Masonic Medical Research Laboratory, Utica, New York 13501, USA.
Heart Rhythm. 2010 Sep;7(9):1273-9. doi: 10.1016/j.hrthm.2010.05.019. Epub 2010 May 15.
Dronedarone is approved by the U.S. Food and Drug Administration for the treatment of patients with atrial fibrillation (AF) as a safe alternative to amiodarone. There are no full-length published reports describing the effectiveness of acute dronedarone use against AF in experimental or clinical studies.
The purpose of this study was to determine the effect of acute dronedarone and amiodarone on electrophysiological parameters, and their anti-AF efficacy in canine isolated arterially perfused right atria.
Transmembrane action potentials and pseudoelectrocardiograms were recorded. Acetylcholine (ACh, 1.0 muM) was used to induce persistent AF.
Amiodarone-induced changes were much more pronounced than those of dronedarone on (1) action potential duration (DeltaAPD(90), +51 +/- 17 ms vs. 4 +/- 6 ms, P >.01), (2) effective refractory period (DeltaERP, +84 +/- 23 ms vs. 18 +/- 9 ms, P <.001), (3) diastolic threshold of excitation (DeltaDTE, +0.32 +/- 0.11 mA vs. 0.03 +/- 0.02 mA, P <.001), and (4) V(max) (DeltaV(max), -43 +/- 14% vs. -11 +/- 4%, P <.01, n = 5 to 6; all recorded at 10 muM, cycle length = 500 ms). Persistent AF was induced in 10 of 10 atria exposed to ACh alone; subsequent addition of dronedarone or amiodarone terminated AF in 1 of 7 and 4 of 5 atria, respectively. Persistent ACh-mediated AF was induced in 5 of 6 and 0 of 5 atria pretreated with dronedarone and amiodarone, respectively.
The electrophysiological effects and anti-AF efficacy of acute dronedarone are much weaker than those of amiodarone in a canine model of AF. The efficacy of acute dronedarone to prevent induction of acetylcholine-mediated AF as well as to terminate persistent AF in canine right atria is relatively poor. Our data suggest that acute dronedarone is a poor substitute for amiodarone for acute cardioversion of AF or prevention of AF recurrence.
在美国食品和药物管理局批准的胺碘酮治疗心房颤动(AF)患者,作为一种安全的替代。没有完整的发表的报告描述了急性使用多非利特对 AF 在实验或临床研究中的有效性。
本研究的目的是确定急性多非利特和胺碘酮对电生理参数的影响,以及它们在犬离体动脉灌注右心房对抗 AF 的疗效。
记录跨膜动作电位和伪心电图。乙酰胆碱(ACh,1.0 μM)用于诱导持续 AF。
胺碘酮引起的变化比多非利特更明显(1)动作电位时程(DeltaAPD(90),+51 +/- 17 ms 对 4 +/- 6 ms,P >.01),(2)有效不应期(DeltaERP,+84 +/- 23 ms 对 18 +/- 9 ms,P <.001),(3)舒张期兴奋阈(DeltaDTE,+0.32 +/- 0.11 mA 对 0.03 +/- 0.02 mA,P <.001),和(4)V(max)(DeltaV(max),-43 +/- 14%对-11 +/- 4%,P <.01,n = 5 至 6;均在 10 μM 时记录,周长 = 500 ms)。单独用 ACh 暴露的 10 个心房中有 10 个诱导出持续 AF;随后加入多非利特或胺碘酮分别终止了 7 个和 5 个心房中的 AF。用多非利特和胺碘酮预处理的 6 个心房中有 5 个和 5 个心房中有 0 个诱导出持续的 ACh 介导的 AF。
在犬 AF 模型中,急性多非利特的电生理效应和抗 AF 疗效明显弱于胺碘酮。多非利特预防乙酰胆碱介导的 AF 诱导和终止犬右心房持续性 AF 的疗效相对较差。我们的数据表明,急性多非利特是胺碘酮治疗 AF 急性转复或预防 AF 复发的不良替代品。