The role of inositol 1,4,5,-trisphosphate receptors in Ca2+ signalling and the generation of arrhythmias in rat atrial myocytes

Lauren Mackenzie, Martin D. Bootman, Mika Laine, Michael J. Berridge, Jan Thuring, Andrew Holmes, Wen Hong Li, Peter Lipp

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179 Scopus citations

Abstract

Various cardio-active stimuli, including endothelin-1 (ET-1), exhibit potent arrhythmogenicity, but the underlying cellular mechanisms of their actions are largely unclear. We used isolated rat atrial myocytes and related changes in their subcellular Ca2+ signalling to the ability of various stimuli to induce diastolic, premature extra Ca2+ transients (ECTs). For this, we recorded global and spatially resolved Ca2+ signals in indo-1 - and fluo-4-loaded atrial myocytes during electrical pacing. ET-1 exhibited a higher arrhythmogenicity (arrhythmogenic index; ratio of number of ECTs over fold-increase in Ca2+ response, 8.60; n = 8 cells) when compared with concentrations of cardiac glycosides (arrhythmogenic index, 4.10; n = 8 cells) or the β-adrenergic agonist isoproterenol (arrhythmogenic index, 0. 11; n = 6 cells) that gave similar increases in the global Ca2+ responses. Seventy-five percent of the ET-1-induced arrhythmogenic Ca2+ transients were accompanied by premature action potentials, while for digoxin this proportion was 25 %. The β-adrenergic agonist failed to elicit a significant number of ECTs. Direct activation of inositol 1,4,5-trisphosphate (InsP3) receptors with a membrane-permeable InSP3 ester (InsP3 BM) mimicked the effect of ET-1 (arrhythmogenic index, 14.70; n = 6 cells). Inhibition of InsP3 receptors using 2 μM 2-amino-ethoxydiphenyl borate, which did not display any effects on Ca2+ signalling under control conditions, specifically suppressed the arrhythmogenic action of ET-1 and InsP3 BM. Immunocytochemistry indicated a co-localisation of peripheral, junctional ryanodine receptors with InsP3Rs. Thus, the pronounced arrhythmogenic potency of ET-1 is due to the spatially specific recruitment of Ca2+ sparks by subsarcolemmal InsP3Rs. Summation of such sparks efficiently generates delayed afterdepolarisations that trigger premature action potentials. We conclude that the particular spatial profile of cellular Ca2+ signals is a major, previously unrecognised, determinant for arrhythmogenic potency and that the InsP3 signalling cassette might therefore be a promising new target for understanding and managing atrial arrhythmia.

Original languageEnglish (US)
Pages (from-to)395-409
Number of pages15
JournalJournal of Physiology
Volume541
Issue number2
DOIs
Publication statusPublished - Jun 1 2002

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ASJC Scopus subject areas

  • Physiology

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