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Cefaclor causes vagus nerve-mediated depression-like symptoms with gut dysbiosis in mice
Antibiotics are increasingly recognized as causing neuropsychiatric side effects including depression and anxiety. Alterations in central serotonin and 5-HT receptor expression are implicated in the pathogenesis of anxiety and depression, which are highly comorbid with gastrointestinal disorders. Ne...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509198/ https://www.ncbi.nlm.nih.gov/pubmed/37726354 http://dx.doi.org/10.1038/s41598-023-42690-1 |
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author | Joo, Min-Kyung Shin, Yoon-Jung Kim, Dong-Hyun |
author_facet | Joo, Min-Kyung Shin, Yoon-Jung Kim, Dong-Hyun |
author_sort | Joo, Min-Kyung |
collection | PubMed |
description | Antibiotics are increasingly recognized as causing neuropsychiatric side effects including depression and anxiety. Alterations in central serotonin and 5-HT receptor expression are implicated in the pathogenesis of anxiety and depression, which are highly comorbid with gastrointestinal disorders. Nevertheless, it is still unclear how antibiotics can cause anxiety and depression. In this study, oral administration of cefaclor, a second-generation cephalosporin antibiotic, induced anxiety- and depression-like behaviors and colitis with gut microbiota alteration in mice. Cefaclor reduced serotonin levels and fluctuated 5-HT receptor mRNA expressions such as Htr1a, Htr1b, and Htr6 in the hippocampus. Vagotomy attenuated the cefaclor-induced anxiety- and depression-like symptoms, while the cefaclor-induced changes in gut bacteria alteration and colitis were not affected. Fluoxetine attenuated cefaclor-induced anxiety- and depression-like behaviors. Furthermore, fluoxetine decreased cefaclor-resistant Enterobacteriaceae and Enterococcaceae. Taken together, our findings suggest that the use of antibiotics, particularly, cefaclor may cause gut dysbiosis-dependent anxiety and depression through the microbiota-gut-blood–brain and microbiota-gut-vagus nerve-brain pathway. Targeting antibiotics-resistant pathogenic bacteria may be a promising therapeutic strategy for the treatment of anxiety and depression. |
format | Online Article Text |
id | pubmed-10509198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105091982023-09-21 Cefaclor causes vagus nerve-mediated depression-like symptoms with gut dysbiosis in mice Joo, Min-Kyung Shin, Yoon-Jung Kim, Dong-Hyun Sci Rep Article Antibiotics are increasingly recognized as causing neuropsychiatric side effects including depression and anxiety. Alterations in central serotonin and 5-HT receptor expression are implicated in the pathogenesis of anxiety and depression, which are highly comorbid with gastrointestinal disorders. Nevertheless, it is still unclear how antibiotics can cause anxiety and depression. In this study, oral administration of cefaclor, a second-generation cephalosporin antibiotic, induced anxiety- and depression-like behaviors and colitis with gut microbiota alteration in mice. Cefaclor reduced serotonin levels and fluctuated 5-HT receptor mRNA expressions such as Htr1a, Htr1b, and Htr6 in the hippocampus. Vagotomy attenuated the cefaclor-induced anxiety- and depression-like symptoms, while the cefaclor-induced changes in gut bacteria alteration and colitis were not affected. Fluoxetine attenuated cefaclor-induced anxiety- and depression-like behaviors. Furthermore, fluoxetine decreased cefaclor-resistant Enterobacteriaceae and Enterococcaceae. Taken together, our findings suggest that the use of antibiotics, particularly, cefaclor may cause gut dysbiosis-dependent anxiety and depression through the microbiota-gut-blood–brain and microbiota-gut-vagus nerve-brain pathway. Targeting antibiotics-resistant pathogenic bacteria may be a promising therapeutic strategy for the treatment of anxiety and depression. Nature Publishing Group UK 2023-09-19 /pmc/articles/PMC10509198/ /pubmed/37726354 http://dx.doi.org/10.1038/s41598-023-42690-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Joo, Min-Kyung Shin, Yoon-Jung Kim, Dong-Hyun Cefaclor causes vagus nerve-mediated depression-like symptoms with gut dysbiosis in mice |
title | Cefaclor causes vagus nerve-mediated depression-like symptoms with gut dysbiosis in mice |
title_full | Cefaclor causes vagus nerve-mediated depression-like symptoms with gut dysbiosis in mice |
title_fullStr | Cefaclor causes vagus nerve-mediated depression-like symptoms with gut dysbiosis in mice |
title_full_unstemmed | Cefaclor causes vagus nerve-mediated depression-like symptoms with gut dysbiosis in mice |
title_short | Cefaclor causes vagus nerve-mediated depression-like symptoms with gut dysbiosis in mice |
title_sort | cefaclor causes vagus nerve-mediated depression-like symptoms with gut dysbiosis in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509198/ https://www.ncbi.nlm.nih.gov/pubmed/37726354 http://dx.doi.org/10.1038/s41598-023-42690-1 |
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