ELECTROPHARMACOLOGY OF DOFETILIDE - A NEW CLASS-III AGENT, IN ANESTHETIZED DOGS

被引:32
作者
GWILT, M
BLACKBURN, KJ
BURGES, RA
HIGGINS, AJ
MILNE, AA
SOLCA, AM
机构
[1] Pfizer Central Research, Sandwich
关键词
ANTIARRHYTHMIC AGENTS; K+ CHANNELS; VENTRICULAR FIBRILLATION;
D O I
10.1016/0014-2999(92)90021-U
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In open chest anaesthetised dogs, dofetilide increased the ventricular effective refractory period over the dose range 1-100-mu-g/kg i.v. and the ventricular fibrillation threshold at doses between 3-100-mu-g/kg and was 80-1000 times more potent than sematilide, racemic sotalol, d-sotalol or quinidine. The maximal increases in ventricular fibrillation threshold induced by sematilide and quinidine were less than that induced by the other drugs. A change in the character of the induced arrhythmia from true ventricular fibrillation to a rapid ventricular flutter, with frequent spontaneous conversion, was observed following all drugs. No adverse haemodynamic effects of dofetilide, sematilide or d-sotalol were observed, but quinidine induced marked cardiac depression and racemic sotalol also impaired left ventricular contractility. All drugs reduced heart rate, though the effect of racemic sotalol was clearly greater than that of the other agents. Dofetilide is a potent class III antiarrhythmic agent with antifibrillatory properties and a favourable haemodynamic profile.
引用
收藏
页码:137 / 144
页数:8
相关论文
共 29 条