Gymnemic acid (GA) isolated from gymnema sylvestre (Retz.) Schult has been shown to display anti-diabetic activity, however the molecular mechanisms governing these effects are unclear. In this study, GA (40,… Click to show full abstract
Gymnemic acid (GA) isolated from gymnema sylvestre (Retz.) Schult has been shown to display anti-diabetic activity, however the molecular mechanisms governing these effects are unclear. In this study, GA (40, 80 mg/kg/day) was evaluated by type 2 diabetes mellitus (T2DM) rats to explore its hypoglycemic activity and underlying mechanisms of action. The results indicated that GA decreased fasting blood glucose (FBG) concentrations by 26.7 %, and lowered insulin concentrations by 16.1 % after oral administration of GA at a dose of 80 mg/kg/day for 6 weeks in T2DM rats. Our data showed that RT-PCR and Western blot analysis indicated that GA up-regulated the expression of phosphatidylinositol-3-kinase (PI3K) and glycogen synthesis (GS), promoted the phosphorylation of protein kinase B (Akt), while down-regulated the expression of glycogen synthesis kinase-3β (GSK-3β) in T2DM rats. In addition, key proteins involved in AMPK-mediated gluconeogenesis (such as phosphoenolpyruvate carboxy kinase (PEPCK) and glucose-6-phosphatase (G6Pase)) were down-regulated in GA-treated T2DM rats. In summary, the hypoglycemic mechanisms of GA may be related to promoting insulin signal transduction and activating PI3K/Akt and AMPK-mediated signaling pathway in T2DM rats.
               
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