# Ketone ester supplementation protects from experimental colitis via improved goblet cell differentiation and function

**Authors:** Nadine Rohwer, Anika Sander, Soeren Ocvirk, Michelle Wiebel, Anja A. Kühl, Nils Helge Schebb, Tilman Grune, Karsten-H. Weylandt

PMC · DOI: 10.1007/s00394-025-03833-4 · European Journal of Nutrition · 2025-11-12

## TL;DR

Ketone ester supplements may help reduce intestinal inflammation by improving mucus barrier function and gut bacteria balance in mice with colitis.

## Contribution

This study demonstrates that ketone esters, not a ketogenic diet, reduce colitis severity through goblet cell and mucus barrier enhancement.

## Key findings

- Ketone ester supplementation reduced colitis severity in murine models.
- KE increased mucin2 expression and goblet cell differentiation.
- KE increased abundance of Akkermansia, a gut bacteria linked to intestinal health.

## Abstract

A ketogenic diet (KD), high in fat and low in carbohydrates, induces ketosis characterized by elevated circulating ketone bodies. While both KD and ketone bodies have demonstrated therapeutic potential in various pathophysiological conditions, their effect on inflammatory bowel diseases remains controversial. This study aimed to investigate the impact of a KD and ketone ester (KE), an ingestible form of ketone bodies, on intestinal inflammation.

Acute dextran sodium sulfate (DSS)- and 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced murine colitis models were used to evaluate and compare the effects of KD feeding and KE supplementation on intestinal inflammation, the mucus barrier and gut microbiota composition.

KD feeding did not significantly affect colitis activity, whereas KE supplementation alleviated colitis in both models investigated. KE-induced mitigation of colitis was associated with increased mucin2 expression, indicating enhanced colonic mucus barrier integrity. KE supplementation also improved goblet cell function and differentiation, as evidenced by increased goblet cell numbers and the upregulation of goblet cell differentiation markers. Furthermore, 16S rRNA sequencing analysis revealed that KE supplementation resulted in higher abundances of mucus-degrading Akkermansia, a genus believed to play a key role in maintaining intestinal homeostasis.

The present study suggests that KE represent an effective anti-inflammatory dietary supplement in the context of acute colitis, potentially by modulating mucin2 expression, goblet cell differentiation, and the abundance of Akkermansia. Although promising, these findings remain preliminary, and further investigations are needed to explore the therapeutic potential of KE as a dietary supplement in patients with inflammatory bowel disease.

The online version contains supplementary material available at 10.1007/s00394-025-03833-4.

## Linked entities

- **Chemicals:** 2,4,6-trinitrobenzene sulfonic acid (PubChem CID 11045)
- **Diseases:** colitis (MONDO:0005292), inflammatory bowel disease (MONDO:0005265)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** MUC2 (mucin 2, oligomeric mucus/gel-forming) [NCBI Gene 4583] {aka MLP, MUC-2, SMUC}
- **Diseases:** inflammatory bowel disease (MESH:D015212), inflammatory (MESH:D007249), colitis (MESH:D003092), ketosis (MESH:D007662)
- **Chemicals:** carbohydrates (MESH:D002241), ketone bodies (MESH:D007657), 2,4,6-trinitrobenzene sulfonic acid (-)
- **Species:** Akkermansia (genus) [taxon 239934], Homo sapiens (human, species) [taxon 9606], 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/PMC12611996/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12611996/full.md

---
Source: https://tomesphere.com/paper/PMC12611996