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Scaling of recovery rates influences T-type Ca(2+) channel availability following IPSPs

The excitability of neuronal membranes is crucially modulated by T-type Ca(2+) channels (I(CaT)) due to their low threshold of activation. I(CaT) inactivates steeply at potentials close to the resting membrane potential. Therefore, the availability of I(CaT) following changes in membrane potential d...

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Detalles Bibliográficos
Autores principales: Schaub, Christina, Uebachs, Mischa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395784/
https://www.ncbi.nlm.nih.gov/pubmed/30886927
http://dx.doi.org/10.1016/j.heliyon.2019.e01278
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author Schaub, Christina
Uebachs, Mischa
author_facet Schaub, Christina
Uebachs, Mischa
author_sort Schaub, Christina
collection PubMed
description The excitability of neuronal membranes is crucially modulated by T-type Ca(2+) channels (I(CaT)) due to their low threshold of activation. I(CaT) inactivates steeply at potentials close to the resting membrane potential. Therefore, the availability of I(CaT) following changes in membrane potential depends on the time course of the onset of inactivation as well as on the time course of recovery from inactivation. It was previously shown that the time course of recovery from inactivation depends on the duration of the conditioning pulse in cloned T-type Ca(2+) channel subunits (Ca(v)3.1-Ca(v)3.3(Uebachs et al., 2006)). This provides a potential mechanism for an intrinsic form of short term plasticity. Here, we address the question, whether this mechanism results in altered availability of I(CaT) following physiological changes in membrane potential. We found that the recovery of I(CaT) during an IPSP depends on the duration of a preceding depolarized period.
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spelling pubmed-63957842019-03-18 Scaling of recovery rates influences T-type Ca(2+) channel availability following IPSPs Schaub, Christina Uebachs, Mischa Heliyon Article The excitability of neuronal membranes is crucially modulated by T-type Ca(2+) channels (I(CaT)) due to their low threshold of activation. I(CaT) inactivates steeply at potentials close to the resting membrane potential. Therefore, the availability of I(CaT) following changes in membrane potential depends on the time course of the onset of inactivation as well as on the time course of recovery from inactivation. It was previously shown that the time course of recovery from inactivation depends on the duration of the conditioning pulse in cloned T-type Ca(2+) channel subunits (Ca(v)3.1-Ca(v)3.3(Uebachs et al., 2006)). This provides a potential mechanism for an intrinsic form of short term plasticity. Here, we address the question, whether this mechanism results in altered availability of I(CaT) following physiological changes in membrane potential. We found that the recovery of I(CaT) during an IPSP depends on the duration of a preceding depolarized period. Elsevier 2019-02-27 /pmc/articles/PMC6395784/ /pubmed/30886927 http://dx.doi.org/10.1016/j.heliyon.2019.e01278 Text en © 2019 The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Schaub, Christina
Uebachs, Mischa
Scaling of recovery rates influences T-type Ca(2+) channel availability following IPSPs
title Scaling of recovery rates influences T-type Ca(2+) channel availability following IPSPs
title_full Scaling of recovery rates influences T-type Ca(2+) channel availability following IPSPs
title_fullStr Scaling of recovery rates influences T-type Ca(2+) channel availability following IPSPs
title_full_unstemmed Scaling of recovery rates influences T-type Ca(2+) channel availability following IPSPs
title_short Scaling of recovery rates influences T-type Ca(2+) channel availability following IPSPs
title_sort scaling of recovery rates influences t-type ca(2+) channel availability following ipsps
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395784/
https://www.ncbi.nlm.nih.gov/pubmed/30886927
http://dx.doi.org/10.1016/j.heliyon.2019.e01278
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