# Traditional Chinese medicine in the treatment of diabetic kidney disease: the mechanisms of signaling pathways regulations

**Authors:** Wencan Li, Chaoqi Lei, Qinxuan Wu, Keqian Chen, Zheng Liu, Qichang Xing, Xiang Liu, Jiani Zhang

PMC · DOI: 10.3389/fendo.2026.1792000 · 2026-02-25

## TL;DR

This paper reviews how traditional Chinese medicine may treat diabetic kidney disease by targeting specific cellular signaling pathways.

## Contribution

The paper systematically reviews TCM's therapeutic potential in DKD through signaling pathways and identifies promising targets and drugs.

## Key findings

- TCM offers multi-target and multi-pathway intervention with low toxicity for DKD.
- Key signaling pathways like Nrf2, TGF-β/Smad, and NF-κB/NLRP3 are highlighted as important in TCM treatment of DKD.
- Several TCM agents such as astragaloside IV and Shengqing Jiangzhuo formula are identified as potentially effective.

## Abstract

Diabetic kidney disease (DKD) represents a diabetes-driven microvascular complication characterized by renal physiological and metabolic disorders and is considered a top-ranking trigger of progression to end-stage renal disease and death in diabetic patients. Although the drugs commonly used in clinical practice for DKD provide some renal protection, their toxic side effects and limited ability to halt further progression of the disease remain unsatisfactory. Traditional Chinese medicine (TCM) brings centuries of accumulated practice and distinct therapeutic strengths to the management of chronic diseases with complex pathogenesis such as DKD. Its characteristics of multi-target and multi-pathway intervention establish a solid material basis for DKD therapy, while its low toxicity profile aligns well with the chronic nature of DKD. This review elaborates on the therapeutic potential of examining TCM’s impact on DKD through the prism of cellular signaling pathways and reveals that the Nrf2, TGF-β/Smad, NF-κB/NLRP3, MAPK, and PI3K/AKT signaling pathways warrant particular attention in the TCM treatment of DKD. The TCM agents involved include astragaloside IV, Shengqing Jiangzhuo formula, Huangkui capsule, Fuxin granules, Liuwei Dihuang pill, Taxus chinensis, Burdock fructooligosaccharide, baicalin, hirudin, rutin, and fermented seaweed extracts. This review aims to refresh and consolidate the signaling pathways engaged by TCM in DKD, sift for promising targets and drugs, and supply both conceptual and experimental scaffolding for future anti-DKD therapeutics.

## Linked entities

- **Proteins:** GABPA (GA binding protein transcription factor subunit alpha), MAPK (mitogen activated kinase-like protein)
- **Chemicals:** astragaloside IV (PubChem CID 158694), baicalin (PubChem CID 64982), hirudin (PubChem CID 72941487), rutin (PubChem CID 5280805)
- **Diseases:** diabetic kidney disease (MONDO:0005016), end-stage renal disease (MONDO:0004375)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}
- **Diseases:** diabetes (MESH:D003920), renal physiological and metabolic disorders (MESH:D012735), death (MESH:D003643), toxicity (MESH:D064420), end-stage renal disease (MESH:D007676), chronic diseases (MESH:D002908), DKD (MESH:D003928)
- **Chemicals:** rutin (MESH:D012431), fructooligosaccharide (MESH:C116580), Huangkui capsule (-), astragaloside IV (MESH:C052064), baicalin (MESH:C038044)
- **Species:** Taxus chinensis (Chinese yew, species) [taxon 29808], Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12975479/full.md

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Source: https://tomesphere.com/paper/PMC12975479