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Effects of regulating gut microbiota on the serotonin metabolism in the chronic unpredictable mild stress rat model

OBJECTIVE: This study was to inspect the antidepressant‑like effect of prebiotics and probiotics, and to explore the effect of modulating gut microbiota on the serotonin (5‐HT) metabolism. METHODS: Fifty rats were separated into control and other four groups randomly. The four groups underwent the c...

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Autores principales: Li, Huawei, Wang, Peng, Huang, Luqiao, Li, Ping, Zhang, Dianliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852474/
https://www.ncbi.nlm.nih.gov/pubmed/31323174
http://dx.doi.org/10.1111/nmo.13677
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author Li, Huawei
Wang, Peng
Huang, Luqiao
Li, Ping
Zhang, Dianliang
author_facet Li, Huawei
Wang, Peng
Huang, Luqiao
Li, Ping
Zhang, Dianliang
author_sort Li, Huawei
collection PubMed
description OBJECTIVE: This study was to inspect the antidepressant‑like effect of prebiotics and probiotics, and to explore the effect of modulating gut microbiota on the serotonin (5‐HT) metabolism. METHODS: Fifty rats were separated into control and other four groups randomly. The four groups underwent the chronic unpredictable mild stress (CUMS) intervention with or without prebiotics and probiotics (Bifidobacterium longum, L. rhamnosus) treatment. After weighted, the animals underwent a series of behavioral tests comprising the sucrose preference test (SPT) and the forced swimming test (FST). Central and colonic serotonin levels and relative metabolism factors were measured and analyzed. Microbiota was examined by 16S rRNA gene pyrosequencing. RESULTS: CUMS intervention caused a decrease in body weight, an increase in FST, and a decrease in SPT. Prebiotics and probiotics all ameliorated the CUMS‐induced loss of weight and depressive‐like behaviors to a certain extent, especially L. rhamnosus. Compared with the group of CUMS intervention, the rats of probiotics and probiotics treatment had a tendency to reduce colonic 5‐HT and increase 5‐HT in frontal cortex and hippocampus. However, there was no significant difference in peripheral blood 5‐HT among these groups. Furthermore, CUMS caused noteworthy gut microbiota variations at the phylum and other levels in rats. Remarkably, there were considerable relations of perturbed gut microbiota with the changed metabolism of 5‐HT. CONCLUSION: In conclusion, these findings implied that prebiotics and probiotics have antidepressive effects, and a considerable effect on the regulation of 5‐HT metabolism, especially L. rhamnosus.
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spelling pubmed-68524742019-11-20 Effects of regulating gut microbiota on the serotonin metabolism in the chronic unpredictable mild stress rat model Li, Huawei Wang, Peng Huang, Luqiao Li, Ping Zhang, Dianliang Neurogastroenterol Motil Original Articles OBJECTIVE: This study was to inspect the antidepressant‑like effect of prebiotics and probiotics, and to explore the effect of modulating gut microbiota on the serotonin (5‐HT) metabolism. METHODS: Fifty rats were separated into control and other four groups randomly. The four groups underwent the chronic unpredictable mild stress (CUMS) intervention with or without prebiotics and probiotics (Bifidobacterium longum, L. rhamnosus) treatment. After weighted, the animals underwent a series of behavioral tests comprising the sucrose preference test (SPT) and the forced swimming test (FST). Central and colonic serotonin levels and relative metabolism factors were measured and analyzed. Microbiota was examined by 16S rRNA gene pyrosequencing. RESULTS: CUMS intervention caused a decrease in body weight, an increase in FST, and a decrease in SPT. Prebiotics and probiotics all ameliorated the CUMS‐induced loss of weight and depressive‐like behaviors to a certain extent, especially L. rhamnosus. Compared with the group of CUMS intervention, the rats of probiotics and probiotics treatment had a tendency to reduce colonic 5‐HT and increase 5‐HT in frontal cortex and hippocampus. However, there was no significant difference in peripheral blood 5‐HT among these groups. Furthermore, CUMS caused noteworthy gut microbiota variations at the phylum and other levels in rats. Remarkably, there were considerable relations of perturbed gut microbiota with the changed metabolism of 5‐HT. CONCLUSION: In conclusion, these findings implied that prebiotics and probiotics have antidepressive effects, and a considerable effect on the regulation of 5‐HT metabolism, especially L. rhamnosus. John Wiley and Sons Inc. 2019-07-19 2019-10 /pmc/articles/PMC6852474/ /pubmed/31323174 http://dx.doi.org/10.1111/nmo.13677 Text en © 2019 The Authors. Neurogastroenterology & Motility Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Li, Huawei
Wang, Peng
Huang, Luqiao
Li, Ping
Zhang, Dianliang
Effects of regulating gut microbiota on the serotonin metabolism in the chronic unpredictable mild stress rat model
title Effects of regulating gut microbiota on the serotonin metabolism in the chronic unpredictable mild stress rat model
title_full Effects of regulating gut microbiota on the serotonin metabolism in the chronic unpredictable mild stress rat model
title_fullStr Effects of regulating gut microbiota on the serotonin metabolism in the chronic unpredictable mild stress rat model
title_full_unstemmed Effects of regulating gut microbiota on the serotonin metabolism in the chronic unpredictable mild stress rat model
title_short Effects of regulating gut microbiota on the serotonin metabolism in the chronic unpredictable mild stress rat model
title_sort effects of regulating gut microbiota on the serotonin metabolism in the chronic unpredictable mild stress rat model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852474/
https://www.ncbi.nlm.nih.gov/pubmed/31323174
http://dx.doi.org/10.1111/nmo.13677
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