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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...

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Autores principales: 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
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
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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.
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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
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