Komeichi K, Tohse N, Nakaya H, Shimizu M, Zhu M Y, Kanno M
Department of Pharmacology, Hokkaido University School of Medicine, Sapporo, Japan.
Eur J Pharmacol. 1990 Oct 23;187(3):313-22. doi: 10.1016/0014-2999(90)90358-d.
The effects of N-acetylprocainamide (NAPA) and sotalol on membrane current systems of guinea-pig ventricular myocytes were examined and compared with those of quinidine using patch-clamp techniques. All of the drugs prolonged the action potential duration (i.e. Class III effect) in isolated guinea-pig papillary muscles. In isolated ventricular cells. NAPA (300 microM) and sotalol (100 microM) produced a decrease in the delayed outward potassium current (IK) concomitantly with a slight decrease in the calcium current (ICa), which was similar to quinidine (10 microM). NAPA also slightly depressed the inward rectifier potassium current (IKrect). Thus, NAPA and sotalol both inhibited IK, and this action appears to be mainly responsible for their Class III effect.
运用膜片钳技术研究了N - 乙酰普鲁卡因胺(NAPA)和索他洛尔对豚鼠心室肌细胞膜电流系统的影响,并与奎尼丁进行了比较。所有药物均可延长离体豚鼠乳头肌的动作电位时程(即Ⅲ类效应)。在离体心室细胞中,NAPA(300微摩尔)和索他洛尔(100微摩尔)可使延迟外向钾电流(IK)降低,同时钙电流(ICa)略有下降,这与奎尼丁(10微摩尔)相似。NAPA还可轻微抑制内向整流钾电流(IKrect)。因此,NAPA和索他洛尔均抑制IK,且这种作用似乎是其Ⅲ类效应的主要原因。