Winslow E, Campbell J K, Delbressine L
Department of Pharmacology, RL CERM Laboratories, Riom, France.
J Pharm Pharmacol. 1995 Jul;47(7):608-13. doi: 10.1111/j.2042-7158.1995.tb06723.x.
Org 20781, the major metabolite of Org 7797 found in in-vitro experiments was examined for antiarrhythmic and electrophysiological effects in-vivo. Org 20781 (0.5-2.0mg kg-1, i.v.) inhibited the development of early ischaemia-induced arrhythmias in rats, suppressed spontaneous ventricular tachycardia (VT) in conscious dogs with 24-h old infarcts, and prevented electrical induction of VT in dogs with 5-6 day old infarcts, actions associated with slowing of conduction at all levels of the myocardium. Cardiac refractory periods were only modestly prolonged whilst repolarization was unchanged. Peak plasma levels of the parent compound (infused to total doses of 2-4 mg kg-1) associated with suppression of late arrhythmias were 6-18 microM, whilst the mean plasma elimination half-life (in normal dogs) was 107 min. It was concluded that the major metabolite has a similar antiarrhythmic and electrophysiological profile to the parent compound, is at least half as potent and may contribute to the therapeutic effects of Org 7797 administration.
在体外实验中发现的Org 7797的主要代谢产物Org 20781,在体内进行了抗心律失常和电生理效应研究。Org 20781(0.5 - 2.0毫克/千克,静脉注射)可抑制大鼠早期缺血性心律失常的发生,抑制24小时梗死的清醒犬的自发性室性心动过速(VT),并预防5 - 6天梗死犬的VT电诱导,这些作用与心肌各水平传导减慢有关。心脏不应期仅适度延长,而复极化无变化。与抑制晚期心律失常相关的母体化合物(输注至总剂量2 - 4毫克/千克)的血浆峰值水平为6 - 18微摩尔,而平均血浆消除半衰期(在正常犬中)为107分钟。结论是,主要代谢产物具有与母体化合物相似的抗心律失常和电生理特征,效力至少为母体化合物的一半,可能有助于Org 7797给药的治疗效果。