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氟卡尼和E-4031对猫心室肌细胞延迟整流钾电流IK的阻断作用

Block of delayed rectifier potassium current, IK, by flecainide and E-4031 in cat ventricular myocytes.

作者信息

Follmer C H, Colatsky T J

机构信息

Cardiovascular Pharmacology, Wyeth-Ayerst Research, Princeton, NJ 08543-8000.

出版信息

Circulation. 1990 Jul;82(1):289-93. doi: 10.1161/01.cir.82.1.289.

Abstract

Block of the delayed rectifier potassium current, IK, by the class IC antiarrhythmic agent, flecainide, and by the novel selective class III antiarrhythmic agent, E-4031, were compared in isolated cat ventricular myocytes using the single suction-pipette, voltage-clamp technique. Flecainide (10 microM) markedly reduced IK elicited on depolarization steps to plateau voltages (+10 mV) and nearly completely blocked the "tail currents" elicited on repolarization to -40 mV (93 +/- 4% block at +40 mV, n = 3). E-4031 (1 microM) produced similar effects (96 +/- 3% block at +40 mV, n = 3). Slow voltage ramps from -100 to +40 mV confirmed inward rectifying properties of IK and showed that flecainide and E-4031 have no effects on the background potassium current, IK1. Thus, the results demonstrate that block of IK is a common feature of flecainide and E-4031. IK block by E-4031 most likely underlies the drug's potent class III antiarrhythmic properties. On the other hand, flecainide block of IK during an action potential would tend to prolong repolarization, but this effect may be obscured by concomitant block of plateau Na+ channels to produce little or no change in action potential duration, consistent with its class IC classification.

摘要

使用单吸液管电压钳技术,在分离的猫心室肌细胞中比较了ⅠC类抗心律失常药物氟卡尼和新型选择性Ⅲ类抗心律失常药物E - 4031对延迟整流钾电流(IK)的阻断作用。氟卡尼(10微摩尔)显著降低了去极化至平台电压(+10毫伏)时诱发的IK,并几乎完全阻断了复极化至 - 40毫伏时诱发的“尾电流”(在 +40毫伏时阻断率为93±4%,n = 3)。E - 4031(1微摩尔)产生了类似的效果(在 +40毫伏时阻断率为96±3%,n = 3)。从 - 100毫伏到 +40毫伏的缓慢电压斜坡证实了IK的内向整流特性,并表明氟卡尼和E - 4031对背景钾电流IK1没有影响。因此,结果表明阻断IK是氟卡尼和E - 4031的共同特征。E - 4031对IK的阻断很可能是该药物强大的Ⅲ类抗心律失常特性的基础。另一方面,在动作电位期间氟卡尼对IK的阻断会倾向于延长复极化,但这种效应可能会被同时阻断平台期钠通道所掩盖,从而使动作电位持续时间几乎没有变化,这与其ⅠC类分类一致。

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