Journal
EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 721, Issue 1-3, Pages 237-248Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2013.09.029
Keywords
Ajmaline; Antiarrhythmic drug; Cardiac arrhythmia; Cellular excitability; K(2)p channel; Membrane potential; Mexiletine; Propafenone
Categories
Funding
- University of Heidelberg, Faculty of Medicine (Rahel Goitein-Straus Scholarship to CS)
- German Cardiac Society (Otto Hess Scholarship to FW)
- German Heart Foundation/German Foundation of Heart Research
- Joachim Siebeneicher Foundation
- DZHIK (Deutsches Zentrum fiir Herz-Kreislauf-Forschung - German Centre for Cardiovascular Research)
- BMBF
- MaxPlanck-Society
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Class IC antiarrhythmic drugs are commonly used for rhythm control in atrial fibrillation. In addition, class l drugs are administered to suppress ventricular tachyarrhythmia in selected cases. The multichannel blocking profile of class l compounds includes reduction of cardiac potassium currents in addition to their primary mechanism of action, sodium channel inhibition. Blockade of two-pore-domain potassium (K25) channels in the heart causes action potential prolongation and may provide antiarrhythmic action in atrial fibrillation. This study was designed to elucidate inhibitory effects of class I antiarrhythmic drugs on K21, channels. Human K(2p)2.1 (TREK1) and liK21,3.1 (TASK1) channels were systematically tested for their sensitivity to clinically relevant class IA (ajmaline), class IB (mexiletine), and class IC (propafenone) antiarrhythmic compounds using whole cell patch clamp and two electrode voltage clamp electrophysiology in Chinese hamster ovary cells and in Xenopus oocytes. Mexiletine and propafenone inhibited hK252.1 C50. mexile[ine = 173 jiM; ICsojiropaie.one = 7.6 jiM) and liK253.1 channels (1C50(Mrttexileuln) e = 97.3 PM; 1C50,(propafenone) = 5.1 nM) in mammalian cells. Ajrnaline did not significantly reduce current amplitudes. K25 channels were blocked in open and closed states, resulting in resting membrane potential depolarization. Open rectification properties of the channels were not affected by class l drugs. In summary, class l antiarrhythmic drugs target cardiac K25 K channels. Blockade of hK(2p2.1) and hK(2p)3.1 potassium currents provides mechanistic evidence to establish cardiac K25 channels as antiarrhythrnic drug targets. (C) 2013 Elsevier BM. All rights reserved
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