To evaluate the protective effects of
glycosides/
phenol component of
Moutan Cortex (MC) on renal injury of
diabetic nephropathy (DN) rats based on renal function parameters and histopathological examinations(HE staining and transmission electron microscope),and explore its possible mechanism by establishing DN rat models induced by high-
sugar high-fat diet combined with
streptozotocin (STZ). The results showed that compared with the model group, the MC
glycosides/
phenol component high and low dose groups(0.808, 0.404 g•kg⁻¹•d⁻¹) could significantly improve serum
creatinine, blood
urea nitrogen, urine
protein and other abnormal renal function parameters. HE staining and transmission electron microscope results showed thickening of glomerular basement membrane, proliferation of mesangial cells and damages of podocyte structure in major rats of model group. However, the intervention of
glycosides/
phenol component of MC could effectively protect the glomerular injury. To explore its possible mechanism, the expressions of TGF-β1,
fibronectin (FN) and
collagen Ⅳ in renal tissues of rats in each group were detected by Western blot and immunohistochemical assay, and the phosphorylation levels of downstream effect factors (Smad2/3, p38MARK) of TGF-β1 were detected. The results showed that
glycosides/
phenol component of MC could effectively antagonize the activity of TGF-β1, lower the expressions of
fibronectin (FN) and
collagen Ⅳ inextracellular matrix (ECM), and resist against the thickening of glomerular basement membrane. More importantly, its protective effect on renal injury in DN rats may be associated with interfering the conduction of Smad, MARK pathways and resisting against the TGF-β1-induced ECM accumulation.