# Phellodendron amurense Rupr. Polysaccharides protects against diabetic nephropathy via alteration of PI3K/GSK-3β/Nrf2/TGF-β/Smad signaling pathway and gut microbiota

**Authors:** Mei Mei, Huawei Sun, Kai Zhang, Feng Zhang, Shiqing Sun, Yu Zhang

PMC · DOI: 10.1007/s13659-025-00566-z · Natural Products and Bioprospecting · 2026-01-10

## TL;DR

This study shows that Phellodendron amurense Rupr. Polysaccharides (PAP) can protect against diabetic kidney disease by improving antioxidant defenses, reducing inflammation, and altering gut bacteria.

## Contribution

The novel finding is that PAP protects against diabetic nephropathy via multiple mechanisms, including gut microbiota modulation and signaling pathway regulation.

## Key findings

- PAP enhances antioxidant capacity and reduces oxidative damage in diabetic nephropathy.
- PAP mitigates renal fibrosis and inflammation by modulating the TGF-β/Smad and Nrf2 pathways.
- PAP protects against kidney injury by altering gut microbiota composition in diabetic rats.

## Abstract

In this study, a diabetic nephropathy (DN) rat model was established using 2% Streptozocin (STZ) solution, and an in vitro DN model was constructed by stimulating HK-2 cells with 30 mM glucose to investigate the mechanism of Phellodendron amurense Rupr. Polysaccharides (PAP) in ameliorating DN. Results demonstrated that PAP, a neutral homogeneous polysaccharide with molecular weight of 1.98 × 105 Da composed of Rha, GalA, Gal, and D-Xyl, exerted renal protective effects through multiple pathways. It enhanced renal antioxidant capacity and alleviated oxidative damage in DN by upregulating PI3K/AKT pathway-related protein expression. Simultaneously, PAP activated the TGF-β/Smad pathway via Nrf2 to mitigate renal fibrosis symptoms in DN, while inhibiting cellular apoptosis. Furthermore, PAP suppressed renal inflammation through gut microbiota reduction, thereby protecting against renal injury in DN rats. This study reveals that PAP alleviates DN symptoms by modulating gut microbiota, enhancing antioxidant and anti-fibrotic capacities, and inhibiting apoptotic pathways, comprehensively elucidating its multifaceted therapeutic mechanisms against DN.

## Linked entities

- **Proteins:** PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha), AKT1 (AKT serine/threonine kinase 1), GABPA (GA binding protein transcription factor subunit alpha), TGFB1 (transforming growth factor beta 1), Smox (Smad on X), GSK3B (glycogen synthase kinase 3 beta)
- **Chemicals:** Streptozocin (PubChem CID 29327), glucose (PubChem CID 5793)
- **Diseases:** diabetic nephropathy (MONDO:0005016)
- **Species:** Rattus norvegicus (taxon 10116), Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** renal inflammation (MESH:D007249), renal fibrosis (MESH:D005355), renal injury (MESH:D007674), DN (MESH:D003928)
- **Chemicals:** PAP (MESH:D010724), Polysaccharides (MESH:D011134), D-Xyl (-), Gal (MESH:C101993), STZ (MESH:D013311), glucose (MESH:D005947), GalA (MESH:C066951)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12790561/full.md

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Source: https://tomesphere.com/paper/PMC12790561