# Comparison of Anti-Renal Fibrosis Activity of Eucommiae cortex Extract and Its Microbial Fermentation Products

**Authors:** Zhengyou He, Wenyi Jiang, Ruijiao Yao, Wenyan Xiao, Zhiyang Chen, Miao Zheng, Xia Zeng, Jia Li, Zhengwen Li, Yong Jiang

PMC · DOI: 10.3390/ph18050747 · Pharmaceuticals · 2025-05-19

## TL;DR

This study compares the effects of Eucommiae cortex extract and its fermented form on reducing kidney fibrosis in mice with chronic kidney disease.

## Contribution

The study demonstrates that microbial fermentation of Eucommiae cortex enhances its anti-renal fibrosis activity.

## Key findings

- EC and ECF reduced creatinine and urea nitrogen levels in mice with CKD.
- Both treatments down-regulated TGF-β1/Smad signaling pathway markers linked to fibrosis.
- ECF showed reno-protective effects, suggesting potential for clinical drug development.

## Abstract

Background: Renal fibrosis is a common pathological feature of all progressive chronic kidney disease (CKD). Eucommiae cortex (EC) is a valuable economic tree species endemic to China. The microbial fermentation of Chinese medicines can release their active ingredients as effectively as possible or produce new active ingredients with enhanced efficacy and reduced toxic side effects; Methods: The microbial fermentation of EC can produce pinoresinol (Pin) and dehydrodiconiferyl alcohol (DA). In this study, C57 BL/6 mice were fed a diet containing 0.2% adenine, resulting in a model of chronic kidney disease. The effects of EC and EC ferment (ECF) on CKD were explored by the exogenous supplementation of EC and ECF; Results: The results of the study showed that exogenous supplementation with EC and ECF suc-cessfully reduced creatinine and urea nitrogen levels, down-regulated the expression levels of TGF-β1, α-SMA, Smad3, and phospho-Smad3 in the TGF-β1/Smad signaling pathway, and ameliorated renal fibrosis; Conclusions: Both EC and ECF may have reno-protective effects and provide a reference for relevant clinical drug development.

## Linked entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040], ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58], SMAD3 (SMAD family member 3) [NCBI Gene 4088]
- **Chemicals:** pinoresinol (PubChem CID 73399), dehydrodiconiferyl alcohol (PubChem CID 5372367), creatinine (PubChem CID 588), urea nitrogen (PubChem CID 31295)
- **Diseases:** chronic kidney disease (MONDO:0005300), renal fibrosis (MONDO:0000494)

## Full-text entities

- **Genes:** Ighmbp2 (immunoglobulin mu DNA binding protein 2) [NCBI Gene 20589] {aka AEP, Catf1, RIPE3b1, Smbp-2, Smbp2, Smubp2}, Smad3 (SMAD family member 3) [NCBI Gene 17127] {aka Madh3}
- **Diseases:** Renal Fibrosis (MESH:D005355), CKD (MESH:D051436)
- **Chemicals:** creatinine (MESH:D003404), Chinese medicines (-), urea (MESH:D014508), nitrogen (MESH:D009584), DA (MESH:C080686), Pin (MESH:C103298), adenine (MESH:D000225)
- **Species:** 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/PMC12114716/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12114716/full.md

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Source: https://tomesphere.com/paper/PMC12114716