Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autor principal: Bondarenko, Vladimir E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
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
_version_ 1782304696816369664
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
work_keys_str_mv AT bondarenkovladimire acompartmentalizedmathematicalmodeloftheb1adrenergicsignalingsysteminmouseventricularmyocytes
AT bondarenkovladimire compartmentalizedmathematicalmodeloftheb1adrenergicsignalingsysteminmouseventricularmyocytes