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Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system

Depression is the leading cause of disability worldwide. Recent observations have revealed an association between mood disorders and alterations of the intestinal microbiota. Here, using unpredictable chronic mild stress (UCMS) as a mouse model of depression, we show that UCMS mice display phenotypi...

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Autores principales: Chevalier, Grégoire, Siopi, Eleni, Guenin-Macé, Laure, Pascal, Maud, Laval, Thomas, Rifflet, Aline, Boneca, Ivo Gomperts, Demangel, Caroline, Colsch, Benoit, Pruvost, Alain, Chu-Van, Emeline, Messager, Aurélie, Leulier, François, Lepousez, Gabriel, Eberl, Gérard, Lledo, Pierre-Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732982/
https://www.ncbi.nlm.nih.gov/pubmed/33311466
http://dx.doi.org/10.1038/s41467-020-19931-2
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author Chevalier, Grégoire
Siopi, Eleni
Guenin-Macé, Laure
Pascal, Maud
Laval, Thomas
Rifflet, Aline
Boneca, Ivo Gomperts
Demangel, Caroline
Colsch, Benoit
Pruvost, Alain
Chu-Van, Emeline
Messager, Aurélie
Leulier, François
Lepousez, Gabriel
Eberl, Gérard
Lledo, Pierre-Marie
author_facet Chevalier, Grégoire
Siopi, Eleni
Guenin-Macé, Laure
Pascal, Maud
Laval, Thomas
Rifflet, Aline
Boneca, Ivo Gomperts
Demangel, Caroline
Colsch, Benoit
Pruvost, Alain
Chu-Van, Emeline
Messager, Aurélie
Leulier, François
Lepousez, Gabriel
Eberl, Gérard
Lledo, Pierre-Marie
author_sort Chevalier, Grégoire
collection PubMed
description Depression is the leading cause of disability worldwide. Recent observations have revealed an association between mood disorders and alterations of the intestinal microbiota. Here, using unpredictable chronic mild stress (UCMS) as a mouse model of depression, we show that UCMS mice display phenotypic alterations, which could be transferred from UCMS donors to naïve recipient mice by fecal microbiota transplantation. The cellular and behavioral alterations observed in recipient mice were accompanied by a decrease in the endocannabinoid (eCB) signaling due to lower peripheral levels of fatty acid precursors of eCB ligands. The adverse effects of UCMS-transferred microbiota were alleviated by selectively enhancing the central eCB or by complementation with a strain of the Lactobacilli genus. Our findings provide a mechanistic scenario for how chronic stress, diet and gut microbiota generate a pathological feed-forward loop that contributes to despair behavior via the central eCB system.
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spelling pubmed-77329822020-12-17 Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system Chevalier, Grégoire Siopi, Eleni Guenin-Macé, Laure Pascal, Maud Laval, Thomas Rifflet, Aline Boneca, Ivo Gomperts Demangel, Caroline Colsch, Benoit Pruvost, Alain Chu-Van, Emeline Messager, Aurélie Leulier, François Lepousez, Gabriel Eberl, Gérard Lledo, Pierre-Marie Nat Commun Article Depression is the leading cause of disability worldwide. Recent observations have revealed an association between mood disorders and alterations of the intestinal microbiota. Here, using unpredictable chronic mild stress (UCMS) as a mouse model of depression, we show that UCMS mice display phenotypic alterations, which could be transferred from UCMS donors to naïve recipient mice by fecal microbiota transplantation. The cellular and behavioral alterations observed in recipient mice were accompanied by a decrease in the endocannabinoid (eCB) signaling due to lower peripheral levels of fatty acid precursors of eCB ligands. The adverse effects of UCMS-transferred microbiota were alleviated by selectively enhancing the central eCB or by complementation with a strain of the Lactobacilli genus. Our findings provide a mechanistic scenario for how chronic stress, diet and gut microbiota generate a pathological feed-forward loop that contributes to despair behavior via the central eCB system. Nature Publishing Group UK 2020-12-11 /pmc/articles/PMC7732982/ /pubmed/33311466 http://dx.doi.org/10.1038/s41467-020-19931-2 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chevalier, Grégoire
Siopi, Eleni
Guenin-Macé, Laure
Pascal, Maud
Laval, Thomas
Rifflet, Aline
Boneca, Ivo Gomperts
Demangel, Caroline
Colsch, Benoit
Pruvost, Alain
Chu-Van, Emeline
Messager, Aurélie
Leulier, François
Lepousez, Gabriel
Eberl, Gérard
Lledo, Pierre-Marie
Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system
title Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system
title_full Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system
title_fullStr Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system
title_full_unstemmed Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system
title_short Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system
title_sort effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732982/
https://www.ncbi.nlm.nih.gov/pubmed/33311466
http://dx.doi.org/10.1038/s41467-020-19931-2
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