Kunxian capsule alleviates podocyte injury and proteinuria by inactivating & beta;-catenin in db/db mice

Background: Diabetic kidney disease (DKD) remains the primary cause of endstage renal disease (ESRD) globally, but treatment options are limited. Kunxian capsule (KXC) has been utilized for the treatment of autoimmune diseases and IgA nephropathy in China. However, its effect on DKD remains poorly investigated. Therefore, this study aimed to explore the protective effect of KXC in db/db mice and elucidate its underlying mechanism. Methods: The renoprotective effects of KXC were assessed in a DKD mouse model using male BKS db/db diabetic mice. After 8 weeks of treatment, the urinary albumin-to-creatinine ratio (UACR), blood biochemical parameters, renal histopathological manifestation, and podocyte ultrastructural changes were evaluated. Additionally, the expression of podocyte epithelial-to-mesenchymal transition (EMT) markers [WT1, ZO-1, and collogen I (Col1a1)] was quantitatively analyzed. Furthermore, we explored the role of KXC in the ss-catenin signaling pathway to elucidate the underlying mechanism of KXC's renoprotective effect. Results: KXC treatment effectively reduced albuminuria and attenuated renal structural abnormalities in db/db mice. Additionally, KXC restored the protein and mRNA expression of WT1 and ZO-1 while suppressing the expression of Col1a1 in db/db mice, indicating its ability to alleviate podocyte EMT. Mechanistically, KXC exerted a significant suppressive effect on the activation of ss-catenin signaling in diabetic kidneys. Conclusion: KXC has the potential to protect podocytes during DKD by alleviating podocyte EMT through inactivating ss-catenin signaling.

Automated summary

This study investigated the protective effect of Kunxian capsule (KXC) in a diabetic kidney disease (DKD) mouse model and elucidated its underlying mechanism. The results showed that KXC effectively reduced albuminuria and attenuated renal structural abnormalities in the mice. Furthermore, KXC restored the expression of podocyte markers and suppressed the activation of the β-catenin signaling pathway. In conclusion, KXC has the potential to protect podocytes during DKD by alleviating podocyte epithelial-to-mesenchymal transition (EMT) through inactivating β-catenin signaling.