Tuna I C, Qi A C, Gornick C, Bolman R M, Benditt D G
Circulation. 1985 Dec;72(6):1380-5. doi: 10.1161/01.cir.72.6.1380.
We examined the temporal kinetics of onset and offset of the cardiac electrophysiologic effects of orally administered amiodarone in chronically instrumented, unsedated adult dogs (n = 8). Right atrial (RA), atrioventricular nodal (AVN), and right ventricular (RV) effective refractory period (ERP), and AVN functional refractory period (FRP), were determined daily for 21 days during amiodarone loading (24 mg/kg/day) and for 21 days after cessation of amiodarone. Left ventricular (LV) ERP was assessed in four of eight animals. Group mean RA-ERP peaked and plateaued early during amiodarone loading (time to reach one-half observed peak change [t1/2 onset] = 1.2 +/- 0.5 days) and rapidly returned toward baseline after cessation of drug (decay time to one-half peak value [t1/2 offset] = 2.0 +/- 1.7 days). Group mean RV-ERP rose in a linear manner throughout the loading period (t1/2 onset = 9.3 +/- 2.1 days) and remained elevated after cessation of drug (t1/2 offset greater than 21.0 days). Group mean AVN-ERP and FRP exhibited temporal kinetics intermediate between those of the RA-ERP and RV-ERP, both during amiodarone loading and after cessation of the drug. Group mean LV-ERP onset kinetics (assessed in a limited number of animals, n = 4) appeared to differ from RV-ERP onset kinetics (t1/2 onset = 2.5 +/- 2.5 days), whereas LV-ERP and RV-ERP offset kinetics appeared similar (t1/2 offset greater than 21 days). In summary, our findings demonstrate that during oral loading, the temporal sequence of onset of amiodarone-induced electrophysiologic effects is site dependent. Similarly, after cessation of amiodarone, the persistence of drug-induced electrophysiologic effects is both variable and site dependent.
我们研究了口服胺碘酮对长期植入仪器、未使用镇静剂的成年犬(n = 8)心脏电生理效应的起始和消退的时间动力学。在胺碘酮负荷期(24 mg/kg/天)的21天以及胺碘酮停药后的21天内,每天测定右心房(RA)、房室结(AVN)和右心室(RV)的有效不应期(ERP)以及AVN的功能不应期(FRP)。对八只动物中的四只评估左心室(LV)ERP。在胺碘酮负荷期,组平均RA-ERP在早期达到峰值并保持平稳(达到观察到的峰值变化一半的时间[t1/2起始] = 1.2 +/- 0.5天),停药后迅速恢复至基线水平(衰减至峰值一半的时间[t1/2消退] = 2.0 +/- 1.7天)。在整个负荷期,组平均RV-ERP呈线性上升(t1/2起始 = 9.3 +/- 2.1天),停药后仍保持升高(t1/2消退大于21.0天)。在胺碘酮负荷期及停药后,组平均AVN-ERP和FRP的时间动力学介于RA-ERP和RV-ERP之间。组平均LV-ERP的起始动力学(在有限数量的动物中评估,n = 4)似乎与RV-ERP的起始动力学不同(t1/2起始 = 2.5 +/- 2.5天),而LV-ERP和RV-ERP的消退动力学似乎相似(t1/2消退大于21天)。总之,我们的研究结果表明,在口服负荷期间,胺碘酮诱导的电生理效应起始的时间顺序取决于部位。同样,胺碘酮停药后,药物诱导的电生理效应的持续存在既可变又取决于部位。