# Improvement effect of compound Ento-PB on oxazolone-induced ulcerative colitis in rats

**Authors:** Zhi Fan, Jinhu Chen, Jia Wei, ZhiBin Yang, Huai Xiao, Heng Liu

PMC · DOI: 10.1590/acb395524 · Acta Cirúrgica Brasileira · 2024-09-02

## TL;DR

This study shows that the compound Ento-PB reduces inflammation and improves colon damage in rats with ulcerative colitis.

## Contribution

The novel contribution is demonstrating the anti-inflammatory and tissue-repair effects of Ento-PB in a rat model of UC.

## Key findings

- Ento-PB significantly reduced disease activity and macroscopic lesion scores in UC rats.
- Ento-PB inhibited proinflammatory cytokines and promoted anti-inflammatory cytokines.
- Ento-PB enhanced intestinal epithelial repair by increasing EGF expression.

## Abstract

To investigate the impact of the Chinese medicine compound Ento-PB on oxazolone (OXZ)-induced ulcerative colitis (UC) in rats.

UC rats induced by OXZ were treated with Ento-PB. The damage to the colon was assessed using several measures, including the disease activity index (DAI), colon length, colon weight/length ratio, colonic mucosal damage index, and histological score. The levels of interleukin-4 (IL-4), interleukin-10 (IL-10), interleukin-13 (IL-13), epidermal growth factor (EGF), inducible nitric oxide synthase, and total nitric oxide synthase (tNOS) in rat serum, as well as the levels of tumor necrosis factor-α (TNF-α) and myeloperoxidase (MPO) in rat colon tissue, were determined using enzyme-linked immunosorbent assay and conventional kits.

After being treated with Ento-PB, the DAI score and macroscopic lesion score of OXZ-induced UC rats were significantly reduced. Ento-PB prevented the shortening of rat colons, reduced the ratio of colon weight to length, and improved colon tissue lesions. Meanwhile, Ento-PB could significantly inhibit the activities of proinflammatory cytokines TNF-α, IL-13, and MPO, as well as tNOS and iNOS, while upregulating the expression of anti-inflammatory cytokines IL-4 and IL-10. Moreover, a significant increase in the expression level of EGF was observed in UC rats treated with Ento-PB, indicating that Ento-PB could enhance the repair of damaged intestinal epithelial tissue.

Ento-PB demonstrates significant anti-UC activities in OXZ-induced UC rats by regulating the expression levels of inflammatory factors and promoting the repair of colon tissue. This study provides scientific evidence to support the further development of Ento-PB.

## Linked entities

- **Proteins:** IL4 (interleukin 4), IL10 (interleukin 10), IL13 (interleukin 13), EGF (epidermal growth factor), TNF (tumor necrosis factor), MPO (myeloperoxidase)
- **Chemicals:** oxazolone (PubChem CID 1712094)
- **Diseases:** ulcerative colitis (MONDO:0005101)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Il4 (interleukin 4) [NCBI Gene 287287] {aka Il4e12}, Il10 (interleukin 10) [NCBI Gene 25325] {aka IL10X, If2a}, EGF [NCBI Gene 108348113], Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Mpo (myeloperoxidase) [NCBI Gene 303413], Il13 (interleukin 13) [NCBI Gene 116553], Nos2 (nitric oxide synthase 2) [NCBI Gene 24599] {aka Nos2a, iNos}
- **Diseases:** UC (MESH:D003093), inflammatory (MESH:D007249), colon tissue lesions (MESH:D003108), mucosal damage (MESH:D052016)
- **Chemicals:** OXZ (MESH:D010081), Ento-PB (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11368207/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11368207/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC11368207/full.md

---
Source: https://tomesphere.com/paper/PMC11368207