Temporal changes in atrial EC-coupling during prolonged stimulation with endothelin-1

被引:26
作者
Bootman, Martin D.
Harzheim, Dagmar
Smyrnias, Loannis
Conway, Stuart J.
Roderick, H. Llewelyn
机构
[1] Babraham Inst, Mol Signalling Lab, Cambridge CB22 3AT, England
[2] Univ St Andrews, Sch Chem, Dept Chem, St Andrews KY16 9ST, Fife, Scotland
[3] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1PD, England
基金
英国生物技术与生命科学研究理事会;
关键词
calcium; contraction; atrial; myocyte; inositol; endothelin;
D O I
10.1016/j.ceca.2007.05.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Endothelin-1 (ET-1) is a potent G(q)-coupled agonist with important physiological effects on the heart. In the present study, we characterised the effect of prolonged ET-1 stimulation on Ca2+ signalling within acutely isolated atrial myocytes. ET-1 induced a reproducible and complex sequence of effects, including negative inotropy, positive inotropy and pro-arrhythmic spontaneous Ca2+ transients (SCTs). The negative and positive inotropic effects correlated with the ability of Ca2+ to propagate from the subsarcolemmal sites where EC-coupling initiates into the centre of the atrial cells. We examined the spatial and temporal properties of the SCTs and observed them to range from elementary Ca2+ sparks, flurries of Ca2+ sparks, to Ca2+ waves and action potential-evoked global Ca2+ transients. The positive inotropic effect of ET-1 and its ability to trigger SCTs were mimicked by direct stimulation of InsP(3)Rs. An antagonist of InsP(3)Rs prevented the generation of SCTs and partially reduced the positive inotropy evoked by ET-1. Our data suggest that ET-1 engages multiple signal transduction pathways to provoke a plethora of different responses within an atrial myocyte. Some of the actions of ET-1 appear to be due to stimulation of InsP(3)Rs. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:489 / 501
页数:13
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