In this study, we demonstrate the use of 2H2O, in a manner analogous to 3H2O, to study gluconeogenic flux (deuterium labeling at the carbon-6 position of glucose) relative to overall flux through glucose 6-phosphate (deuterium labeling at the carbon-2 position of glucose) into glucose output and glycogen synthesis during hyperglycemia. Before the study (4 days), jugular and carotid catheters were placed. Rats were fasted for 17 h before the study. 2H2O was infused for 2 h at 3 ml/h, with a subsequent 1-h equilibration period. A hyperglycemic clamp at 180 mg/dl (10 mM) was then performed for 90 min (plasma samples obtained at 10-min intervals). At the end of the experiment, anesthesia was induced and the liver removed. Gas chromatography-mass spectroscopy isotopomer analysis of four different mass clusters from glucose was used to determine deuterium enrichment on the carbon-2 (E2D) and carbon-6 (E6D) positions of plasma glucose and glycogen-glucose. The results show that the labeling pattern in glycogen and plasma glucose was virtually identical. In addition, the E6D-to-E2D ratio in plasma glucose did not change during hyperglycemia. Additional studies were performed to show that the E6D-to-E2D ratio was decreased in the fed state and that the fed animal, compared with the fasted rat, had a marked increase in the ratio when given an epinephrine infusion. Thus it was concluded that this was a robust new technique for analyzing glucose and glycogen metabolism in rats.(ABSTRACT TRUNCATED AT 250 WORDS)