Adamantidis M M, Kerram P, Caron J F, Dupuis B A
Laboratoire de Pharmacologie, Institut National de la Santé et de la Recherche Médicale, Faculté de Médecine, Lille, France.
J Pharmacol Exp Ther. 1993 Aug;266(2):884-93.
This study was designed to clarify discrepancies concerning the effects of droperidol on cardiac repolarization. Myocardial electrical activity was recorded by using microelectrode technique in rabbit Purkinje fibers and guinea pig ventricular muscle. In Purkinje fibers stimulated at 60 pulses/min, low concentrations (0.01-0.3 microM) of droperidol increased in a dose-dependent fashion action potential duration (APD) without altering the other parameters. At 1 and 3 microM, droperidol led to the reversal of the prolonging effect. The highest concentrations used (10 and 30 microM), produced shortening in APD at 50% repolarization concomitantly with a significant decrease in Vmax, action potential amplitude and resting membrane potential. Inexcitability occurred in 4 of 15 preparations exposed to 30 microM. In 8 of 15 Purkinje fibers, the prolonging effect induced by low concentrations was so important that APD exceeded the 1000-msec period of basal stimulation and early afterdepolarizations (EADs) and triggered activity developed. In guinea pig ventricular muscle, these effects were notably less pronounced. Prolongation of action potential showed a reverse use-dependence (i.e., much greater at the lowest stimulation frequencies), whereas Vmax depression was use-dependent. Decreasing extracellular K concentration from 4.0 to 2.7 mM enhanced the incidence of EADs in Purkinje fibers, whereas elevating the K concentration from 2.7 to 5.4 mM abolished them completely and shortened drastically APD. EADs were also eliminated by increasing magnesium concentration from 1 to 5 mM. Addition of isoproterenol favored EADs, whereas these were suppressed at plateau level by exposure to 0.3 microM nifedipine. The results indicate that in rabbit Purkinje fibers, droperidol exerts a dual effect on repolarization, prolongation with low concentrations with development of EADs and subsequent triggered activity. These abnormalities were suppressed at high concentrations concomitantly with a marked depression of other characteristics. These observations suggest multiple ionic channel activities and further studies are required to precise the underlying mechanisms at channel level.
本研究旨在阐明有关氟哌利多对心脏复极化影响的差异。采用微电极技术记录家兔浦肯野纤维和豚鼠心室肌的心肌电活动。在以60次脉冲/分钟刺激的浦肯野纤维中,低浓度(0.01 - 0.3微摩尔)的氟哌利多以剂量依赖性方式增加动作电位时程(APD),而不改变其他参数。在1和3微摩尔时,氟哌利多导致延长效应的逆转。使用的最高浓度(10和30微摩尔),在复极化50%时使APD缩短,同时Vmax、动作电位幅度和静息膜电位显著降低。在暴露于30微摩尔的15个标本中,有4个出现了兴奋性丧失。在15个浦肯野纤维中的8个中,低浓度诱导的延长效应非常显著,以至于APD超过了基础刺激的1000毫秒周期,并出现了早期后去极化(EADs)和触发活动。在豚鼠心室肌中,这些效应明显不那么显著。动作电位的延长表现出反向使用依赖性(即,在最低刺激频率时更大),而Vmax的降低是使用依赖性的。将细胞外钾浓度从4.0毫摩尔降低到2.7毫摩尔会增加浦肯野纤维中EADs的发生率,而将钾浓度从2.7毫摩尔提高到5.4毫摩尔则会完全消除它们并大幅缩短APD。通过将镁浓度从1毫摩尔增加到5毫摩尔也可消除EADs。加入异丙肾上腺素有利于EADs的发生,而在平台期通过暴露于0.3微摩尔硝苯地平可抑制EADs。结果表明,在家兔浦肯野纤维中,氟哌利多对复极化有双重作用,低浓度时延长并伴有EADs的发生和随后的触发活动。这些异常在高浓度时被抑制,同时其他特征也明显降低。这些观察结果提示存在多种离子通道活动,需要进一步研究以明确通道水平的潜在机制。