Literature DB >> 28257761

Membrane potential determines calcium alternans through modulation of SR Ca2+ load and L-type Ca2+ current.

Giedrius Kanaporis1, Lothar A Blatter2.   

Abstract

Alternans is a risk factor for cardiac arrhythmia, including atrial fibrillation. At the cellular level alternans is observed as beat-to-beat alternations in contraction, action potential (AP) morphology and magnitude of the Ca2+ transient (CaT). It is widely accepted that the bi-directional interplay between membrane voltage and Ca2+ is crucial for the development of alternans, however recently the attention has shifted to instabilities in cellular Ca2+ handling, while the role of AP alternation remains poorly understood. This study provides new insights how beat- to-beat alternation in AP morphology affects occurrence of CaT alternans in atrial myocytes. Pacing-induced AP and CaT alternans were studied in rabbit atrial myocytes using combined Ca2+ imaging and electrophysiological measurements. To determine the role of AP morphology for the generation of CaT alternans, trains of two voltage commands in form of APs recorded during large and small alternans CaTs were applied to voltage-clamped cells. APs of longer duration (as observed during small amplitude alternans CaT) and especially beat-to-beat alternations in AP morphology (AP alternans) reduced the pacing frequency threshold and increased the degree of CaT alternans. AP morphology contributes to the development of CaT alternans by two mechanisms. First, the AP waveform observed during small alternans CaTs coincided with higher end-diastolic sarcoplasmic reticulum Ca2+ levels ([Ca2+]SR), and AP alternans resulted in beat-to-beat alternations in end-diastolic [Ca2+]SR. Second, L-type Ca2+ current was significantly affected by AP morphology, where the AP waveform observed during large CaT elicited L-type Ca2+ currents of higher magnitude and faster kinetics, resulting in more efficient triggering of SR Ca2+ release. In conclusion, alternation in AP morphology plays a significant role in the development and stabilization of atrial alternans. The demonstration that CaT alternans can be controlled or even prevented by modulating AP morphology has important ramifications for arrhythmia prevention and therapy strategies.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Action potential; Alternans; Arrhythmia; Ca(2+) signaling; Excitation-contraction coupling

Mesh:

Substances:

Year:  2017        PMID: 28257761      PMCID: PMC5410220          DOI: 10.1016/j.yjmcc.2017.02.004

Source DB:  PubMed          Journal:  J Mol Cell Cardiol        ISSN: 0022-2828            Impact factor:   5.000


  42 in total

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Journal:  J Mol Cell Cardiol       Date:  2011-09-29       Impact factor: 5.000

5.  A graphic method for the study of alternation in cardiac action potentials.

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7.  Refractoriness of sarcoplasmic reticulum Ca2+ release determines Ca2+ alternans in atrial myocytes.

Authors:  Vyacheslav M Shkryl; Joshua T Maxwell; Timothy L Domeier; Lothar A Blatter
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8.  Differential expression of small-conductance Ca2+-activated K+ channels SK1, SK2, and SK3 in mouse atrial and ventricular myocytes.

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Journal:  Am J Physiol Heart Circ Physiol       Date:  2005-07-29       Impact factor: 4.733

9.  Profile and kinetics of L-type calcium current during the cardiac ventricular action potential compared in guinea-pigs, rats and rabbits.

Authors:  K W Linz; R Meyer
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2.  Action potential shortening rescues atrial calcium alternans.

Authors:  Giedrius Kanaporis; Zane M Kalik; Lothar A Blatter
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Review 3.  Diabetic Cardiomyopathy: An Update of Mechanisms Contributing to This Clinical Entity.

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5.  AP and Ca2+ alternans: An inseparable couple.

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6.  Mechanistic investigation of Ca2+ alternans in human heart failure and its modulation by fibroblasts.

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7.  Increased Vulnerability to Atrial Fibrillation Is Associated With Increased Susceptibility to Alternans in Old Sheep.

Authors:  Charles M Pearman; George W P Madders; Emma J Radcliffe; Graeme J Kirkwood; Michael Lawless; Amy Watkins; Charlotte E R Smith; Andrew W Trafford; David A Eisner; Katharine M Dibb
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Review 8.  Impact of peroxisome proliferator-activated receptor-α on diabetic cardiomyopathy.

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Review 9.  Excitation-contraction coupling and calcium release in atrial muscle.

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Review 10.  The Mystery of Diabetic Cardiomyopathy: From Early Concepts and Underlying Mechanisms to Novel Therapeutic Possibilities.

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