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Brachial plexus avulsion induced changes in gut microbiota promotes pain related anxiety-like behavior in mice

INTRODUCTION: Brachial plexus avulsion (BPA) injury develops frequent and intense neuropathic pain, involving in both peripheral and central nervous systems. The incidence of anxiety or depression caused by BPA-induced neuropathic pain is high, but the underlying mechanism remains unclear. METHODS:...

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Autores principales: Zhang, Jian-lei, Xian, Hang, Zhao, Rui, Luo, Ceng, Xie, Rou-gang, Tian, Tong, Cong, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944865/
https://www.ncbi.nlm.nih.gov/pubmed/36846129
http://dx.doi.org/10.3389/fneur.2023.1084494
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author Zhang, Jian-lei
Xian, Hang
Zhao, Rui
Luo, Ceng
Xie, Rou-gang
Tian, Tong
Cong, Rui
author_facet Zhang, Jian-lei
Xian, Hang
Zhao, Rui
Luo, Ceng
Xie, Rou-gang
Tian, Tong
Cong, Rui
author_sort Zhang, Jian-lei
collection PubMed
description INTRODUCTION: Brachial plexus avulsion (BPA) injury develops frequent and intense neuropathic pain, involving in both peripheral and central nervous systems. The incidence of anxiety or depression caused by BPA-induced neuropathic pain is high, but the underlying mechanism remains unclear. METHODS: We established a BPA mice model and assessed its negative emotions through behavioral tests. To further explore the role of the microbiota-gut-brain axis in the unique emotional behavior after BPA, we performed intestinal fecal 16s and metabolomics assays. Psychobiotics (PB) supplementation was administered to BPA mice to check the probiotics effects on BPA-induced anxiety behaviors. RESULTS: Pain related anxiety-like behavior was observed at the early stage after BPA (7 days), while no depression-like behavior was detected. Intriguingly, gut microbiota diversity was increased in BPA mice, and the most abundant probiotics, Lactobacillus, showed obvious changes. Lactobacillus_reuteri was significantly decreased in BPA mice. Metabolomics analysis showed that Lactobacillus_reuteri-related bile acid pathway and some neurotransmitter amino acids were significantly altered. Further PB (dominated by Lactobacillus_reuteri) supplementation could significantly relieve BPA-induced anxiety-like behaviors in mice. CONCLUSION: Our study suggests that pathological neuralgia after BPA could alter intestinal microbiota diversity, especially Lactobacillus, and the changes in neurotransmitter amino acid metabolites may be the key reason for the onset of anxiety-like behaviors in BPA mice.
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spelling pubmed-99448652023-02-23 Brachial plexus avulsion induced changes in gut microbiota promotes pain related anxiety-like behavior in mice Zhang, Jian-lei Xian, Hang Zhao, Rui Luo, Ceng Xie, Rou-gang Tian, Tong Cong, Rui Front Neurol Neurology INTRODUCTION: Brachial plexus avulsion (BPA) injury develops frequent and intense neuropathic pain, involving in both peripheral and central nervous systems. The incidence of anxiety or depression caused by BPA-induced neuropathic pain is high, but the underlying mechanism remains unclear. METHODS: We established a BPA mice model and assessed its negative emotions through behavioral tests. To further explore the role of the microbiota-gut-brain axis in the unique emotional behavior after BPA, we performed intestinal fecal 16s and metabolomics assays. Psychobiotics (PB) supplementation was administered to BPA mice to check the probiotics effects on BPA-induced anxiety behaviors. RESULTS: Pain related anxiety-like behavior was observed at the early stage after BPA (7 days), while no depression-like behavior was detected. Intriguingly, gut microbiota diversity was increased in BPA mice, and the most abundant probiotics, Lactobacillus, showed obvious changes. Lactobacillus_reuteri was significantly decreased in BPA mice. Metabolomics analysis showed that Lactobacillus_reuteri-related bile acid pathway and some neurotransmitter amino acids were significantly altered. Further PB (dominated by Lactobacillus_reuteri) supplementation could significantly relieve BPA-induced anxiety-like behaviors in mice. CONCLUSION: Our study suggests that pathological neuralgia after BPA could alter intestinal microbiota diversity, especially Lactobacillus, and the changes in neurotransmitter amino acid metabolites may be the key reason for the onset of anxiety-like behaviors in BPA mice. Frontiers Media S.A. 2023-02-08 /pmc/articles/PMC9944865/ /pubmed/36846129 http://dx.doi.org/10.3389/fneur.2023.1084494 Text en Copyright © 2023 Zhang, Xian, Zhao, Luo, Xie, Tian and Cong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Zhang, Jian-lei
Xian, Hang
Zhao, Rui
Luo, Ceng
Xie, Rou-gang
Tian, Tong
Cong, Rui
Brachial plexus avulsion induced changes in gut microbiota promotes pain related anxiety-like behavior in mice
title Brachial plexus avulsion induced changes in gut microbiota promotes pain related anxiety-like behavior in mice
title_full Brachial plexus avulsion induced changes in gut microbiota promotes pain related anxiety-like behavior in mice
title_fullStr Brachial plexus avulsion induced changes in gut microbiota promotes pain related anxiety-like behavior in mice
title_full_unstemmed Brachial plexus avulsion induced changes in gut microbiota promotes pain related anxiety-like behavior in mice
title_short Brachial plexus avulsion induced changes in gut microbiota promotes pain related anxiety-like behavior in mice
title_sort brachial plexus avulsion induced changes in gut microbiota promotes pain related anxiety-like behavior in mice
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944865/
https://www.ncbi.nlm.nih.gov/pubmed/36846129
http://dx.doi.org/10.3389/fneur.2023.1084494
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