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A role for gut microbiota in early-life stress-induced widespread muscle pain in the adult rat

Adult rats that experienced neonatal limited bedding (NLB), a form of early-life stress, experience persistent muscle mechanical hyperalgesia. Since there is a growing recognition that the gut microbiome regulates pain and nociception, and that early-life stress produces a long-lasting impact on the...

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Autores principales: Green, Paul G, Alvarez, Pedro, Levine, Jon D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186117/
https://www.ncbi.nlm.nih.gov/pubmed/34096398
http://dx.doi.org/10.1177/17448069211022952
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author Green, Paul G
Alvarez, Pedro
Levine, Jon D
author_facet Green, Paul G
Alvarez, Pedro
Levine, Jon D
author_sort Green, Paul G
collection PubMed
description Adult rats that experienced neonatal limited bedding (NLB), a form of early-life stress, experience persistent muscle mechanical hyperalgesia. Since there is a growing recognition that the gut microbiome regulates pain and nociception, and that early-life stress produces a long-lasting impact on the gut microbiome, we tested the hypothesis that persistent muscle hyperalgesia seen in adult NLB rats could be ameliorated by interventions that modify the gut microbiome. Adult NLB rats received probiotics, either Lactobacillus rhamnosus GG (10 billion CFU/150 ml) or De Simone Formulation (DSF) (112.5 billion CFU/150 ml mixture of 8 bacterial species), in their drinking water, or non-absorbable antibiotics, rifaximin or neomycin, admixed with cookie dough, to provide 50 mg/kg. Mechanical nociceptive threshold in the gastrocnemius muscle was evaluated before and at several time points after administration of probiotics or antibiotics. Adult NLB rats fed probiotics L. Rhamnosus or DSF, antibiotics, as well as rats fed non-absorbable antibiotics rifaximin or neomycin, had markedly attenuated muscle mechanical hyperalgesia. We hypothesize that persistent skeletal muscle hyperalgesia produced by NLB stress may be, at least in part, due to a contribution of the gut microbiome, and that modulation of gut microbiome using probiotics or non-absorbable antibiotics, may be novel therapeutic approaches for the treatment of chronic musculoskeletal pain.
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spelling pubmed-81861172021-06-21 A role for gut microbiota in early-life stress-induced widespread muscle pain in the adult rat Green, Paul G Alvarez, Pedro Levine, Jon D Mol Pain Short Report Adult rats that experienced neonatal limited bedding (NLB), a form of early-life stress, experience persistent muscle mechanical hyperalgesia. Since there is a growing recognition that the gut microbiome regulates pain and nociception, and that early-life stress produces a long-lasting impact on the gut microbiome, we tested the hypothesis that persistent muscle hyperalgesia seen in adult NLB rats could be ameliorated by interventions that modify the gut microbiome. Adult NLB rats received probiotics, either Lactobacillus rhamnosus GG (10 billion CFU/150 ml) or De Simone Formulation (DSF) (112.5 billion CFU/150 ml mixture of 8 bacterial species), in their drinking water, or non-absorbable antibiotics, rifaximin or neomycin, admixed with cookie dough, to provide 50 mg/kg. Mechanical nociceptive threshold in the gastrocnemius muscle was evaluated before and at several time points after administration of probiotics or antibiotics. Adult NLB rats fed probiotics L. Rhamnosus or DSF, antibiotics, as well as rats fed non-absorbable antibiotics rifaximin or neomycin, had markedly attenuated muscle mechanical hyperalgesia. We hypothesize that persistent skeletal muscle hyperalgesia produced by NLB stress may be, at least in part, due to a contribution of the gut microbiome, and that modulation of gut microbiome using probiotics or non-absorbable antibiotics, may be novel therapeutic approaches for the treatment of chronic musculoskeletal pain. SAGE Publications 2021-06-06 /pmc/articles/PMC8186117/ /pubmed/34096398 http://dx.doi.org/10.1177/17448069211022952 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Short Report
Green, Paul G
Alvarez, Pedro
Levine, Jon D
A role for gut microbiota in early-life stress-induced widespread muscle pain in the adult rat
title A role for gut microbiota in early-life stress-induced widespread muscle pain in the adult rat
title_full A role for gut microbiota in early-life stress-induced widespread muscle pain in the adult rat
title_fullStr A role for gut microbiota in early-life stress-induced widespread muscle pain in the adult rat
title_full_unstemmed A role for gut microbiota in early-life stress-induced widespread muscle pain in the adult rat
title_short A role for gut microbiota in early-life stress-induced widespread muscle pain in the adult rat
title_sort role for gut microbiota in early-life stress-induced widespread muscle pain in the adult rat
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186117/
https://www.ncbi.nlm.nih.gov/pubmed/34096398
http://dx.doi.org/10.1177/17448069211022952
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