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Reconfigurations in brain networks upon awakening from slow wave sleep: Interventions and implications in neural communication
Sleep inertia is the brief period of impaired alertness and performance experienced immediately after waking. Little is known about the neural mechanisms underlying this phenomenon. A better understanding of the neural processes during sleep inertia may offer insight into the awakening process. We o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MIT Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270716/ https://www.ncbi.nlm.nih.gov/pubmed/37334002 http://dx.doi.org/10.1162/netn_a_00272 |
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author | Hilditch, Cassie J. Bansal, Kanika Chachad, Ravi Wong, Lily R. Bathurst, Nicholas G. Feick, Nathan H. Santamaria, Amanda Shattuck, Nita L. Garcia, Javier O. Flynn-Evans, Erin E. |
author_facet | Hilditch, Cassie J. Bansal, Kanika Chachad, Ravi Wong, Lily R. Bathurst, Nicholas G. Feick, Nathan H. Santamaria, Amanda Shattuck, Nita L. Garcia, Javier O. Flynn-Evans, Erin E. |
author_sort | Hilditch, Cassie J. |
collection | PubMed |
description | Sleep inertia is the brief period of impaired alertness and performance experienced immediately after waking. Little is known about the neural mechanisms underlying this phenomenon. A better understanding of the neural processes during sleep inertia may offer insight into the awakening process. We observed brain activity every 15 min for 1 hr following abrupt awakening from slow wave sleep during the biological night. Using 32-channel electroencephalography, a network science approach, and a within-subject design, we evaluated power, clustering coefficient, and path length across frequency bands under both a control and a polychromatic short-wavelength-enriched light intervention condition. We found that under control conditions, the awakening brain is typified by an immediate reduction in global theta, alpha, and beta power. Simultaneously, we observed a decrease in the clustering coefficient and an increase in path length within the delta band. Exposure to light immediately after awakening ameliorated changes in clustering. Our results suggest that long-range network communication within the brain is crucial to the awakening process and that the brain may prioritize these long-range connections during this transitional state. Our study highlights a novel neurophysiological signature of the awakening brain and provides a potential mechanism by which light improves performance after waking. |
format | Online Article Text |
id | pubmed-10270716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MIT Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102707162023-06-16 Reconfigurations in brain networks upon awakening from slow wave sleep: Interventions and implications in neural communication Hilditch, Cassie J. Bansal, Kanika Chachad, Ravi Wong, Lily R. Bathurst, Nicholas G. Feick, Nathan H. Santamaria, Amanda Shattuck, Nita L. Garcia, Javier O. Flynn-Evans, Erin E. Netw Neurosci Research Article Sleep inertia is the brief period of impaired alertness and performance experienced immediately after waking. Little is known about the neural mechanisms underlying this phenomenon. A better understanding of the neural processes during sleep inertia may offer insight into the awakening process. We observed brain activity every 15 min for 1 hr following abrupt awakening from slow wave sleep during the biological night. Using 32-channel electroencephalography, a network science approach, and a within-subject design, we evaluated power, clustering coefficient, and path length across frequency bands under both a control and a polychromatic short-wavelength-enriched light intervention condition. We found that under control conditions, the awakening brain is typified by an immediate reduction in global theta, alpha, and beta power. Simultaneously, we observed a decrease in the clustering coefficient and an increase in path length within the delta band. Exposure to light immediately after awakening ameliorated changes in clustering. Our results suggest that long-range network communication within the brain is crucial to the awakening process and that the brain may prioritize these long-range connections during this transitional state. Our study highlights a novel neurophysiological signature of the awakening brain and provides a potential mechanism by which light improves performance after waking. MIT Press 2023-01-01 /pmc/articles/PMC10270716/ /pubmed/37334002 http://dx.doi.org/10.1162/netn_a_00272 Text en © 2022 Massachusetts Institute of Technology https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. For a full description of the license, please visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Hilditch, Cassie J. Bansal, Kanika Chachad, Ravi Wong, Lily R. Bathurst, Nicholas G. Feick, Nathan H. Santamaria, Amanda Shattuck, Nita L. Garcia, Javier O. Flynn-Evans, Erin E. Reconfigurations in brain networks upon awakening from slow wave sleep: Interventions and implications in neural communication |
title | Reconfigurations in brain networks upon awakening from slow wave sleep: Interventions and implications in neural communication |
title_full | Reconfigurations in brain networks upon awakening from slow wave sleep: Interventions and implications in neural communication |
title_fullStr | Reconfigurations in brain networks upon awakening from slow wave sleep: Interventions and implications in neural communication |
title_full_unstemmed | Reconfigurations in brain networks upon awakening from slow wave sleep: Interventions and implications in neural communication |
title_short | Reconfigurations in brain networks upon awakening from slow wave sleep: Interventions and implications in neural communication |
title_sort | reconfigurations in brain networks upon awakening from slow wave sleep: interventions and implications in neural communication |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270716/ https://www.ncbi.nlm.nih.gov/pubmed/37334002 http://dx.doi.org/10.1162/netn_a_00272 |
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