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雷米普利对糖尿病大鼠心肌缺血/再灌注损伤的保护作用
引用本文:吴艳娜,张喆,陈艳,焦建杰,康毅,高卫真,娄建石,刘艳霞.雷米普利对糖尿病大鼠心肌缺血/再灌注损伤的保护作用[J].中国药理学通报,2008,24(7):924-928.
作者姓名:吴艳娜  张喆  陈艳  焦建杰  康毅  高卫真  娄建石  刘艳霞
作者单位:天津医科大学药理学教研室,天津,300070
基金项目:天津市科委资助项目 , 天津医科大学重点基金 , 天津医科大学校科研和教改项目
摘    要:目的研究雷米普利(RAM)对糖尿病大鼠心肌缺血/再灌注损伤的保护作用。方法链脲佐菌素致糖尿病大鼠被随机分为缺血/再灌注(I/R)、缺血预适应(IPC)和RAM3组。RAM组每天用RAM(1mg·kg-1)灌胃,IPC和I/R组用等体积生理盐水灌胃。4wk后各组动物均经历心肌缺血/再灌注损伤,IPC组于缺血前行心肌缺血预适应。连续监测心电图,检测心肌梗死范围、心肌细胞凋亡、凋亡蛋白Bcl-2与Bax表达,光镜下观察心肌形态学改变。结果与I/R组比较,RAM及IPC组ST-段抬高幅度降低,室早出现时间推迟,持续时间缩短,室速、室颤发生率降低,心肌梗死范围缩小,心肌细胞凋亡减轻,Bcl-2/Bax比值升高。结论连续4wk应用RAM可减轻糖尿病大鼠心肌缺血/再灌注损伤。

关 键 词:雷米普利  糖尿病  缺血/再灌注  凋亡  缺血预适应

Study on cardioprotection of ramipril against ischemia/reperfusion injury in diabetic rats
WU Yan-na,ZHANG Zhe,CHEN Yan,JIAO Jian-jie,KANG Yi,GAO Wei-zhen,LOU Jian-shi,LIU Yan-xia.Study on cardioprotection of ramipril against ischemia/reperfusion injury in diabetic rats[J].Chinese Pharmacological Bulletin,2008,24(7):924-928.
Authors:WU Yan-na  ZHANG Zhe  CHEN Yan  JIAO Jian-jie  KANG Yi  GAO Wei-zhen  LOU Jian-shi  LIU Yan-xia
Abstract:Aim To investigate the effect of ramipril on myocardial ischemia-reperfusion injury in diabetic rats.Methods Streptozotocin induced diabetic rats were divided randomly into ischemia/reperfusion(I/R),ischemic preconditioning(IPC) and ramipril(RAM) groups.Rats in RAM group were administered RAM(1 mg·kg-1) orally for 4 weeks,the others were administered normal saline.Then all rats were subjected to myocardial ischemia/reperfusion injury.Rats in IPC group were preconditioned before ischemia.ECG,myocardial infarct size,apoptosis and expressions of Bcl-2 and Bax,changes of myocardial morphology were examined.Results Compared with those of I/R group,the elevation of ST segment and the incidence of ventricular tachycardia and ventricular fibrillation during ischemia were significantly decreased,myocardial infarct size and cardiomyocyte apoptosis index were remarkably reduced,ratio of Bcl-2/Bax was increased in both IPC and RAM groups.Conclusion Myocardial ischemia/reperfusion injury was decreased in diabetic rats after ramipril orally administered for 4 weeks.
Keywords:ramipril  diabetes mellitus  ischemia/reperfusion  apoptosis  ischemic preconditioning
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