Shih J Y, Gillette P C, Kugler J D, Garson A, Fukushige J, Zinner A, Driscoll D J
Pediatr Pharmacol (New York). 1982;2(1):65-73.
The electrophysiologic effects of procainamide in young animals have not been established. To test the effects of this drug on the immature heart, we studied eight nonsedated, chronically instrumented puppies (age range 12-28 days, median 16 days; weight range 0.7-1.1 kg, median 0.8 kg). The electrophysiologic study was performed before and 30 minutes after procainamide was given intravenously (20 mg/kg infusion). At the time of the study, the serum concentrations of procainamide (8.2 +/- 1.7 micrograms/ml to 6.2 +/- 1.6 micrograms/ml; mean +/- SEM) were in the usual adult human therapeutic range (4-10 microgram/ml). Procainamide in puppies caused a significant lengthening of the atrial and ventricular refractory periods, a significant decrease of the sinus node recovery time and the sinus of atrial echo zone, a significant decrease in the heart rate, and a significant increase in the sinoatrial conduction time.
普鲁卡因胺对幼龄动物的电生理效应尚未明确。为了测试该药物对未成熟心脏的影响,我们研究了8只未使用镇静剂、长期植入仪器的幼犬(年龄范围12 - 28天,中位数16天;体重范围0.7 - 1.1千克,中位数0.8千克)。在静脉注射普鲁卡因胺(20毫克/千克输注)前及给药后30分钟进行电生理研究。在研究时,普鲁卡因胺的血清浓度(8.2±1.7微克/毫升至6.2±1.6微克/毫升;均值±标准误)处于成人通常的治疗范围内(4 - 10微克/毫升)。幼犬使用普鲁卡因胺后导致心房和心室不应期显著延长,窦房结恢复时间和心房回波区显著缩短,心率显著降低,以及窦房传导时间显著延长。