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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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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. |
format | Online Article Text |
id | pubmed-5763326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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