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Sex difference in prebiotics on gut and blood–brain barrier dysfunction underlying stress‐induced anxiety and depression

BACKGROUND: Most of the previous studies have demonstrated the potential antidepressive and anxiolytic role of prebiotic supplement in male subjects, yet few have females enrolled. Herein, we explored whether prebiotics administration during chronic stress prevented depression‐like and anxiety‐like...

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Autores principales: Jiang, Jiajun, Fu, Yaoyang, Tang, Anying, Gao, Xingle, Zhang, Danhua, Shen, Yuting, Mou, Tingting, Hu, Shaohua, Gao, Jingfang, Lai, Jianbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314104/
https://www.ncbi.nlm.nih.gov/pubmed/36650644
http://dx.doi.org/10.1111/cns.14091
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author Jiang, Jiajun
Fu, Yaoyang
Tang, Anying
Gao, Xingle
Zhang, Danhua
Shen, Yuting
Mou, Tingting
Hu, Shaohua
Gao, Jingfang
Lai, Jianbo
author_facet Jiang, Jiajun
Fu, Yaoyang
Tang, Anying
Gao, Xingle
Zhang, Danhua
Shen, Yuting
Mou, Tingting
Hu, Shaohua
Gao, Jingfang
Lai, Jianbo
author_sort Jiang, Jiajun
collection PubMed
description BACKGROUND: Most of the previous studies have demonstrated the potential antidepressive and anxiolytic role of prebiotic supplement in male subjects, yet few have females enrolled. Herein, we explored whether prebiotics administration during chronic stress prevented depression‐like and anxiety‐like behavior in a sex‐specific manner and the mechanism of behavioral differences caused by sex. METHODS: Female and male C57 BL/J mice on normal diet were supplemented with or without a combination of fructo‐oligosaccharides (FOS) and galacto‐oligosaccharides (GOS) during 3‐ and 4‐week chronic restraint stress (CRS) treatment, respectively. C57 BL/J mice on normal diet without CRS were used as controls. Behavior consequences, gut microbiota, dysfunction of gut and brain–blood barriers, and inflammatory profiles were measured. RESULTS: In the 3rd week, FOS + GOS administration attenuated stress‐induced anxiety‐like behavior in female, but not in male mice, and the anxiolytic effects in males were observed until the 4th week. However, protective effects of prebiotics on CRS‐induced depression were not observed. Changes in the gene expression of tight junction proteins in the distal colon and hippocampus, and decreased number of colon goblet cells following CRS were restored by prebiotics only in females. In both female and male mice, prebiotics alleviated stress‐induced BBB dysfunction and elevation in pro‐inflammatory cytokines levels, and modulated gut microbiota caused by stress. Furthermore, correlation analysis revealed that anxiety‐like behaviors were significantly correlated with levels of pro‐inflammatory cytokines and gene expression of tight junction proteins in the hippocampus of female mice, and the abundance of specific gut microbes was also correlated with anxiety‐like behaviors, pro‐inflammatory cytokines, and gene expression of tight junction proteins in the hippocampus of female mice. CONCLUSION: Female mice were more vulnerable to stress and prebiotics than males. The gut microbiota, gut and blood–brain barrier, and inflammatory response may mediate the protective effects of prebiotics on anxiety‐like behaviors in female mice.
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spelling pubmed-103141042023-07-02 Sex difference in prebiotics on gut and blood–brain barrier dysfunction underlying stress‐induced anxiety and depression Jiang, Jiajun Fu, Yaoyang Tang, Anying Gao, Xingle Zhang, Danhua Shen, Yuting Mou, Tingting Hu, Shaohua Gao, Jingfang Lai, Jianbo CNS Neurosci Ther Original Articles BACKGROUND: Most of the previous studies have demonstrated the potential antidepressive and anxiolytic role of prebiotic supplement in male subjects, yet few have females enrolled. Herein, we explored whether prebiotics administration during chronic stress prevented depression‐like and anxiety‐like behavior in a sex‐specific manner and the mechanism of behavioral differences caused by sex. METHODS: Female and male C57 BL/J mice on normal diet were supplemented with or without a combination of fructo‐oligosaccharides (FOS) and galacto‐oligosaccharides (GOS) during 3‐ and 4‐week chronic restraint stress (CRS) treatment, respectively. C57 BL/J mice on normal diet without CRS were used as controls. Behavior consequences, gut microbiota, dysfunction of gut and brain–blood barriers, and inflammatory profiles were measured. RESULTS: In the 3rd week, FOS + GOS administration attenuated stress‐induced anxiety‐like behavior in female, but not in male mice, and the anxiolytic effects in males were observed until the 4th week. However, protective effects of prebiotics on CRS‐induced depression were not observed. Changes in the gene expression of tight junction proteins in the distal colon and hippocampus, and decreased number of colon goblet cells following CRS were restored by prebiotics only in females. In both female and male mice, prebiotics alleviated stress‐induced BBB dysfunction and elevation in pro‐inflammatory cytokines levels, and modulated gut microbiota caused by stress. Furthermore, correlation analysis revealed that anxiety‐like behaviors were significantly correlated with levels of pro‐inflammatory cytokines and gene expression of tight junction proteins in the hippocampus of female mice, and the abundance of specific gut microbes was also correlated with anxiety‐like behaviors, pro‐inflammatory cytokines, and gene expression of tight junction proteins in the hippocampus of female mice. CONCLUSION: Female mice were more vulnerable to stress and prebiotics than males. The gut microbiota, gut and blood–brain barrier, and inflammatory response may mediate the protective effects of prebiotics on anxiety‐like behaviors in female mice. John Wiley and Sons Inc. 2023-01-17 /pmc/articles/PMC10314104/ /pubmed/36650644 http://dx.doi.org/10.1111/cns.14091 Text en © 2023 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Jiang, Jiajun
Fu, Yaoyang
Tang, Anying
Gao, Xingle
Zhang, Danhua
Shen, Yuting
Mou, Tingting
Hu, Shaohua
Gao, Jingfang
Lai, Jianbo
Sex difference in prebiotics on gut and blood–brain barrier dysfunction underlying stress‐induced anxiety and depression
title Sex difference in prebiotics on gut and blood–brain barrier dysfunction underlying stress‐induced anxiety and depression
title_full Sex difference in prebiotics on gut and blood–brain barrier dysfunction underlying stress‐induced anxiety and depression
title_fullStr Sex difference in prebiotics on gut and blood–brain barrier dysfunction underlying stress‐induced anxiety and depression
title_full_unstemmed Sex difference in prebiotics on gut and blood–brain barrier dysfunction underlying stress‐induced anxiety and depression
title_short Sex difference in prebiotics on gut and blood–brain barrier dysfunction underlying stress‐induced anxiety and depression
title_sort sex difference in prebiotics on gut and blood–brain barrier dysfunction underlying stress‐induced anxiety and depression
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314104/
https://www.ncbi.nlm.nih.gov/pubmed/36650644
http://dx.doi.org/10.1111/cns.14091
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