Bertrix L, Timour Chah Q, Lang J, Lakhal M, Bouzouita K, Faucon G
Arch Int Pharmacodyn Ther. 1985 Mar;274(1):97-110.
The efficacy of verapamil and propranolol was studied in comparison with disopyramide on the atrial fibrillation experimentally induced in the dog heart in situ by electrical stimulation combined with intra-aortic injection of acetylcholine (ACh). After reducing the amplitude and duration of the monophasic action potential (MAP) and the duration of the effective refractory period (ERP) of the atrial contractile fibres, ACh lowered the fibrillation threshold (FT), and, when fibrillation had been elicited, it accelerated the fibrillation rate (FR). Verapamil and propranolol failed to prevent atrial fibrillation: they did not counteract any of the alterations in the electrophysiological properties of the atrial contractile fibres due to ACh. In contrast, disopyramide, at doses within the therapeutic range, prevented fibrillation. The fibrillation threshold, which fell from 50 mA to 1 mA in the presence of ACh, was restored to control values by disopyramide. Disopyramide also antagonized the reduction in amplitude of MAP caused by ACh before the triggering of fibrillation and the reductions by ACh of the durations of MAP and ERP. Disopyramide first slowed FR, in association with an increase in amplitude of fibrillation waves and a tendency to synchronous activity, and ultimately terminated the fibrillation.
在通过电刺激联合主动脉内注射乙酰胆碱(ACh)在犬原位心脏实验性诱发房颤的模型中,对比研究了维拉帕米、普萘洛尔与丙吡胺的疗效。ACh降低心房收缩纤维的单相动作电位(MAP)幅度和时程以及有效不应期(ERP)时程后,降低了房颤阈值(FT),且在诱发房颤后,加快了房颤频率(FR)。维拉帕米和普萘洛尔未能预防房颤:它们未抵消因ACh导致的心房收缩纤维电生理特性的任何改变。相比之下,治疗范围内剂量的丙吡胺可预防房颤。在ACh存在下从50 mA降至1 mA的房颤阈值,被丙吡胺恢复至对照值。丙吡胺还可拮抗在诱发房颤前由ACh引起的MAP幅度降低以及由ACh引起的MAP和ERP时程缩短。丙吡胺首先减慢FR,同时伴有房颤波幅度增加和同步活动倾向,最终终止房颤。