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Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations
The two-process model of sleep-wake regulation posits that sleep-wake-dependent homeostatic processes interact with the circadian timing system to affect human behavior. The circadian timing system is fundamental to maintaining stable cognitive performance, as it counteracts growing homeostatic slee...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514145/ https://www.ncbi.nlm.nih.gov/pubmed/28717201 http://dx.doi.org/10.1038/s41598-017-05695-1 |
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author | Reichert, Carolin F. Maire, Micheline Gabel, Virginie Viola, Antoine U. Götz, Thomas Scheffler, Klaus Klarhöfer, Markus Berthomier, Christian Strobel, Werner Phillips, Christophe Salmon, Eric Cajochen, Christian Schmidt, Christina |
author_facet | Reichert, Carolin F. Maire, Micheline Gabel, Virginie Viola, Antoine U. Götz, Thomas Scheffler, Klaus Klarhöfer, Markus Berthomier, Christian Strobel, Werner Phillips, Christophe Salmon, Eric Cajochen, Christian Schmidt, Christina |
author_sort | Reichert, Carolin F. |
collection | PubMed |
description | The two-process model of sleep-wake regulation posits that sleep-wake-dependent homeostatic processes interact with the circadian timing system to affect human behavior. The circadian timing system is fundamental to maintaining stable cognitive performance, as it counteracts growing homeostatic sleep pressure during daytime. Using magnetic resonance imaging, we explored brain responses underlying working memory performance during the time of maximal circadian wake-promotion under varying sleep pressure conditions. Circadian wake-promoting strength was derived from the ability to sleep during an evening nap. Hypothalamic BOLD activity was positively linked to circadian wake-promoting strength under normal, but not under disproportionally high or low sleep pressure levels. Furthermore, higher hypothalamic activity under normal sleep pressure levels predicted better performance under sleep loss. Our results reappraise the two-process model by revealing a homeostatic-dose-dependent association between circadian wake-promotion and cognition-related hypothalamic activity. |
format | Online Article Text |
id | pubmed-5514145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55141452017-07-19 Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations Reichert, Carolin F. Maire, Micheline Gabel, Virginie Viola, Antoine U. Götz, Thomas Scheffler, Klaus Klarhöfer, Markus Berthomier, Christian Strobel, Werner Phillips, Christophe Salmon, Eric Cajochen, Christian Schmidt, Christina Sci Rep Article The two-process model of sleep-wake regulation posits that sleep-wake-dependent homeostatic processes interact with the circadian timing system to affect human behavior. The circadian timing system is fundamental to maintaining stable cognitive performance, as it counteracts growing homeostatic sleep pressure during daytime. Using magnetic resonance imaging, we explored brain responses underlying working memory performance during the time of maximal circadian wake-promotion under varying sleep pressure conditions. Circadian wake-promoting strength was derived from the ability to sleep during an evening nap. Hypothalamic BOLD activity was positively linked to circadian wake-promoting strength under normal, but not under disproportionally high or low sleep pressure levels. Furthermore, higher hypothalamic activity under normal sleep pressure levels predicted better performance under sleep loss. Our results reappraise the two-process model by revealing a homeostatic-dose-dependent association between circadian wake-promotion and cognition-related hypothalamic activity. Nature Publishing Group UK 2017-07-17 /pmc/articles/PMC5514145/ /pubmed/28717201 http://dx.doi.org/10.1038/s41598-017-05695-1 Text en © The Author(s) 2017 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 Reichert, Carolin F. Maire, Micheline Gabel, Virginie Viola, Antoine U. Götz, Thomas Scheffler, Klaus Klarhöfer, Markus Berthomier, Christian Strobel, Werner Phillips, Christophe Salmon, Eric Cajochen, Christian Schmidt, Christina Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations |
title | Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations |
title_full | Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations |
title_fullStr | Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations |
title_full_unstemmed | Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations |
title_short | Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations |
title_sort | cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514145/ https://www.ncbi.nlm.nih.gov/pubmed/28717201 http://dx.doi.org/10.1038/s41598-017-05695-1 |
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