STEADY-STATE AND NON-STEADY-STATE MEASUREMENTS OF PLASMA GLUTAMINE TURNOVER IN HUMANS

To compare steady-state glutamine turnover using nitrogen, carbon, and hydrogen tracers and to test the validity of monocompartmental equati ons to determine plasma glutamine turnover under non-steady-state cond itions, we infused 10 normal postabsorptive volunteers simultaneously with [3,4-H-3]glutamine, [2-N-15]glutamine, and [U-C-14]glutamine for 4 h to isotopic steady state. Eight of the ten subjects were subsequen tly infused in a stepwise fashion with exogenous glutamine. Plasma glu tamine enrichment and specific activities fit a monoexponential model well (r = 0.89, 0.92, and 0.92 for [2-N-15]-, [U-C-14]-, and [3,4-H-3] glutamine, respectively). Volumes of distribution for each tracer (362 +/- 58, 433 +/- 51, and 446 +/- 63 ml/kg) and the transfer rate const ants (0.0224 +/- 0.0020, 0.0222 +/- 0.0020, and 0.0240 +/- 0.0023 min( -1)) for [2-N-15]-, [U-C-14]-, and [3,4-H-3]glutamine, respectively, w ere not significantly different from one another. However, turnover of glutamine determined with [3,4-H-3]glutamine (6.14 +/- 0.54 mu mol . kg(-1). min(-1)) exceeded that determined with [U-C-14]glutamine (5.72 +/- 0.541 mu mol . kg(-1). min(-1); P < 0.03), which in turn exceeded that determined with [2-N-15]glutamine (4.67 +/- 0.39 mu mol . kg(-1) . min(-1), P < 0.01). The monocompartmental non-steady-state equations of both DeBodo et al. (DeBodo, R., R. Steele, A. Dunn, and J. Bishop. Rec. Prog. Horm. Res. 19: 445-448, 1963) and Finegood et al. (Finegoo d, D., R. Bergman, and M. Vranic. Diabetes 36: 914-924, 1987) yielded acceptable approximations of predicted rates of glutamine plasma appea rance with deviations from predicted rates from 0.2 to 1.6% (Finegood et al.) and from 0.1 to 8.2% (DeBodo et al.). Use of a 0.75 pool fract ion most closely approximated predicted rates.