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Molecular candidates for cardiac stretch-activated ion channels
The heart is a mechanically-active organ that dynamically senses its own mechanical environment. This environment is constantly changing, on a beat-by-beat basis, with additional modulation by respiratory activity and changes in posture or physical activity, and further overlaid with more slowly occ...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bloomsbury Qatar Foundation Journals
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220428/ https://www.ncbi.nlm.nih.gov/pubmed/25405172 http://dx.doi.org/10.5339/gcsp.2014.19 |
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author | Reed, Alistair Kohl, Peter Peyronnet, Rémi |
author_facet | Reed, Alistair Kohl, Peter Peyronnet, Rémi |
author_sort | Reed, Alistair |
collection | PubMed |
description | The heart is a mechanically-active organ that dynamically senses its own mechanical environment. This environment is constantly changing, on a beat-by-beat basis, with additional modulation by respiratory activity and changes in posture or physical activity, and further overlaid with more slowly occurring physiological (e.g. pregnancy, endurance training) or pathological challenges (e.g. pressure or volume overload). Far from being a simple pump, the heart detects changes in mechanical demand and adjusts its performance accordingly, both via heart rate and stroke volume alteration. Many of the underlying regulatory processes are encoded intracardially, and are thus maintained even in heart transplant recipients. Over the last three decades, molecular substrates of cardiac mechanosensitivity have gained increasing recognition in the scientific and clinical communities. Nonetheless, the processes underlying this phenomenon are still poorly understood. Stretch-activated ion channels (SAC) have been identified as one contributor to mechanosensitive autoregulation of the heartbeat. They also appear to play important roles in the development of cardiac pathologies – most notably stretch-induced arrhythmias. As recently discovered, some established cardiac drugs act, in part at least, via mechanotransduction pathways suggesting SAC as potential therapeutic targets. Clearly, identification of the molecular substrate of cardiac SAC is of clinical importance and a number of candidate proteins have been identified. At the same time, experimental studies have revealed variable–and at times contrasting–results regarding their function. Further complication arises from the fact that many ion channels that are not classically defined as SAC, including voltage and ligand-gated ion channels, can respond to mechanical stimulation. Here, we summarise what is known about the molecular substrate of the main candidates for cardiac SAC, before identifying potential further developments in this area of translational research. |
format | Online Article Text |
id | pubmed-4220428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Bloomsbury Qatar Foundation Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-42204282014-11-17 Molecular candidates for cardiac stretch-activated ion channels Reed, Alistair Kohl, Peter Peyronnet, Rémi Glob Cardiol Sci Pract Review Article The heart is a mechanically-active organ that dynamically senses its own mechanical environment. This environment is constantly changing, on a beat-by-beat basis, with additional modulation by respiratory activity and changes in posture or physical activity, and further overlaid with more slowly occurring physiological (e.g. pregnancy, endurance training) or pathological challenges (e.g. pressure or volume overload). Far from being a simple pump, the heart detects changes in mechanical demand and adjusts its performance accordingly, both via heart rate and stroke volume alteration. Many of the underlying regulatory processes are encoded intracardially, and are thus maintained even in heart transplant recipients. Over the last three decades, molecular substrates of cardiac mechanosensitivity have gained increasing recognition in the scientific and clinical communities. Nonetheless, the processes underlying this phenomenon are still poorly understood. Stretch-activated ion channels (SAC) have been identified as one contributor to mechanosensitive autoregulation of the heartbeat. They also appear to play important roles in the development of cardiac pathologies – most notably stretch-induced arrhythmias. As recently discovered, some established cardiac drugs act, in part at least, via mechanotransduction pathways suggesting SAC as potential therapeutic targets. Clearly, identification of the molecular substrate of cardiac SAC is of clinical importance and a number of candidate proteins have been identified. At the same time, experimental studies have revealed variable–and at times contrasting–results regarding their function. Further complication arises from the fact that many ion channels that are not classically defined as SAC, including voltage and ligand-gated ion channels, can respond to mechanical stimulation. Here, we summarise what is known about the molecular substrate of the main candidates for cardiac SAC, before identifying potential further developments in this area of translational research. Bloomsbury Qatar Foundation Journals 2014-06-18 /pmc/articles/PMC4220428/ /pubmed/25405172 http://dx.doi.org/10.5339/gcsp.2014.19 Text en © 2014 Reed, Kohl, Peyronnet, licensee Bloomsbury Qatar Foundation Journals. This is an open access article distributed under the terms of the Creative Commons Attribution license CC BY 4.0, which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Reed, Alistair Kohl, Peter Peyronnet, Rémi Molecular candidates for cardiac stretch-activated ion channels |
title | Molecular candidates for cardiac stretch-activated ion channels |
title_full | Molecular candidates for cardiac stretch-activated ion channels |
title_fullStr | Molecular candidates for cardiac stretch-activated ion channels |
title_full_unstemmed | Molecular candidates for cardiac stretch-activated ion channels |
title_short | Molecular candidates for cardiac stretch-activated ion channels |
title_sort | molecular candidates for cardiac stretch-activated ion channels |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220428/ https://www.ncbi.nlm.nih.gov/pubmed/25405172 http://dx.doi.org/10.5339/gcsp.2014.19 |
work_keys_str_mv | AT reedalistair molecularcandidatesforcardiacstretchactivatedionchannels AT kohlpeter molecularcandidatesforcardiacstretchactivatedionchannels AT peyronnetremi molecularcandidatesforcardiacstretchactivatedionchannels |