# Effect of Dealcoholized Muscadine Wine on the Development of Spontaneous Colitis and Gut Microbiome in IL-10−/− Mice

**Authors:** Hao Li, Liwei Gu

PMC · DOI: 10.3390/nu17142327 · Nutrients · 2025-07-16

## TL;DR

Dealcoholized muscadine wine may help reduce colitis symptoms in mice by interacting with genes and gut microbes.

## Contribution

This study shows that dealcoholized muscadine wine polyphenols can moderate colitis in IL-10−/− mice through gene-microbe interactions.

## Key findings

- DMW reduced intestinal permeability and inflammatory cytokines in IL-10−/− mice.
- DMW altered gut microbiome beta-diversity in wild-type mice and reduced Akkermansia in both genotypes.
- DMW decreased Parasutterella abundance only in IL-10−/− mice.

## Abstract

Background/Objectives: Colitis is a chronic condition affecting millions worldwide. Purple muscadine wine polyphenols have a unique composition and possible disease-preventive properties. This study aims to determine how dealcoholized muscadine wine (DMW) affects the development of colitis and gut microbiome in IL-10−/− mice, compared to wild types (WT). Methods: Six-week-old male IL-10−/− and WT C57BL/6 mice were fed either a DMW-supplemented diet (4.8% v/w) or a control diet based on AIN-93M for 154 days. Colitis severity was evaluated by disease activity, intestinal permeability, gene expression of cytokines and tight junction proteins in the colon, and inflammatory cytokines in the serum. Fecal samples were collected for gut microbiome profiling via 16S rRNA gene sequencing. Results: DMW contained predominantly anthocyanins and a significant amount of ellagic acid. IL-10−/− mice developed mild colitis as indicated by the disease activity index. DMW × gene interactions decreased intestinal permeability, colonic mRNA levels of IL-1β, and serum TNF-α in the IL-10−/− mice. DMW suppressed the colonic mRNA levels of IL-6, enhanced the gene expression of ZO-1, but did not influence the mRNA level of TNF-α or occludin. While DMW did not alter α-diversity of the gut microbiome, it significantly influenced β-diversity in the WT mice. DMW significantly reduced the relative abundances of Akkermansia in the IL-10−/− and WT mice. DMW and DMW×gene interaction decreased the relative abundance of Parasutterella only in IL-10−/− mice. Conclusions: These results suggested that polyphenols from DMW interacted with genes to moderately alleviate the development of colitis in IL-10−/− mice and could be a useful dietary strategy for IBD prevention.

## Linked entities

- **Genes:** IL10 (interleukin 10) [NCBI Gene 3586], IL1B (interleukin 1 beta) [NCBI Gene 3553], IL6 (interleukin 6) [NCBI Gene 3569], TNF (tumor necrosis factor) [NCBI Gene 7124], TJP1 (tight junction protein 1) [NCBI Gene 7082], si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3) [NCBI Gene 103182021]
- **Chemicals:** anthocyanins (PubChem CID 145858), ellagic acid (PubChem CID 5281855)
- **Diseases:** colitis (MONDO:0005292), IBD (MONDO:0005265)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Ocln (occludin) [NCBI Gene 18260] {aka Ocl}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}
- **Diseases:** Colitis (MESH:D003092), IBD (MESH:D015212)
- **Chemicals:** AIN-93M (-), anthocyanins (MESH:D000872), polyphenols (MESH:D059808), ellagic acid (MESH:D004610)
- **Species:** gut metagenome (species) [taxon 749906], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12298891/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12298891/full.md

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Source: https://tomesphere.com/paper/PMC12298891