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The Effects of Anodal Transcranial Direct Current Stimulation on Sleep Time and Efficiency

A single session of anodal transcranial direct current stimulation (tDCS) has been shown to increase arousal in healthy participants for up to 24 h post-stimulation. However, little is known about the effects of tDCS on subsequent sleep in this population. Based on previous clinical studies, we hypo...

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Autores principales: McIntire, Lindsey K., McKinley, R. Andy, Goodyear, Chuck, McIntire, John P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481387/
https://www.ncbi.nlm.nih.gov/pubmed/33192380
http://dx.doi.org/10.3389/fnhum.2020.00357
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author McIntire, Lindsey K.
McKinley, R. Andy
Goodyear, Chuck
McIntire, John P.
author_facet McIntire, Lindsey K.
McKinley, R. Andy
Goodyear, Chuck
McIntire, John P.
author_sort McIntire, Lindsey K.
collection PubMed
description A single session of anodal transcranial direct current stimulation (tDCS) has been shown to increase arousal in healthy participants for up to 24 h post-stimulation. However, little is known about the effects of tDCS on subsequent sleep in this population. Based on previous clinical studies, we hypothesized that anodal stimulation to the left dorsolateral prefrontal cortex (lDLPFC) would produce higher arousal with decreased sleep time and stimulation to the primary motor cortex (M1) would have the converse effect. Thirty-six active duty military were randomized into one of three groups (n = 12/group); active anodal tDCS over the lDLPFC, active anodal tDCS over left M1, or sham tDCS. Participants answered questionnaires 3 times a day and wore a wrist activity monitor (WAM) to measure sleep time and efficiency for 3 weeks. On weeks 2 and 3 (order counterbalance), participants received stimulation at 1800 h before 26 h of sustained wakefulness testing (sleep deprived) and at 1800 h without sleep deprivation (non-sleep deprived). There were no significant effects for the non-sleep deprived portion of testing. For the sleep deprived portion of testing, there were main effects of group and night on sleep time. The DLPFC group slept less than the other groups on the second and third night following stimulation. There is no negative effect on mood or sleep quality from a single dose of tDCS when participants have normal sleep patterns (i.e., non-sleep deprived portion of testing). The results suggest that stimulation may result in faster recovery from fatigue caused by acute periods of sleep deprivation, as their recovery sleep periods were less.
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spelling pubmed-74813872020-11-12 The Effects of Anodal Transcranial Direct Current Stimulation on Sleep Time and Efficiency McIntire, Lindsey K. McKinley, R. Andy Goodyear, Chuck McIntire, John P. Front Hum Neurosci Neuroscience A single session of anodal transcranial direct current stimulation (tDCS) has been shown to increase arousal in healthy participants for up to 24 h post-stimulation. However, little is known about the effects of tDCS on subsequent sleep in this population. Based on previous clinical studies, we hypothesized that anodal stimulation to the left dorsolateral prefrontal cortex (lDLPFC) would produce higher arousal with decreased sleep time and stimulation to the primary motor cortex (M1) would have the converse effect. Thirty-six active duty military were randomized into one of three groups (n = 12/group); active anodal tDCS over the lDLPFC, active anodal tDCS over left M1, or sham tDCS. Participants answered questionnaires 3 times a day and wore a wrist activity monitor (WAM) to measure sleep time and efficiency for 3 weeks. On weeks 2 and 3 (order counterbalance), participants received stimulation at 1800 h before 26 h of sustained wakefulness testing (sleep deprived) and at 1800 h without sleep deprivation (non-sleep deprived). There were no significant effects for the non-sleep deprived portion of testing. For the sleep deprived portion of testing, there were main effects of group and night on sleep time. The DLPFC group slept less than the other groups on the second and third night following stimulation. There is no negative effect on mood or sleep quality from a single dose of tDCS when participants have normal sleep patterns (i.e., non-sleep deprived portion of testing). The results suggest that stimulation may result in faster recovery from fatigue caused by acute periods of sleep deprivation, as their recovery sleep periods were less. Frontiers Media S.A. 2020-08-27 /pmc/articles/PMC7481387/ /pubmed/33192380 http://dx.doi.org/10.3389/fnhum.2020.00357 Text en Copyright © 2020 McIntire, McKinley, Goodyear and McIntire. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
McIntire, Lindsey K.
McKinley, R. Andy
Goodyear, Chuck
McIntire, John P.
The Effects of Anodal Transcranial Direct Current Stimulation on Sleep Time and Efficiency
title The Effects of Anodal Transcranial Direct Current Stimulation on Sleep Time and Efficiency
title_full The Effects of Anodal Transcranial Direct Current Stimulation on Sleep Time and Efficiency
title_fullStr The Effects of Anodal Transcranial Direct Current Stimulation on Sleep Time and Efficiency
title_full_unstemmed The Effects of Anodal Transcranial Direct Current Stimulation on Sleep Time and Efficiency
title_short The Effects of Anodal Transcranial Direct Current Stimulation on Sleep Time and Efficiency
title_sort effects of anodal transcranial direct current stimulation on sleep time and efficiency
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481387/
https://www.ncbi.nlm.nih.gov/pubmed/33192380
http://dx.doi.org/10.3389/fnhum.2020.00357
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