[钙通道阻滞剂对实验性大鼠心肌梗死的影响]。

Ceskoslovenska farmacie Pub Date : 1993-06-01
M Kuzelová, P Svec
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引用次数: 0

摘要

观察钙通道阻滞剂对冠状动脉闭塞大鼠心肌缺血发展的影响。用戊巴比妥麻醉大鼠,在结扎前7天将游离于左冠状动脉室支下的结扎末端收紧,对冠状动脉进行封堵。用心电图记录缺血后r波和st段的变化。冠状动脉闭塞导致心律失常,st段明显升高,心率轻微增加。不同药理学性质的钙通道阻滞剂维拉帕米、硝苯地平和地尔硫卓对缺血的影响程度不同。硝苯地平(0.02 mg。Kg-1,静脉注射,闭塞前30分钟),维拉帕米(0.2 mg。Kg-1,缺血前10分钟静脉注射),地尔硫卓(0.3 mg。kg-1, i.v.,缺血前10分钟)显著降低st段升高。维拉帕米对上述模型的影响最大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The effect of calcium channel blockers in experimental myocardial infarct in rats].

The effect of the blockers of calcium channels on the development of myocardial ischaemia in rats with an occlusion of the coronary artery was examined. An occlusion of the coronary artery was carried out in rats anaesthetized with pentobarbital by tightening the ends of the ligature freely placed under the left coronary artery - ramus interventricularis seven days prior to ligation. The ischaemia-induced changes in the R-wave and ST-segment were recorded using ECG. The occlusion of the coronary artery produced arrhythmias, a significant elevation of the ST-segment and a slight increase in the heart rate. The blockers of calcium channels with different pharmacological properties - verapamil, nifedipine and diltiazem influenced the ischaemia-induced changes with different intensity. Nifedipine (0.02 mg.kg-1, i.v., 30 min prior to occlusion), verapamil (0.2 mg.kg-1, i.v., 10 mins prior to ischaemia), and diltiazem (0.3 mg.kg-1, i.v., 10 mins prior to ischemia) significantly reduced the increased elevation of the ST-segment. The highest effect on the above-mentioned model was shown by verapamil.

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