# A New Strategy for Treating Renal Fibrosis Based on a Drug‐Food Homogeneous Formula of Traditional Chinese Medicine

**Authors:** Gao Zitian, Tang Yuyan, Huang Luyan, Xu Jiahui, Huang Lusheng, Sun Weiqian, He Haidong, Chen Yu

PMC · DOI: 10.1002/fsn3.71186 · 2025-11-14

## TL;DR

A new traditional Chinese medicine formulation delivered to the colon shows promise in treating kidney fibrosis by improving gut health and reducing inflammation.

## Contribution

A novel medicinal-edible homologous formulation for renal fibrosis via colon administration is proposed and tested.

## Key findings

- Colon administration of the formulation repaired intestinal barriers and reduced systemic inflammation.
- The treatment improved kidney function and reduced fibrosis markers via the PI3K/AKT pathway.
- The formulation shows potential as a therapeutic strategy for renal fibrosis through the gut-kidney axis.

## Abstract

Renal fibrosis is a common pathological feature of chronic kidney disease (CKD) as it progresses to the end stage. Currently, about 10% of adults worldwide are affected by this disease. In recent years, significant progress has been made in the field of renal fibrosis treatment, with both traditional drugs and innovative therapies showing new hope. In this study, we propose a novel therapeutic strategy for renal fibrosis based on the traditional Chinese medicine concept of “medicinal and edible homology”. This involves the use of a compound formulation comprising red ginseng, dandelion, and oyster shell, and evaluating its therapeutic effect on renal fibrosis through the colon administration route. Through integrated network pharmacology and molecular docking analyses, we identified AKT1, JUN, TNF, HSP90AA1, and IL‐6 as core targets, with the PI3K/AKT signaling pathway playing a key role. Colon administration of the formulation significantly restored intestinal barrier function by upregulating tight junction proteins ZO‐1 and occludin, thereby reducing circulating endotoxin (LPS) and systemic inflammatory markers (IL‐6, IL‐1β). Concurrently, the treatment intervened in the renal PI3K/AKT pathway, upregulated expressions of PI3KR1, PKCa, and AKT1/2/3, improved renal function (reduced creatinine and urea nitrogen), and ameliorated fibrosis markers (reduced fibronectin and α‐SMA, increased E‐cadherin). These findings demonstrate that the medicinal‐edible homologous formulation alleviates renal fibrosis via modulation of the gut–kidney axis, combining intestinal barrier repair with suppression of pro‐fibrotic signaling. This study supports the use of colon‐delivered traditional Chinese medicine as a promising therapeutic strategy for renal fibrosis.

Renal fibrosis is a common pathological feature of chronic kidney disease as it progresses to the end stage. This study explores a novel medicinal‐edible homologous formulation delivered via colon to target the gut–kidney axis. The formulation repaired the intestinal barrier, reduced systemic LPS and inflammation, and subsequently suppressed renal fibrosis by modulating the PI3K/AKT pathway, ultimately improving renal function. Our work demonstrates that the colon‐delivered herbal strategy is a promising therapeutic approach for combating renal fibrosis.

## Linked entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], JUN (Jun proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3725], TNF (tumor necrosis factor) [NCBI Gene 7124], HSP90AA1 (heat shock protein 90 alpha family class A member 1) [NCBI Gene 3320], IL6 (interleukin 6) [NCBI Gene 3569], PRKCA (protein kinase C alpha) [NCBI Gene 5578], TJP1 (tight junction protein 1) [NCBI Gene 7082], si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3) [NCBI Gene 103182021], IL6 (interleukin 6) [NCBI Gene 3569], IL1B (interleukin 1 beta) [NCBI Gene 3553], fn1.S (fibronectin 1 S homeolog) [NCBI Gene 397744], ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58], shg (shotgun) [NCBI Gene 37386]
- **Diseases:** renal fibrosis (MONDO:0000494), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Diseases:** CKD (MESH:D051436), inflammatory (MESH:D007249), Renal Fibrosis (MESH:D005355)
- **Chemicals:** LPS (MESH:D008070), nitrogen (MESH:D009584), creatinine (MESH:D003404), urea (MESH:D014508)
- **Species:** Taraxacum officinale (dandelion, species) [taxon 50225]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12616506/full.md

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Source: https://tomesphere.com/paper/PMC12616506