학술논문

Electrophysiologic Antiarrhythmic and Cardioprotective Effects of N35 Dichlorophenyl 44Hydroxy2MethoxyPhenyl Piperazine Carboxamidine Dihydrochloride RS87337
Document Type
Article
Source
Journal of Cardiovascular Pharmacology; August 1989, Vol. 14 Issue: 2 p184-193, 10p
Subject
Language
ISSN
01602446; 15334023
Abstract
N-[3,5-Dichlorophenyl] 4-[4-hydroxy-2-methoxy-phenyl] piperazine carboxamidine dihydrochloride (RS-87337) is a chemically novel antiarrhythmic agent with an electrophysiologic profile characteristic of both class III and class la compounds as defined by Vaughan-Williams and Campbell. In isolated superfused guinea pig papillary muscles, RS-87337 (0.1–10 μM) prolonged the duration of the action potential (class III effect) and at higher concentrations (10–30 μM) reduced the maximum rate of membrane depolarisation (class I effect). The rate of onset and of recovery from the latter activity was similar to that of disopyramide, between that of lignocaine and flecainide, which allowed its placement in subclass la. When perfused into isolated working rat hearts, RS-87337 (10–1,000 nM) reduced the incidence of ventricular fibrillation that followed coronary artery re-perfusion and in anaesthetised rats [RS-87337, 1–5 mg/kg intravenously (i.v.)] enabled more animals to survive the tachycardia, fibrillation, and mortality produced by a similar procedure. In conscious dogs, i.v. (3–10 mg/kg) and oral (15–60 mg/kg) doses of RS-87337 reduced the number of the ectopic electrocardiogram (ECG) complexes observed 24 h after a two-stage coronary ligation. In anaesthetised dogs with paced hearts, i.v. doses of RS-87337 (0.02–5.0 mg/kg) reduced the elevated ECG S-T segment evoked by brief coronary artery occlusion without altering baseline haemodynamic values. We assume that the class III and la effects of RS-87337 made an important contribution to the compound's antiarrhythmic and cardioprotective effects.