Amerini S, Carbonin P, Cerbai E, Giotti A, Mugelli A, Pahor M
Br J Pharmacol. 1985 Dec;86(4):805-15. doi: 10.1111/j.1476-5381.1985.tb11102.x.
The antiarrhythmic potency of mexiletine was evaluated on three groups of guinea-pig isolated hearts. Arrhythmias were induced (a) with digitalis intoxication, (b) with hypoxia followed by reoxygenation and (c) with ischaemia followed by reperfusion. Mexiletine 10 microM was found to be very effective against all three types of arrhythmias in all three groups. The electrophysiological effects of mexiletine were then studied on sheep cardiac Purkinje fibres manifesting oscillatory afterpotentials and triggered automaticity induced by barium or strophanthidin. Mexiletine 10 microM consistently decreased the amplitude of oscillatory afterpotentials and blocked subsequent triggered activity in sheep Purkinje fibres. In contrast, mexiletine 10 microM had no significant effect on Vmax in normal, barium- and strophanthidin-treated preparations. The results are discussed in relation to the mechanisms of antiarrhythmic action of mexiletine.
在三组豚鼠离体心脏上评估了美西律的抗心律失常效力。心律失常通过以下方式诱发:(a) 洋地黄中毒,(b) 缺氧后再给氧,以及 (c) 缺血后再灌注。发现在所有三组中,10微摩尔的美西律对所有三种类型的心律失常都非常有效。然后在表现出振荡后电位和由钡或毒毛花苷诱导的触发自律性的绵羊心脏浦肯野纤维上研究了美西律的电生理效应。10微摩尔的美西律持续降低振荡后电位的幅度,并阻断绵羊浦肯野纤维随后的触发活动。相比之下,10微摩尔的美西律对正常、经钡和毒毛花苷处理的制剂中的最大动作电位速率(Vmax)没有显著影响。结合美西律抗心律失常作用的机制对结果进行了讨论。