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Changes in hepatic glycogen cycling during a glucose load in healthy humans
Authors:H. Stingl  V. Chandramouli  W. C. Schumann  A. Brehm  P. Nowotny  W. Waldhäusl  B. R. Landau  M. Roden
Affiliation:(1) Division of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria;(2) Departments of Medicine and Biochemistry, Case Western Reserve University, Cleveland, OH, USA;(3) First Medical Department, Hanusch Hospital, Heinrich Collin Strasse 30, A-1140 Vienna, Austria
Abstract:Aims/hypothesis Glycogen cycling, i.e. simultaneous glycogen synthesis and glycogenolysis, affects estimates of glucose fluxes using tracer techniques and may contribute to hyperglycaemia in diabetic conditions. This study presents a new method for quantifying hepatic glycogen cycling in the fed state. Glycogen is synthesised from glucose by the direct and indirect (gluconeogenic) pathways. Since glycogen is also synthesised from glycogen, i.e. glycogen→glucose 1-phosphate→glycogen, that synthesised through the direct and indirect pathways does not account for 100% of glycogen synthesis. The percentage contribution of glycogen cycling to glycogen synthesis then equals the difference between the sum of the percentage contributions of the direct and indirect pathways and 100. Materials and methods The indirect and direct pathways were measured independently in nine healthy volunteers who had fasted overnight. They ingested 2H2O (5 ml/kg body water) and were infused with [5-3H]glucose and acetaminophen (paracetamol; 1 g) during hyperglycaemic clamps (7.8 mmol/l) lasting 8 h. The percentage contribution of the indirect pathway was calculated from the ratio of 2H enrichments at carbon 5 to that at carbon 2, and the contribution of the direct pathway was determined from the 3H-specific activity, relative to plasma glucose, of the urinary glucuronide excreted between 2 and 4, 4 and 6, and 6 and 8 h. Results Glucose infusion rates increased (p<0.01) to ∼50 μmol kg−1 min−1. Plasma insulin and the insulin : glucagon ratio rose ∼3.6- and ∼8.3-fold (p<0.001), respectively. From the difference between 100% and the sum of the direct (2–4 h, 54±6%; 4–6 h, 59±5%; 6–8 h, 63±4%) and indirect (32±3, 38±4, 36±3%) pathways, glycogen cycling was seen to be decreased (p<0.05) from 14±4% (2–4 h) to 4±3% (4–6 h) and 1±3% (6–8 h). Conclusions/interpretation This method allows measurement of hepatic glycogen cycling in the fed state and demonstrates that glycogen cycling occurs most in the early hours after glucose loading subsequent to a fast.
Keywords:Deuterated water  Gluconeogenesis  Glucose fluxes  Glycogenolysis  Hepatic glycogen cycling
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