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The human gut microbiome includes a diverse array of microbial species, including beneficial commensals and opportunistic pathogens, which interact to support host health. These microbes contribute to essential functions such as nutrient metabolism, immune system modulation, and maintenance of intestinal barrier integrity. However, disruptions to this equilibrium—referred to as dysbiosis—can have widespread physiological consequences.Dysbiosis is often characterized by reduced microbial...

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Studying the Epithelial Effects of Intestinal Inflammation In Vitro on Established Murine Colonoids
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Butyrate enemas upregulate Muc genes expression but decrease adherent mucus thickness in mice colon.

E Gaudier1, M Rival, M-P Buisine

  • 1UMR - PhAN & CRNH, Physiologie des Adaptations Nutritionnelles, Nantes Cedex 1, France.

Physiological Research
|January 18, 2008
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Summary
This summary is machine-generated.

Butyrate, a product of carbohydrate fermentation, increases the expression of colonic mucin genes but decreases the thickness of the protective mucus layer in mice.

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Area of Science:

  • Gastroenterology
  • Molecular Biology
  • Cell Biology

Background:

  • The colonic mucus gel, primarily mucins, protects the gut lining.
  • Butyrate, a fermentation product, influences mucin production, but its specific effects are unclear.

Purpose of the Study:

  • To investigate butyrate's impact on colonic mucin gene expression in vivo.
  • To determine if butyrate affects mucus synthesis and mucus layer thickness.

Main Methods:

  • Mice received daily rectal enemas of butyrate (100 mM) or saline for 7 days.
  • Gene expression of colonic mucins (Muc1, Muc2, Muc3, Muc4) was analyzed.
  • Muc2 protein levels and adherent mucus layer thickness were assessed.

Main Results:

  • Butyrate significantly stimulated the gene expression of both secreted (Muc2) and membrane-linked (Muc1, Muc3, Muc4) mucins.
  • A 6-fold increase in Muc2 gene expression was observed in the proximal colon.
  • Despite increased MUC2 gene expression, the number of Muc2-containing cells remained unchanged, and the adherent mucus layer thickness decreased twofold.

Conclusions:

  • Butyrate upregulates colonic mucin gene expression in vivo.
  • The decrease in adherent mucus layer thickness warrants further investigation into its functional implications for mucosal protection.