Cargando…

Commensal Microbiota Regulation of Metabolic Networks During Olfactory Dysfunction in Mice

INTRODUCTION: Recently, an increasing number of studies have focused on commensal microbiota. These microorganisms have been suggested to impact human health and disease. However, only a small amount of data exists to support the assessment of the influences that commensal microbiota exert on olfacto...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Haiyang, Liu, Lanxiang, Rao, Xuechen, Chai, Tingjia, Zeng, Benhua, Zhang, Xiaotong, Yu, Ying, Zhou, Chanjuan, Pu, Juncai, Zhou, Wei, Li, Wenxia, Zhang, Hanping, Wei, Hong, Xie, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090175/
https://www.ncbi.nlm.nih.gov/pubmed/32256072
http://dx.doi.org/10.2147/NDT.S236541
_version_ 1783509877581152256
author Wang, Haiyang
Liu, Lanxiang
Rao, Xuechen
Chai, Tingjia
Zeng, Benhua
Zhang, Xiaotong
Yu, Ying
Zhou, Chanjuan
Pu, Juncai
Zhou, Wei
Li, Wenxia
Zhang, Hanping
Wei, Hong
Xie, Peng
author_facet Wang, Haiyang
Liu, Lanxiang
Rao, Xuechen
Chai, Tingjia
Zeng, Benhua
Zhang, Xiaotong
Yu, Ying
Zhou, Chanjuan
Pu, Juncai
Zhou, Wei
Li, Wenxia
Zhang, Hanping
Wei, Hong
Xie, Peng
author_sort Wang, Haiyang
collection PubMed
description INTRODUCTION: Recently, an increasing number of studies have focused on commensal microbiota. These microorganisms have been suggested to impact human health and disease. However, only a small amount of data exists to support the assessment of the influences that commensal microbiota exert on olfactory function. METHODS: We used a buried food pellet test (BFPT) to investigate and compare olfactory functions in adult, male, germ-free (GF) and specific-pathogen-free (SPF) mice, then examined and compared the metabolomic profiles for olfactory bulbs (OBs) isolated from GF and SPF mice to uncover the mechanisms associated with olfactory dysfunction. RESULTS: We found that the absence of commensal microbiota was able to influence olfactory function and the metabolic signatures of OBs, with 38 metabolites presenting significant differences between the two groups. These metabolites were primarily associated with disturbances in glycolysis, the tricarboxylic acid (TCA) cycle, amino acid metabolism, and purine catabolism. Finally, the commensal microbiota regulation of metabolic networks during olfactory dysfunction was identified, based on an integrated analysis of metabolite, protein, and mRNA levels. CONCLUSION: This study demonstrated that the absence of commensal microbiota may impair olfactory function and disrupt metabolic networks. These findings provide a new entry-point for understanding olfactory-associated disorders and their potential underlying mechanisms.
format Online
Article
Text
id pubmed-7090175
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-70901752020-04-01 Commensal Microbiota Regulation of Metabolic Networks During Olfactory Dysfunction in Mice Wang, Haiyang Liu, Lanxiang Rao, Xuechen Chai, Tingjia Zeng, Benhua Zhang, Xiaotong Yu, Ying Zhou, Chanjuan Pu, Juncai Zhou, Wei Li, Wenxia Zhang, Hanping Wei, Hong Xie, Peng Neuropsychiatr Dis Treat Original Research INTRODUCTION: Recently, an increasing number of studies have focused on commensal microbiota. These microorganisms have been suggested to impact human health and disease. However, only a small amount of data exists to support the assessment of the influences that commensal microbiota exert on olfactory function. METHODS: We used a buried food pellet test (BFPT) to investigate and compare olfactory functions in adult, male, germ-free (GF) and specific-pathogen-free (SPF) mice, then examined and compared the metabolomic profiles for olfactory bulbs (OBs) isolated from GF and SPF mice to uncover the mechanisms associated with olfactory dysfunction. RESULTS: We found that the absence of commensal microbiota was able to influence olfactory function and the metabolic signatures of OBs, with 38 metabolites presenting significant differences between the two groups. These metabolites were primarily associated with disturbances in glycolysis, the tricarboxylic acid (TCA) cycle, amino acid metabolism, and purine catabolism. Finally, the commensal microbiota regulation of metabolic networks during olfactory dysfunction was identified, based on an integrated analysis of metabolite, protein, and mRNA levels. CONCLUSION: This study demonstrated that the absence of commensal microbiota may impair olfactory function and disrupt metabolic networks. These findings provide a new entry-point for understanding olfactory-associated disorders and their potential underlying mechanisms. Dove 2020-03-19 /pmc/articles/PMC7090175/ /pubmed/32256072 http://dx.doi.org/10.2147/NDT.S236541 Text en © 2020 Wang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wang, Haiyang
Liu, Lanxiang
Rao, Xuechen
Chai, Tingjia
Zeng, Benhua
Zhang, Xiaotong
Yu, Ying
Zhou, Chanjuan
Pu, Juncai
Zhou, Wei
Li, Wenxia
Zhang, Hanping
Wei, Hong
Xie, Peng
Commensal Microbiota Regulation of Metabolic Networks During Olfactory Dysfunction in Mice
title Commensal Microbiota Regulation of Metabolic Networks During Olfactory Dysfunction in Mice
title_full Commensal Microbiota Regulation of Metabolic Networks During Olfactory Dysfunction in Mice
title_fullStr Commensal Microbiota Regulation of Metabolic Networks During Olfactory Dysfunction in Mice
title_full_unstemmed Commensal Microbiota Regulation of Metabolic Networks During Olfactory Dysfunction in Mice
title_short Commensal Microbiota Regulation of Metabolic Networks During Olfactory Dysfunction in Mice
title_sort commensal microbiota regulation of metabolic networks during olfactory dysfunction in mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090175/
https://www.ncbi.nlm.nih.gov/pubmed/32256072
http://dx.doi.org/10.2147/NDT.S236541
work_keys_str_mv AT wanghaiyang commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT liulanxiang commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT raoxuechen commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT chaitingjia commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT zengbenhua commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT zhangxiaotong commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT yuying commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT zhouchanjuan commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT pujuncai commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT zhouwei commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT liwenxia commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT zhanghanping commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT weihong commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice
AT xiepeng commensalmicrobiotaregulationofmetabolicnetworksduringolfactorydysfunctioninmice