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Progression to deep sleep is characterized by changes to BOLD dynamics in sensory cortices

Sleep has been shown to subtly disrupt the spatial organization of functional connectivity networks in the brain, but in a way that largely preserves the connectivity within sensory cortices. Here we evaluated the hypothesis that sleep does impact sensory cortices, but through alteration of activity...

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Detalles Bibliográficos
Autores principales: Davis, Ben, Tagliazucchi, Enzo, Jovicich, Jorge, Laufs, Helmut, Hasson, Uri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819724/
https://www.ncbi.nlm.nih.gov/pubmed/26724779
http://dx.doi.org/10.1016/j.neuroimage.2015.12.034
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author Davis, Ben
Tagliazucchi, Enzo
Jovicich, Jorge
Laufs, Helmut
Hasson, Uri
author_facet Davis, Ben
Tagliazucchi, Enzo
Jovicich, Jorge
Laufs, Helmut
Hasson, Uri
author_sort Davis, Ben
collection PubMed
description Sleep has been shown to subtly disrupt the spatial organization of functional connectivity networks in the brain, but in a way that largely preserves the connectivity within sensory cortices. Here we evaluated the hypothesis that sleep does impact sensory cortices, but through alteration of activity dynamics. We therefore examined the impact of sleep on hemodynamics using a method for quantifying non-random, high frequency signatures of the blood-oxygen-level dependent (BOLD) signal (amplitude variance asymmetry; AVA). We found that sleep was associated with the elimination of these dynamics in a manner that is restricted to auditory, motor and visual cortices. This elimination was concurrent with increased variance of activity in these regions. Functional connectivity between regions showing AVA during wakefulness maintained a relatively consistent hierarchical structure during wakefulness and N1 and N2 sleep, despite a gradual reduction of connectivity strength as sleep progressed. Thus, sleep is related to elimination of high frequency non-random activity signatures in sensory cortices that are robust during wakefulness. The elimination of these AVA signatures conjointly with preservation of the structure of functional connectivity patterns may be linked to the need to suppress sensory inputs during sleep while still maintaining the capacity to react quickly to complex multimodal inputs.
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spelling pubmed-48197242016-04-15 Progression to deep sleep is characterized by changes to BOLD dynamics in sensory cortices Davis, Ben Tagliazucchi, Enzo Jovicich, Jorge Laufs, Helmut Hasson, Uri Neuroimage Article Sleep has been shown to subtly disrupt the spatial organization of functional connectivity networks in the brain, but in a way that largely preserves the connectivity within sensory cortices. Here we evaluated the hypothesis that sleep does impact sensory cortices, but through alteration of activity dynamics. We therefore examined the impact of sleep on hemodynamics using a method for quantifying non-random, high frequency signatures of the blood-oxygen-level dependent (BOLD) signal (amplitude variance asymmetry; AVA). We found that sleep was associated with the elimination of these dynamics in a manner that is restricted to auditory, motor and visual cortices. This elimination was concurrent with increased variance of activity in these regions. Functional connectivity between regions showing AVA during wakefulness maintained a relatively consistent hierarchical structure during wakefulness and N1 and N2 sleep, despite a gradual reduction of connectivity strength as sleep progressed. Thus, sleep is related to elimination of high frequency non-random activity signatures in sensory cortices that are robust during wakefulness. The elimination of these AVA signatures conjointly with preservation of the structure of functional connectivity patterns may be linked to the need to suppress sensory inputs during sleep while still maintaining the capacity to react quickly to complex multimodal inputs. Academic Press 2016-04-15 /pmc/articles/PMC4819724/ /pubmed/26724779 http://dx.doi.org/10.1016/j.neuroimage.2015.12.034 Text en © 2015 The Authors 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
Davis, Ben
Tagliazucchi, Enzo
Jovicich, Jorge
Laufs, Helmut
Hasson, Uri
Progression to deep sleep is characterized by changes to BOLD dynamics in sensory cortices
title Progression to deep sleep is characterized by changes to BOLD dynamics in sensory cortices
title_full Progression to deep sleep is characterized by changes to BOLD dynamics in sensory cortices
title_fullStr Progression to deep sleep is characterized by changes to BOLD dynamics in sensory cortices
title_full_unstemmed Progression to deep sleep is characterized by changes to BOLD dynamics in sensory cortices
title_short Progression to deep sleep is characterized by changes to BOLD dynamics in sensory cortices
title_sort progression to deep sleep is characterized by changes to bold dynamics in sensory cortices
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819724/
https://www.ncbi.nlm.nih.gov/pubmed/26724779
http://dx.doi.org/10.1016/j.neuroimage.2015.12.034
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