Villafane J, Gelband H, Xu H, McCormack J, Stolfi A, Pickoff A S
Pediatr Res. 1987 Jul;22(1):50-4. doi: 10.1203/00006450-198707000-00013.
The electrophysiologic effects of the new antiarrhythmic agent, propafenone, were investigated in 10 mongrel canine neonates, ages 5 to 11 days. Utilizing standard His bundle recording and stimulation techniques, assessments of sinus and atrioventricular (AV) node function and atrial, AV nodal, and ventricular refractory periods were performed prior to (control) and after cumulative intravenous doses of 1, 2, and 4 mg/kg of propafenone. Propafenone depressed the spontaneous heart rate and prolonged the postatrial pacing recovery times. AV nodal function was depressed as manifested by Wenckebach periodicity occurring at slower pacing rates, increases in AV nodal conduction time, and increases in AV nodal refractoriness. Atrial and ventricular refractory periods were prolonged significantly in a dose-dependent fashion. Prolongation of the His-Purkinje conduction time occurred at the highest dose. Thus, propafenone exerts a generalized depressant effect on neonatal myocardial conduction and refractoriness which suggests that this agent may be useful in the therapy of atrial and ventricular dysrhythmias in the immature heart.
在10只年龄为5至11天的杂种犬新生幼犬中研究了新型抗心律失常药物普罗帕酮的电生理效应。利用标准的希氏束记录和刺激技术,在静脉注射累积剂量为1、2和4mg/kg普罗帕酮之前(对照)和之后,对窦房结和房室(AV)结功能以及心房、房室结和心室不应期进行了评估。普罗帕酮降低了自发心率并延长了心房起搏后恢复时间。房室结功能受到抑制,表现为在较慢的起搏频率下出现文氏周期、房室结传导时间增加以及房室结不应期增加。心房和心室不应期以剂量依赖方式显著延长。在最高剂量时发生希氏-浦肯野传导时间延长。因此,普罗帕酮对新生儿心肌传导和不应期产生普遍的抑制作用,这表明该药物可能对治疗未成熟心脏的心房和心室心律失常有用。