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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9481532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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