Cargando…

fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep

System-specific brain responses—time-locked to rapid eye movements (REMs) in sleep—are characteristically widespread, with robust and clear activation in the primary visual cortex and other structures involved in multisensory integration. This pattern suggests that REMs underwrite hierarchical proce...

Descripción completa

Detalles Bibliográficos
Autores principales: Hong, Charles Chong-Hwa, Fallon, James H., Friston, Karl J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615877/
https://www.ncbi.nlm.nih.gov/pubmed/34827529
http://dx.doi.org/10.3390/brainsci11111528
_version_ 1784604211845005312
author Hong, Charles Chong-Hwa
Fallon, James H.
Friston, Karl J.
author_facet Hong, Charles Chong-Hwa
Fallon, James H.
Friston, Karl J.
author_sort Hong, Charles Chong-Hwa
collection PubMed
description System-specific brain responses—time-locked to rapid eye movements (REMs) in sleep—are characteristically widespread, with robust and clear activation in the primary visual cortex and other structures involved in multisensory integration. This pattern suggests that REMs underwrite hierarchical processing of visual information in a time-locked manner, where REMs index the generation and scanning of virtual-world models, through multisensory integration in dreaming—as in awake states. Default mode network (DMN) activity increases during rest and reduces during various tasks including visual perception. The implicit anticorrelation between the DMN and task-positive network (TPN)—that persists in REM sleep—prompted us to focus on DMN responses to temporally-precise REM events. We timed REMs during sleep from the video recordings and quantified the neural correlates of REMs—using functional MRI (fMRI)—in 24 independent studies of 11 healthy participants. A reanalysis of these data revealed that the cortical areas exempt from widespread REM-locked brain activation were restricted to the DMN. Furthermore, our analysis revealed a modest temporally-precise REM-locked decrease—phasic deactivation—in key DMN nodes, in a subset of independent studies. These results are consistent with hierarchical predictive coding; namely, permissive deactivation of DMN at the top of the hierarchy (leading to the widespread cortical activation at lower levels; especially the primary visual cortex). Additional findings indicate REM-locked cerebral vasodilation and suggest putative mechanisms for dream forgetting.
format Online
Article
Text
id pubmed-8615877
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-86158772021-11-26 fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep Hong, Charles Chong-Hwa Fallon, James H. Friston, Karl J. Brain Sci Article System-specific brain responses—time-locked to rapid eye movements (REMs) in sleep—are characteristically widespread, with robust and clear activation in the primary visual cortex and other structures involved in multisensory integration. This pattern suggests that REMs underwrite hierarchical processing of visual information in a time-locked manner, where REMs index the generation and scanning of virtual-world models, through multisensory integration in dreaming—as in awake states. Default mode network (DMN) activity increases during rest and reduces during various tasks including visual perception. The implicit anticorrelation between the DMN and task-positive network (TPN)—that persists in REM sleep—prompted us to focus on DMN responses to temporally-precise REM events. We timed REMs during sleep from the video recordings and quantified the neural correlates of REMs—using functional MRI (fMRI)—in 24 independent studies of 11 healthy participants. A reanalysis of these data revealed that the cortical areas exempt from widespread REM-locked brain activation were restricted to the DMN. Furthermore, our analysis revealed a modest temporally-precise REM-locked decrease—phasic deactivation—in key DMN nodes, in a subset of independent studies. These results are consistent with hierarchical predictive coding; namely, permissive deactivation of DMN at the top of the hierarchy (leading to the widespread cortical activation at lower levels; especially the primary visual cortex). Additional findings indicate REM-locked cerebral vasodilation and suggest putative mechanisms for dream forgetting. MDPI 2021-11-18 /pmc/articles/PMC8615877/ /pubmed/34827529 http://dx.doi.org/10.3390/brainsci11111528 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hong, Charles Chong-Hwa
Fallon, James H.
Friston, Karl J.
fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep
title fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep
title_full fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep
title_fullStr fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep
title_full_unstemmed fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep
title_short fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep
title_sort fmri evidence for default mode network deactivation associated with rapid eye movements in sleep
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615877/
https://www.ncbi.nlm.nih.gov/pubmed/34827529
http://dx.doi.org/10.3390/brainsci11111528
work_keys_str_mv AT hongcharleschonghwa fmrievidencefordefaultmodenetworkdeactivationassociatedwithrapideyemovementsinsleep
AT fallonjamesh fmrievidencefordefaultmodenetworkdeactivationassociatedwithrapideyemovementsinsleep
AT fristonkarlj fmrievidencefordefaultmodenetworkdeactivationassociatedwithrapideyemovementsinsleep