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喷替索胺(CM 7857)对心肌兴奋、传导、复极化和不应期的影响。一项人体电生理研究。

Effect of pentisomide (CM 7857) on myocardial excitation, conduction, repolarization, and refractoriness. An electrophysiological study in humans.

作者信息

Olsson S B, Edvardsson N, Newell P A, Yuan S, Zeng Z

机构信息

Department of Cardiology, Lund University Hospital, Sweden.

出版信息

J Cardiovasc Pharmacol. 1991 Dec;18(6):849-54. doi: 10.1097/00005344-199112000-00010.

Abstract

The electrophysiological effects of pentisomide upon the intact human heart were evaluated using programmed stimulation and recording of intracardiac monophasic action potentials (MAP) in 17 patients with various ventricular arrhythmias. After i.v. administration of pentisomide, 85-135 mg, the atrial-His interval increased by 8 +/- 12 ms (p less than 0.05) during sinus rhythm and by 13 +/- 21 ms (p less than 0.05) at atrial pacing of 600 ms cycle length (600 ms pacing). The His-ventricular interval also increased by 6 +/- 10 ms during sinus rhythm (p less than 0.05) and by 5 +/- 9 ms at 600 ms pacing (NS). The QRS duration prolonged by 9 +/- 10 ms (p less than 0.01) and 6 +/- 8 ms (p less than 0.01) during 600 and 500 ms ventricular pacing, respectively. The right ventricular MAP duration to 90% repolarization was significantly shortened, by 20 +/- 21 ms (p less than 0.01) during sinus rhythm, by 16 +/- 17 ms (p less than 0.01) at 600 ms ventricular pacing, and by 11 +/- 16 ms (p less than 0.01) at 500 ms ventricular pacing. The corrected QT interval was shortened by 21 +/- 28 ms (p less than 0.01). The present study supports that pentisomide is a class-I antiarrhythmic agent with a marked effect on depolarization (action of class Ia and Ic) and on repolarization (action of class Ib). This unique combination of cellular electrophysiological properties indicates that the clinical antiarrhythmic efficacy of pentisomide may differ from that of hitherto available antiarrhythmic drugs.

摘要

采用程序刺激和记录心内单相动作电位(MAP)的方法,对17例患有各种室性心律失常的患者,评估了喷替米特对完整人体心脏的电生理效应。静脉注射85 - 135mg喷替米特后,窦性心律时心房 - 希氏束间期增加8±12毫秒(p<0.05),在600毫秒周期长度的心房起搏(600毫秒起搏)时增加13±21毫秒(p<0.05)。希氏束 - 心室间期在窦性心律时也增加6±10毫秒(p<0.05),在600毫秒起搏时增加5±9毫秒(无显著性差异)。在600毫秒和500毫秒心室起搏时,QRS时限分别延长9±10毫秒(p<0.01)和6±8毫秒(p<0.01)。右心室MAP复极化至90%时的时限显著缩短,窦性心律时缩短20±21毫秒(p<0.01),600毫秒心室起搏时缩短16±17毫秒(p<0.01),500毫秒心室起搏时缩短11±16毫秒(p<0.01)。校正QT间期缩短21±28毫秒(p<0.01)。本研究支持喷替米特是一种I类抗心律失常药物,对去极化(Ia类和Ic类作用)和复极化(Ib类作用)均有显著影响。这种独特的细胞电生理特性组合表明,喷替米特的临床抗心律失常疗效可能与迄今可用的抗心律失常药物不同。

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