Furuya M, Yoshida K
Department of Anesthesiology, Kanagawa Dental College, Yokosuka.
Masui. 1999 Oct;48(10):1074-82.
This study was designed to investigate whether two L-type calcium antagonists, verapamil and nicardipine reduce the myocardial necrosis (infarct size) following ischemia and reperfusion. Rabbits (n = 52) were subjected to regional myocardial ischemia by 30 min of the left anterior descending artery occlusion followed by 3 hrs of reperfusion under ketamine/xylazine anesthesia. The animals were randomly assigned to a control group, and verapamil or nicardipine treatment groups. A continuous infusion of verapamil (0.1 mg.kg-1.h-1) or nicardipine (0.06 mg.kg-1.h-1) was initiated 5 min prior to ischemia, immediately after ischemia, 5 min after ischemia, 5 min prior to reperfusion, immediately after reperfusion, and 5 min after reperfusion. A lead II ECG was recorded throughout the experiment for determining ventricular arrhythmias. The area at risk was delineated by Evans blue, and infarct size was determined by triphenyl tetrazolium chloride staining at the end of the experiment in the heart (the left anterior descending artery was religated). The area at risk showed no significant differences among all the groups tested; infarct size in the rabbits to which verapamil was given 5 min before subjecting to ischemia was significantly reduced to 41.7 +/- 4.3% from 65.9 +/- 1.7% in control rabbits. The treatment with nicardipine at any period of time did not reduce infarct size. On the other hand, the incidence of reperfusion-induced arrhythmias was decreased by nicardipine infusion, when started 5 min prior to ischemia, immediately after ischemia, 5 min after ischemia, 5 min prior to reperfusion, and immediately after reperfusion. These results suggest that verapamil given before coronary artery occlusion has an infarct limiting effect in the myocardium, and that nicardipine has an antiarrhythmic effect during reperfusion in the rabbit heart.
本研究旨在调查两种L型钙拮抗剂维拉帕米和尼卡地平是否能减少缺血再灌注后的心肌坏死(梗死面积)。52只兔子在氯胺酮/赛拉嗪麻醉下,通过左前降支动脉闭塞30分钟,随后再灌注3小时,造成局部心肌缺血。动物被随机分为对照组、维拉帕米治疗组或尼卡地平治疗组。在缺血前5分钟、缺血后即刻、缺血后5分钟、再灌注前5分钟、再灌注后即刻和再灌注后5分钟开始持续输注维拉帕米(0.1mg·kg-1·h-1)或尼卡地平(0.06mg·kg-1·h-1)。在整个实验过程中记录II导联心电图以确定室性心律失常。用伊文思蓝勾勒出危险区域,实验结束时在心脏(重新结扎左前降支动脉)用氯化三苯基四氮唑染色确定梗死面积。所有测试组的危险区域无显著差异;在缺血前5分钟给予维拉帕米的兔子梗死面积从对照组兔子的65.9±1.7%显著降低至41.7±4.3%。在任何时间段给予尼卡地平治疗均未减少梗死面积。另一方面,在缺血前5分钟、缺血后即刻、缺血后5分钟、再灌注前5分钟和再灌注后即刻开始输注尼卡地平,可降低再灌注诱导的心律失常发生率。这些结果表明,冠状动脉闭塞前给予维拉帕米对心肌有梗死限制作用,而尼卡地平在兔心脏再灌注期间有抗心律失常作用。