Fig. 15From: Elucidation of possible mechanisms of the antidiabetic potential of Zn-loaded Bryophyllum pinnatum (Lam.) extracts in experimental animal modelsMechanism of action of extracts through AMPK activation results in increase in glucose uptake, inhibition of gluconeogenesis and fatty acid synthesis. Phosphoenolpyruvate carboxykinase = PEPCK, Protein kinase A = PKA, Glucose 6-phosphatase = G6Pase, Phosphodiesterase 4B = PDE4B, AMP-activated protein kinase = AMPK, Liver kinase B1 = LKB1, Mouse protein-25 = MO-25, Lep R = Leptin R, Protein Phosphatase 2A = PP 2A, Sterol regulatory element-binding proteins = SREBPs, Stearoyl-CoA Desaturase-1 = SCD1, HMG-CoA Reductase = 3-hydroxy-3-methyl-glutaryl-CoA reductase = HMGR, Carnitine Palmitoyl-transferase I = CPT1, Phosphofructokinase 2 = PFK2, Phosphoenolpyruvate carboxykinase = PEPCK, Mammalian target of rapamycin = mTORBack to article page