摘要
目的 探讨心肌缺血预处理(IPC)保护该心肌被以后较长时间缺血损伤的作用。方法 给Wistar大鼠在90min缺血和180min再灌注(I/R)前3次、每次5min、间隔5min再灌注的心肌缺血预处理;I/R前静脉注射Bre.、PMA观察它们对心肌I/R损伤的影响作用。结果 IPC、PMA可保护心肌被I/R的损伤;Bre.则可消除IPC对心肌的保护作用。结论 IPC可保护心肌被长达90min.I/180min.R损伤,其保护机制作者正在研究之中,可能与蛋白激酶C被激活有关。
Objective To explore IPC(ischemic preconditioning) and PMA reduce the size of infarcts compared with control and breviscapini(Bre.). Methods and Results Anesthetized open-chest wistar rats underwent three 5- minute episodes of preconditioning ischemia in IPC group or after administration of Bre. in Bre.group; Control group had no episodes of ischemic preconditioning; PMA was injected 5 minutes before sustained occlusion; Afte- r 90 minutes of CAO and 3 hours of reperfusion, infarct size was significantly reduced in IPC rats' compared with control group and Bre.+IPC groups, P<0.01. Conclusion The wistar rats IPC model was stable, TTC can obviously distinguish the AN(area of necrosis) from normal myocardium. The IPC、PMA protected the myocardium from sustained ischemia-reperfusion injury.Bre. blunted the protective role of IPC. PMA imitated the protective role of IPC. Their protective mechanism will be disscused in detail in next article.
出处
《重庆医科大学学报》
CAS
CSCD
2000年第3期268-269,共2页
Journal of Chongqing Medical University
关键词
缺血预处理
心肌保护
心肌缺血
大鼠
Myocardium infarct
Ischemic preconditioning
Myocardial protection