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Ion channels, long QT syndrome and arrhythmogenesis in ageing

Ageing is associated with increased prevalences of both atrial and ventricular arrhythmias, reflecting disruption of the normal sequence of ion channel activation and inactivation generating the propagated cardiac action potential. Experimental models with specific ion channel genetic modifications...

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Autores principales: Jeevaratnam, Kamalan, Chadda, Karan R, Salvage, Samantha C, Valli, Haseeb, Ahmad, Shiraz, Grace, Andrew A, Huang, Christopher L‐H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763326/
https://www.ncbi.nlm.nih.gov/pubmed/28024120
http://dx.doi.org/10.1111/1440-1681.12721
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author Jeevaratnam, Kamalan
Chadda, Karan R
Salvage, Samantha C
Valli, Haseeb
Ahmad, Shiraz
Grace, Andrew A
Huang, Christopher L‐H
author_facet Jeevaratnam, Kamalan
Chadda, Karan R
Salvage, Samantha C
Valli, Haseeb
Ahmad, Shiraz
Grace, Andrew A
Huang, Christopher L‐H
author_sort Jeevaratnam, Kamalan
collection PubMed
description Ageing is associated with increased prevalences of both atrial and ventricular arrhythmias, reflecting disruption of the normal sequence of ion channel activation and inactivation generating the propagated cardiac action potential. Experimental models with specific ion channel genetic modifications have helped clarify the interacting functional roles of ion channels and how their dysregulation contributes to arrhythmogenic processes at the cellular and systems level. They have also investigated interactions between these ion channel abnormalities and age‐related processes in producing arrhythmic tendency. Previous reviews have explored the relationships between age and loss‐of‐function Na(v)1.5 mutations in producing arrhythmogenicity. The present review now explores complementary relationships arising from gain‐of‐function Na(v)1.5 mutations associated with long QT3 (LQTS3). LQTS3 patients show increased risks of life‐threatening ventricular arrhythmias, particularly after 40 years of age, consistent with such interactions between the ion channel abnormailities and ageing. In turn clinical evidence suggests that ageing is accompanied by structural, particularly fibrotic, as well as electrophysiological change. These abnormalities may result from biochemical changes producing low‐grade inflammation resulting from increased production of reactive oxygen species and superoxide. Experimental studies offer further insights into the underlying mechanisms underlying these phenotypes. Thus, studies in genetically modified murine models for LQTS implicated action potential recovery processes in arrhythmogenesis resulting from functional ion channel abnormalities. In addition, ageing wild type (WT) murine models demonstrated both ion channel alterations and fibrotic changes with ageing. Murine models then suggested evidence for interactions between ageing and ion channel mutations and provided insights into potential arrhythmic mechanisms inviting future exploration.
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spelling pubmed-57633262018-01-17 Ion channels, long QT syndrome and arrhythmogenesis in ageing Jeevaratnam, Kamalan Chadda, Karan R Salvage, Samantha C Valli, Haseeb Ahmad, Shiraz Grace, Andrew A Huang, Christopher L‐H Clin Exp Pharmacol Physiol Special Articles Ageing is associated with increased prevalences of both atrial and ventricular arrhythmias, reflecting disruption of the normal sequence of ion channel activation and inactivation generating the propagated cardiac action potential. Experimental models with specific ion channel genetic modifications have helped clarify the interacting functional roles of ion channels and how their dysregulation contributes to arrhythmogenic processes at the cellular and systems level. They have also investigated interactions between these ion channel abnormalities and age‐related processes in producing arrhythmic tendency. Previous reviews have explored the relationships between age and loss‐of‐function Na(v)1.5 mutations in producing arrhythmogenicity. The present review now explores complementary relationships arising from gain‐of‐function Na(v)1.5 mutations associated with long QT3 (LQTS3). LQTS3 patients show increased risks of life‐threatening ventricular arrhythmias, particularly after 40 years of age, consistent with such interactions between the ion channel abnormailities and ageing. In turn clinical evidence suggests that ageing is accompanied by structural, particularly fibrotic, as well as electrophysiological change. These abnormalities may result from biochemical changes producing low‐grade inflammation resulting from increased production of reactive oxygen species and superoxide. Experimental studies offer further insights into the underlying mechanisms underlying these phenotypes. Thus, studies in genetically modified murine models for LQTS implicated action potential recovery processes in arrhythmogenesis resulting from functional ion channel abnormalities. In addition, ageing wild type (WT) murine models demonstrated both ion channel alterations and fibrotic changes with ageing. Murine models then suggested evidence for interactions between ageing and ion channel mutations and provided insights into potential arrhythmic mechanisms inviting future exploration. John Wiley and Sons Inc. 2017-09-20 2017-12 /pmc/articles/PMC5763326/ /pubmed/28024120 http://dx.doi.org/10.1111/1440-1681.12721 Text en © 2017 The Authors. Clinical and Experimental Pharmacology and Physiology Published by John Wiley & Sons Australia, Ltd.© 2017 The Authors. Clinical and Experimental Pharmacology and Physiology Published by John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Articles
Jeevaratnam, Kamalan
Chadda, Karan R
Salvage, Samantha C
Valli, Haseeb
Ahmad, Shiraz
Grace, Andrew A
Huang, Christopher L‐H
Ion channels, long QT syndrome and arrhythmogenesis in ageing
title Ion channels, long QT syndrome and arrhythmogenesis in ageing
title_full Ion channels, long QT syndrome and arrhythmogenesis in ageing
title_fullStr Ion channels, long QT syndrome and arrhythmogenesis in ageing
title_full_unstemmed Ion channels, long QT syndrome and arrhythmogenesis in ageing
title_short Ion channels, long QT syndrome and arrhythmogenesis in ageing
title_sort ion channels, long qt syndrome and arrhythmogenesis in ageing
topic Special Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763326/
https://www.ncbi.nlm.nih.gov/pubmed/28024120
http://dx.doi.org/10.1111/1440-1681.12721
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