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Alterations in gut microbiota are related to metabolite profiles in spinal cord injury

Studies have shown that gut microbiota metabolites can enter the central nervous system via the blood-spinal cord barrier and cause neuroinflammation, thus constituting secondary injury after spinal cord injury. To investigate the correlation between gut microbiota and metabolites and the possible m...

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Autores principales: Kang, Jian-Ning, Sun, Zheng-Fang, Li, Xin-Yu, Zhang, Xiao-Di, Jin, Zheng-Xin, Zhang, Ce, Zhang, Ying, Wang, Hui-Yun, Huang, Na-Na, Jiang, Jian-Hao, Ning, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827763/
https://www.ncbi.nlm.nih.gov/pubmed/36254996
http://dx.doi.org/10.4103/1673-5374.355769
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author Kang, Jian-Ning
Sun, Zheng-Fang
Li, Xin-Yu
Zhang, Xiao-Di
Jin, Zheng-Xin
Zhang, Ce
Zhang, Ying
Wang, Hui-Yun
Huang, Na-Na
Jiang, Jian-Hao
Ning, Bin
author_facet Kang, Jian-Ning
Sun, Zheng-Fang
Li, Xin-Yu
Zhang, Xiao-Di
Jin, Zheng-Xin
Zhang, Ce
Zhang, Ying
Wang, Hui-Yun
Huang, Na-Na
Jiang, Jian-Hao
Ning, Bin
author_sort Kang, Jian-Ning
collection PubMed
description Studies have shown that gut microbiota metabolites can enter the central nervous system via the blood-spinal cord barrier and cause neuroinflammation, thus constituting secondary injury after spinal cord injury. To investigate the correlation between gut microbiota and metabolites and the possible mechanism underlying the effects of gut microbiota on secondary injury after spinal cord injury, in this study, we established mouse models of T8–T10 traumatic spinal cord injury. We used 16S rRNA gene amplicon sequencing and metabolomics to reveal the changes in gut microbiota and metabolites in fecal samples from the mouse model. Results showed a severe gut microbiota disturbance after spinal cord injury, which included marked increases in pro-inflammatory bacteria, such as Shigella, Bacteroides, Rikenella, Staphylococcus, and Mucispirillum and decreases in anti-inflammatory bacteria, such as Lactobacillus, Allobaculum, and Sutterella. Meanwhile, we identified 27 metabolites that decreased and 320 metabolites that increased in the injured spinal cord. Combined with pathway enrichment analysis, five markedly differential amino acids (L-leucine, L-methionine, L-phenylalanine, L-isoleucine and L-valine) were screened out, which play a pivotal role in activating oxidative stress and inflammatory responses following spinal cord injury. Integrated correlation analysis indicated that the alteration of gut microbiota was related to the differences in amino acids, which suggests that disturbances in gut microbiota might participate in the secondary injury through the accumulation of partial metabolites that activate oxidative stress and inflammatory responses. Findings from this study provide a new theoretical basis for improving the secondary injury after spinal cord injury through fecal microbial transplantation.
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spelling pubmed-98277632023-01-10 Alterations in gut microbiota are related to metabolite profiles in spinal cord injury Kang, Jian-Ning Sun, Zheng-Fang Li, Xin-Yu Zhang, Xiao-Di Jin, Zheng-Xin Zhang, Ce Zhang, Ying Wang, Hui-Yun Huang, Na-Na Jiang, Jian-Hao Ning, Bin Neural Regen Res Research Article Studies have shown that gut microbiota metabolites can enter the central nervous system via the blood-spinal cord barrier and cause neuroinflammation, thus constituting secondary injury after spinal cord injury. To investigate the correlation between gut microbiota and metabolites and the possible mechanism underlying the effects of gut microbiota on secondary injury after spinal cord injury, in this study, we established mouse models of T8–T10 traumatic spinal cord injury. We used 16S rRNA gene amplicon sequencing and metabolomics to reveal the changes in gut microbiota and metabolites in fecal samples from the mouse model. Results showed a severe gut microbiota disturbance after spinal cord injury, which included marked increases in pro-inflammatory bacteria, such as Shigella, Bacteroides, Rikenella, Staphylococcus, and Mucispirillum and decreases in anti-inflammatory bacteria, such as Lactobacillus, Allobaculum, and Sutterella. Meanwhile, we identified 27 metabolites that decreased and 320 metabolites that increased in the injured spinal cord. Combined with pathway enrichment analysis, five markedly differential amino acids (L-leucine, L-methionine, L-phenylalanine, L-isoleucine and L-valine) were screened out, which play a pivotal role in activating oxidative stress and inflammatory responses following spinal cord injury. Integrated correlation analysis indicated that the alteration of gut microbiota was related to the differences in amino acids, which suggests that disturbances in gut microbiota might participate in the secondary injury through the accumulation of partial metabolites that activate oxidative stress and inflammatory responses. Findings from this study provide a new theoretical basis for improving the secondary injury after spinal cord injury through fecal microbial transplantation. Wolters Kluwer - Medknow 2022-10-10 /pmc/articles/PMC9827763/ /pubmed/36254996 http://dx.doi.org/10.4103/1673-5374.355769 Text en Copyright: © Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Kang, Jian-Ning
Sun, Zheng-Fang
Li, Xin-Yu
Zhang, Xiao-Di
Jin, Zheng-Xin
Zhang, Ce
Zhang, Ying
Wang, Hui-Yun
Huang, Na-Na
Jiang, Jian-Hao
Ning, Bin
Alterations in gut microbiota are related to metabolite profiles in spinal cord injury
title Alterations in gut microbiota are related to metabolite profiles in spinal cord injury
title_full Alterations in gut microbiota are related to metabolite profiles in spinal cord injury
title_fullStr Alterations in gut microbiota are related to metabolite profiles in spinal cord injury
title_full_unstemmed Alterations in gut microbiota are related to metabolite profiles in spinal cord injury
title_short Alterations in gut microbiota are related to metabolite profiles in spinal cord injury
title_sort alterations in gut microbiota are related to metabolite profiles in spinal cord injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827763/
https://www.ncbi.nlm.nih.gov/pubmed/36254996
http://dx.doi.org/10.4103/1673-5374.355769
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