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Sake yeast induces the sleep-promoting effects under the stress-induced acute insomnia in mice
Sleep deprivation induces adverse effects on the health, productivity, and performance. The individuals who could not get enough sleep temporarily experience the symptoms of an induced acute insomnia. This study investigated the efficacy of sake yeast in treatment of acute insomnia in mice. The resu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531297/ https://www.ncbi.nlm.nih.gov/pubmed/34675261 http://dx.doi.org/10.1038/s41598-021-00271-0 |
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author | Nishimon, Shohei Sakai, Noriaki Nishino, Seiji |
author_facet | Nishimon, Shohei Sakai, Noriaki Nishino, Seiji |
author_sort | Nishimon, Shohei |
collection | PubMed |
description | Sleep deprivation induces adverse effects on the health, productivity, and performance. The individuals who could not get enough sleep temporarily experience the symptoms of an induced acute insomnia. This study investigated the efficacy of sake yeast in treatment of acute insomnia in mice. The results of this study showed that sake yeast induced a significant dose-dependent wake reduction, a rapid eye movement (REM) and a non-REM (NREM) sleep enhancement during the first 6 h after the oral administration of sake yeast with locomotor activity and core body temperature decreases under the stressful environment in a new cage. In fact, the wake amounts at 3 h and 6 h were significantly reduced after the oral administration of sake yeast compared with the vehicle. The NREM sleep amounts at 3 h and 6 h significantly increased after the administration of sake yeast compared with the vehicle. The REM amount at 6 h significantly increased after the administration of sake yeast compared with the vehicle, but not at 3 h. The previous study suggested that the sleep-promoting effects of sake yeast could be referred from the activating effect of adenosine A(2A) receptor (A(2A)R). In summary, the sake yeast is an A(2A)R agonist and may induce sleep due to its stress-reducing and anti-anxiety properties. Further verification of the involvement of adenosine in the pathophysiology of insomnia is needed. |
format | Online Article Text |
id | pubmed-8531297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85312972021-10-22 Sake yeast induces the sleep-promoting effects under the stress-induced acute insomnia in mice Nishimon, Shohei Sakai, Noriaki Nishino, Seiji Sci Rep Article Sleep deprivation induces adverse effects on the health, productivity, and performance. The individuals who could not get enough sleep temporarily experience the symptoms of an induced acute insomnia. This study investigated the efficacy of sake yeast in treatment of acute insomnia in mice. The results of this study showed that sake yeast induced a significant dose-dependent wake reduction, a rapid eye movement (REM) and a non-REM (NREM) sleep enhancement during the first 6 h after the oral administration of sake yeast with locomotor activity and core body temperature decreases under the stressful environment in a new cage. In fact, the wake amounts at 3 h and 6 h were significantly reduced after the oral administration of sake yeast compared with the vehicle. The NREM sleep amounts at 3 h and 6 h significantly increased after the administration of sake yeast compared with the vehicle. The REM amount at 6 h significantly increased after the administration of sake yeast compared with the vehicle, but not at 3 h. The previous study suggested that the sleep-promoting effects of sake yeast could be referred from the activating effect of adenosine A(2A) receptor (A(2A)R). In summary, the sake yeast is an A(2A)R agonist and may induce sleep due to its stress-reducing and anti-anxiety properties. Further verification of the involvement of adenosine in the pathophysiology of insomnia is needed. Nature Publishing Group UK 2021-10-21 /pmc/articles/PMC8531297/ /pubmed/34675261 http://dx.doi.org/10.1038/s41598-021-00271-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Nishimon, Shohei Sakai, Noriaki Nishino, Seiji Sake yeast induces the sleep-promoting effects under the stress-induced acute insomnia in mice |
title | Sake yeast induces the sleep-promoting effects under the stress-induced acute insomnia in mice |
title_full | Sake yeast induces the sleep-promoting effects under the stress-induced acute insomnia in mice |
title_fullStr | Sake yeast induces the sleep-promoting effects under the stress-induced acute insomnia in mice |
title_full_unstemmed | Sake yeast induces the sleep-promoting effects under the stress-induced acute insomnia in mice |
title_short | Sake yeast induces the sleep-promoting effects under the stress-induced acute insomnia in mice |
title_sort | sake yeast induces the sleep-promoting effects under the stress-induced acute insomnia in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531297/ https://www.ncbi.nlm.nih.gov/pubmed/34675261 http://dx.doi.org/10.1038/s41598-021-00271-0 |
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