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Antibiotic Treatment Induces Long-Lasting Effects on Gut Microbiota and the Enteric Nervous System in Mice

The side effects of antibiotic treatment directly correlate with intestinal dysbiosis. However, a balanced gut microbiota supports the integrity of the enteric nervous system (ENS), which controls gastrointestinal neuromuscular functions. In this study, we investigated the long-term effects of antib...

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Autores principales: Bernabè, Giulia, Shalata, Mahmoud Elsayed Mosaad, Zatta, Veronica, Bellato, Massimo, Porzionato, Andrea, Castagliuolo, Ignazio, Brun, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295661/
https://www.ncbi.nlm.nih.gov/pubmed/37370319
http://dx.doi.org/10.3390/antibiotics12061000
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author Bernabè, Giulia
Shalata, Mahmoud Elsayed Mosaad
Zatta, Veronica
Bellato, Massimo
Porzionato, Andrea
Castagliuolo, Ignazio
Brun, Paola
author_facet Bernabè, Giulia
Shalata, Mahmoud Elsayed Mosaad
Zatta, Veronica
Bellato, Massimo
Porzionato, Andrea
Castagliuolo, Ignazio
Brun, Paola
author_sort Bernabè, Giulia
collection PubMed
description The side effects of antibiotic treatment directly correlate with intestinal dysbiosis. However, a balanced gut microbiota supports the integrity of the enteric nervous system (ENS), which controls gastrointestinal neuromuscular functions. In this study, we investigated the long-term effects of antibiotic-induced microbial dysbiosis on the ENS and the impact of the spontaneous re-establishment of the gut microbiota on gastrointestinal functions. C57BL/6J mice were treated daily for two weeks with antibiotics. After 0–6 weeks of antibiotics wash-out, we determined (a) gut microbiota composition, (b) gastrointestinal motility, (c) integrity of the ENS, (d) neurochemical code, and (e) inflammation. Two weeks of antibiotic treatment significantly altered gut microbial composition; the genera Clostridium, Lachnoclostridium, and Akkermansia did not regain their relative abundance following six weeks of antibiotic discontinuation. Mice treated with antibiotics experienced delayed gastrointestinal transit and altered expression of neuronal markers. The anomalies of the ENS persisted for up to 4 weeks after the antibiotic interruption; the expression of neuronal HuC/D, glial-derived neurotrophic factor (Gdnf), and nerve growth factor (Ngf) mRNA transcripts did not recover. In this study, we strengthened the idea that antibiotic-induced gastrointestinal dysmotility directly correlates with gut dysbiosis as well as structural and functional damage to the ENS.
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spelling pubmed-102956612023-06-28 Antibiotic Treatment Induces Long-Lasting Effects on Gut Microbiota and the Enteric Nervous System in Mice Bernabè, Giulia Shalata, Mahmoud Elsayed Mosaad Zatta, Veronica Bellato, Massimo Porzionato, Andrea Castagliuolo, Ignazio Brun, Paola Antibiotics (Basel) Article The side effects of antibiotic treatment directly correlate with intestinal dysbiosis. However, a balanced gut microbiota supports the integrity of the enteric nervous system (ENS), which controls gastrointestinal neuromuscular functions. In this study, we investigated the long-term effects of antibiotic-induced microbial dysbiosis on the ENS and the impact of the spontaneous re-establishment of the gut microbiota on gastrointestinal functions. C57BL/6J mice were treated daily for two weeks with antibiotics. After 0–6 weeks of antibiotics wash-out, we determined (a) gut microbiota composition, (b) gastrointestinal motility, (c) integrity of the ENS, (d) neurochemical code, and (e) inflammation. Two weeks of antibiotic treatment significantly altered gut microbial composition; the genera Clostridium, Lachnoclostridium, and Akkermansia did not regain their relative abundance following six weeks of antibiotic discontinuation. Mice treated with antibiotics experienced delayed gastrointestinal transit and altered expression of neuronal markers. The anomalies of the ENS persisted for up to 4 weeks after the antibiotic interruption; the expression of neuronal HuC/D, glial-derived neurotrophic factor (Gdnf), and nerve growth factor (Ngf) mRNA transcripts did not recover. In this study, we strengthened the idea that antibiotic-induced gastrointestinal dysmotility directly correlates with gut dysbiosis as well as structural and functional damage to the ENS. MDPI 2023-06-01 /pmc/articles/PMC10295661/ /pubmed/37370319 http://dx.doi.org/10.3390/antibiotics12061000 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bernabè, Giulia
Shalata, Mahmoud Elsayed Mosaad
Zatta, Veronica
Bellato, Massimo
Porzionato, Andrea
Castagliuolo, Ignazio
Brun, Paola
Antibiotic Treatment Induces Long-Lasting Effects on Gut Microbiota and the Enteric Nervous System in Mice
title Antibiotic Treatment Induces Long-Lasting Effects on Gut Microbiota and the Enteric Nervous System in Mice
title_full Antibiotic Treatment Induces Long-Lasting Effects on Gut Microbiota and the Enteric Nervous System in Mice
title_fullStr Antibiotic Treatment Induces Long-Lasting Effects on Gut Microbiota and the Enteric Nervous System in Mice
title_full_unstemmed Antibiotic Treatment Induces Long-Lasting Effects on Gut Microbiota and the Enteric Nervous System in Mice
title_short Antibiotic Treatment Induces Long-Lasting Effects on Gut Microbiota and the Enteric Nervous System in Mice
title_sort antibiotic treatment induces long-lasting effects on gut microbiota and the enteric nervous system in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295661/
https://www.ncbi.nlm.nih.gov/pubmed/37370319
http://dx.doi.org/10.3390/antibiotics12061000
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