# Long-term regulatory effects of high-fiber low-fat diet on gut microbiota diversity and inflammatory marker expression in DSS-induced recurrent colitis in mice

**Authors:** Jie Tang, Dongyun Hang, Xiaotong He, Qingyu Wang, Lingling Chen, Lingmei Feng, Qin Li, Ming Xu

PMC · DOI: 10.1515/med-2025-1350 · Open Medicine · 2026-01-21

## TL;DR

A high-fiber low-fat diet helps manage colitis in mice by improving gut bacteria diversity and reducing inflammation over time.

## Contribution

The study reveals the long-term benefits of a high-fiber low-fat diet in modulating gut microbiota and inflammation during recurrent colitis.

## Key findings

- HFLF diet improved clinical symptoms and gut microbiota diversity in mice with recurrent colitis.
- The diet increased beneficial bacteria and short-chain fatty acid production.
- It modulated inflammation and barrier-related markers during recurrence-remission cycles.

## Abstract

To evaluate the long-term regulatory effects of high-fiber low-fat (HFLF) diet on gut microbiota diversity and inflammation/barrier-related markers in DSS-induced recurrent colitis mice.

A recurrent DSS model was established through multiple cycles of DSS administration. Mice were randomly assigned to HFLF diet vs. control/standard chow ± positive control groups. Multi-timepoint sampling was conducted throughout the study. 16S rRNA sequencing, SCFA quantification, and qPCR/ELISA/immunohistochemistry/Western blot analyses were performed.

HFLF diet significantly improved clinical phenotype, increased gut microbiota diversity, promoted beneficial bacterial genera, enhanced SCFA production, and modulated inflammation/barrier indicators throughout the recurrence-remission cycles.

HFLF diet provides sustained protection during recurrence-remission processes through microbiota-SCFA-inflammation axis modulation, offering potential translational applications for IBD management.

## Linked entities

- **Diseases:** colitis (MONDO:0005292), IBD (MONDO:0005265)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** COX2 (cytochrome c oxidase subunit II) [NCBI Gene 17709], Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Rela (Rela proto-oncogene, NFKB subunit) [NCBI Gene 19697] {aka p65, p65 NF-kappa B, p65 NFkB}, Hcar2 (hydroxycarboxylic acid receptor 2) [NCBI Gene 80885] {aka Gpr109a, Gpr109b, HM74, Niacr1, PUMA-G, Pumag}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, Cldn3 (claudin 3) [NCBI Gene 12739] {aka Cpetr2, mRVP1}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Ocln (occludin) [NCBI Gene 18260] {aka Ocl}, Mpo (myeloperoxidase) [NCBI Gene 17523] {aka mKIAA4033}, Cldn1 (claudin 1) [NCBI Gene 12737], Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, 16S (DNA segment, 16S) [NCBI Gene 27471], Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Muc2 (mucin 2) [NCBI Gene 17831] {aka 2010015E03Rik, MCM, wnn}
- **Diseases:** HFLF (MESH:D009800), IBD (MESH:D015212), ulcerative colitis (MESH:D003093), dislocation (MESH:D004204), immune dysregulation (OMIM:614878), bloating (MESH:C535647), Inflammation (MESH:D007249), rectal bleeding (MESH:D012002), weight loss (MESH:D015431), CD (MESH:D003424), dysbiosis (MESH:D064806), DSS (MESH:C562576), colitis (MESH:D003092)
- **Chemicals:** LPS (MESH:D008070), sucrose (MESH:D013395), acetyl-CoA (MESH:D000105), lipid (MESH:D008055), TRIzol (MESH:C411644), agarose (MESH:D012685), isobutyrate (MESH:D058610), water (MESH:D014867), CO2 (MESH:D002245), luminal (MESH:D010634), formalin (MESH:D005557), diethyl ether (MESH:D004986), SCFA (MESH:D005232), NaOH (MESH:D012972), Alcian blue (MESH:D000423), valerate (MESH:D014631), eosin (MESH:D004801), acetate (MESH:D000085), conjugated linoleic acid (MESH:D044243), alcohols (MESH:D000438), HCl (MESH:D006851), cellulose (MESH:D002482), inulin (MESH:D007444), dietary fiber (MESH:D004043), hematoxylin (MESH:D006416), pyruvate (MESH:D019289), 2-ethylbutyric acid (-), paraffin (MESH:D010232), methanol (MESH:D000432), bile acid (MESH:D001647), 5-ASA (MESH:D019804), propionate (MESH:D011422), MTBSTFA (MESH:C059151), starch (MESH:D013213), carbohydrate (MESH:D002241), Butyrate (MESH:D002087), xylene (MESH:D014992), pectin (MESH:D010368), nitrogen (MESH:D009584)
- **Species:** Pseudomonadota (proteobacteria, phylum) [taxon 1224], Bacillota (clostridial firmicutes, phylum) [taxon 1239], gut metagenome (species) [taxon 749906], Roseburia hominis (species) [taxon 301301], Helicobacter (genus) [taxon 209], Bifidobacterium (genus) [taxon 1678], Lactobacillus (genus) [taxon 1578], Homo sapiens (human, species) [taxon 9606], Faecalibacterium prausnitzii (species) [taxon 853], Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12917597/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12917597/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12917597/full.md

---
Source: https://tomesphere.com/paper/PMC12917597