Cargando…

Rapid eye movement sleep patterns of brain activation and deactivation occur within unique functional networks

Rapid eye movement (REM) sleep is a paradoxical state where the individual appears asleep while the electroencephalogram pattern resembles that of wakefulness. Regional differences in brain metabolism have been observed during REM sleep compared to wakefulness, but it is not known whether the spatia...

Descripción completa

Detalles Bibliográficos
Autores principales: Uitermarkt, Brandt D., Bruss, Joel, Hwang, Kai, Boes, Aaron D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469766/
https://www.ncbi.nlm.nih.gov/pubmed/32573885
http://dx.doi.org/10.1002/hbm.25102
_version_ 1783578460623470592
author Uitermarkt, Brandt D.
Bruss, Joel
Hwang, Kai
Boes, Aaron D.
author_facet Uitermarkt, Brandt D.
Bruss, Joel
Hwang, Kai
Boes, Aaron D.
author_sort Uitermarkt, Brandt D.
collection PubMed
description Rapid eye movement (REM) sleep is a paradoxical state where the individual appears asleep while the electroencephalogram pattern resembles that of wakefulness. Regional differences in brain metabolism have been observed during REM sleep compared to wakefulness, but it is not known whether the spatial distribution of metabolic differences corresponds to known functional networks in the brain. Here, we use a combination of techniques to evaluate the networks associated with sites of REM sleep activation and deactivation from previously published positron emission tomography studies. We use seed‐based functional connectivity from healthy adults acquired during quiet rest to show that REM‐activation regions are functionally connected in a network that includes retrosplenial cingulate cortex, parahippocampal gyrus, and extrastriate visual cortices, corresponding to components of the default mode network and visual networks. Regions deactivated during REM sleep localize to right‐lateralized fronto‐parietal and salience networks. A negatively correlated relationship was observed between REM‐activation and deactivation networks. Together, these findings show that regional activation and deactivation patterns of REM sleep tend to occur in distinct functional connectivity networks that are present during wakefulness, providing insights regarding the differential contributions of brain regions to the distinct subjective experiences that occur during REM sleep (dreaming) relative to wakefulness.
format Online
Article
Text
id pubmed-7469766
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-74697662020-09-09 Rapid eye movement sleep patterns of brain activation and deactivation occur within unique functional networks Uitermarkt, Brandt D. Bruss, Joel Hwang, Kai Boes, Aaron D. Hum Brain Mapp Research Articles Rapid eye movement (REM) sleep is a paradoxical state where the individual appears asleep while the electroencephalogram pattern resembles that of wakefulness. Regional differences in brain metabolism have been observed during REM sleep compared to wakefulness, but it is not known whether the spatial distribution of metabolic differences corresponds to known functional networks in the brain. Here, we use a combination of techniques to evaluate the networks associated with sites of REM sleep activation and deactivation from previously published positron emission tomography studies. We use seed‐based functional connectivity from healthy adults acquired during quiet rest to show that REM‐activation regions are functionally connected in a network that includes retrosplenial cingulate cortex, parahippocampal gyrus, and extrastriate visual cortices, corresponding to components of the default mode network and visual networks. Regions deactivated during REM sleep localize to right‐lateralized fronto‐parietal and salience networks. A negatively correlated relationship was observed between REM‐activation and deactivation networks. Together, these findings show that regional activation and deactivation patterns of REM sleep tend to occur in distinct functional connectivity networks that are present during wakefulness, providing insights regarding the differential contributions of brain regions to the distinct subjective experiences that occur during REM sleep (dreaming) relative to wakefulness. John Wiley & Sons, Inc. 2020-06-23 /pmc/articles/PMC7469766/ /pubmed/32573885 http://dx.doi.org/10.1002/hbm.25102 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Uitermarkt, Brandt D.
Bruss, Joel
Hwang, Kai
Boes, Aaron D.
Rapid eye movement sleep patterns of brain activation and deactivation occur within unique functional networks
title Rapid eye movement sleep patterns of brain activation and deactivation occur within unique functional networks
title_full Rapid eye movement sleep patterns of brain activation and deactivation occur within unique functional networks
title_fullStr Rapid eye movement sleep patterns of brain activation and deactivation occur within unique functional networks
title_full_unstemmed Rapid eye movement sleep patterns of brain activation and deactivation occur within unique functional networks
title_short Rapid eye movement sleep patterns of brain activation and deactivation occur within unique functional networks
title_sort rapid eye movement sleep patterns of brain activation and deactivation occur within unique functional networks
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469766/
https://www.ncbi.nlm.nih.gov/pubmed/32573885
http://dx.doi.org/10.1002/hbm.25102
work_keys_str_mv AT uitermarktbrandtd rapideyemovementsleeppatternsofbrainactivationanddeactivationoccurwithinuniquefunctionalnetworks
AT brussjoel rapideyemovementsleeppatternsofbrainactivationanddeactivationoccurwithinuniquefunctionalnetworks
AT hwangkai rapideyemovementsleeppatternsofbrainactivationanddeactivationoccurwithinuniquefunctionalnetworks
AT boesaarond rapideyemovementsleeppatternsofbrainactivationanddeactivationoccurwithinuniquefunctionalnetworks