects of fluvastatin on the left ventricular function, MHC gene expression and collagen remodeling after myocardial infarction
LIU Yu-hong,ZENG Qiu-tang,CHEN bin.Effects of fluvastatin on the left ventricular function, MHC gene expression and collagen remodeling after myocardial infarction[J].Chinese Journal of Pathophysiology,2005,21(12):2341-2345.
Authors:LIU Yu-hong  ZENG Qiu-tang  CHEN bin
Institution:1Department of Cardiology, Union Hospital,2Department of Ultrasound, Tongji Hospital, Tongji Medical Collage, Huazhong University of Science & Technology, Wuhan 430022, China
Abstract:AIM: To observe the effects of fluvastatin (FV) on the left ventricular (LV) function, MHC mRNA and collagen remodeling of non-infarcted area after acute myocardial infarction (AMI). METHODS: Six hours after ligating left coronary artery, survivors of AMI female SD rats were randomly assigned to: ①AMI control; ②FV; ③sham-operated groups. After 8 weeks of therapy, the LV function, hemodynamics, expression of non-infarcted myocardial MHC mRNA, collagen volume fraction (CVF) and the ratio of type Ⅰ/Ⅲ collagen of non-infarcted area were assessed. RESULTS: Compared with sham-operated group, E wave, E wave deceleration, E/A ratio, LV end diastolic pressure (LVEDP), β MHC mRNA, CVF and the ratio of type Ⅰ/Ⅲ collagen were all significantly increased in AMI group, while fractional shortening (FS), ejection fraction (EF), mean arterial pressure (MAP) and α MHC mRNA were all significantly decreased. In comparison with AMI group, E wave, E wave deceleration, E/A, LVEDP, β MHC mRNA, CVF and the ratio of type Ⅰ/Ⅲ collagen were all significantly decreased, while FS, EF, MAP and α MHC mRNA were all significantly increased in FV group. CONCLUSION: FV improves the LV function after AMI and has beneficial effects on reversing LV myocardial pathologic switching of MHC isoform and collagen remodeling.
Keywords:Fluvastatin  Myocardial infarction  Myosin heavy chains  Collagen
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