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Robust switches in thalamic network activity require a timescale separation between sodium and T-type calcium channel activations

Switches in brain states, synaptic plasticity and neuromodulation are fundamental processes in our brain that take place concomitantly across several spatial and timescales. All these processes target neuron intrinsic properties and connectivity to achieve specific physiological goals, raising the q...

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Detalles Bibliográficos
Autores principales: Jacquerie, Kathleen, Drion, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162675/
https://www.ncbi.nlm.nih.gov/pubmed/34003841
http://dx.doi.org/10.1371/journal.pcbi.1008997
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author Jacquerie, Kathleen
Drion, Guillaume
author_facet Jacquerie, Kathleen
Drion, Guillaume
author_sort Jacquerie, Kathleen
collection PubMed
description Switches in brain states, synaptic plasticity and neuromodulation are fundamental processes in our brain that take place concomitantly across several spatial and timescales. All these processes target neuron intrinsic properties and connectivity to achieve specific physiological goals, raising the question of how they can operate without interfering with each other. Here, we highlight the central importance of a timescale separation in the activation of sodium and T-type calcium channels to sustain robust switches in brain states in thalamic neurons that are compatible with synaptic plasticity and neuromodulation. We quantify the role of this timescale separation by comparing the robustness of rhythms of six published conductance-based models at the cellular, circuit and network levels. We show that robust rhythm generation requires a T-type calcium channel activation whose kinetics are situated between sodium channel activation and T-type calcium channel inactivation in all models despite their quantitative differences.
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spelling pubmed-81626752021-06-10 Robust switches in thalamic network activity require a timescale separation between sodium and T-type calcium channel activations Jacquerie, Kathleen Drion, Guillaume PLoS Comput Biol Research Article Switches in brain states, synaptic plasticity and neuromodulation are fundamental processes in our brain that take place concomitantly across several spatial and timescales. All these processes target neuron intrinsic properties and connectivity to achieve specific physiological goals, raising the question of how they can operate without interfering with each other. Here, we highlight the central importance of a timescale separation in the activation of sodium and T-type calcium channels to sustain robust switches in brain states in thalamic neurons that are compatible with synaptic plasticity and neuromodulation. We quantify the role of this timescale separation by comparing the robustness of rhythms of six published conductance-based models at the cellular, circuit and network levels. We show that robust rhythm generation requires a T-type calcium channel activation whose kinetics are situated between sodium channel activation and T-type calcium channel inactivation in all models despite their quantitative differences. Public Library of Science 2021-05-18 /pmc/articles/PMC8162675/ /pubmed/34003841 http://dx.doi.org/10.1371/journal.pcbi.1008997 Text en © 2021 Jacquerie, Drion https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Jacquerie, Kathleen
Drion, Guillaume
Robust switches in thalamic network activity require a timescale separation between sodium and T-type calcium channel activations
title Robust switches in thalamic network activity require a timescale separation between sodium and T-type calcium channel activations
title_full Robust switches in thalamic network activity require a timescale separation between sodium and T-type calcium channel activations
title_fullStr Robust switches in thalamic network activity require a timescale separation between sodium and T-type calcium channel activations
title_full_unstemmed Robust switches in thalamic network activity require a timescale separation between sodium and T-type calcium channel activations
title_short Robust switches in thalamic network activity require a timescale separation between sodium and T-type calcium channel activations
title_sort robust switches in thalamic network activity require a timescale separation between sodium and t-type calcium channel activations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162675/
https://www.ncbi.nlm.nih.gov/pubmed/34003841
http://dx.doi.org/10.1371/journal.pcbi.1008997
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