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Alterations in the gut microbiota and metabolite profiles in the context of neuropathic pain

The aim of this study was to explore the relationships among gut microbiota disturbances and serum and spinal cord metabolic disorders in neuropathic pain. 16S rDNA amplicon sequencing and serum and spinal cord metabolomics were used to identify alterations in the microbiota and metabolite profiles...

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Autores principales: Chen, Peng, Wang, Chen, Ren, Yan-na, Ye, Zeng-jie, Jiang, Chao, Wu, Zhi-bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941960/
https://www.ncbi.nlm.nih.gov/pubmed/33750430
http://dx.doi.org/10.1186/s13041-021-00765-y
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author Chen, Peng
Wang, Chen
Ren, Yan-na
Ye, Zeng-jie
Jiang, Chao
Wu, Zhi-bing
author_facet Chen, Peng
Wang, Chen
Ren, Yan-na
Ye, Zeng-jie
Jiang, Chao
Wu, Zhi-bing
author_sort Chen, Peng
collection PubMed
description The aim of this study was to explore the relationships among gut microbiota disturbances and serum and spinal cord metabolic disorders in neuropathic pain. 16S rDNA amplicon sequencing and serum and spinal cord metabolomics were used to identify alterations in the microbiota and metabolite profiles in the sham rats and the chronic constriction injury (CCI) model rats. Correlations between the abundances of gut microbiota components at the genus level, the levels of serum metabolites, and pain-related behavioural parameters were analysed. Ingenuity pathway analysis (IPA) was applied to analyse the interaction networks of the differentially expressed serum metabolites. First, we found that the composition of the gut microbiota was different between rats with CCI-induced neuropathic pain and sham controls. At the genus level, the abundances of Helicobacter, Phascolarctobacterium, Christensenella, Blautia, Streptococcus, Rothia and Lactobacillus were significantly increased, whereas the abundances of Ignatzschineria, Butyricimonas, Escherichia, AF12, and Corynebacterium were significantly decreased. Additionally, 72 significantly differentially expressed serum metabolites and 17 significantly differentially expressed spinal cord metabolites were identified between the CCI rats and the sham rats. Finally, correlation analysis showed that changes in the gut microbiota was significantly correlated with changes in serum metabolite levels, suggesting that dysbiosis of the gut microbiota is an important factor in modulating metabolic disturbances in the context of neuropathic pain. In conclusion, our research provides a novel perspective on the potential roles of the gut microbiota and related metabolites in neuropathic pain.
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spelling pubmed-79419602021-03-09 Alterations in the gut microbiota and metabolite profiles in the context of neuropathic pain Chen, Peng Wang, Chen Ren, Yan-na Ye, Zeng-jie Jiang, Chao Wu, Zhi-bing Mol Brain Research The aim of this study was to explore the relationships among gut microbiota disturbances and serum and spinal cord metabolic disorders in neuropathic pain. 16S rDNA amplicon sequencing and serum and spinal cord metabolomics were used to identify alterations in the microbiota and metabolite profiles in the sham rats and the chronic constriction injury (CCI) model rats. Correlations between the abundances of gut microbiota components at the genus level, the levels of serum metabolites, and pain-related behavioural parameters were analysed. Ingenuity pathway analysis (IPA) was applied to analyse the interaction networks of the differentially expressed serum metabolites. First, we found that the composition of the gut microbiota was different between rats with CCI-induced neuropathic pain and sham controls. At the genus level, the abundances of Helicobacter, Phascolarctobacterium, Christensenella, Blautia, Streptococcus, Rothia and Lactobacillus were significantly increased, whereas the abundances of Ignatzschineria, Butyricimonas, Escherichia, AF12, and Corynebacterium were significantly decreased. Additionally, 72 significantly differentially expressed serum metabolites and 17 significantly differentially expressed spinal cord metabolites were identified between the CCI rats and the sham rats. Finally, correlation analysis showed that changes in the gut microbiota was significantly correlated with changes in serum metabolite levels, suggesting that dysbiosis of the gut microbiota is an important factor in modulating metabolic disturbances in the context of neuropathic pain. In conclusion, our research provides a novel perspective on the potential roles of the gut microbiota and related metabolites in neuropathic pain. BioMed Central 2021-03-09 /pmc/articles/PMC7941960/ /pubmed/33750430 http://dx.doi.org/10.1186/s13041-021-00765-y Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Peng
Wang, Chen
Ren, Yan-na
Ye, Zeng-jie
Jiang, Chao
Wu, Zhi-bing
Alterations in the gut microbiota and metabolite profiles in the context of neuropathic pain
title Alterations in the gut microbiota and metabolite profiles in the context of neuropathic pain
title_full Alterations in the gut microbiota and metabolite profiles in the context of neuropathic pain
title_fullStr Alterations in the gut microbiota and metabolite profiles in the context of neuropathic pain
title_full_unstemmed Alterations in the gut microbiota and metabolite profiles in the context of neuropathic pain
title_short Alterations in the gut microbiota and metabolite profiles in the context of neuropathic pain
title_sort alterations in the gut microbiota and metabolite profiles in the context of neuropathic pain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941960/
https://www.ncbi.nlm.nih.gov/pubmed/33750430
http://dx.doi.org/10.1186/s13041-021-00765-y
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