Effect of ethanol at clinically relevant concentrations on atrial inward rectifier potassium current sensitive to acetylcholine

. 2016 Oct ; 389 (10) : 1049-58. [epub] 20160701

Jazyk angličtina Země Německo Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid27369777
Odkazy

PubMed 27369777
DOI 10.1007/s00210-016-1265-z
PII: 10.1007/s00210-016-1265-z
Knihovny.cz E-zdroje

Alcohol intoxication tends to induce arrhythmias, most often the atrial fibrillation. To elucidate arrhythmogenic mechanisms related to alcohol consumption, the effect of ethanol on main components of the ionic membrane current is investigated step by step. Considering limited knowledge, we aimed to examine the effect of clinically relevant concentrations of ethanol (0.8-80 mM) on acetylcholine-sensitive inward rectifier potassium current I K(Ach). Experiments were performed by the whole-cell patch clamp technique at 23 ± 1 °C on isolated rat and guinea-pig atrial myocytes, and on expressed human Kir3.1/3.4 channels. Ethanol induced changes of I K(Ach) in the whole range of concentrations applied; the effect was not voltage dependent. The constitutively active component of I K(Ach) was significantly increased by ethanol with the maximum effect (an increase by ∼100 %) between 8 and 20 mM. The changes were comparable in rat and guinea-pig atrial myocytes and also in expressed human Kir3.1/3.4 channels (i.e., structural correlate of I K(Ach)). In the case of the acetylcholine-induced component of I K(Ach), a dual ethanol effect was apparent with a striking heterogeneity of changes in individual cells. The effect correlated with the current magnitude in control: the current was increased by eth-anol in the cells showing small current in control and vice versa. The average effect peaked at 20 mM ethanol (an increase of the current by ∼20 %). Observed changes of action potential duration agreed well with the voltage clamp data. Ethanol significantly affected both components of I K(Ach) even in concentrations corresponding to light alcohol consumption.

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Alcohol Clin Exp Res. 2012 Dec;36(12):2036-46 PubMed

J Pharmacol Toxicol Methods. 2007 Sep-Oct;56(2):145-58 PubMed

J Physiol Pharmacol. 2014 Aug;65(4):497-509 PubMed

Eur Biophys J. 2012 Jun;41(6):491-503 PubMed

Nat Neurosci. 1999 Dec;2(12):1091-7 PubMed

Circ Res. 1997 Jun;80(6):772-81 PubMed

J Am Coll Cardiol. 2007 Mar 27;49(12):1340-8 PubMed

Proc Natl Acad Sci U S A. 2013 Nov 5;110(45):18309-14 PubMed

Cardiovasc Res. 2007 Jun 1;74(3):426-37 PubMed

J Cardiovasc Pharmacol. 2008 Aug;52(2):129-35 PubMed

Alcohol Clin Exp Res. 2009 Oct;33(10):1697-703 PubMed

Adv Pharmacol. 2014;70:393-409 PubMed

Europace. 2017 Mar 1;19(3):346-355 PubMed

J Am Coll Cardiol. 2011 Jan 25;57(4):427-36 PubMed

Circ Res. 2014 Apr 25;114(9):1483-99 PubMed

Nat Neurosci. 2009 Aug;12(8):988-95 PubMed

Eur J Pharmacol. 1995 Jan 13;292(2):143-9 PubMed

J Mol Cell Cardiol. 2013 Aug;61:142-52 PubMed

Cardiovasc Res. 2003 Aug 1;59(2):328-38 PubMed

Cardiovasc Res. 2002 Jan;53(1):59-67 PubMed

Circ Arrhythm Electrophysiol. 2010 Oct;3(5):472-80 PubMed

PLoS Comput Biol. 2012;8(10):e1002710 PubMed

Circulation. 2005 Dec 13;112(24):3697-706 PubMed

Cardiovasc Res. 2003 Oct 1;59(4):863-73 PubMed

Sheng Li Xue Bao. 2011 Jun 25;63(3):219-24 PubMed

Acta Physiol (Oxf). 2010 Dec;200(4):301-14 PubMed

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