Effect of glutamine on leucine metabolism in humans. Hankard, R[acute]egis G., Morey W. Haymond, and Dominique Darmaun. Nemours Children's Clinic, Jacksonville, Florida
APStracts 3:0115E, 1996.
The aim of this study was to determine whether the putative protein anabolic effect of glutamine: 1) is mediated by increased protein synthesis or decreased protein breakdown, and 2) is specific to glutamine. Seven healthy adults were administered 5-h intravenous infusions of L-[1-14C]leucine in the postabsorptive state while receiving in a randomized order an enteral infusion of saline on one day or L-glutamine (800 [mu]mol.kg-1.h-1, equivalent to 0.11 g of nitrogen per kg) on the other day. Seven additional subjects were studied using the same protocol except they received isonitrogenous infusion of glycine. The rates of leucine appearance (RaLEU), an index of protein degradation, leucine oxidation (OxLEU), and non oxidative leucine disposal (NOLD), an index of protein synthesis, were measured using the 14C-specific activity of plasma [alpha] -ketoisocaproate and the excretion rate of 14CO2 in breath. During glutamine infusion, plasma glutamine concentration doubled (673 +/- 66 v 1184 +/- 37 [mu]M (p&LT0.05) whereas RaLEU did not change (122 +/- 9 v 122 +/- 7 [mu]mol.kg-1.h-1), OxLEU decreased (19 +/- 2 v 11 +/- 1 [mu]mol.kg-1.h-1, p&LT0.01), and NOLD increased (103 +/-8 v 111+/- 6 [mu]mol.kg-1.h-1, p&LT0.01). During glycine infusion, plasma glycine increased 14-fold (268 +/- 62 v 3806 +/- 546 [mu]M (p&LT0.01), but in contrast with glutamine, RaLEU (124 +/- 6 v 110 +/- 4 [mu]mol.kg-1.h-1, p=0.02), OxLEU (17 +/- 1 v 14 +/- 1 [mu]mol.kg-1.h-1, p=0.03), and NOLD (106 +/- 5 v 96 +/- 3 [mu]mol.kg -1.h-1, p&LT0.05) all decreased. We conclude that glutamine enteral infusion may exert its protein anabolic effect by increasing protein synthesis whereas an isonitrogenous amount of glycine merely decreases protein turnover with only a small anabolic effect resulting from a greater decrease in proteolysis than protein synthesis.

Received 20 February 1996; accepted in final form 5 June 1996.
APS Manuscript Number E88-6.
Article publication pending Am. J. Physiol. (Endocrinol. Metab.).
ISSN 1080-4757 Copyright 1996 The American Physiological Society.
Published in APStracts on 28 June 96