Sex-dependent effects of a high fat diet on metabolic disorders, intestinal barrier function and gut microbiota in mouse

Abstract Obesity is often associated with sex-dependent metabolic complications, in which altered intestinal barrier function and gut microbiota contribute. We aimed to characterize in mice the sex-dependent effects of a high fat diet on these parameters. Male and female C57BL/6 mice received a stan...

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Published in:Scientific Reports
Main Authors: Candice Lefebvre, Adam Tiffay, Charles-Edward Breemeersch, Virginie Dreux, Christine Bôle-Feysot, Charlène Guérin, Jonathan Breton, Elise Maximin, Magali Monnoye, Pierre Déchelotte, Véronique Douard, Alexis Goichon, Moïse Coëffier
Format: Article
Language:English
Published: Nature Portfolio 2024-08-01
Online Access:https://doi.org/10.1038/s41598-024-70931-4
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author Candice Lefebvre
Adam Tiffay
Charles-Edward Breemeersch
Virginie Dreux
Christine Bôle-Feysot
Charlène Guérin
Jonathan Breton
Elise Maximin
Magali Monnoye
Pierre Déchelotte
Véronique Douard
Alexis Goichon
Moïse Coëffier
author_facet Candice Lefebvre
Adam Tiffay
Charles-Edward Breemeersch
Virginie Dreux
Christine Bôle-Feysot
Charlène Guérin
Jonathan Breton
Elise Maximin
Magali Monnoye
Pierre Déchelotte
Véronique Douard
Alexis Goichon
Moïse Coëffier
author_sort Candice Lefebvre
collection DOAJ
container_title Scientific Reports
description Abstract Obesity is often associated with sex-dependent metabolic complications, in which altered intestinal barrier function and gut microbiota contribute. We aimed to characterize in mice the sex-dependent effects of a high fat diet on these parameters. Male and female C57BL/6 mice received a standard (SD) or high fat diet (HFD; 60% kcal from fat) during 14 weeks (W14). Body composition, glucose tolerance, insulin sensitivity, intestinal permeability, colonic expression of 44 genes encoding factors involved in inflammatory response and gut barrier function, cecal microbiota, plasma adipokines and white adipose tissue response have been assessed. Both male and female HFD mice exhibited an increase of body weight and fat mass gain and glucose intolerance compared to SD mice. However, only male HFD mice tended to develop insulin resistance associated to increased Tnfα and Ccl2 mRNA expression in perigonadal adipose tissue. By contrast, only female HFD mice showed significant intestinal hyperpermeability that was associated with more markedly altered colonic inflammatory response. Cecal microbiota richness was markedly reduced in both sexes (Observed species) with sex-dependent modifications at the phyla or family level, e.g. decreased relative abundance of Bacillota and Lachnospiraceae in females, increased of Bacteroidaceae in males. Interestingly, some of these microbiota alterations were correlated with peripheral metabolic and inflammatory markers. In conclusions, male and female mice exhibit different responses to a high fat diet with specific changes of gut microbiota, intestinal barrier function, colonic and white adipose tissue inflammation, metabolic markers and body weight gain. The underlying mechanisms should be deciphered in further investigations.
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spelling doaj-art-7597ddd6a7ef42e2b7a01ae2c68acb2d2025-08-20T00:55:15ZengNature PortfolioScientific Reports2045-23222024-08-0114111610.1038/s41598-024-70931-4Sex-dependent effects of a high fat diet on metabolic disorders, intestinal barrier function and gut microbiota in mouseCandice Lefebvre0Adam Tiffay1Charles-Edward Breemeersch2Virginie Dreux3Christine Bôle-Feysot4Charlène Guérin5Jonathan Breton6Elise Maximin7Magali Monnoye8Pierre Déchelotte9Véronique Douard10Alexis Goichon11Moïse Coëffier12Univ Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéINRAE, AgroParisTech, Micalis Institute, Université Paris-SaclayINRAE, AgroParisTech, Micalis Institute, Université Paris-SaclayUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéINRAE, AgroParisTech, Micalis Institute, Université Paris-SaclayUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 “Nutrition, Inflammation and Microbiota-Gut-Brain Axis”, UFR SantéAbstract Obesity is often associated with sex-dependent metabolic complications, in which altered intestinal barrier function and gut microbiota contribute. We aimed to characterize in mice the sex-dependent effects of a high fat diet on these parameters. Male and female C57BL/6 mice received a standard (SD) or high fat diet (HFD; 60% kcal from fat) during 14 weeks (W14). Body composition, glucose tolerance, insulin sensitivity, intestinal permeability, colonic expression of 44 genes encoding factors involved in inflammatory response and gut barrier function, cecal microbiota, plasma adipokines and white adipose tissue response have been assessed. Both male and female HFD mice exhibited an increase of body weight and fat mass gain and glucose intolerance compared to SD mice. However, only male HFD mice tended to develop insulin resistance associated to increased Tnfα and Ccl2 mRNA expression in perigonadal adipose tissue. By contrast, only female HFD mice showed significant intestinal hyperpermeability that was associated with more markedly altered colonic inflammatory response. Cecal microbiota richness was markedly reduced in both sexes (Observed species) with sex-dependent modifications at the phyla or family level, e.g. decreased relative abundance of Bacillota and Lachnospiraceae in females, increased of Bacteroidaceae in males. Interestingly, some of these microbiota alterations were correlated with peripheral metabolic and inflammatory markers. In conclusions, male and female mice exhibit different responses to a high fat diet with specific changes of gut microbiota, intestinal barrier function, colonic and white adipose tissue inflammation, metabolic markers and body weight gain. The underlying mechanisms should be deciphered in further investigations.https://doi.org/10.1038/s41598-024-70931-4
spellingShingle Candice Lefebvre
Adam Tiffay
Charles-Edward Breemeersch
Virginie Dreux
Christine Bôle-Feysot
Charlène Guérin
Jonathan Breton
Elise Maximin
Magali Monnoye
Pierre Déchelotte
Véronique Douard
Alexis Goichon
Moïse Coëffier
Sex-dependent effects of a high fat diet on metabolic disorders, intestinal barrier function and gut microbiota in mouse
title Sex-dependent effects of a high fat diet on metabolic disorders, intestinal barrier function and gut microbiota in mouse
title_full Sex-dependent effects of a high fat diet on metabolic disorders, intestinal barrier function and gut microbiota in mouse
title_fullStr Sex-dependent effects of a high fat diet on metabolic disorders, intestinal barrier function and gut microbiota in mouse
title_full_unstemmed Sex-dependent effects of a high fat diet on metabolic disorders, intestinal barrier function and gut microbiota in mouse
title_short Sex-dependent effects of a high fat diet on metabolic disorders, intestinal barrier function and gut microbiota in mouse
title_sort sex dependent effects of a high fat diet on metabolic disorders intestinal barrier function and gut microbiota in mouse
url https://doi.org/10.1038/s41598-024-70931-4
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