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The alerting effect of the wake maintenance zone during 40 hours of sleep deprivation

Under entrained conditions, the accumulation of homeostatic sleep pressure in the evening is opposed by a strong circadian arousal signal prior to the dim light melatonin onset, called the Wake Maintenance Zone (WMZ). This study aimed at investigating the impact of the WMZ on different cognitive per...

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Autores principales: Zeeuw, Jan de, Wisniewski, Sophia, Papakonstantinou, Alexandra, Bes, Frederik, Wahnschaffe, Amely, Zaleska, Mandy, Kunz, Dieter, Münch, Mirjam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054682/
https://www.ncbi.nlm.nih.gov/pubmed/30030487
http://dx.doi.org/10.1038/s41598-018-29380-z
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author Zeeuw, Jan de
Wisniewski, Sophia
Papakonstantinou, Alexandra
Bes, Frederik
Wahnschaffe, Amely
Zaleska, Mandy
Kunz, Dieter
Münch, Mirjam
author_facet Zeeuw, Jan de
Wisniewski, Sophia
Papakonstantinou, Alexandra
Bes, Frederik
Wahnschaffe, Amely
Zaleska, Mandy
Kunz, Dieter
Münch, Mirjam
author_sort Zeeuw, Jan de
collection PubMed
description Under entrained conditions, the accumulation of homeostatic sleep pressure in the evening is opposed by a strong circadian arousal signal prior to the dim light melatonin onset, called the Wake Maintenance Zone (WMZ). This study aimed at investigating the impact of the WMZ on different cognitive performance tests, as well as on subjective and objective sleepiness. Twelve young male participants completed a constant routine protocol with 40 h of extended wakefulness that included two WMZs. Cognitive tests and saliva samples were assessed hourly, while the electroencephalogram (EEG) was recorded continuously. Participants improved in cognitive response inhibition during WMZ1 (13.5 h awake) and sustained attention during WMZ2 (37.5 h awake), but not in higher executive function tests. There were significant EEG power density reductions in the delta/theta frequency range during WMZ1 and in delta/theta, alpha, and sigma/beta ranges during WMZ2, with a greater change in the sigma/beta range during WMZ2 compared to WMZ1. EEG power reductions coincided during WMZ1 with stable subjective sleepiness and sustained attention. During WMZ2, EEG power reductions were more pronounced and coincided with improved sustained attention. Our results suggest the circadian arousal signal in the evening differently modulates cognitive functions and EEG power depending on the duration of prior wakefulness.
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spelling pubmed-60546822018-07-23 The alerting effect of the wake maintenance zone during 40 hours of sleep deprivation Zeeuw, Jan de Wisniewski, Sophia Papakonstantinou, Alexandra Bes, Frederik Wahnschaffe, Amely Zaleska, Mandy Kunz, Dieter Münch, Mirjam Sci Rep Article Under entrained conditions, the accumulation of homeostatic sleep pressure in the evening is opposed by a strong circadian arousal signal prior to the dim light melatonin onset, called the Wake Maintenance Zone (WMZ). This study aimed at investigating the impact of the WMZ on different cognitive performance tests, as well as on subjective and objective sleepiness. Twelve young male participants completed a constant routine protocol with 40 h of extended wakefulness that included two WMZs. Cognitive tests and saliva samples were assessed hourly, while the electroencephalogram (EEG) was recorded continuously. Participants improved in cognitive response inhibition during WMZ1 (13.5 h awake) and sustained attention during WMZ2 (37.5 h awake), but not in higher executive function tests. There were significant EEG power density reductions in the delta/theta frequency range during WMZ1 and in delta/theta, alpha, and sigma/beta ranges during WMZ2, with a greater change in the sigma/beta range during WMZ2 compared to WMZ1. EEG power reductions coincided during WMZ1 with stable subjective sleepiness and sustained attention. During WMZ2, EEG power reductions were more pronounced and coincided with improved sustained attention. Our results suggest the circadian arousal signal in the evening differently modulates cognitive functions and EEG power depending on the duration of prior wakefulness. Nature Publishing Group UK 2018-07-20 /pmc/articles/PMC6054682/ /pubmed/30030487 http://dx.doi.org/10.1038/s41598-018-29380-z 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
Zeeuw, Jan de
Wisniewski, Sophia
Papakonstantinou, Alexandra
Bes, Frederik
Wahnschaffe, Amely
Zaleska, Mandy
Kunz, Dieter
Münch, Mirjam
The alerting effect of the wake maintenance zone during 40 hours of sleep deprivation
title The alerting effect of the wake maintenance zone during 40 hours of sleep deprivation
title_full The alerting effect of the wake maintenance zone during 40 hours of sleep deprivation
title_fullStr The alerting effect of the wake maintenance zone during 40 hours of sleep deprivation
title_full_unstemmed The alerting effect of the wake maintenance zone during 40 hours of sleep deprivation
title_short The alerting effect of the wake maintenance zone during 40 hours of sleep deprivation
title_sort alerting effect of the wake maintenance zone during 40 hours of sleep deprivation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054682/
https://www.ncbi.nlm.nih.gov/pubmed/30030487
http://dx.doi.org/10.1038/s41598-018-29380-z
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