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不同物种的心脏心室肌中各种钾电流的抑制作用及其对复极化的影响存在差异。

Species-dependent differences in the inhibition of various potassium currents and in their effects on repolarization in cardiac ventricular muscle.

机构信息

Department of Pharmacology and Pharmacotherapy, Albert Szent-Györgyi Medical School, University of Szeged, H-6721 Szeged, Hungary.

Department of Cardiac Surgery, Second Department of Internal Medicine and Cardiology Center, Albert Szent-Györgyi Health Center, University of Szeged, H-6725 Szeged, Hungary.

出版信息

Can J Physiol Pharmacol. 2022 Sep 1;100(9):880-889. doi: 10.1139/cjpp-2022-0028. Epub 2022 Apr 20.

DOI:10.1139/cjpp-2022-0028
PMID:35442802
Abstract

Even though rodents are accessible model animals, their electrophysiological properties are deeply different from those of humans, making the translation of rat studies to humans rather difficult. We compared the mechanisms of ventricular repolarization in various animal models to those of humans by measuring cardiac ventricular action potentials from ventricular papillary muscle preparations using conventional microelectrodes and applying selective inhibitors of various potassium transmembrane ion currents. Inhibition of the current (10 µmol/L barium chloride) significantly prolonged rat ventricular repolarization, but only slightly prolonged it in dogs, and did not affect it in humans. On the contrary, inhibition (50 nmol/L dofetilide) significantly prolonged repolarization in humans, rabbits, and dogs, but not in rats. Inhibition of the current (1 µmol/L XEN-D0101) only prolonged rat ventricular repolarization and had no effect in humans or dogs. Inhibition of the (500 nmol/L HMR-1556) and currents (100 µmol/L chromanol-293B) elicited similar effects in all investigated species. We conclude that dog ventricular preparations have the strongest translational value and rat ventricular preparations have the weakest translational value in cardiac electrophysiological experiments.

摘要

尽管啮齿类动物是可获得的模型动物,但它们的电生理特性与人类有很大的不同,使得将大鼠研究转化为人类研究相当困难。我们通过使用常规微电极从心室乳头肌标本测量心脏心室动作电位,并应用各种钾跨膜离子电流的选择性抑制剂,比较了各种动物模型的心室复极机制与人类的心室复极机制。抑制 电流(10µmol/L 氯化钡)显著延长大鼠心室复极,但在犬中仅轻度延长,在人中无影响。相反,抑制 电流(50nmol/L 多非利特)显著延长人中、兔中和犬中的复极,但在大鼠中无影响。抑制 电流(1µmol/L XEN-D0101)仅延长大鼠心室复极,在人和犬中无影响。抑制 电流(500nmol/L HMR-1556)和 电流(100µmol/L chromanol-293B)在所有研究的物种中产生相似的效果。我们得出结论,在心脏电生理实验中,犬心室标本具有最强的转化价值,而大鼠心室标本具有最弱的转化价值。

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