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High-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome

Diets rich in added sugars are associated with metabolic diseases, and studies have shown a link between these pathologies and changes in the microbiome. Given the reported associations in animal models between the microbiome and brown adipose tissue (BAT) function, and the alterations in the microb...

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Autores principales: Richard, Gabriel, Blondin, Denis P., Syed, Saad A., Rossi, Laura, Fontes, Michelle E., Fortin, Mélanie, Phoenix, Serge, Frisch, Frédérique, Dubreuil, Stéphanie, Guérin, Brigitte, Turcotte, Éric E., Lepage, Martin, Surette, Michael G., Schertzer, Jonathan D., Steinberg, Gregory R., Morrison, Katherine M., Carpentier, André C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512695/
https://www.ncbi.nlm.nih.gov/pubmed/36130480
http://dx.doi.org/10.1016/j.xcrm.2022.100742
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author Richard, Gabriel
Blondin, Denis P.
Syed, Saad A.
Rossi, Laura
Fontes, Michelle E.
Fortin, Mélanie
Phoenix, Serge
Frisch, Frédérique
Dubreuil, Stéphanie
Guérin, Brigitte
Turcotte, Éric E.
Lepage, Martin
Surette, Michael G.
Schertzer, Jonathan D.
Steinberg, Gregory R.
Morrison, Katherine M.
Carpentier, André C.
author_facet Richard, Gabriel
Blondin, Denis P.
Syed, Saad A.
Rossi, Laura
Fontes, Michelle E.
Fortin, Mélanie
Phoenix, Serge
Frisch, Frédérique
Dubreuil, Stéphanie
Guérin, Brigitte
Turcotte, Éric E.
Lepage, Martin
Surette, Michael G.
Schertzer, Jonathan D.
Steinberg, Gregory R.
Morrison, Katherine M.
Carpentier, André C.
author_sort Richard, Gabriel
collection PubMed
description Diets rich in added sugars are associated with metabolic diseases, and studies have shown a link between these pathologies and changes in the microbiome. Given the reported associations in animal models between the microbiome and brown adipose tissue (BAT) function, and the alterations in the microbiome induced by high-glucose or high-fructose diets, we investigated the potential causal link between high-glucose or -fructose diets and BAT dysfunction in humans. Primary outcomes are changes in BAT cold-induced thermogenesis and the fecal microbiome (clinicaltrials.gov, NCT03188835). We show that BAT glucose uptake, but not thermogenesis, is impaired by a high-fructose but not high-glucose diet, in the absence of changes in the gastrointestinal microbiome. We conclude that decreased BAT glucose metabolism occurs earlier than other pathophysiological abnormalities during fructose overconsumption in humans. This is a potential confounding factor for studies relying on (18)F-FDG to assess BAT thermogenesis.
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spelling pubmed-95126952022-09-28 High-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome Richard, Gabriel Blondin, Denis P. Syed, Saad A. Rossi, Laura Fontes, Michelle E. Fortin, Mélanie Phoenix, Serge Frisch, Frédérique Dubreuil, Stéphanie Guérin, Brigitte Turcotte, Éric E. Lepage, Martin Surette, Michael G. Schertzer, Jonathan D. Steinberg, Gregory R. Morrison, Katherine M. Carpentier, André C. Cell Rep Med Article Diets rich in added sugars are associated with metabolic diseases, and studies have shown a link between these pathologies and changes in the microbiome. Given the reported associations in animal models between the microbiome and brown adipose tissue (BAT) function, and the alterations in the microbiome induced by high-glucose or high-fructose diets, we investigated the potential causal link between high-glucose or -fructose diets and BAT dysfunction in humans. Primary outcomes are changes in BAT cold-induced thermogenesis and the fecal microbiome (clinicaltrials.gov, NCT03188835). We show that BAT glucose uptake, but not thermogenesis, is impaired by a high-fructose but not high-glucose diet, in the absence of changes in the gastrointestinal microbiome. We conclude that decreased BAT glucose metabolism occurs earlier than other pathophysiological abnormalities during fructose overconsumption in humans. This is a potential confounding factor for studies relying on (18)F-FDG to assess BAT thermogenesis. Elsevier 2022-09-20 /pmc/articles/PMC9512695/ /pubmed/36130480 http://dx.doi.org/10.1016/j.xcrm.2022.100742 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Richard, Gabriel
Blondin, Denis P.
Syed, Saad A.
Rossi, Laura
Fontes, Michelle E.
Fortin, Mélanie
Phoenix, Serge
Frisch, Frédérique
Dubreuil, Stéphanie
Guérin, Brigitte
Turcotte, Éric E.
Lepage, Martin
Surette, Michael G.
Schertzer, Jonathan D.
Steinberg, Gregory R.
Morrison, Katherine M.
Carpentier, André C.
High-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome
title High-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome
title_full High-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome
title_fullStr High-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome
title_full_unstemmed High-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome
title_short High-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome
title_sort high-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512695/
https://www.ncbi.nlm.nih.gov/pubmed/36130480
http://dx.doi.org/10.1016/j.xcrm.2022.100742
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