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The Fate of Incoming Stimuli during NREM Sleep is Determined by Spindles and the Phase of the Slow Oscillation

The present study aimed at identifying the neurophysiological responses associated with auditory stimulation during non-rapid eye movement (NREM) sleep using simultaneous electroencephalography (EEG)/functional magnetic resonance imaging (fMRI) recordings. It was reported earlier that auditory stimu...

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Autores principales: Schabus, Manuel, Dang-Vu, Thien Thanh, Heib, Dominik Philip Johannes, Boly, Mélanie, Desseilles, Martin, Vandewalle, Gilles, Schmidt, Christina, Albouy, Geneviève, Darsaud, Annabelle, Gais, Steffen, Degueldre, Christian, Balteau, Evelyne, Phillips, Christophe, Luxen, André, Maquet, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319907/
https://www.ncbi.nlm.nih.gov/pubmed/22493589
http://dx.doi.org/10.3389/fneur.2012.00040
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author Schabus, Manuel
Dang-Vu, Thien Thanh
Heib, Dominik Philip Johannes
Boly, Mélanie
Desseilles, Martin
Vandewalle, Gilles
Schmidt, Christina
Albouy, Geneviève
Darsaud, Annabelle
Gais, Steffen
Degueldre, Christian
Balteau, Evelyne
Phillips, Christophe
Luxen, André
Maquet, Pierre
author_facet Schabus, Manuel
Dang-Vu, Thien Thanh
Heib, Dominik Philip Johannes
Boly, Mélanie
Desseilles, Martin
Vandewalle, Gilles
Schmidt, Christina
Albouy, Geneviève
Darsaud, Annabelle
Gais, Steffen
Degueldre, Christian
Balteau, Evelyne
Phillips, Christophe
Luxen, André
Maquet, Pierre
author_sort Schabus, Manuel
collection PubMed
description The present study aimed at identifying the neurophysiological responses associated with auditory stimulation during non-rapid eye movement (NREM) sleep using simultaneous electroencephalography (EEG)/functional magnetic resonance imaging (fMRI) recordings. It was reported earlier that auditory stimuli produce bilateral activation in auditory cortex, thalamus, and caudate during both wakefulness and NREM sleep. However, due to the spontaneous membrane potential fluctuations cortical responses may be highly variable during NREM. Here we now examine the modulation of cerebral responses to tones depending on the presence or absence of sleep spindles and the phase of the slow oscillation. Thirteen healthy young subjects were scanned successfully during stage 2–4 NREM sleep in the first half of the night in a 3 T scanner. Subjects were not sleep-deprived and sounds were post hoc classified according to (i) the presence of sleep spindles or (ii) the phase of the slow oscillation during (±300 ms) tone delivery. These detected sounds were then entered as regressors of interest in fMRI analyses. Interestingly wake-like responses – although somewhat altered in size and location – persisted during NREM sleep, except during present spindles (as previously published in Dang-Vu et al., 2011) and the negative going phase of the slow oscillation during which responses became less consistent or even absent. While the phase of the slow oscillation did not alter brain responses in primary sensory cortex, it did modulate responses at higher cortical levels. In addition EEG analyses show a distinct N550 response to tones during the presence of light sleep spindles and suggest that in deep NREM sleep the brain is more responsive during the positive going slope of the slow oscillation. The presence of short temporal windows during which the brain is open to external stimuli is consistent with the fact that even during deep sleep meaningful events can be detected. Altogether, our results emphasize the notion that spontaneous fluctuations of brain activity profoundly modify brain responses to external information across all behavioral states, including deep NREM sleep.
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spelling pubmed-33199072012-04-10 The Fate of Incoming Stimuli during NREM Sleep is Determined by Spindles and the Phase of the Slow Oscillation Schabus, Manuel Dang-Vu, Thien Thanh Heib, Dominik Philip Johannes Boly, Mélanie Desseilles, Martin Vandewalle, Gilles Schmidt, Christina Albouy, Geneviève Darsaud, Annabelle Gais, Steffen Degueldre, Christian Balteau, Evelyne Phillips, Christophe Luxen, André Maquet, Pierre Front Neurol Neuroscience The present study aimed at identifying the neurophysiological responses associated with auditory stimulation during non-rapid eye movement (NREM) sleep using simultaneous electroencephalography (EEG)/functional magnetic resonance imaging (fMRI) recordings. It was reported earlier that auditory stimuli produce bilateral activation in auditory cortex, thalamus, and caudate during both wakefulness and NREM sleep. However, due to the spontaneous membrane potential fluctuations cortical responses may be highly variable during NREM. Here we now examine the modulation of cerebral responses to tones depending on the presence or absence of sleep spindles and the phase of the slow oscillation. Thirteen healthy young subjects were scanned successfully during stage 2–4 NREM sleep in the first half of the night in a 3 T scanner. Subjects were not sleep-deprived and sounds were post hoc classified according to (i) the presence of sleep spindles or (ii) the phase of the slow oscillation during (±300 ms) tone delivery. These detected sounds were then entered as regressors of interest in fMRI analyses. Interestingly wake-like responses – although somewhat altered in size and location – persisted during NREM sleep, except during present spindles (as previously published in Dang-Vu et al., 2011) and the negative going phase of the slow oscillation during which responses became less consistent or even absent. While the phase of the slow oscillation did not alter brain responses in primary sensory cortex, it did modulate responses at higher cortical levels. In addition EEG analyses show a distinct N550 response to tones during the presence of light sleep spindles and suggest that in deep NREM sleep the brain is more responsive during the positive going slope of the slow oscillation. The presence of short temporal windows during which the brain is open to external stimuli is consistent with the fact that even during deep sleep meaningful events can be detected. Altogether, our results emphasize the notion that spontaneous fluctuations of brain activity profoundly modify brain responses to external information across all behavioral states, including deep NREM sleep. Frontiers Research Foundation 2012-04-05 /pmc/articles/PMC3319907/ /pubmed/22493589 http://dx.doi.org/10.3389/fneur.2012.00040 Text en Copyright © 2012 Schabus, Dang-Vu, Heib, Boly, Desseilles, Vandewalle, Schmidt, Albouy, Darsaud, Gais, Degueldre, Balteau, Phillips, Luxen and Maquet. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Neuroscience
Schabus, Manuel
Dang-Vu, Thien Thanh
Heib, Dominik Philip Johannes
Boly, Mélanie
Desseilles, Martin
Vandewalle, Gilles
Schmidt, Christina
Albouy, Geneviève
Darsaud, Annabelle
Gais, Steffen
Degueldre, Christian
Balteau, Evelyne
Phillips, Christophe
Luxen, André
Maquet, Pierre
The Fate of Incoming Stimuli during NREM Sleep is Determined by Spindles and the Phase of the Slow Oscillation
title The Fate of Incoming Stimuli during NREM Sleep is Determined by Spindles and the Phase of the Slow Oscillation
title_full The Fate of Incoming Stimuli during NREM Sleep is Determined by Spindles and the Phase of the Slow Oscillation
title_fullStr The Fate of Incoming Stimuli during NREM Sleep is Determined by Spindles and the Phase of the Slow Oscillation
title_full_unstemmed The Fate of Incoming Stimuli during NREM Sleep is Determined by Spindles and the Phase of the Slow Oscillation
title_short The Fate of Incoming Stimuli during NREM Sleep is Determined by Spindles and the Phase of the Slow Oscillation
title_sort fate of incoming stimuli during nrem sleep is determined by spindles and the phase of the slow oscillation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319907/
https://www.ncbi.nlm.nih.gov/pubmed/22493589
http://dx.doi.org/10.3389/fneur.2012.00040
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