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Stretch-activated current in human atrial myocytes and Na(+) current and mechano-gated channels’ current in myofibroblasts alter myocyte mechanical behavior: a computational study
BACKGROUND: The activation of stretch-activated channels (SACs) in cardiac myocytes, which changes the phases of action potential repolarization, is proven to be highly efficient for the conversion of atrial fibrillation. The expression of Na(+) current in myofibroblasts (Mfbs) regenerates myocytes’...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814973/ https://www.ncbi.nlm.nih.gov/pubmed/31653259 http://dx.doi.org/10.1186/s12938-019-0723-5 |
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author | Zhan, Heqing Zhang, Jingtao Jiao, Anquan Wang, Qin |
author_facet | Zhan, Heqing Zhang, Jingtao Jiao, Anquan Wang, Qin |
author_sort | Zhan, Heqing |
collection | PubMed |
description | BACKGROUND: The activation of stretch-activated channels (SACs) in cardiac myocytes, which changes the phases of action potential repolarization, is proven to be highly efficient for the conversion of atrial fibrillation. The expression of Na(+) current in myofibroblasts (Mfbs) regenerates myocytes’ action potentials, suggesting that Mfbs play an active role in triggering cardiac rhythm disturbances. Moreover, the excitation of mechano-gated channels (MGCs) in Mfbs depolarizes their membrane potential and contributes to the increased risk of post-infarct arrhythmia. Although these electrophysiological mechanisms have been largely known, the roles of these currents in cardiac mechanics are still debated. In this study, we aimed to investigate the mechanical influence of these currents via mathematical modeling. A novel mathematical model was developed by integrating models of human atrial myocyte (including the stretch-activated current, Ca(2+)–force relation, and mechanical behavior of a single segment) and Mfb (including our formulation of Na(+) current and mechano-gated channels’ current). The effects of the changes in basic cycle length, number of coupled Mfbs and intercellular coupling conductance on myocyte mechanical properties were compared. RESULTS: Our results indicated that these three currents significantly regulated myocyte mechanical parameters. In isosarcometric contraction, these currents increased segment force by 13.8–36.6% and dropped element length by 12.1–31.5%. In isotonic contraction, there are 2.7–5.9% growth and 0.9–24% reduction. Effects of these currents on the extremum of myocyte mechanical parameters become more significant with the increase of basic cycle length, number of coupled Mfbs and intercellular coupling conductance. CONCLUSIONS: The results demonstrated that stretch-activated current in myocytes and Na(+) current and mechano-gated channels’ current in Mfbs significantly influenced myocyte mechanical behavior and should be considered in future cardiac mechanical mathematical modeling. |
format | Online Article Text |
id | pubmed-6814973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68149732019-10-31 Stretch-activated current in human atrial myocytes and Na(+) current and mechano-gated channels’ current in myofibroblasts alter myocyte mechanical behavior: a computational study Zhan, Heqing Zhang, Jingtao Jiao, Anquan Wang, Qin Biomed Eng Online Research BACKGROUND: The activation of stretch-activated channels (SACs) in cardiac myocytes, which changes the phases of action potential repolarization, is proven to be highly efficient for the conversion of atrial fibrillation. The expression of Na(+) current in myofibroblasts (Mfbs) regenerates myocytes’ action potentials, suggesting that Mfbs play an active role in triggering cardiac rhythm disturbances. Moreover, the excitation of mechano-gated channels (MGCs) in Mfbs depolarizes their membrane potential and contributes to the increased risk of post-infarct arrhythmia. Although these electrophysiological mechanisms have been largely known, the roles of these currents in cardiac mechanics are still debated. In this study, we aimed to investigate the mechanical influence of these currents via mathematical modeling. A novel mathematical model was developed by integrating models of human atrial myocyte (including the stretch-activated current, Ca(2+)–force relation, and mechanical behavior of a single segment) and Mfb (including our formulation of Na(+) current and mechano-gated channels’ current). The effects of the changes in basic cycle length, number of coupled Mfbs and intercellular coupling conductance on myocyte mechanical properties were compared. RESULTS: Our results indicated that these three currents significantly regulated myocyte mechanical parameters. In isosarcometric contraction, these currents increased segment force by 13.8–36.6% and dropped element length by 12.1–31.5%. In isotonic contraction, there are 2.7–5.9% growth and 0.9–24% reduction. Effects of these currents on the extremum of myocyte mechanical parameters become more significant with the increase of basic cycle length, number of coupled Mfbs and intercellular coupling conductance. CONCLUSIONS: The results demonstrated that stretch-activated current in myocytes and Na(+) current and mechano-gated channels’ current in Mfbs significantly influenced myocyte mechanical behavior and should be considered in future cardiac mechanical mathematical modeling. BioMed Central 2019-10-25 /pmc/articles/PMC6814973/ /pubmed/31653259 http://dx.doi.org/10.1186/s12938-019-0723-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zhan, Heqing Zhang, Jingtao Jiao, Anquan Wang, Qin Stretch-activated current in human atrial myocytes and Na(+) current and mechano-gated channels’ current in myofibroblasts alter myocyte mechanical behavior: a computational study |
title | Stretch-activated current in human atrial myocytes and Na(+) current and mechano-gated channels’ current in myofibroblasts alter myocyte mechanical behavior: a computational study |
title_full | Stretch-activated current in human atrial myocytes and Na(+) current and mechano-gated channels’ current in myofibroblasts alter myocyte mechanical behavior: a computational study |
title_fullStr | Stretch-activated current in human atrial myocytes and Na(+) current and mechano-gated channels’ current in myofibroblasts alter myocyte mechanical behavior: a computational study |
title_full_unstemmed | Stretch-activated current in human atrial myocytes and Na(+) current and mechano-gated channels’ current in myofibroblasts alter myocyte mechanical behavior: a computational study |
title_short | Stretch-activated current in human atrial myocytes and Na(+) current and mechano-gated channels’ current in myofibroblasts alter myocyte mechanical behavior: a computational study |
title_sort | stretch-activated current in human atrial myocytes and na(+) current and mechano-gated channels’ current in myofibroblasts alter myocyte mechanical behavior: a computational study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814973/ https://www.ncbi.nlm.nih.gov/pubmed/31653259 http://dx.doi.org/10.1186/s12938-019-0723-5 |
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