tailieunhanh - Báo cáo Y học: Elucidation of the role of fructose 2,6-bisphosphate in the regulation of glucose fluxes in mice usingin vivo 13 C NMR measurements of hepatic carbohydrate metabolism

Fructose 2,6-bisphosphate (Fru-2,6-P2 ) plays an important role in the regulation of major carbohydrate fluxes as both allosteric activator and inhibitor of target enzymes. To examine the role of Fru-2,6-P2in the regulation of hepatic carbohydrate metabolism in vivo,Fru-2,6-P2 levels were elevated in ADM mice with adenovirus-mediated overex-pression of a double mutant bifunctional enzyme, 6-phos-phofructo-2-kinase/fructose-2,6-bisphosphatase (n¼6), in comparison to normal control mice (control,n¼6). . | Eur. J. Biochem. 269 4418-4426 2002 FEBS 2002 doi Elucidation of the role of fructose 2 6-bisphosphate in the regulation of glucose fluxes in mice using in vivo 13C NMR measurements of hepatic carbohydrate metabolism In-Youna Choi1 Chaodona Wu2 David A Okar2 Alex J. Lanae2 and Rolf Gruetter1 3 Bl . Departments of Radiology1 Biochemistry Molecular Biology and Biophysics2 Neuroscience3 University of Minnesota Medical School Minneapolis MN USA Fructose 2 6-bisphosphate Fru-2 6-P2 plays an important role in the regulation of major carbohydrate fluxes as both allosteric activator and inhibitor of target enzymes. To examine the role of Fru-2 6-P2 in the regulation of hepatic carbohydrate metabolism in vivo Fru-2 6-P2 levels were elevated in ADM mice with adenovirus-mediated overexpression of a double mutant bifunctional enzyme 6-phos-phofructo-2-kinase fructose-2 6-bisphosphatase n 6 in comparison to normal control mice control n 6 . The rates of hepatic glycogen synthesis in the ADM and control mouse liver in vivo were measured using new advances in 13C NMR including 3D localization in conjunction with 1-13C glucose infusion. In addition to glycogen C1 the C6 and C2-C5 signals were measured simultaneously for the first time in vivo which provide the basis for the estimation of direct and indirect synthesis of glycogen in the liver. The rate of label incorporation into glycogen C1 was not different between the control and ADM group whereas the rate of label incorporation into glycogen C6 signals was in the ADM group pmol-g_1-h-1 which was higher than that of the control group of pmol-g_1-h-1 P . The rates of net glycogen synthesis determined by the glycogen C2-C5 signal changes were twofold higher in the ADM group P . The results provide direct in vivo evidence that the effects of elevated Fru-2 6-P2 levels in the liver include increased glycogen storage through indirect synthesis of glycogen. These observations

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