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Propagated infra-slow intrinsic brain activity reorganizes across wake and slow wave sleep
Propagation of slow intrinsic brain activity has been widely observed in electrophysiogical studies of slow wave sleep (SWS). However, in human resting state fMRI (rs-fMRI), intrinsic activity has been understood predominantly in terms of zero-lag temporal synchrony (functional connectivity) within...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737658/ https://www.ncbi.nlm.nih.gov/pubmed/26551562 http://dx.doi.org/10.7554/eLife.10781 |
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author | Mitra, Anish Snyder, Abraham Z Tagliazucchi, Enzo Laufs, Helmut Raichle, Marcus E |
author_facet | Mitra, Anish Snyder, Abraham Z Tagliazucchi, Enzo Laufs, Helmut Raichle, Marcus E |
author_sort | Mitra, Anish |
collection | PubMed |
description | Propagation of slow intrinsic brain activity has been widely observed in electrophysiogical studies of slow wave sleep (SWS). However, in human resting state fMRI (rs-fMRI), intrinsic activity has been understood predominantly in terms of zero-lag temporal synchrony (functional connectivity) within systems known as resting state networks (RSNs). Prior rs-fMRI studies have found that RSNs are generally preserved across wake and sleep. Here, we use a recently developed analysis technique to study propagation of infra-slow intrinsic blood oxygen level dependent (BOLD) signals in normal adults during wake and SWS. This analysis reveals marked changes in propagation patterns in SWS vs. wake. Broadly, ordered propagation is preserved within traditionally defined RSNs but lost between RSNs. Additionally, propagation between cerebral cortex and subcortical structures reverses directions, and intra-cortical propagation becomes reorganized, especially in visual and sensorimotor cortices. These findings show that propagated rs-fMRI activity informs theoretical accounts of the neural functions of sleep. DOI: http://dx.doi.org/10.7554/eLife.10781.001 |
format | Online Article Text |
id | pubmed-4737658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47376582016-02-04 Propagated infra-slow intrinsic brain activity reorganizes across wake and slow wave sleep Mitra, Anish Snyder, Abraham Z Tagliazucchi, Enzo Laufs, Helmut Raichle, Marcus E eLife Human Biology and Medicine Propagation of slow intrinsic brain activity has been widely observed in electrophysiogical studies of slow wave sleep (SWS). However, in human resting state fMRI (rs-fMRI), intrinsic activity has been understood predominantly in terms of zero-lag temporal synchrony (functional connectivity) within systems known as resting state networks (RSNs). Prior rs-fMRI studies have found that RSNs are generally preserved across wake and sleep. Here, we use a recently developed analysis technique to study propagation of infra-slow intrinsic blood oxygen level dependent (BOLD) signals in normal adults during wake and SWS. This analysis reveals marked changes in propagation patterns in SWS vs. wake. Broadly, ordered propagation is preserved within traditionally defined RSNs but lost between RSNs. Additionally, propagation between cerebral cortex and subcortical structures reverses directions, and intra-cortical propagation becomes reorganized, especially in visual and sensorimotor cortices. These findings show that propagated rs-fMRI activity informs theoretical accounts of the neural functions of sleep. DOI: http://dx.doi.org/10.7554/eLife.10781.001 eLife Sciences Publications, Ltd 2015-11-09 /pmc/articles/PMC4737658/ /pubmed/26551562 http://dx.doi.org/10.7554/eLife.10781 Text en © 2015, Mitra et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Human Biology and Medicine Mitra, Anish Snyder, Abraham Z Tagliazucchi, Enzo Laufs, Helmut Raichle, Marcus E Propagated infra-slow intrinsic brain activity reorganizes across wake and slow wave sleep |
title | Propagated infra-slow intrinsic brain activity reorganizes across wake and slow wave sleep |
title_full | Propagated infra-slow intrinsic brain activity reorganizes across wake and slow wave sleep |
title_fullStr | Propagated infra-slow intrinsic brain activity reorganizes across wake and slow wave sleep |
title_full_unstemmed | Propagated infra-slow intrinsic brain activity reorganizes across wake and slow wave sleep |
title_short | Propagated infra-slow intrinsic brain activity reorganizes across wake and slow wave sleep |
title_sort | propagated infra-slow intrinsic brain activity reorganizes across wake and slow wave sleep |
topic | Human Biology and Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737658/ https://www.ncbi.nlm.nih.gov/pubmed/26551562 http://dx.doi.org/10.7554/eLife.10781 |
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