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Impact of high-fat diet on ovarian epigenetics: Insights from altered intestinal butyric acid levels. | LitMetric

AI Article Synopsis

  • - The study aimed to explore how a high-fat diet (HFD) affects a specific gut bacterium, Roseburia intestinalis, and butyric acid levels, as well as their implications for ovarian function and gene regulation in female mice.
  • - Mice fed an HFD for 36 weeks experienced increased body weight, reduced levels of Roseburia intestinalis and butyric acid, decreased intestinal goblet cells, and signs of inflammation, along with impaired development of ovarian follicles and altered epigenetic markers.
  • - The findings suggest that a long-term high-fat diet can harm female reproductive health by disrupting gut bacteria and inflammation, which negatively influences both ovarian function and epigenetic processes.

Article Abstract

Objective: To investigate the effects of a high-fat diet (HFD) on the gut bacterium Roseburia intestinalis and butyric acid levels, and to assess their impact on ovarian function and epigenetic markers in mice.

Methods: A total of 20 female ICR mice aged 4 weeks were randomly assigned to two groups and fed either a control diet (CD) or an HFD for 36 weeks. Post-intervention, ileal contents were analyzed for the quantification of butyric acid using ELISA, while feces were obtained for Roseburia intestinalis expression assessment via qPCR. Histological evaluations of intestinal and ovarian tissues included H&E and Alcian Blue-Periodic Acid Schiff (AB-PAS) staining, alongside immunohistochemical analysis for F4/80, and immunofluorescent detection of Occludin, ZO-1, 5 mC, and H3K36me3. Ovarian health was assessed through follicle counts and morphological evaluations. Statistical analyses were performed using GraphPad Prism 8.0, with P < 0.05 considered significant.

Results: After 36 weeks, the HFD group showed significantly higher body weight compared to the CD group (P < 0.01). The HFD led to a decrease in Roseburia intestinalis and butyric acid levels, a reduction in intestinal goblet cells, and an increase in intestinal inflammation. Histological analyses revealed impaired ovarian follicular development and enhanced inflammation in the HFD mice, with immunofluorescent staining showing downregulation of the ovarian epigenetic markers 5 mC and H3K36me3.

Conclusion: Our study demonstrates that long-term HFD negatively impacts ovarian function and epigenetic regulation. We found decreased levels of the gut bacterium Roseburia intestinalis and its metabolite, butyric acid, which contribute to these adverse effects. Additionally, the associated intestinal inflammation and compromised mucosal barrier may contribute to these adverse outcomes on female reproductive health.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11252756PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e33170DOI Listing

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