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β-肾上腺素能刺激对新型III类抗心律失常药多非利特、氨巴利特和色满醇293B频率依赖性电生理作用的差异效应。

Differential effect of beta-adrenergic stimulation on the frequency-dependent electrophysiologic actions of the new class III antiarrhythmics dofetilide, ambasilide, and chromanol 293B.

作者信息

Schreieck J, Wang Y, Gjini V, Korth M, Zrenner B, Schömig A, Schmitt C

机构信息

I. Medizinische Klinik, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

出版信息

J Cardiovasc Electrophysiol. 1997 Dec;8(12):1420-30. doi: 10.1111/j.1540-8167.1997.tb01039.x.

Abstract

INTRODUCTION

Blockade of the rapid delayed rectifier potassium current (IKr) as an important mechanism for current Class III antiarrhythmics is less effective in action potential prolongation during beta-adrenergic activation. We hypothesized that blockade of the increased slow IK (IKs) current during beta-adrenergic stimulation could improve action potential prolongation and tested this hypothesis by comparison of three different IK blockers: dofetilide, a selective blocker of IKr; ambasilide, a nonselective blocker of IK; and chromanol 293B, a selective blocker of IKs.

METHODS AND RESULTS

Transmembrane action potential duration was determined in guinea pig papillary muscles. After equilibration with the potassium channel blockers (dofetilide 10 nM, ambasilide 10 microM, chromanol 293B 10 microM), isoproterenol (10 and 100 nM) was added. The action potential prolonging effect of dofetilide was reduced in the presence of increasing concentrations of isoproterenol whereas the effect of ambasilide was much less reduced. In contrast, the effect of chromanol 293B clearly was increased in the presence of both concentrations of isoproterenol. No afterdepolarizations were observed after application of isoproterenol in control. Following isoproterenol, but not before, dofetilide and chromanol 293B induced early afterdepolarizations in 20% and 17% of the papillary muscles, whereas ambasilide and chromanol 293B induced delayed afterdepolarizations in 27% and 33%, respectively.

CONCLUSION

In contrast to dofetilide, the Class III effect of ambasilide is less reduced and the effect of chromanol 293B is enhanced during beta-adrenergic stimulation. Our data support the hypothesis that IKs blockade improves the efficacy of antiarrhythmics in action potential prolongation during beta-adrenergic activation; however, this effect may increase the risk of afterdepolarizations.

摘要

引言

快速延迟整流钾电流(IKr)的阻断作为Ⅲ类抗心律失常药物的重要作用机制,在β肾上腺素能激活期间对动作电位延长的作用效果较差。我们推测,在β肾上腺素能刺激期间阻断增加的慢IK(IKs)电流可改善动作电位延长,并通过比较三种不同的IK阻断剂来验证这一假设:多非利特,一种选择性IKr阻断剂;氨巴利特,一种非选择性IK阻断剂;以及色满醇293B,一种选择性IKs阻断剂。

方法与结果

在豚鼠乳头肌中测定跨膜动作电位持续时间。在用钾通道阻断剂(多非利特10 nM、氨巴利特10 μM、色满醇293B 10 μM)平衡后,加入异丙肾上腺素(10和100 nM)。随着异丙肾上腺素浓度增加,多非利特的动作电位延长作用减弱,而氨巴利特的作用减弱程度小得多。相反,在两种浓度的异丙肾上腺素存在下,色满醇293B的作用明显增强。在对照中应用异丙肾上腺素后未观察到后去极化。在应用异丙肾上腺素后,但不是之前,多非利特和色满醇293B分别在20%和17%的乳头肌中诱导早期后去极化,而氨巴利特和色满醇293B分别在27%和33%的乳头肌中诱导延迟后去极化。

结论

与多非利特不同,在β肾上腺素能刺激期间,氨巴利特的Ⅲ类作用减弱程度较小,而色满醇293B的作用增强。我们的数据支持以下假设:在β肾上腺素能激活期间,IKs阻断可提高抗心律失常药物在动作电位延长方面的疗效;然而,这种作用可能会增加后去极化的风险。

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