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Deprivation and Recovery of Sleep in Succession Enhances Reflexive Motor Behavior
Sleep deprivation impairs inhibitory control over reflexive behavior, and this impairment is commonly assumed to dissipate after recovery sleep. Contrary to this belief, here we show that fast reflexive behaviors, when practiced during sleep deprivation, is consolidated across recovery sleep and, th...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816803/ https://www.ncbi.nlm.nih.gov/pubmed/26048955 http://dx.doi.org/10.1093/cercor/bhv115 |
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author | Sprenger, Andreas Weber, Frederik D. Machner, Bjoern Talamo, Silke Scheffelmeier, Sabine Bethke, Judith Helmchen, Christoph Gais, Steffen Kimmig, Hubert Born, Jan |
author_facet | Sprenger, Andreas Weber, Frederik D. Machner, Bjoern Talamo, Silke Scheffelmeier, Sabine Bethke, Judith Helmchen, Christoph Gais, Steffen Kimmig, Hubert Born, Jan |
author_sort | Sprenger, Andreas |
collection | PubMed |
description | Sleep deprivation impairs inhibitory control over reflexive behavior, and this impairment is commonly assumed to dissipate after recovery sleep. Contrary to this belief, here we show that fast reflexive behaviors, when practiced during sleep deprivation, is consolidated across recovery sleep and, thereby, becomes preserved. As a model for the study of sleep effects on prefrontal cortex-mediated inhibitory control in humans, we examined reflexive saccadic eye movements (express saccades), as well as speeded 2-choice finger motor responses. Different groups of subjects were trained on a standard prosaccade gap paradigm before periods of nocturnal sleep and sleep deprivation. Saccade performance was retested in the next morning and again 24 h later. The rate of express saccades was not affected by sleep after training, but slightly increased after sleep deprivation. Surprisingly, this increase augmented even further after recovery sleep and was still present 4 weeks later. Additional experiments revealed that the short testing after sleep deprivation was sufficient to increase express saccades across recovery sleep. An increase in speeded responses across recovery sleep was likewise found for finger motor responses. Our findings indicate that recovery sleep can consolidate motor disinhibition for behaviors practiced during prior sleep deprivation, thereby persistently enhancing response automatization. |
format | Online Article Text |
id | pubmed-4816803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48168032016-04-04 Deprivation and Recovery of Sleep in Succession Enhances Reflexive Motor Behavior Sprenger, Andreas Weber, Frederik D. Machner, Bjoern Talamo, Silke Scheffelmeier, Sabine Bethke, Judith Helmchen, Christoph Gais, Steffen Kimmig, Hubert Born, Jan Cereb Cortex Articles Sleep deprivation impairs inhibitory control over reflexive behavior, and this impairment is commonly assumed to dissipate after recovery sleep. Contrary to this belief, here we show that fast reflexive behaviors, when practiced during sleep deprivation, is consolidated across recovery sleep and, thereby, becomes preserved. As a model for the study of sleep effects on prefrontal cortex-mediated inhibitory control in humans, we examined reflexive saccadic eye movements (express saccades), as well as speeded 2-choice finger motor responses. Different groups of subjects were trained on a standard prosaccade gap paradigm before periods of nocturnal sleep and sleep deprivation. Saccade performance was retested in the next morning and again 24 h later. The rate of express saccades was not affected by sleep after training, but slightly increased after sleep deprivation. Surprisingly, this increase augmented even further after recovery sleep and was still present 4 weeks later. Additional experiments revealed that the short testing after sleep deprivation was sufficient to increase express saccades across recovery sleep. An increase in speeded responses across recovery sleep was likewise found for finger motor responses. Our findings indicate that recovery sleep can consolidate motor disinhibition for behaviors practiced during prior sleep deprivation, thereby persistently enhancing response automatization. Oxford University Press 2015-11 2015-06-05 /pmc/articles/PMC4816803/ /pubmed/26048955 http://dx.doi.org/10.1093/cercor/bhv115 Text en © The Author 2015. Published by Oxford University Press http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Articles Sprenger, Andreas Weber, Frederik D. Machner, Bjoern Talamo, Silke Scheffelmeier, Sabine Bethke, Judith Helmchen, Christoph Gais, Steffen Kimmig, Hubert Born, Jan Deprivation and Recovery of Sleep in Succession Enhances Reflexive Motor Behavior |
title | Deprivation and Recovery of Sleep in Succession Enhances Reflexive Motor Behavior |
title_full | Deprivation and Recovery of Sleep in Succession Enhances Reflexive Motor Behavior |
title_fullStr | Deprivation and Recovery of Sleep in Succession Enhances Reflexive Motor Behavior |
title_full_unstemmed | Deprivation and Recovery of Sleep in Succession Enhances Reflexive Motor Behavior |
title_short | Deprivation and Recovery of Sleep in Succession Enhances Reflexive Motor Behavior |
title_sort | deprivation and recovery of sleep in succession enhances reflexive motor behavior |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816803/ https://www.ncbi.nlm.nih.gov/pubmed/26048955 http://dx.doi.org/10.1093/cercor/bhv115 |
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