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Oral Administration of Human-Gut-Derived Prevotella histicola Improves Sleep Architecture in Rats
(1) Background: The human gut microbiome may regulate sleep through the gut–brain axis. However, the sleep-promoting effects of gut microbiota remain unclear. (2) Methods: We obtained sleep–wake profiles from 25 rats receiving P. histicola (P. histicola group), 5 rats receiving P. stercorea (P. ster...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223264/ https://www.ncbi.nlm.nih.gov/pubmed/37317125 http://dx.doi.org/10.3390/microorganisms11051151 |
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author | Yoon, Dae Wui Baik, Inkyung |
author_facet | Yoon, Dae Wui Baik, Inkyung |
author_sort | Yoon, Dae Wui |
collection | PubMed |
description | (1) Background: The human gut microbiome may regulate sleep through the gut–brain axis. However, the sleep-promoting effects of gut microbiota remain unclear. (2) Methods: We obtained sleep–wake profiles from 25 rats receiving P. histicola (P. histicola group), 5 rats receiving P. stercorea (P. stercorea group), 4 rats not receiving bacteria (No administration group), and 8 rats receiving P. histicola extracellular vesicles (EV) (EV group) during the baseline, administration, and withdrawal periods. (3) Results: The P. histicola group showed increased total sleep, rapid eye movement (REM) sleep, and non-rapid eye movement (NREM) sleep time during the administration and withdrawal periods; on the last day of administration, we found significant increases of 52 min for total sleep (p < 0.01), 13 min for REM sleep (p < 0.05), and 39 min for NREM sleep (p < 0.01) over the baseline. EV administration also increased NREM sleep time on Day 3 of administration (p = 0.05). We observed a linear trend in the dose–response relationship for total sleep and NREM sleep in the P. histicola group. However, neither the no-administration group nor the P. stercorea group showed significant findings. (4) Conclusions: Oral administration of probiotic P. histicola may improve sleep and could be a potential sleep aid. Further rigorous evaluations for the safety and efficacy of P. histicola supplementation are warranted. |
format | Online Article Text |
id | pubmed-10223264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102232642023-05-28 Oral Administration of Human-Gut-Derived Prevotella histicola Improves Sleep Architecture in Rats Yoon, Dae Wui Baik, Inkyung Microorganisms Article (1) Background: The human gut microbiome may regulate sleep through the gut–brain axis. However, the sleep-promoting effects of gut microbiota remain unclear. (2) Methods: We obtained sleep–wake profiles from 25 rats receiving P. histicola (P. histicola group), 5 rats receiving P. stercorea (P. stercorea group), 4 rats not receiving bacteria (No administration group), and 8 rats receiving P. histicola extracellular vesicles (EV) (EV group) during the baseline, administration, and withdrawal periods. (3) Results: The P. histicola group showed increased total sleep, rapid eye movement (REM) sleep, and non-rapid eye movement (NREM) sleep time during the administration and withdrawal periods; on the last day of administration, we found significant increases of 52 min for total sleep (p < 0.01), 13 min for REM sleep (p < 0.05), and 39 min for NREM sleep (p < 0.01) over the baseline. EV administration also increased NREM sleep time on Day 3 of administration (p = 0.05). We observed a linear trend in the dose–response relationship for total sleep and NREM sleep in the P. histicola group. However, neither the no-administration group nor the P. stercorea group showed significant findings. (4) Conclusions: Oral administration of probiotic P. histicola may improve sleep and could be a potential sleep aid. Further rigorous evaluations for the safety and efficacy of P. histicola supplementation are warranted. MDPI 2023-04-28 /pmc/articles/PMC10223264/ /pubmed/37317125 http://dx.doi.org/10.3390/microorganisms11051151 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yoon, Dae Wui Baik, Inkyung Oral Administration of Human-Gut-Derived Prevotella histicola Improves Sleep Architecture in Rats |
title | Oral Administration of Human-Gut-Derived Prevotella histicola Improves Sleep Architecture in Rats |
title_full | Oral Administration of Human-Gut-Derived Prevotella histicola Improves Sleep Architecture in Rats |
title_fullStr | Oral Administration of Human-Gut-Derived Prevotella histicola Improves Sleep Architecture in Rats |
title_full_unstemmed | Oral Administration of Human-Gut-Derived Prevotella histicola Improves Sleep Architecture in Rats |
title_short | Oral Administration of Human-Gut-Derived Prevotella histicola Improves Sleep Architecture in Rats |
title_sort | oral administration of human-gut-derived prevotella histicola improves sleep architecture in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223264/ https://www.ncbi.nlm.nih.gov/pubmed/37317125 http://dx.doi.org/10.3390/microorganisms11051151 |
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