Sonoda Kazumasa, Watanabe Ichiro, Ohkubo Kimie, Okumura Yasuo, Kofune Masayoshi, Sasaki Naoko, Kogawa Rikitake, Mano Hiroaki, Nakai Toshiko, Hirayama Atsushi
Division of Cardiology, Department of Medicine, Nihon University School of Medicine.
Int Heart J. 2013;54(5):279-84. doi: 10.1536/ihj.54.279.
Persistent atrial fibrillation (AF) is characterized by electrical remodeling, ie, marked decreases in the atrial effective refractory period (ERP), ERP rate adaptation, and atrial conduction velocity. Little information is available on the effects of class III antiarrhythmic drugs on the remodeled atrium. We studied the effects of the class III antiarrhythmic drugs nifekalant, ibutilide, and amiodarone on rate-dependent changes in atrial action potential duration in patients with persistent AF. Right atrial (RA) monophasic action potential duration (MAPD) and intra-atrial conduction time (IACT) were measured at pacing cycle lengths (CLs) of 800, 700, 600, 500, 400, 350, 300, and 250 ms before and after administration of nifekalant (0.4 mg/kg + 0.3 mg/kg/hr, iv), amiodarone (5 mg/kg, iv), or ibutilide (0.01 mg/kg, iv) in 31 patients after successful internal cardioversion of chronic AF of > 2 months duration. Nifekalant and ibutilide significantly increased RA MAPD and the ERP at each CL in a reverse rate-dependent manner. Amiodarone did not affect RA MAPD. Nifekalant did not affect IACT, whereas amiodarone increased IACT at each CL in a rate-dependent manner, and ibutilide increased IACT at CLs ≤ 350 ms. The atrial electrophysiologic effects of the class III antiarrhythmic drugs nifekalant, amiodarone, and ibutilide differ, depending on the degree of electrical and structural remodeling and the effects of the drugs on the depolarizing and repolarizing currents.
持续性心房颤动(AF)的特征是电重构,即心房有效不应期(ERP)、ERP频率适应性和心房传导速度显著降低。关于Ⅲ类抗心律失常药物对重构心房的影响,目前所知甚少。我们研究了Ⅲ类抗心律失常药物尼非卡兰、伊布利特和胺碘酮对持续性AF患者心房动作电位持续时间的频率依赖性变化的影响。在31例慢性AF持续时间超过2个月且成功进行体内心脏复律的患者中,在给予尼非卡兰(0.4mg/kg + 0.3mg/kg/小时,静脉注射)、胺碘酮(5mg/kg,静脉注射)或伊布利特(0.01mg/kg,静脉注射)前后,分别在800、700、600、500、400、350、300和250ms的起搏周期长度(CLs)下测量右心房(RA)单相动作电位持续时间(MAPD)和心房内传导时间(IACT)。尼非卡兰和伊布利特以反向频率依赖性方式显著增加每个CL下的RA MAPD和ERP。胺碘酮不影响RA MAPD。尼非卡兰不影响IACT,而胺碘酮以频率依赖性方式增加每个CL下的IACT,伊布利特在CLs≤350ms时增加IACT。Ⅲ类抗心律失常药物尼非卡兰、胺碘酮和伊布利特的心房电生理效应不同,这取决于电重构和结构重构的程度以及药物对去极化电流和复极化电流的影响。