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A four-component model of the action potential in mouse detrusor smooth muscle cell

BACKGROUND AND HYPOTHESIS: Detrusor smooth muscle cells (DSMCs) of the urinary bladder are electrically connected to one another via gap junctions and form a three dimensional syncytium. DSMCs exhibit spontaneous electrical activity, including passive depolarizations and action potentials. The shape...

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Detalles Bibliográficos
Autores principales: Padmakumar, Mithun, Brain, Keith L., Young, John S., Manchanda, Rohit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774707/
https://www.ncbi.nlm.nih.gov/pubmed/29351282
http://dx.doi.org/10.1371/journal.pone.0190016
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author Padmakumar, Mithun
Brain, Keith L.
Young, John S.
Manchanda, Rohit
author_facet Padmakumar, Mithun
Brain, Keith L.
Young, John S.
Manchanda, Rohit
author_sort Padmakumar, Mithun
collection PubMed
description BACKGROUND AND HYPOTHESIS: Detrusor smooth muscle cells (DSMCs) of the urinary bladder are electrically connected to one another via gap junctions and form a three dimensional syncytium. DSMCs exhibit spontaneous electrical activity, including passive depolarizations and action potentials. The shapes of spontaneous action potentials (sAPs) observed from a single DSM cell can vary widely. The biophysical origins of this variability, and the precise components which contribute to the complex shapes observed are not known. To address these questions, the basic components which constitute the sAPs were investigated. We hypothesized that linear combinations of scaled versions of these basic components can produce sAP shapes observed in the syncytium. METHODS AND RESULTS: The basic components were identified as spontaneous evoked junction potentials (sEJP), native AP (nAP), slow after hyperpolarization (sAHP) and very slow after hyperpolarization (vsAHP). The experimental recordings were grouped into two sets: a training data set and a testing data set. A training set was used to estimate the components, and a test set to evaluate the efficiency of the estimated components. We found that a linear combination of the identified components when appropriately amplified and time shifted replicated various AP shapes to a high degree of similarity, as quantified by the root mean square error (RMSE) measure. CONCLUSIONS: We conclude that the four basic components—sEJP, nAP, sAHP, and vsAHP—identified and isolated in this work are necessary and sufficient to replicate all varieties of the sAPs recorded experimentally in DSMCs. This model has the potential to generate testable hypotheses that can help identify the physiological processes underlying various features of the sAPs. Further, this model also provides a means to classify the sAPs into various shape classes.
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spelling pubmed-57747072018-01-26 A four-component model of the action potential in mouse detrusor smooth muscle cell Padmakumar, Mithun Brain, Keith L. Young, John S. Manchanda, Rohit PLoS One Research Article BACKGROUND AND HYPOTHESIS: Detrusor smooth muscle cells (DSMCs) of the urinary bladder are electrically connected to one another via gap junctions and form a three dimensional syncytium. DSMCs exhibit spontaneous electrical activity, including passive depolarizations and action potentials. The shapes of spontaneous action potentials (sAPs) observed from a single DSM cell can vary widely. The biophysical origins of this variability, and the precise components which contribute to the complex shapes observed are not known. To address these questions, the basic components which constitute the sAPs were investigated. We hypothesized that linear combinations of scaled versions of these basic components can produce sAP shapes observed in the syncytium. METHODS AND RESULTS: The basic components were identified as spontaneous evoked junction potentials (sEJP), native AP (nAP), slow after hyperpolarization (sAHP) and very slow after hyperpolarization (vsAHP). The experimental recordings were grouped into two sets: a training data set and a testing data set. A training set was used to estimate the components, and a test set to evaluate the efficiency of the estimated components. We found that a linear combination of the identified components when appropriately amplified and time shifted replicated various AP shapes to a high degree of similarity, as quantified by the root mean square error (RMSE) measure. CONCLUSIONS: We conclude that the four basic components—sEJP, nAP, sAHP, and vsAHP—identified and isolated in this work are necessary and sufficient to replicate all varieties of the sAPs recorded experimentally in DSMCs. This model has the potential to generate testable hypotheses that can help identify the physiological processes underlying various features of the sAPs. Further, this model also provides a means to classify the sAPs into various shape classes. Public Library of Science 2018-01-19 /pmc/articles/PMC5774707/ /pubmed/29351282 http://dx.doi.org/10.1371/journal.pone.0190016 Text en © 2018 Padmakumar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Padmakumar, Mithun
Brain, Keith L.
Young, John S.
Manchanda, Rohit
A four-component model of the action potential in mouse detrusor smooth muscle cell
title A four-component model of the action potential in mouse detrusor smooth muscle cell
title_full A four-component model of the action potential in mouse detrusor smooth muscle cell
title_fullStr A four-component model of the action potential in mouse detrusor smooth muscle cell
title_full_unstemmed A four-component model of the action potential in mouse detrusor smooth muscle cell
title_short A four-component model of the action potential in mouse detrusor smooth muscle cell
title_sort four-component model of the action potential in mouse detrusor smooth muscle cell
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774707/
https://www.ncbi.nlm.nih.gov/pubmed/29351282
http://dx.doi.org/10.1371/journal.pone.0190016
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