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Human brain patterns underlying vigilant attention: impact of sleep debt, circadian phase and attentional engagement

Sleepiness and cognitive function vary over the 24-h day due to circadian and sleep-wake-dependent mechanisms. However, the underlying cerebral hallmarks associated with these variations remain to be fully established. Using functional magnetic resonance imaging (fMRI), we investigated brain respons...

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Autores principales: Maire, Micheline, Reichert, Carolin F., Gabel, Virginie, Viola, Antoine U., Phillips, Christophe, Berthomier, Christian, Borgwardt, Stefan, Cajochen, Christian, Schmidt, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772468/
https://www.ncbi.nlm.nih.gov/pubmed/29343686
http://dx.doi.org/10.1038/s41598-017-17022-9
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author Maire, Micheline
Reichert, Carolin F.
Gabel, Virginie
Viola, Antoine U.
Phillips, Christophe
Berthomier, Christian
Borgwardt, Stefan
Cajochen, Christian
Schmidt, Christina
author_facet Maire, Micheline
Reichert, Carolin F.
Gabel, Virginie
Viola, Antoine U.
Phillips, Christophe
Berthomier, Christian
Borgwardt, Stefan
Cajochen, Christian
Schmidt, Christina
author_sort Maire, Micheline
collection PubMed
description Sleepiness and cognitive function vary over the 24-h day due to circadian and sleep-wake-dependent mechanisms. However, the underlying cerebral hallmarks associated with these variations remain to be fully established. Using functional magnetic resonance imaging (fMRI), we investigated brain responses associated with circadian and homeostatic sleep-wake-driven dynamics of subjective sleepiness throughout day and night. Healthy volunteers regularly performed a psychomotor vigilance task (PVT) in the MR-scanner during a 40-h sleep deprivation (high sleep pressure) and a 40-h multiple nap protocol (low sleep pressure). When sleep deprived, arousal-promoting thalamic activation during optimal PVT performance paralleled the time course of subjective sleepiness with peaks at night and troughs on the subsequent day. Conversely, task-related cortical activation decreased when sleepiness increased as a consequence of higher sleep debt. Under low sleep pressure, we did not observe any significant temporal association between PVT-related brain activation and subjective sleepiness. Thus, a circadian modulation in brain correlates of vigilant attention was only detectable under high sleep pressure conditions. Our data indicate that circadian and sleep homeostatic processes impact on vigilant attention via specific mechanisms; mirrored in a decline of cortical resources under high sleep pressure, opposed by a subcortical “rescuing” at adverse circadian times.
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spelling pubmed-57724682018-01-26 Human brain patterns underlying vigilant attention: impact of sleep debt, circadian phase and attentional engagement Maire, Micheline Reichert, Carolin F. Gabel, Virginie Viola, Antoine U. Phillips, Christophe Berthomier, Christian Borgwardt, Stefan Cajochen, Christian Schmidt, Christina Sci Rep Article Sleepiness and cognitive function vary over the 24-h day due to circadian and sleep-wake-dependent mechanisms. However, the underlying cerebral hallmarks associated with these variations remain to be fully established. Using functional magnetic resonance imaging (fMRI), we investigated brain responses associated with circadian and homeostatic sleep-wake-driven dynamics of subjective sleepiness throughout day and night. Healthy volunteers regularly performed a psychomotor vigilance task (PVT) in the MR-scanner during a 40-h sleep deprivation (high sleep pressure) and a 40-h multiple nap protocol (low sleep pressure). When sleep deprived, arousal-promoting thalamic activation during optimal PVT performance paralleled the time course of subjective sleepiness with peaks at night and troughs on the subsequent day. Conversely, task-related cortical activation decreased when sleepiness increased as a consequence of higher sleep debt. Under low sleep pressure, we did not observe any significant temporal association between PVT-related brain activation and subjective sleepiness. Thus, a circadian modulation in brain correlates of vigilant attention was only detectable under high sleep pressure conditions. Our data indicate that circadian and sleep homeostatic processes impact on vigilant attention via specific mechanisms; mirrored in a decline of cortical resources under high sleep pressure, opposed by a subcortical “rescuing” at adverse circadian times. Nature Publishing Group UK 2018-01-17 /pmc/articles/PMC5772468/ /pubmed/29343686 http://dx.doi.org/10.1038/s41598-017-17022-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Maire, Micheline
Reichert, Carolin F.
Gabel, Virginie
Viola, Antoine U.
Phillips, Christophe
Berthomier, Christian
Borgwardt, Stefan
Cajochen, Christian
Schmidt, Christina
Human brain patterns underlying vigilant attention: impact of sleep debt, circadian phase and attentional engagement
title Human brain patterns underlying vigilant attention: impact of sleep debt, circadian phase and attentional engagement
title_full Human brain patterns underlying vigilant attention: impact of sleep debt, circadian phase and attentional engagement
title_fullStr Human brain patterns underlying vigilant attention: impact of sleep debt, circadian phase and attentional engagement
title_full_unstemmed Human brain patterns underlying vigilant attention: impact of sleep debt, circadian phase and attentional engagement
title_short Human brain patterns underlying vigilant attention: impact of sleep debt, circadian phase and attentional engagement
title_sort human brain patterns underlying vigilant attention: impact of sleep debt, circadian phase and attentional engagement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772468/
https://www.ncbi.nlm.nih.gov/pubmed/29343686
http://dx.doi.org/10.1038/s41598-017-17022-9
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