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NREM sleep stages specifically alter dynamical integration of large-scale brain networks
Functional dissociations in the brain observed during non-rapid eye movement (NREM) sleep have been associated with reduced information integration and impaired consciousness that accompany increasing sleep depth. Here, we explored the dynamical properties of large-scale functional brain networks de...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773861/ https://www.ncbi.nlm.nih.gov/pubmed/33409474 http://dx.doi.org/10.1016/j.isci.2020.101923 |
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author | Tarun, Anjali Wainstein-Andriano, Danyal Sterpenich, Virginie Bayer, Laurence Perogamvros, Lampros Solms, Mark Axmacher, Nikolai Schwartz, Sophie Van De Ville, Dimitri |
author_facet | Tarun, Anjali Wainstein-Andriano, Danyal Sterpenich, Virginie Bayer, Laurence Perogamvros, Lampros Solms, Mark Axmacher, Nikolai Schwartz, Sophie Van De Ville, Dimitri |
author_sort | Tarun, Anjali |
collection | PubMed |
description | Functional dissociations in the brain observed during non-rapid eye movement (NREM) sleep have been associated with reduced information integration and impaired consciousness that accompany increasing sleep depth. Here, we explored the dynamical properties of large-scale functional brain networks derived from transient brain activity using functional magnetic resonance imaging. Spatial brain maps generally display significant modifications in terms of their tendency to occur across wakefulness and NREM sleep. Unexpectedly, almost all networks predominated in activity during NREM stage 2 before an abrupt loss of activity is observed in NREM stage 3. Yet, functional connectivity and mutual dependencies between these networks progressively broke down with increasing sleep depth. Thus, the efficiency of information transfer during NREM stage 2 is low despite the high attempt to communicate. Critically, our approach provides relevant data for evaluating functional brain network integrity and our findings robustly support a significant advance in our neural models of human sleep and consciousness. |
format | Online Article Text |
id | pubmed-7773861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-77738612021-01-05 NREM sleep stages specifically alter dynamical integration of large-scale brain networks Tarun, Anjali Wainstein-Andriano, Danyal Sterpenich, Virginie Bayer, Laurence Perogamvros, Lampros Solms, Mark Axmacher, Nikolai Schwartz, Sophie Van De Ville, Dimitri iScience Article Functional dissociations in the brain observed during non-rapid eye movement (NREM) sleep have been associated with reduced information integration and impaired consciousness that accompany increasing sleep depth. Here, we explored the dynamical properties of large-scale functional brain networks derived from transient brain activity using functional magnetic resonance imaging. Spatial brain maps generally display significant modifications in terms of their tendency to occur across wakefulness and NREM sleep. Unexpectedly, almost all networks predominated in activity during NREM stage 2 before an abrupt loss of activity is observed in NREM stage 3. Yet, functional connectivity and mutual dependencies between these networks progressively broke down with increasing sleep depth. Thus, the efficiency of information transfer during NREM stage 2 is low despite the high attempt to communicate. Critically, our approach provides relevant data for evaluating functional brain network integrity and our findings robustly support a significant advance in our neural models of human sleep and consciousness. Elsevier 2020-12-10 /pmc/articles/PMC7773861/ /pubmed/33409474 http://dx.doi.org/10.1016/j.isci.2020.101923 Text en © 2020 The Author(s) 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 Tarun, Anjali Wainstein-Andriano, Danyal Sterpenich, Virginie Bayer, Laurence Perogamvros, Lampros Solms, Mark Axmacher, Nikolai Schwartz, Sophie Van De Ville, Dimitri NREM sleep stages specifically alter dynamical integration of large-scale brain networks |
title | NREM sleep stages specifically alter dynamical integration of large-scale brain networks |
title_full | NREM sleep stages specifically alter dynamical integration of large-scale brain networks |
title_fullStr | NREM sleep stages specifically alter dynamical integration of large-scale brain networks |
title_full_unstemmed | NREM sleep stages specifically alter dynamical integration of large-scale brain networks |
title_short | NREM sleep stages specifically alter dynamical integration of large-scale brain networks |
title_sort | nrem sleep stages specifically alter dynamical integration of large-scale brain networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773861/ https://www.ncbi.nlm.nih.gov/pubmed/33409474 http://dx.doi.org/10.1016/j.isci.2020.101923 |
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