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The Journal of Clinical Endocrinology & Metabolism Vol. 86, No. 5 2220-2226
Copyright © 2001 by The Endocrine Society


Original Studies

The Quantification of Gluconeogenesis in Healthy Men by 2H2O and [2-13C]Glycerol Yields Different Results: Rates of Gluconeogenesis in Healthy Men Measured with 2H2O Are Higher Than Those Measured with [2-13C]Glycerol1

M. T. Ackermans, A. M. Pereira Arias, P. H. Bisschop, E. Endert, H. P. Sauerwein and J. A. Romijn

Department of Clinical Chemistry, Laboratory of Endocrinology and Radiochemistry (M.T.A., E.E.), and Department of Internal Medicine and Endocrinology (P.H.B., H.P.S.), Academic Medical Center, University of Amsterdam, 1100 DD Amsterdam; and Department of Endocrinology, Leiden University Medical Center (A.M.P.A., P.H.B., J.A.R.), Leiden, 2300 RC The Netherlands

Address all correspondence and requests for reprints to: M. T. Ackermans, Ph.D., Department of Clinical Chemistry, Laboratory of Endocrinology and Radiochemistry, F2-111, Academic Medical Center, P.O. Box 22660, 1100 DD Amsterdam, The Netherlands. E-mail: m.t.ackermans{at}amc.uva.nl

The quantification of gluconeogenesis (GNG) by 2H2O and [2-13C]glycerol and the mass isotopomer dilution analysis of glucose does not involve assumptions regarding the enrichment of the oxaloacetate precursor pool. To compare these two methods we measured GNG in six healthy postabsorptive males under identical, strictly standardized, eucaloric conditions, once after oral administration of 2H2O and once during a primed continuous infusion of [2-13C]glycerol. Endogenous glucose production (EGP) was measured by infusion of [6,6-2H2]glucose. EGP was not different after 2H2O administration or during [2-13C]glycerol infusion (12.2 ± 0.7 vs. 11.7 ± 0.3 µmol/kg·min). However, GNG measured after 2H2O administration was significantly higher than that during [2-13C]glycerol infusion (7.4 ± 0.7 vs. 4.9 ± 0.6 µmol/kg·min; P = 0.03), representing approximately 60% and 41% of EGP, respectively. The 2H2O study was repeated during primed continuous infusion of unlabeled glycerol, showing that infusion of glycerol at the rate used in the [2-13C]glycerol method does not affect the measurement of GNG with 2H2O, viz. 7.4 ± 0.7 without glycerol vs. 7.6 ± 0.9 µmol/kg·min with glycerol, representing approximately 60% vs. 62% of EGP. In conclusion, GNG measured by 2H2O yields higher results than those measured by [2-13C]glycerol. This discrepancy is not merely caused by infusion of glycerol per se. Rather, the discrepancy between both methods probably relates to conceptual problems in underlying assumptions in one or both methods.




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