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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...

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Autores principales: Sprenger, Andreas, Weber, Frederik D., Machner, Bjoern, Talamo, Silke, Scheffelmeier, Sabine, Bethke, Judith, Helmchen, Christoph, Gais, Steffen, Kimmig, Hubert, Born, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
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.
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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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