Przywara D A, Dambach G E
Department of Pharmacology, Wayne State University School of Medicine, Detroit, Michigan 48201.
Circ Res. 1989 Jul;65(1):185-92. doi: 10.1161/01.res.65.1.185.
The hypothesis that cocaine has Class I-type antiarrhythmic drug effects was tested in tissues isolated from rabbit heart with standard microelectrode methods. Propranolol (1 microM) was used to block beta-adrenergic effects. The actions of cocaine on cellular electrophysiology were concentration- and time-dependent and were reversible. In paced right atrial (RA) and right ventricular papillary (RVP) tissues, cocaine produced a profound prolongation of the effective refractory period (ERP) assessed by either premature stimulation or minimum pacing interval. ERP was increased up to eightfold in RA tissue and doubled in RVP tissue by 60 microM cocaine. This concentration of cocaine depressed action potential phase 0 depolarization 80% in RA tissue and 53% in RVP tissue but had no effect on resting membrane potentials. Automaticity was moderately depressed in sinus node (34% decrease in rate) but not in tricuspid valve cells. Phase 0 depolarization was not altered in these spontaneously active slow-response cells. Repolarization was depressed in RA, tricuspid valve, and sinus node cells leading to a twofold increase in action potential duration during exposure to cocaine. Evidence from the effects on cellular action potentials suggests that cocaine affects both fast Na+ channels and repolarizing K+ but not Ca2+ channels. We conclude that cocaine has Class I-type activity and the effects on ERP are extreme.
采用标准微电极方法,在从兔心脏分离的组织中测试了可卡因具有I类抗心律失常药物作用的假说。使用普萘洛尔(1微摩尔)阻断β-肾上腺素能效应。可卡因对细胞电生理的作用具有浓度和时间依赖性,并且是可逆的。在起搏的右心房(RA)和右心室乳头肌(RVP)组织中,可卡因通过过早刺激或最小起搏间隔评估,使有效不应期(ERP)显著延长。在RA组织中,60微摩尔可卡因使ERP增加高达八倍,在RVP组织中使ERP增加一倍。该浓度的可卡因使RA组织中动作电位0期去极化降低80%,RVP组织中降低53%,但对静息膜电位无影响。窦房结的自律性中度降低(速率降低34%),但三尖瓣细胞的自律性未降低。在这些自发活动的慢反应细胞中,0期去极化未改变。在RA、三尖瓣和窦房结细胞中复极化受到抑制,导致在暴露于可卡因期间动作电位持续时间增加两倍。对细胞动作电位影响的证据表明,可卡因影响快速Na+通道和复极化K+通道,但不影响Ca2+通道。我们得出结论,可卡因具有I类活性,并且对ERP的影响非常显著。