Glucose production, gluconeogenesis, and hepatic tricarboxylic acid cycle fluxes measured by nuclear magnetic resonance analysis of a single glucose derivative

ES Jin, JG Jones, M Merritt, SC Burgess, CR Malloy… - Analytical …, 2004 - Elsevier
ES Jin, JG Jones, M Merritt, SC Burgess, CR Malloy, AD Sherry
Analytical biochemistry, 2004Elsevier
A triple-tracer method was developed to provide absolute fluxes contributing to endogenous
glucose production and hepatic tricarboxylic acid (TCA) cycle fluxes in 24-h-fasted rats by
2H and 13C nuclear magnetic resonance (NMR) analysis of a single glucose derivative. A
primed, intravenous [3, 4-13C2] glucose infusion was used to measure endogenous glucose
production; intraperitoneal 2H2O (to enrich total body water) was used to quantify sources of
glucose (TCA cycle, glycerol, and glycogen), and intraperitoneal [U-13C3] propionate was …
A triple-tracer method was developed to provide absolute fluxes contributing to endogenous glucose production and hepatic tricarboxylic acid (TCA) cycle fluxes in 24-h-fasted rats by 2H and 13C nuclear magnetic resonance (NMR) analysis of a single glucose derivative. A primed, intravenous [3,4-13C2]glucose infusion was used to measure endogenous glucose production; intraperitoneal 2H2O (to enrich total body water) was used to quantify sources of glucose (TCA cycle, glycerol, and glycogen), and intraperitoneal [U-13C3] propionate was used to quantify hepatic anaplerosis, pyruvate cycling, and TCA cycle flux. Plasma glucose was converted to monoacetone glucose (MAG), and a single 2H and 13C NMR spectrum of MAG provided the following metabolic data (all in units of μmol/kg/min; n=6): endogenous glucose production (40.4±2.9), gluconeogenesis from glycerol (11.5±3.5), gluconeogenesis from the TCA cycle (67.3±5.6), glycogenolysis (1.0±0.8), pyruvate cycling (154.4±43.4), PEPCK flux (221.7±47.6), and TCA cycle flux (49.1±16.8). In a separate group of rats, glucose production was not different in the absence of 2H2O and [U-13C]propionate, demonstrating that these tracers do not alter the measurement of glucose turnover.
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