Open AccessIon currents, action potentials, and noradrenergic responses in rat pulmonary vein and left atrial cardiomyocytes
Author(s) -
Bond Richard C.,
Choisy Stéphanie C.,
Bryant Simon M.,
Hancox Jules C.,
James Andrew F.
Publication year - 2020
Publication title -
physiological reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 39
ISSN - 2051-817X
DOI - 10.14814/phy2.14432
Subject(s) - afterdepolarization , electrophysiology , pulmonary vein , medicine , inward rectifier potassium ion channel , membrane potential , patch clamp , myocyte , atrium (architecture) , cardiology , endocrinology , ion channel , chemistry , biology , atrial fibrillation , repolarization , biophysics , receptor
Abstract The electrophysiological properties of pulmonary vein (PV)‐cardiomyocytes, and their responses to the sympathetic neurotransmitter, noradrenaline (NA), are thought to differ from those of the left atrium (LA) and contribute to atrial ectopy. The aim of this study was to examine rat PV cardiomyocyte electrophysiology and responses to NA in comparison with LA cells. LA and PV cardiomyocytes were isolated from adult male Wistar rat hearts, and membrane potentials and ion currents recorded at 36°C using whole‐cell patch‐clamp techniques. PV and LA cardiomyocytes did not differ in size. In control, there were no differences between the two cell‐types in zero‐current potential or action potential duration (APD) at 1 Hz, although the incidence of early afterdepolarizations (EADs) was greater in PV than LA cardiomyocytes. The L‐type Ca 2+ current ( I CaL ) was ~×1.5 smaller ( p = .0029, Student's t test) and the steady‐state K + current ( I Kss ) was ~×1.4 larger ( p = .0028, Student's t test) in PV than in LA cardiomyocytes. PV cardiomyocyte inward‐rectifier current ( I K1 ) was slightly smaller than LA cardiomyocyte I K1 . In LA cardiomyocytes, NA significantly prolonged APD 30 . In PV cells, APD 30 responses to 1 μM NA were heterogeneous: while the mean percentage change in APD 30 was not different from 0 (16.5 ± 9.7%, n cells/N animals = 12/10, p = .1177, one‐sample t test), three cells showed shortening (‐18.8 ± 6.0%) whereas nine showed prolongation (28.3 ± 10.1%, p = .008, Student's t test). NA had no effect on I K1 in either cell‐type but inhibited PV I Kss by 41.9 ± 4.1% ( n/N = 23/11 p < .0001), similar to LA cells. NA increased I CaL in most PV cardiomyocytes (median × 2.2‐increase, p < .0001, n/N = 32/14, Wilcoxon‐signed‐rank test), although in 7/32 PV cells I CaL was decreased following NA. PV cardiomyocytes differ from LA cells and respond heterogeneously to NA.