Evidence map›Paper›PMID 39191839›Full record

ArticleScientific reports2024

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

Candice Lefebvre, Adam Tiffay, Charles-Edward Breemeersch, Virginie Dreux, Christine Bôle-Feysot, Charlène Guérin, Jonathan Breton, Elise Maximin, Magali Monnoye, Pierre Déchelotte and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. Gut microbes · 2026
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  18. Weight Cycling Deregulates Eating Behavior in Mice via the Induction of Durable Gut Dysbiosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Candice LefebvreUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France.
Adam TiffayUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France.
Charles-Edward BreemeerschUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France.
Virginie DreuxUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France.
Christine Bôle-FeysotUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France.
Charlène GuérinUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France.
Jonathan BretonUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France.
Elise MaximinINRAE, AgroParisTech, Micalis Institute, Université Paris-Saclay, Domaine de Vilvert, 78350, Jouy-en-Josas, France.
Magali MonnoyeINRAE, AgroParisTech, Micalis Institute, Université Paris-Saclay, Domaine de Vilvert, 78350, Jouy-en-Josas, France.
Pierre DéchelotteUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France.
Véronique DouardINRAE, AgroParisTech, Micalis Institute, Université Paris-Saclay, Domaine de Vilvert, 78350, Jouy-en-Josas, France.
Alexis GoichonUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France.
Moïse CoëffierUniv Rouen Normandie, INSERM, Normandie Univ, ADEN UMR1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", UFR Santé, 22 Boulevard Gambetta, 76000, Rouen, France. moise.coeffier@univ-rouen.fr.

Funding

Agence Nationale de la Recherche AAPG2020-CE17-0012
6 · The paper itself

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.

Indexed as

Diet, High-FatGastrointestinal MicrobiomeMice, Inbred C57BLAdipose Tissue, WhiteAnimalsBody WeightFemaleInsulin ResistanceIntestinal Barrier FunctionIntestinal MucosaMaleMetabolic DiseasesMiceObesityPermeabilitySex Factors

Identifiers

PMID39191839
PMCPMC11349972

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.