Gandi Capsule Improved Podocyte Lipid Metabolism of Diabetic Nephropathy Mice through SIRT1/AMPK/HNF4A Pathway.
Ying ZhangHuijuan YaoChao LiWei SunXiaofei ChenYan CaoYue LiuYan LiuJihui ChenJia QiQiqiang ZhangHai ZhangA-Jing XuJian ZhangPublished in: Oxidative medicine and cellular longevity (2022)
Podocyte lipid accumulation is a potential therapeutic target for diabetic nephropathy (DN). This study was aimed at clarifying the mechanism of Gandi capsule (GDC) ameliorating DN by regulating the lipid metabolism of podocytes. Network pharmacology methods were performed to screen the key molecules and potential targets of GDC for constructing the molecular-protein interaction network of GDC and conducting signal pathway enrichment analysis. GDC was predicted to ameliorate DN through SIRT1/AMPK/HNF4A pathway. Our results showed that GDC improved renal function in db/db mice. Besides, GDC exhibited effectiveness in relieving kidney tissue damage and renal lipid accumulation in db/db mice, and same effects were present in GDC-active ingredient baicalin. We further proved the new role of HNF4A in the lipid metabolism of DN mediated by SIRT1 and AMPK signaling pathways. The results suggested decreased expression of SIRT1 and p-AMPK α in the kidney tissue and increased expression of HNF4A of db/db mice compared with the control group. GDC and baicalin could reverse these expression changes. Furthermore, similar expression changes were observed in the murine podocyte cell line (MPC-5) treated with different concentrations of GDC and baicalin. Our research suggested that GDC and its active ingredient baicalin could alleviate the abnormal lipid metabolism in the kidney of db/db mice and might exert renal protection through the SIRT1/AMPK/HNF4A pathway.
Keyphrases
- diabetic nephropathy
- poor prognosis
- high fat diet induced
- oxidative stress
- skeletal muscle
- ischemia reperfusion injury
- binding protein
- protein kinase
- systematic review
- signaling pathway
- fatty acid
- type diabetes
- insulin resistance
- high glucose
- adipose tissue
- epithelial mesenchymal transition
- high throughput
- inflammatory response
- cell proliferation
- protein protein
- metabolic syndrome
- amino acid
- pi k akt