Cargando…
Microbiota alteration is associated with the development of stress-induced despair behavior
Depressive disorders often run in families, which, in addition to the genetic component, may point to the microbiome as a causative agent. Here, we employed a combination of behavioral, molecular and computational techniques to test the role of the microbiota in mediating despair behavior. In chroni...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339726/ https://www.ncbi.nlm.nih.gov/pubmed/28266612 http://dx.doi.org/10.1038/srep43859 |
_version_ | 1782512716049547264 |
---|---|
author | Marin, Ioana A. Goertz, Jennifer E. Ren, Tiantian Rich, Stephen S. Onengut-Gumuscu, Suna Farber, Emily Wu, Martin Overall, Christopher C. Kipnis, Jonathan Gaultier, Alban |
author_facet | Marin, Ioana A. Goertz, Jennifer E. Ren, Tiantian Rich, Stephen S. Onengut-Gumuscu, Suna Farber, Emily Wu, Martin Overall, Christopher C. Kipnis, Jonathan Gaultier, Alban |
author_sort | Marin, Ioana A. |
collection | PubMed |
description | Depressive disorders often run in families, which, in addition to the genetic component, may point to the microbiome as a causative agent. Here, we employed a combination of behavioral, molecular and computational techniques to test the role of the microbiota in mediating despair behavior. In chronically stressed mice displaying despair behavior, we found that the microbiota composition and the metabolic signature dramatically change. Specifically, we observed reduced Lactobacillus and increased circulating kynurenine levels as the most prominent changes in stressed mice. Restoring intestinal Lactobacillus levels was sufficient to improve the metabolic alterations and behavioral abnormalities. Mechanistically, we identified that Lactobacillus-derived reactive oxygen species may suppress host kynurenine metabolism, by inhibiting the expression of the metabolizing enzyme, IDO1, in the intestine. Moreover, maintaining elevated kynurenine levels during Lactobacillus supplementation diminished the treatment benefits. Collectively, our data provide a mechanistic scenario for how a microbiota player (Lactobacillus) may contribute to regulating metabolism and resilience during stress. |
format | Online Article Text |
id | pubmed-5339726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53397262017-03-10 Microbiota alteration is associated with the development of stress-induced despair behavior Marin, Ioana A. Goertz, Jennifer E. Ren, Tiantian Rich, Stephen S. Onengut-Gumuscu, Suna Farber, Emily Wu, Martin Overall, Christopher C. Kipnis, Jonathan Gaultier, Alban Sci Rep Article Depressive disorders often run in families, which, in addition to the genetic component, may point to the microbiome as a causative agent. Here, we employed a combination of behavioral, molecular and computational techniques to test the role of the microbiota in mediating despair behavior. In chronically stressed mice displaying despair behavior, we found that the microbiota composition and the metabolic signature dramatically change. Specifically, we observed reduced Lactobacillus and increased circulating kynurenine levels as the most prominent changes in stressed mice. Restoring intestinal Lactobacillus levels was sufficient to improve the metabolic alterations and behavioral abnormalities. Mechanistically, we identified that Lactobacillus-derived reactive oxygen species may suppress host kynurenine metabolism, by inhibiting the expression of the metabolizing enzyme, IDO1, in the intestine. Moreover, maintaining elevated kynurenine levels during Lactobacillus supplementation diminished the treatment benefits. Collectively, our data provide a mechanistic scenario for how a microbiota player (Lactobacillus) may contribute to regulating metabolism and resilience during stress. Nature Publishing Group 2017-03-07 /pmc/articles/PMC5339726/ /pubmed/28266612 http://dx.doi.org/10.1038/srep43859 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Marin, Ioana A. Goertz, Jennifer E. Ren, Tiantian Rich, Stephen S. Onengut-Gumuscu, Suna Farber, Emily Wu, Martin Overall, Christopher C. Kipnis, Jonathan Gaultier, Alban Microbiota alteration is associated with the development of stress-induced despair behavior |
title | Microbiota alteration is associated with the development of stress-induced despair behavior |
title_full | Microbiota alteration is associated with the development of stress-induced despair behavior |
title_fullStr | Microbiota alteration is associated with the development of stress-induced despair behavior |
title_full_unstemmed | Microbiota alteration is associated with the development of stress-induced despair behavior |
title_short | Microbiota alteration is associated with the development of stress-induced despair behavior |
title_sort | microbiota alteration is associated with the development of stress-induced despair behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339726/ https://www.ncbi.nlm.nih.gov/pubmed/28266612 http://dx.doi.org/10.1038/srep43859 |
work_keys_str_mv | AT marinioanaa microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior AT goertzjennifere microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior AT rentiantian microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior AT richstephens microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior AT onengutgumuscusuna microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior AT farberemily microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior AT wumartin microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior AT overallchristopherc microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior AT kipnisjonathan microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior AT gaultieralban microbiotaalterationisassociatedwiththedevelopmentofstressinduceddespairbehavior |