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A Compartmentalized Mathematical Model of the β(1)-Adrenergic Signaling System in Mouse Ventricular Myocytes
The β(1)-adrenergic signaling system plays an important role in the functioning of cardiac cells. Experimental data shows that the activation of this system produces inotropy, lusitropy, and chronotropy in the heart, such as increased magnitude and relaxation rates of [Ca(2+)](i) transients and cont...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931689/ https://www.ncbi.nlm.nih.gov/pubmed/24586529 http://dx.doi.org/10.1371/journal.pone.0089113 |
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author | Bondarenko, Vladimir E. |
author_facet | Bondarenko, Vladimir E. |
author_sort | Bondarenko, Vladimir E. |
collection | PubMed |
description | The β(1)-adrenergic signaling system plays an important role in the functioning of cardiac cells. Experimental data shows that the activation of this system produces inotropy, lusitropy, and chronotropy in the heart, such as increased magnitude and relaxation rates of [Ca(2+)](i) transients and contraction force, and increased heart rhythm. However, excessive stimulation of β(1)-adrenergic receptors leads to heart dysfunction and heart failure. In this paper, a comprehensive, experimentally based mathematical model of the β(1)-adrenergic signaling system for mouse ventricular myocytes is developed, which includes major subcellular functional compartments (caveolae, extracaveolae, and cytosol). The model describes biochemical reactions that occur during stimulation of β(1)-adrenoceptors, changes in ionic currents, and modifications of Ca(2+) handling system. Simulations describe the dynamics of major signaling molecules, such as cyclic AMP and protein kinase A, in different subcellular compartments; the effects of inhibition of phosphodiesterases on cAMP production; kinetics and magnitudes of phosphorylation of ion channels, transporters, and Ca(2+) handling proteins; modifications of action potential shape and duration; magnitudes and relaxation rates of [Ca(2+)](i) transients; changes in intracellular and transmembrane Ca(2+) fluxes; and [Na(+)](i) fluxes and dynamics. The model elucidates complex interactions of ionic currents upon activation of β(1)-adrenoceptors at different stimulation frequencies, which ultimately lead to a relatively modest increase in action potential duration and significant increase in [Ca(2+)](i) transients. In particular, the model includes two subpopulations of the L-type Ca(2+) channels, in caveolae and extracaveolae compartments, and their effects on the action potential and [Ca(2+)](i) transients are investigated. The presented model can be used by researchers for the interpretation of experimental data and for the developments of mathematical models for other species or for pathological conditions. |
format | Online Article Text |
id | pubmed-3931689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39316892014-02-25 A Compartmentalized Mathematical Model of the β(1)-Adrenergic Signaling System in Mouse Ventricular Myocytes Bondarenko, Vladimir E. PLoS One Research Article The β(1)-adrenergic signaling system plays an important role in the functioning of cardiac cells. Experimental data shows that the activation of this system produces inotropy, lusitropy, and chronotropy in the heart, such as increased magnitude and relaxation rates of [Ca(2+)](i) transients and contraction force, and increased heart rhythm. However, excessive stimulation of β(1)-adrenergic receptors leads to heart dysfunction and heart failure. In this paper, a comprehensive, experimentally based mathematical model of the β(1)-adrenergic signaling system for mouse ventricular myocytes is developed, which includes major subcellular functional compartments (caveolae, extracaveolae, and cytosol). The model describes biochemical reactions that occur during stimulation of β(1)-adrenoceptors, changes in ionic currents, and modifications of Ca(2+) handling system. Simulations describe the dynamics of major signaling molecules, such as cyclic AMP and protein kinase A, in different subcellular compartments; the effects of inhibition of phosphodiesterases on cAMP production; kinetics and magnitudes of phosphorylation of ion channels, transporters, and Ca(2+) handling proteins; modifications of action potential shape and duration; magnitudes and relaxation rates of [Ca(2+)](i) transients; changes in intracellular and transmembrane Ca(2+) fluxes; and [Na(+)](i) fluxes and dynamics. The model elucidates complex interactions of ionic currents upon activation of β(1)-adrenoceptors at different stimulation frequencies, which ultimately lead to a relatively modest increase in action potential duration and significant increase in [Ca(2+)](i) transients. In particular, the model includes two subpopulations of the L-type Ca(2+) channels, in caveolae and extracaveolae compartments, and their effects on the action potential and [Ca(2+)](i) transients are investigated. The presented model can be used by researchers for the interpretation of experimental data and for the developments of mathematical models for other species or for pathological conditions. Public Library of Science 2014-02-21 /pmc/articles/PMC3931689/ /pubmed/24586529 http://dx.doi.org/10.1371/journal.pone.0089113 Text en © 2014 Vladimir E http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bondarenko, Vladimir E. A Compartmentalized Mathematical Model of the β(1)-Adrenergic Signaling System in Mouse Ventricular Myocytes |
title | A Compartmentalized Mathematical Model of the β(1)-Adrenergic Signaling System in Mouse Ventricular Myocytes |
title_full | A Compartmentalized Mathematical Model of the β(1)-Adrenergic Signaling System in Mouse Ventricular Myocytes |
title_fullStr | A Compartmentalized Mathematical Model of the β(1)-Adrenergic Signaling System in Mouse Ventricular Myocytes |
title_full_unstemmed | A Compartmentalized Mathematical Model of the β(1)-Adrenergic Signaling System in Mouse Ventricular Myocytes |
title_short | A Compartmentalized Mathematical Model of the β(1)-Adrenergic Signaling System in Mouse Ventricular Myocytes |
title_sort | compartmentalized mathematical model of the β(1)-adrenergic signaling system in mouse ventricular myocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931689/ https://www.ncbi.nlm.nih.gov/pubmed/24586529 http://dx.doi.org/10.1371/journal.pone.0089113 |
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