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无创性肢体缺血预处理对缺血心肌的保护作用
引用本文:王宁夫,徐坚,夏强,高琴,史笑笑,周占林,王琳琳,童国新,李虹,李佩璋,张雄,凌峰,潘浩,杨建敏.无创性肢体缺血预处理对缺血心肌的保护作用[J].中华医学杂志,2009,89(28):1999-2002.
作者姓名:王宁夫  徐坚  夏强  高琴  史笑笑  周占林  王琳琳  童国新  李虹  李佩璋  张雄  凌峰  潘浩  杨建敏
作者单位:1. 南京医科大学附属杭州医院杭州市第一人民医院心内科,310006
2. 浙江大学医学院生理教研室
基金项目:浙江省科技厅计划项目 
摘    要:目的 验证在远距离预处理中抑制线粒体钙单向转运体对缺血、再灌注心肌的保护作用.方法 结扎冠脉左前降支使心脏局部缺血30 min,然后再灌注120 min形成缺血/再灌注损伤模型.分别应用远距离预处理、线粒体钙单向转运体抑制剂(钌红)、线粒体钙单向转运体激动剂(精胺、SB202190)进行干预.远距离预处理采用右股动脉结扎5 min,再灌注5 min,反复3个循环实现.再灌注过程中测量平均动脉压,心率,血浆乳酸脱氢酶水平,结束后测量心肌梗死面积.结果 与缺血再灌注组相比,远距离预处理使再灌注后心肌梗死面积缩小(20.4±2.5)%比(51.0±6.0)%],乳酸脱氢酶的释放减少(271±9)U/L比(339±39)U/L];而在远距离预处理前给予精胺或SB202190干预后梗死面积、乳酸脱氢酶降幅均减小,分别为(40.8±9.2)%,(383±43)U/L;(44.3±6.8)%,(356±26)U/L].结论 远距离预处理通过抑制线粒体钙单向转运体的开放可以减轻缺血/再灌注对缺血心肌的损伤,起到对缺血心肌的保护作用.

关 键 词:心肌梗死  再灌注损伤  线粒体钙单向转运体

Mechanism of cardioprotection induced by noninvasive limb ischemic preconditioning
WANG Ning-fu,XU Jian,XIA Qiang,GAO Qin,SHI Xiao-xiao,ZHOU Zhan-lin,WANG Lin-lin,TONG Guo-xin,LI Hong,LI Pei-zhang,ZHANG Xiong,LING Feng,PAN Hao,YANG Jian-min.Mechanism of cardioprotection induced by noninvasive limb ischemic preconditioning[J].National Medical Journal of China,2009,89(28):1999-2002.
Authors:WANG Ning-fu  XU Jian  XIA Qiang  GAO Qin  SHI Xiao-xiao  ZHOU Zhan-lin  WANG Lin-lin  TONG Guo-xin  LI Hong  LI Pei-zhang  ZHANG Xiong  LING Feng  PAN Hao  YANG Jian-min
Abstract:Objective To verify the inhibitory effect of mitochondrial calcium uniporter in remote preconditioning-induced cardioprotection. Methods By occlusion and reperfusion of left anterior descending artery, the rat hearts were subjected to 30 min regional ischemia and 120 min reperfusion in vivo. Thus the ischemic reperfusion model was established. The rats were randomly assigned to undergo one of the following maneuvers: (1) remote preconditioning; (2) ruthenium red (an inhibitor of mitochondrial calcium uniporter); (3) spermine or SB202190 (an opener of mitochondrial calcium uniporter) . Remote preconditioning was elicited by three cycles of 5 rain of right femoral artery occlusion interspersed with 5 min of reperfusion. The mean arterial blood pressure, heart rate and lactate dehydrogenase released in plasma were measured during reperfusion but the infarct size was measured after reperfusion. Results In comparison with I/R group, remote preconditioning limited infarct size (20.4±2.5)% vs (51.0± 6.0) %] and lactate dehydrogenase release (271±9) U/L vs (339±39) U/L] during reperfusion. On the contrary, spermine or SB202190 attenuated the reduction of infarct size and lactate dehydrogenase release induced by remote preconditioning. The group of spermine was (40.8±9.2) % vs (20.4±2.5) %] and (383±43)U/L vs (271±9)U/L] while the group of SB202190 was (44.3±6.8)% vs (20.4± 2.5)%] and(356±26)U/L vs(271±9)U/L]. Conclusion Inhibition of mitochondrial calcium uniporter opening is involved in the remote preconditioning-induced cardioprotection.
Keywords:Myocardial infarction  Reperfusion injury  Mitochandrial calcium uniporter
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