# Asiatic Acid Alleviates Renal Damage by Upregulating STBD1-Mediated Glycophagy in Diabetic Kidney Disease

**Authors:** Lei Guo, Peili Wu, Qijian Feng, Xiaochun Lin, Yuan Wang, Minghai Wu, Feifei Cai, Jin Zhang, Chuyi Yang, Xuelin Li, Churan Wen, Yingbei Lin, Nannan Liu, Yuxuan Hu, Huiyun Wang, Xinzhao Fan, Meiping Guan

PMC · DOI: 10.3390/biomedicines13071544 · 2025-06-25

## TL;DR

Asiatic acid may help treat diabetic kidney disease by boosting a protein called STBD1, which helps clear glycogen buildup in the kidneys.

## Contribution

The study identifies STBD1 as a novel therapeutic target for diabetic kidney disease and shows that asiatic acid can modulate glycophagy through this pathway.

## Key findings

- Asiatic acid reduced blood glucose and urinary albumin-to-creatinine ratio in diabetic mice.
- AA reversed glycogen accumulation and restored STBD1 expression in the kidneys.
- STBD1 overexpression in mice produced similar protective effects against kidney damage.

## Abstract

Background/Objectives: The role of glycogen metabolism in diabetic kidney disease (DKD) remains unclear. This study investigated the therapeutic potential of asiatic acid (AA) on glycogen metabolism in DKD and its underlying mechanisms. Methods: A DKD mouse model was established using a high-fat diet and streptozotocin, followed by AA treatment for 8 weeks. Network pharmacology and molecular docking identified STBD1 as a potential target of AA, and its overexpression in mice was performed. Results: AA reduced blood glucose levels and the urinary albumin-to-creatinine ratio (UACR) and downregulated TGFβ-1, KIM-1, and PDK4. Additionally, AA treatment reversed abnormal glycogen accumulation and restored STBD1 expression. Network pharmacology and molecular docking identified STBD1 as a potential target of AA, and its overexpression in mice demonstrated similar beneficial effects. Gene enrichment analysis revealed that STBD1 is involved in key metabolic pathways related to DKD. Conclusions: These findings suggest that AA alleviates renal damage in DKD, possibly through modulation of STBD1, highlighting its therapeutic potential and the critical role of STBD1 in renal glycophagy.

## Linked entities

- **Genes:** STBD1 (starch binding domain 1) [NCBI Gene 8987], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040], HAVCR1 (hepatitis A virus cellular receptor 1) [NCBI Gene 26762], PDK4 (pyruvate dehydrogenase kinase 4) [NCBI Gene 5166]
- **Chemicals:** asiatic acid (PubChem CID 119034)
- **Diseases:** diabetic kidney disease (MONDO:0005016), DKD (MONDO:0005016)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Pdk4 (pyruvate dehydrogenase kinase, isoenzyme 4) [NCBI Gene 27273], Stbd1 (starch binding domain 1) [NCBI Gene 52331] {aka D530019K15Rik, D5Ertd593e}, Alb (albumin) [NCBI Gene 11657] {aka Alb-1, Alb1, BCL001, BCL002, BPL001}, Havcr1 (hepatitis A virus cellular receptor 1) [NCBI Gene 171283] {aka KIM-1, TIM-1, Tim1, Timd1}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}
- **Diseases:** DKD (MESH:D003928), renal (MESH:D006030), Renal Damage (MESH:D007674)
- **Chemicals:** blood glucose (MESH:D001786), glycogen (MESH:D006003), AA (MESH:C017032), streptozotocin (MESH:D013311), creatinine (MESH:D003404)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12293080/full.md

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Source: https://tomesphere.com/paper/PMC12293080