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地塞米松对缺血再灌注大鼠血流动力学和心肌超微结构的影响
引用本文:庄梅,方颖,吴立荣,雷大卫. 地塞米松对缺血再灌注大鼠血流动力学和心肌超微结构的影响[J]. 贵阳医学院学报, 2007, 32(1): 24-28
作者姓名:庄梅  方颖  吴立荣  雷大卫
作者单位:1. 贵阳医学院附院,心内科,贵州,贵阳,550004
2. 贵阳医学院,生物化学教研室,贵州,贵阳,550004
摘    要:目的:探讨地塞米松预处理对缺血再灌注大鼠血流动力学和心肌超微结构的影响.方法:将SD大鼠予地塞米松预处理,生理盐水预处理设为对照.预处理24 h后构建Langendorff离体心脏缺血再灌注动物模型,动态观测缺血前及再灌注期间血流动力学的改变;观察大鼠心肌超微结构及热休克蛋白72(HSP72)表达变化.结果:地塞米松预处理诱导大鼠心肌HSP72的表达较对照组显著增加(P<0.05);地塞米松可改善再灌注期间血流动力学指标(左心室发展压、左心室收缩的最大速率、左心室舒张的最大速率、冠状动脉循环流出量,P<0.01)及减轻缺血再灌注后心肌超微结构的损伤.结论:地塞米松预处理对缺血再灌注大鼠的心脏具有延迟保护作用.

关 键 词:地塞米松  心肌缺血  心肌再灌注  血流动力学  超微结构  热休克蛋白类  大鼠,Sprague-Dowley
文章编号:1000-2707(2007)01-0024-05
修稿时间:2006-10-30

Effects of Dexamethasone on Hemodynamics and Myocardial Ultrastructure in Rats during Ischemia and Reperfusion
ZHUANG Mei,FANG Ying,WU Lirong,LEI Dawei. Effects of Dexamethasone on Hemodynamics and Myocardial Ultrastructure in Rats during Ischemia and Reperfusion[J]. Journal of Guiyang Medical College, 2007, 32(1): 24-28
Authors:ZHUANG Mei  FANG Ying  WU Lirong  LEI Dawei
Affiliation:1. Department of Cardiac Internal Medicine, The Affiliated Hospital of Guiyang Medical College, Guiyang 550004, China ; 2. Department of Biochemistry, Guiyang Medical College, Guiyang 550004, China
Abstract:Objective:To explore the effects of dexamethasone(DEX) on hemodynamics and myocardial ultrastructure in rats during ischemia/reperfusion.Methods: The rats were pretreated with DEX in 24 hours before their hearts were separated for Langendorff perfusion and for ischemia/reperfusion.Rats in control group were pretreated with sodium chloride.The left ventricular functions(LVDP,+dp/dtmax,-dp/dtmax) and coronary artery flow(CF) were observed dynamically before ischemia and during 60-minute reperfusion following 30-minute ischemia.Myocardial ultrastructures were also examined.Heat shock protein 72(HSP72) expression was checked by using immunohistochemistry technique.Results: Compared with control group,in DEX pretreated rats,the expression of HSP72 was significantly increased(P<0.05),the LVDP,+dp/dtmax,-dp/dtmax and CF were greatly improved(P<0.01),and the ischemia/reperfusion injury of myocardial ultrastructure was decreased.Conclusions: DEX induces upregulation of HSP72,which functions to protect myocardium against ischemia/reperfusion injury in rat heart.
Keywords:dexamethasone    myocardial ischemia   myocardial reperfusion    hemodynamics    ultrastructure    heat-shock proteins    rats, Sprague-Dowley
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