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Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward

BACKGROUND: Excessive hedonic consumption is one of the main drivers for weight gain. Identifying contributors of this dysregulation would help to tackle obesity. The gut microbiome is altered during obesity and regulates host metabolism including food intake. RESULTS: By using fecal material transp...

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Autores principales: de Wouters d’Oplinter, Alice, Verce, Marko, Huwart, Sabrina J. P., Lessard-Lord, Jacob, Depommier, Clara, Van Hul, Matthias, Desjardins, Yves, Cani, Patrice D., Everard, Amandine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142783/
https://www.ncbi.nlm.nih.gov/pubmed/37106463
http://dx.doi.org/10.1186/s40168-023-01526-w
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author de Wouters d’Oplinter, Alice
Verce, Marko
Huwart, Sabrina J. P.
Lessard-Lord, Jacob
Depommier, Clara
Van Hul, Matthias
Desjardins, Yves
Cani, Patrice D.
Everard, Amandine
author_facet de Wouters d’Oplinter, Alice
Verce, Marko
Huwart, Sabrina J. P.
Lessard-Lord, Jacob
Depommier, Clara
Van Hul, Matthias
Desjardins, Yves
Cani, Patrice D.
Everard, Amandine
author_sort de Wouters d’Oplinter, Alice
collection PubMed
description BACKGROUND: Excessive hedonic consumption is one of the main drivers for weight gain. Identifying contributors of this dysregulation would help to tackle obesity. The gut microbiome is altered during obesity and regulates host metabolism including food intake. RESULTS: By using fecal material transplantation (FMT) from lean or obese mice into recipient mice, we demonstrated that gut microbes play a role in the regulation of food reward (i.e., wanting and learning processes associated with hedonic food intake) and could be responsible for excessive motivation to obtain sucrose pellets and alterations in dopaminergic and opioid markers in reward-related brain areas. Through untargeted metabolomic approach, we identified the 3-(3’-hydroxyphenyl)propanoic acid (33HPP) as highly positively correlated with the motivation. By administrating 33HPP in mice, we revealed its effects on food reward. CONCLUSIONS: Our data suggest that targeting the gut microbiota and its metabolites would be an interesting therapeutic strategy for compulsive eating, preventing inappropriate hedonic food intake. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01526-w.
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spelling pubmed-101427832023-04-29 Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward de Wouters d’Oplinter, Alice Verce, Marko Huwart, Sabrina J. P. Lessard-Lord, Jacob Depommier, Clara Van Hul, Matthias Desjardins, Yves Cani, Patrice D. Everard, Amandine Microbiome Research BACKGROUND: Excessive hedonic consumption is one of the main drivers for weight gain. Identifying contributors of this dysregulation would help to tackle obesity. The gut microbiome is altered during obesity and regulates host metabolism including food intake. RESULTS: By using fecal material transplantation (FMT) from lean or obese mice into recipient mice, we demonstrated that gut microbes play a role in the regulation of food reward (i.e., wanting and learning processes associated with hedonic food intake) and could be responsible for excessive motivation to obtain sucrose pellets and alterations in dopaminergic and opioid markers in reward-related brain areas. Through untargeted metabolomic approach, we identified the 3-(3’-hydroxyphenyl)propanoic acid (33HPP) as highly positively correlated with the motivation. By administrating 33HPP in mice, we revealed its effects on food reward. CONCLUSIONS: Our data suggest that targeting the gut microbiota and its metabolites would be an interesting therapeutic strategy for compulsive eating, preventing inappropriate hedonic food intake. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01526-w. BioMed Central 2023-04-28 /pmc/articles/PMC10142783/ /pubmed/37106463 http://dx.doi.org/10.1186/s40168-023-01526-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
de Wouters d’Oplinter, Alice
Verce, Marko
Huwart, Sabrina J. P.
Lessard-Lord, Jacob
Depommier, Clara
Van Hul, Matthias
Desjardins, Yves
Cani, Patrice D.
Everard, Amandine
Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward
title Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward
title_full Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward
title_fullStr Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward
title_full_unstemmed Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward
title_short Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward
title_sort obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142783/
https://www.ncbi.nlm.nih.gov/pubmed/37106463
http://dx.doi.org/10.1186/s40168-023-01526-w
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