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新型 I 类抗心律失常药物比地索胺(SC - 40230)对麻醉大鼠冠状动脉闭塞和再灌注诱发的室性心律失常的影响;与美西律和丙吡胺的比较。

Effects of bidisomide (SC-40230), a new class I antiarrhythmic agent, on ventricular arrhythmias induced by coronary artery occlusion and reperfusion in anesthetized rats; comparison with mexiletine and disopyramide.

作者信息

Komori S, Sano S, Li B H, Matsumura K, Naitoh A, Mochizuki S, Ishihara T, Watanabe A, Umetani K, Ijiri H

机构信息

Second Department of Internal Medicine, Yamanashi Medical University, Japan.

出版信息

Heart Vessels. 1995;10(1):7-11. doi: 10.1007/BF01745072.

Abstract

We investigated the antiarrhythmic effects of bidisomide (SC-40230), a new class I antiarrhythmic drug, in early-phase ventricular arrhythmias induced by coronary artery occlusion and reperfusion in anesthetized rats. The effects of bidisomide were compared with those of mexiletine (MXT) and disopyramide (DSP), established class I antiarrhythmic drugs. Drugs were administered intravenously, 5 min before induction of coronary occlusion. Bidisomide (5 mg/kg) reduced the number of premature ventricular complexes and the incidence of ventricular tachycardia and ventricular fibrillation similarly to MXT and DSP in rats with ventricular arrhythmias induced by coronary artery occlusion. In rats with ventricular arrhythmias induced by coronary artery reperfusion following a 5-min coronary occlusion, the antiarrhythmic effects of 5 mg/kg of bidisomide were similar to those of the same doses of MXT and DSP. All three drugs significantly slowed the heart rate. Our results suggest that bidisomide may effectively reduce the severity of life-threatening ventricular arrhythmias that occur during acute coronary syndrome.

摘要

我们研究了新型I类抗心律失常药物比地索胺(SC - 40230)对麻醉大鼠冠状动脉闭塞和再灌注诱发的早期室性心律失常的抗心律失常作用。将比地索胺的作用与已确立的I类抗心律失常药物美西律(MXT)和丙吡胺(DSP)的作用进行了比较。在冠状动脉闭塞诱导前5分钟静脉给药。在冠状动脉闭塞诱发室性心律失常的大鼠中,比地索胺(5毫克/千克)减少室性早搏的数量以及室性心动过速和心室颤动的发生率,其效果与MXT和DSP相似。在冠状动脉闭塞5分钟后进行冠状动脉再灌注诱发室性心律失常的大鼠中,5毫克/千克比地索胺的抗心律失常作用与相同剂量的MXT和DSP相似。所有三种药物均显著减慢心率。我们的结果表明,比地索胺可能有效降低急性冠状动脉综合征期间发生的危及生命的室性心律失常的严重程度。

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