Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Tarun, Anjali, Wainstein-Andriano, Danyal, Sterpenich, Virginie, Bayer, Laurence, Perogamvros, Lampros, Solms, Mark, Axmacher, Nikolai, Schwartz, Sophie, Van De Ville, Dimitri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
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
_version_ 1783630139310997504
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
work_keys_str_mv AT tarunanjali nremsleepstagesspecificallyalterdynamicalintegrationoflargescalebrainnetworks
AT wainsteinandrianodanyal nremsleepstagesspecificallyalterdynamicalintegrationoflargescalebrainnetworks
AT sterpenichvirginie nremsleepstagesspecificallyalterdynamicalintegrationoflargescalebrainnetworks
AT bayerlaurence nremsleepstagesspecificallyalterdynamicalintegrationoflargescalebrainnetworks
AT perogamvroslampros nremsleepstagesspecificallyalterdynamicalintegrationoflargescalebrainnetworks
AT solmsmark nremsleepstagesspecificallyalterdynamicalintegrationoflargescalebrainnetworks
AT axmachernikolai nremsleepstagesspecificallyalterdynamicalintegrationoflargescalebrainnetworks
AT schwartzsophie nremsleepstagesspecificallyalterdynamicalintegrationoflargescalebrainnetworks
AT vandevilledimitri nremsleepstagesspecificallyalterdynamicalintegrationoflargescalebrainnetworks