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Sex-dependent differences in the gut microbiota following chronic nasal inflammation in adult mice
A growing body of evidence suggests a relationship between olfactory dysfunction and the pathogenesis of mental disorders. Our previous studies indicated that chronic nasal inflammation caused loss of olfactory sensory neurons and gross atrophy of the olfactory bulb, which may lead to olfactory dysf...
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/PMC7907122/ https://www.ncbi.nlm.nih.gov/pubmed/33633180 http://dx.doi.org/10.1038/s41598-021-83896-5 |
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author | Mishima, Yuko Osaki, Takako Shimada, Atsuyoshi Kamiya, Shigeru Hasegawa-Ishii, Sanae |
author_facet | Mishima, Yuko Osaki, Takako Shimada, Atsuyoshi Kamiya, Shigeru Hasegawa-Ishii, Sanae |
author_sort | Mishima, Yuko |
collection | PubMed |
description | A growing body of evidence suggests a relationship between olfactory dysfunction and the pathogenesis of mental disorders. Our previous studies indicated that chronic nasal inflammation caused loss of olfactory sensory neurons and gross atrophy of the olfactory bulb, which may lead to olfactory dysfunction. Simultaneously, increasing numbers of reports have elucidated the importance of gut microbiota to maintain brain function and that dysbiosis may be associated with neuropsychiatric disorders. Here we examined whether chronic nasal inflammation perturbed gut microbiota and whether there were sex differences in this pattern. Eight-week-old C57BL/6 mice repeatedly received bilateral nasal administration of lipopolysaccharide (LPS) 3 times/week to cause chronic nasal inflammation or saline as a control. At 9 weeks, cecal feces were used for 16S metagenomic analysis and whole blood and fresh tissue of spleen were used for ELISA analyses. Microbiome analysis demonstrated a remarkable change of the gut microbiota in male mice with chronic nasal inflammation which was different from that in female mice. In both mice, systemic inflammation did not occur. This has shown for the first time that chronic nasal inflammation correlates with sex-dependent changes in the gut microbiota. The detailed mechanism and potential alteration to brain functions await further studies. |
format | Online Article Text |
id | pubmed-7907122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79071222021-02-26 Sex-dependent differences in the gut microbiota following chronic nasal inflammation in adult mice Mishima, Yuko Osaki, Takako Shimada, Atsuyoshi Kamiya, Shigeru Hasegawa-Ishii, Sanae Sci Rep Article A growing body of evidence suggests a relationship between olfactory dysfunction and the pathogenesis of mental disorders. Our previous studies indicated that chronic nasal inflammation caused loss of olfactory sensory neurons and gross atrophy of the olfactory bulb, which may lead to olfactory dysfunction. Simultaneously, increasing numbers of reports have elucidated the importance of gut microbiota to maintain brain function and that dysbiosis may be associated with neuropsychiatric disorders. Here we examined whether chronic nasal inflammation perturbed gut microbiota and whether there were sex differences in this pattern. Eight-week-old C57BL/6 mice repeatedly received bilateral nasal administration of lipopolysaccharide (LPS) 3 times/week to cause chronic nasal inflammation or saline as a control. At 9 weeks, cecal feces were used for 16S metagenomic analysis and whole blood and fresh tissue of spleen were used for ELISA analyses. Microbiome analysis demonstrated a remarkable change of the gut microbiota in male mice with chronic nasal inflammation which was different from that in female mice. In both mice, systemic inflammation did not occur. This has shown for the first time that chronic nasal inflammation correlates with sex-dependent changes in the gut microbiota. The detailed mechanism and potential alteration to brain functions await further studies. Nature Publishing Group UK 2021-02-25 /pmc/articles/PMC7907122/ /pubmed/33633180 http://dx.doi.org/10.1038/s41598-021-83896-5 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Mishima, Yuko Osaki, Takako Shimada, Atsuyoshi Kamiya, Shigeru Hasegawa-Ishii, Sanae Sex-dependent differences in the gut microbiota following chronic nasal inflammation in adult mice |
title | Sex-dependent differences in the gut microbiota following chronic nasal inflammation in adult mice |
title_full | Sex-dependent differences in the gut microbiota following chronic nasal inflammation in adult mice |
title_fullStr | Sex-dependent differences in the gut microbiota following chronic nasal inflammation in adult mice |
title_full_unstemmed | Sex-dependent differences in the gut microbiota following chronic nasal inflammation in adult mice |
title_short | Sex-dependent differences in the gut microbiota following chronic nasal inflammation in adult mice |
title_sort | sex-dependent differences in the gut microbiota following chronic nasal inflammation in adult mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907122/ https://www.ncbi.nlm.nih.gov/pubmed/33633180 http://dx.doi.org/10.1038/s41598-021-83896-5 |
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