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A temporal sequence of thalamic activity unfolds at transitions in behavioral arousal state

Awakening from sleep reflects a profound transformation in neural activity and behavior. The thalamus is a key controller of arousal state, but whether its diverse nuclei exhibit coordinated or distinct activity at transitions in behavioral arousal state is unknown. Using fast fMRI at ultra-high fie...

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Autores principales: Setzer, Beverly, Fultz, Nina E., Gomez, Daniel E. P., Williams, Stephanie D., Bonmassar, Giorgio, Polimeni, Jonathan R., Lewis, Laura D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481532/
https://www.ncbi.nlm.nih.gov/pubmed/36114170
http://dx.doi.org/10.1038/s41467-022-33010-8
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author Setzer, Beverly
Fultz, Nina E.
Gomez, Daniel E. P.
Williams, Stephanie D.
Bonmassar, Giorgio
Polimeni, Jonathan R.
Lewis, Laura D.
author_facet Setzer, Beverly
Fultz, Nina E.
Gomez, Daniel E. P.
Williams, Stephanie D.
Bonmassar, Giorgio
Polimeni, Jonathan R.
Lewis, Laura D.
author_sort Setzer, Beverly
collection PubMed
description Awakening from sleep reflects a profound transformation in neural activity and behavior. The thalamus is a key controller of arousal state, but whether its diverse nuclei exhibit coordinated or distinct activity at transitions in behavioral arousal state is unknown. Using fast fMRI at ultra-high field (7 Tesla), we measured sub-second activity across thalamocortical networks and within nine thalamic nuclei to delineate these dynamics during spontaneous transitions in behavioral arousal state. We discovered a stereotyped sequence of activity across thalamic nuclei and cingulate cortex that preceded behavioral arousal after a period of inactivity, followed by widespread deactivation. These thalamic dynamics were linked to whether participants subsequently fell back into unresponsiveness, with unified thalamic activation reflecting maintenance of behavior. These results provide an outline of the complex interactions across thalamocortical circuits that orchestrate behavioral arousal state transitions, and additionally, demonstrate that fast fMRI can resolve sub-second subcortical dynamics in the human brain.
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spelling pubmed-94815322022-09-18 A temporal sequence of thalamic activity unfolds at transitions in behavioral arousal state Setzer, Beverly Fultz, Nina E. Gomez, Daniel E. P. Williams, Stephanie D. Bonmassar, Giorgio Polimeni, Jonathan R. Lewis, Laura D. Nat Commun Article Awakening from sleep reflects a profound transformation in neural activity and behavior. The thalamus is a key controller of arousal state, but whether its diverse nuclei exhibit coordinated or distinct activity at transitions in behavioral arousal state is unknown. Using fast fMRI at ultra-high field (7 Tesla), we measured sub-second activity across thalamocortical networks and within nine thalamic nuclei to delineate these dynamics during spontaneous transitions in behavioral arousal state. We discovered a stereotyped sequence of activity across thalamic nuclei and cingulate cortex that preceded behavioral arousal after a period of inactivity, followed by widespread deactivation. These thalamic dynamics were linked to whether participants subsequently fell back into unresponsiveness, with unified thalamic activation reflecting maintenance of behavior. These results provide an outline of the complex interactions across thalamocortical circuits that orchestrate behavioral arousal state transitions, and additionally, demonstrate that fast fMRI can resolve sub-second subcortical dynamics in the human brain. Nature Publishing Group UK 2022-09-16 /pmc/articles/PMC9481532/ /pubmed/36114170 http://dx.doi.org/10.1038/s41467-022-33010-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Setzer, Beverly
Fultz, Nina E.
Gomez, Daniel E. P.
Williams, Stephanie D.
Bonmassar, Giorgio
Polimeni, Jonathan R.
Lewis, Laura D.
A temporal sequence of thalamic activity unfolds at transitions in behavioral arousal state
title A temporal sequence of thalamic activity unfolds at transitions in behavioral arousal state
title_full A temporal sequence of thalamic activity unfolds at transitions in behavioral arousal state
title_fullStr A temporal sequence of thalamic activity unfolds at transitions in behavioral arousal state
title_full_unstemmed A temporal sequence of thalamic activity unfolds at transitions in behavioral arousal state
title_short A temporal sequence of thalamic activity unfolds at transitions in behavioral arousal state
title_sort temporal sequence of thalamic activity unfolds at transitions in behavioral arousal state
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481532/
https://www.ncbi.nlm.nih.gov/pubmed/36114170
http://dx.doi.org/10.1038/s41467-022-33010-8
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