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Computational modeling of inhibition of voltage-gated Ca channels: identification of different effects on uterine and cardiac action potentials
The uterus and heart share the important physiological feature whereby contractile activation of the muscle tissue is regulated by the generation of periodic, spontaneous electrical action potentials (APs). Preterm birth arising from premature uterine contractions is a major complication of pregnanc...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199256/ https://www.ncbi.nlm.nih.gov/pubmed/25360118 http://dx.doi.org/10.3389/fphys.2014.00399 |
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author | Tong, Wing-Chiu Ghouri, Iffath Taggart, Michael J. |
author_facet | Tong, Wing-Chiu Ghouri, Iffath Taggart, Michael J. |
author_sort | Tong, Wing-Chiu |
collection | PubMed |
description | The uterus and heart share the important physiological feature whereby contractile activation of the muscle tissue is regulated by the generation of periodic, spontaneous electrical action potentials (APs). Preterm birth arising from premature uterine contractions is a major complication of pregnancy and there remains a need to pursue avenues of research that facilitate the use of drugs, tocolytics, to limit these inappropriate contractions without deleterious actions on cardiac electrical excitation. A novel approach is to make use of mathematical models of uterine and cardiac APs, which incorporate many ionic currents contributing to the AP forms, and test the cell-specific responses to interventions. We have used three such models—of uterine smooth muscle cells (USMC), cardiac sinoatrial node cells (SAN), and ventricular cells—to investigate the relative effects of reducing two important voltage-gated Ca currents—the L-type (I(CaL)) and T-type (I(CaT)) Ca currents. Reduction of I(CaL) (10%) alone, or I(CaT) (40%) alone, blunted USMC APs with little effect on ventricular APs and only mild effects on SAN activity. Larger reductions in either current further attenuated the USMC APs but with also greater effects on SAN APs. Encouragingly, a combination of I(CaL) and I(CaT) reduction did blunt USMC APs as intended with little detriment to APs of either cardiac cell type. Subsequent overlapping maps of I(CaL) and I(CaT) inhibition profiles from each model revealed a range of combined reductions of I(CaL) and I(CaT) over which an appreciable diminution of USMC APs could be achieved with no deleterious action on cardiac SAN or ventricular APs. This novel approach illustrates the potential for computational biology to inform us of possible uterine and cardiac cell-specific mechanisms. Incorporating such computational approaches in future studies directed at designing new, or repurposing existing, tocolytics will be beneficial for establishing a desired uterine specificity of action. |
format | Online Article Text |
id | pubmed-4199256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41992562014-10-30 Computational modeling of inhibition of voltage-gated Ca channels: identification of different effects on uterine and cardiac action potentials Tong, Wing-Chiu Ghouri, Iffath Taggart, Michael J. Front Physiol Physiology The uterus and heart share the important physiological feature whereby contractile activation of the muscle tissue is regulated by the generation of periodic, spontaneous electrical action potentials (APs). Preterm birth arising from premature uterine contractions is a major complication of pregnancy and there remains a need to pursue avenues of research that facilitate the use of drugs, tocolytics, to limit these inappropriate contractions without deleterious actions on cardiac electrical excitation. A novel approach is to make use of mathematical models of uterine and cardiac APs, which incorporate many ionic currents contributing to the AP forms, and test the cell-specific responses to interventions. We have used three such models—of uterine smooth muscle cells (USMC), cardiac sinoatrial node cells (SAN), and ventricular cells—to investigate the relative effects of reducing two important voltage-gated Ca currents—the L-type (I(CaL)) and T-type (I(CaT)) Ca currents. Reduction of I(CaL) (10%) alone, or I(CaT) (40%) alone, blunted USMC APs with little effect on ventricular APs and only mild effects on SAN activity. Larger reductions in either current further attenuated the USMC APs but with also greater effects on SAN APs. Encouragingly, a combination of I(CaL) and I(CaT) reduction did blunt USMC APs as intended with little detriment to APs of either cardiac cell type. Subsequent overlapping maps of I(CaL) and I(CaT) inhibition profiles from each model revealed a range of combined reductions of I(CaL) and I(CaT) over which an appreciable diminution of USMC APs could be achieved with no deleterious action on cardiac SAN or ventricular APs. This novel approach illustrates the potential for computational biology to inform us of possible uterine and cardiac cell-specific mechanisms. Incorporating such computational approaches in future studies directed at designing new, or repurposing existing, tocolytics will be beneficial for establishing a desired uterine specificity of action. Frontiers Media S.A. 2014-10-16 /pmc/articles/PMC4199256/ /pubmed/25360118 http://dx.doi.org/10.3389/fphys.2014.00399 Text en Copyright © 2014 Tong, Ghouri and Taggart. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Tong, Wing-Chiu Ghouri, Iffath Taggart, Michael J. Computational modeling of inhibition of voltage-gated Ca channels: identification of different effects on uterine and cardiac action potentials |
title | Computational modeling of inhibition of voltage-gated Ca channels: identification of different effects on uterine and cardiac action potentials |
title_full | Computational modeling of inhibition of voltage-gated Ca channels: identification of different effects on uterine and cardiac action potentials |
title_fullStr | Computational modeling of inhibition of voltage-gated Ca channels: identification of different effects on uterine and cardiac action potentials |
title_full_unstemmed | Computational modeling of inhibition of voltage-gated Ca channels: identification of different effects on uterine and cardiac action potentials |
title_short | Computational modeling of inhibition of voltage-gated Ca channels: identification of different effects on uterine and cardiac action potentials |
title_sort | computational modeling of inhibition of voltage-gated ca channels: identification of different effects on uterine and cardiac action potentials |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199256/ https://www.ncbi.nlm.nih.gov/pubmed/25360118 http://dx.doi.org/10.3389/fphys.2014.00399 |
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