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Conducted Vasoreactivity: the Dynamical Point of View
Conducted vasodilation is part of the physiological response to increasing metabolic demand of the tissue. Similar responses can be elicited by focal electrical or chemical stimulation. Some evidence suggests an endothelial pathway for nondecremental transmission of hyperpolarizing pulses. However,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303742/ https://www.ncbi.nlm.nih.gov/pubmed/25583354 http://dx.doi.org/10.1007/s11538-014-0058-0 |
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author | Postnov, D. E. Neganova, A. Y. Sosnovtseva, O. V. Holstein-Rathlou, N.-H. Jacobsen, J. C. Brings |
author_facet | Postnov, D. E. Neganova, A. Y. Sosnovtseva, O. V. Holstein-Rathlou, N.-H. Jacobsen, J. C. Brings |
author_sort | Postnov, D. E. |
collection | PubMed |
description | Conducted vasodilation is part of the physiological response to increasing metabolic demand of the tissue. Similar responses can be elicited by focal electrical or chemical stimulation. Some evidence suggests an endothelial pathway for nondecremental transmission of hyperpolarizing pulses. However, the underlying mechanisms are debated. Here, we focus on dynamical aspects of the problem hypothesizing the existence of a bistability-powered mechanism for regenerative pulse transmission along the endothelium. Bistability implies that the cell can have two different stable resting potentials and can switch between those states following an appropriate stimulus. Bistability is possible if the current–voltage curve is N shaped instead of monotonically increasing. Specifically, the presence of an inwardly rectifying potassium current may provide the endothelial cell with such properties. We provide a theoretical analysis as well as numerical simulations of both single- and multiunit bistable systems mimicking endothelial cells to investigate the self-consistence and stability of the proposed mechanism. We find that the individual cell may switch readily between two stable potentials. An array of coupled cells, however, as found in the vascular wall, requires a certain adaptation of the membrane currents after a switch, in order to switch back. Although the formulation is generic, we suggest a combination of specific membrane currents that could underlie the phenomenon. |
format | Online Article Text |
id | pubmed-4303742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-43037422015-01-27 Conducted Vasoreactivity: the Dynamical Point of View Postnov, D. E. Neganova, A. Y. Sosnovtseva, O. V. Holstein-Rathlou, N.-H. Jacobsen, J. C. Brings Bull Math Biol Original Article Conducted vasodilation is part of the physiological response to increasing metabolic demand of the tissue. Similar responses can be elicited by focal electrical or chemical stimulation. Some evidence suggests an endothelial pathway for nondecremental transmission of hyperpolarizing pulses. However, the underlying mechanisms are debated. Here, we focus on dynamical aspects of the problem hypothesizing the existence of a bistability-powered mechanism for regenerative pulse transmission along the endothelium. Bistability implies that the cell can have two different stable resting potentials and can switch between those states following an appropriate stimulus. Bistability is possible if the current–voltage curve is N shaped instead of monotonically increasing. Specifically, the presence of an inwardly rectifying potassium current may provide the endothelial cell with such properties. We provide a theoretical analysis as well as numerical simulations of both single- and multiunit bistable systems mimicking endothelial cells to investigate the self-consistence and stability of the proposed mechanism. We find that the individual cell may switch readily between two stable potentials. An array of coupled cells, however, as found in the vascular wall, requires a certain adaptation of the membrane currents after a switch, in order to switch back. Although the formulation is generic, we suggest a combination of specific membrane currents that could underlie the phenomenon. Springer US 2015-01-13 2015 /pmc/articles/PMC4303742/ /pubmed/25583354 http://dx.doi.org/10.1007/s11538-014-0058-0 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Postnov, D. E. Neganova, A. Y. Sosnovtseva, O. V. Holstein-Rathlou, N.-H. Jacobsen, J. C. Brings Conducted Vasoreactivity: the Dynamical Point of View |
title | Conducted Vasoreactivity: the Dynamical Point of View |
title_full | Conducted Vasoreactivity: the Dynamical Point of View |
title_fullStr | Conducted Vasoreactivity: the Dynamical Point of View |
title_full_unstemmed | Conducted Vasoreactivity: the Dynamical Point of View |
title_short | Conducted Vasoreactivity: the Dynamical Point of View |
title_sort | conducted vasoreactivity: the dynamical point of view |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303742/ https://www.ncbi.nlm.nih.gov/pubmed/25583354 http://dx.doi.org/10.1007/s11538-014-0058-0 |
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