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Electrophysiological effects of dronedarone (SR 33589) a noniodinated amiodarone derivative in the canine heart: comparison with amiodarone

机译:犬心脏中非碘化胺碘酮衍生物决奈达隆(SR 33589)的电生理作用:与胺碘酮的比较

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class="enumerated" style="list-style-type:decimal">The electrophysiological effects of dronedarone, a new nonionidated analogue of amiodarone were studied after chronic and acute administration in dog Purkinje fibres, papillary muscle and isolated ventricular myocytes, and compared with those of amiodarone by applying conventional microelectrode and patch-clamp techniques.Chronic treatment with dronedarone (2×25 mg−1 kg−1 day p.o. for 4 weeks), unlike chronic administration of amiodarone (50 mg−1 kg−1 day p.o. for 4 weeks), did not lengthen significantly the QTc interval of the electrocardiogram or the action potential duration (APD) in papillary muscle. After chronic oral treatment with dronedarone a small, but significant use-dependent Vmax block was noticed, while after chronic amiodarone administration a strong use-dependent Vmax depression was observed.Acute superfusion of dronedarone (10 μM), similar to that of amiodarone (10 μM), moderately lengthened APD in papillary muscle (at 1 Hz from 239.6±5.3 to 248.6±5.3 ms, n=13, P<0.05), but shortened it in Purkinje fibres (at 1 Hz from 309.6±11.8 to 287.1±10.8 ms, n=7, P<0.05).Both dronedarone (10 μM) and amiodarone (10 μM) superfusion reduced the incidence of early and delayed afterdepolarizations evoked by 1 μM dofetilide and 0.2 μM strophantidine in Purkinje fibres.In patch-clamp experiments 10 μM dronedarone markedly reduced the L-type calcium current (76.5±0.7 %, n=6, P<0.05) and the rapid component of the delayed rectifier potassium current (97±1.2 %, n=5, P<0.05) in ventricular myocytes.It is concluded that after acute administration dronedarone exhibits effects on cardiac electrical activity similar to those of amiodarone, but it lacks the ‘amiodarone like' chronic electrophysiological characteristics.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在犬浦肯野纤维,乳头肌和孤立的心室肌细胞中长期和急性给药后,研究了一种新的非去离子的胺碘酮类似物决奈达隆的电生理作用,并通过常规微电极和膜片钳技术将其与胺碘酮进行了比较。 用决奈达隆(2×25 mg −1 kg −1 天口服4周)进行慢性治疗,与胺碘酮的长期给药(50 mg −1 kg −1 日口服4周),未显着延长心电图的QTc间隔或乳头肌的动作电位持续时间(APD)。长期使用决奈达隆口服治疗后,发现一个小的但明显的依赖于使用的Vmax阻滞,而在长期胺碘酮给药后,观察到强烈的依赖于使用的Vmax抑制。 决奈达隆的急性灌注(10μm),与胺碘酮(10μm)相似,乳头肌中的APD适度延长(在1 Hz时从239.6±5.3到248.6±5.3 ms,n = 13,P <0.05),但在Purkinje纤维中缩短了(在1 fromHz时从9 309.6±11.8至287.1±10.8 ms,n = 7,P <0.05)。 决奈达隆(10μM)和胺碘酮(10μM)灌注减少了1μM引起的早期和延迟后去极化的发生。普林肯纤维中的多非利特和0.2μM的鸟嘌呤。 在膜片钳实验中,10μM决奈达隆显着降低L型钙电流(76.5±0.7%,n = 6,P <0.05)和快速成分心室肌细胞中延迟整流钾电流(97±1.2%,n = 5,P <0.05)的变化。 结论:急性给药后dronedaro ne对心脏电活动的影响类似于胺碘酮,但缺乏“胺碘酮样”的慢性电生理特征。

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