Department of Pharmacology and Therapeutics, Faculty of Pharmaceutical Sciences, Toho University.
Biol Pharm Bull. 2013;36(10):1650-2. doi: 10.1248/bpb.b13-00347.
We assessed the effects of oseltamivir on the conduction velocity and effective refractory period in the guinea-pig atrium in comparison with those of a class Ic antiarrhythmic drug pilsicainide. The recording and stimulating electrodes were attached on the epicardium close to the sinus nodal region and on the left atrial appendage. Oseltamivir (10-100 µM) as well as pilsicainide (1-10 µM) decreased the atrial conduction velocity in a frequency-dependent manner. Both drugs also increased the effective refractory period in both atria; but the frequency-dependent property of oseltamivir was lacking in the left atrium, and it was less obvious in the right atrium compared with that of pilsicainide. These results suggest that oseltamivir can directly modify the electrophysiological functions in the guinea-pig atrium possibly via combination of Na(+) and K(+) channel-blocking actions.
我们评估了奥司他韦对豚鼠心房传导速度和有效不应期的影响,并将其与 Ic 类抗心律失常药物吡西卡尼进行了比较。记录和刺激电极分别贴在靠近窦房结区域的心外膜和左心耳上。奥司他韦(10-100μM)和吡西卡尼(1-10μM)均以频率依赖性方式降低心房传导速度。两种药物均使左右心房的有效不应期延长;但奥司他韦在左心房缺乏频率依赖性,与吡西卡尼相比,在右心房的作用也不那么明显。这些结果表明,奥司他韦可能通过钠(+)和钾(+)通道阻断作用的结合,直接改变豚鼠心房的电生理功能。