Summary
In this study, we investigated the biological activities of a novel berberineâmetformin hybrid compound (BMH473) as an antiâdiabetic agent. BMH473 exhibited significant antiâhyperglycaemic and antiâhyperlipidaemic effects on T2DM rats. In white adipose tissue, BMH473 reduced the perirenal and epididymal adipose tissue mass and modulated the lesions in perirenal adipose tissue, by inhibiting the protein expressions of PPARâÆ, C/EBPâα and SREBPâ1c as well as the mRNA expressions of lipogenic genes. Moreover, BMH473 downregulated the levels of proâinflammatory cytokines in perirenal adipose tissue through the suppression of pâNFâÎșB. In liver, BMH473 reduced liver ectopic fat accumulation, by regulating the protein expression levels of SREBPâ1c and PPARâα as well as the mRNA expression levels of lipogenic genes. In addition, BMH473 inhibited hepatic gluconeogenesis by promoting the phosphorylation levels of AMPK α and ACC, and downâregulating the mRNA expression levels of FBPase, G6Pase and PEPCK. Furthermore, BMH473 exhibited significant inhibitory effects on lipogenesis and lipid accumulation in 3T3âL1 adipocytes by modulating the protein expression levels of PPARâÆ, C/EBPâα and SREBPâ1 c as well as the mRNA expression levels of lipogenic genes. In conclusion, our results suggest that the newly synthesized BMH473 is beneficial for maintaining glucose and lipid homeostasis in type 2 diabetic rats, and exhibits better antiâhyperlipidaemic effects compared to metformin and berberine.