Arnsdorf M F, Schmidt G A, Sawicki G J
J Pharmacol Exp Ther. 1985 Jan;232(1):40-8.
Encainide is a benzanilide derivative that is effective against ventricular arrhythmias but, at times, may be arrhythmogenic. The microelectrode technique of intracellular current application and transmembrane voltage recording was used to study the effects of encainide, in a concentration equivalent to a clinically effective antiarrhythmic plasma level, on the determinants of cardiac excitability in sheep Purkinje fibers. A rapid, on-line computerized data analysis system was used to track the alterations in the active and passive membrane properties relevant to excitability in time. Cardiac excitability was defined experimentally in terms of the current required to attain threshold and/or the shift in strength- or change-duration curves. Encainide produced multiphasic changes in cardiac excitability, the final state of excitability depended on the balance between altered passive and active membrane properties. Encainide could enhance excitability by increasing membrane and slope resistance without altering the nonlinearities of the current-voltage relationship despite an actual depression of the sodium system. Encainide could decrease excitability by 1) depressing the sodium system; 2) decreasing membrane resistance without altering the nonlinearities of the subthreshold current-voltage relationship; 3) altering the nonlinearities of the current-voltage relationship; and 4) by a combination of these actions. During washout, excitability could remain altered despite a return of descriptive parameters such as the maximal rate of rise of phase 0, overshoot and action potential duration to normal. The study demonstrated the importance of time-related changes of an antiarrhythmic drug at a constant concentration. The results explain, in part, the antiarrhythmic actions and arrhythmogenic potential of encainide.
恩卡胺是一种苯甲酰苯胺衍生物,对室性心律失常有效,但有时可能致心律失常。采用细胞内电流施加和跨膜电压记录的微电极技术,研究了与临床有效抗心律失常血浆水平相当浓度的恩卡胺对绵羊浦肯野纤维心脏兴奋性决定因素的影响。使用快速在线计算机化数据分析系统及时跟踪与兴奋性相关的主动和被动膜特性的变化。根据达到阈值所需的电流和/或强度 - 或时程曲线的偏移,通过实验定义心脏兴奋性。恩卡胺使心脏兴奋性产生多相变化,兴奋性的最终状态取决于被动和主动膜特性改变之间的平衡。尽管钠系统实际受到抑制,但恩卡胺可通过增加膜电阻和斜率电阻来增强兴奋性,而不改变电流 - 电压关系的非线性。恩卡胺可通过以下方式降低兴奋性:1)抑制钠系统;2)降低膜电阻而不改变阈下电流 - 电压关系的非线性;3)改变电流 - 电压关系的非线性;4)通过这些作用的组合。在洗脱过程中,尽管诸如0期最大上升速率、超射和动作电位时程等描述参数恢复正常,但兴奋性仍可能保持改变。该研究证明了在恒定浓度下抗心律失常药物与时间相关变化的重要性。这些结果部分解释了恩卡胺的抗心律失常作用和致心律失常潜力。