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Department of Diabetes and Endocrinology, GKT School of Medicine, St. Thomas Hospital, London, United Kingdom SE1 7EH
Address all correspondence and requests for reprints to: Dr. James Gibney, Department of Endocrinology, St. Vincents Hospital, Elm Park, Dublin 4, Ireland. E-mail: j.gibney{at}st-vincents.ie.
The anabolic actions of GH in GH-deficient adults and children are well documented. Replacement with GH in such individuals promotes protein synthesis and reduces irreversible loss of protein through oxidation. Although GH is known to be self-administered by athletes, its protein metabolic effects in this context are unknown. This study was designed to determine whether 4 wk of high dose recombinant human GH (r-hGH) administration altered whole body leucine kinetics in endurance-trained athletes at rest and during and after 30 min of exercise at 60% of maximal oxygen uptake. Eleven endurance-trained male athletes were studied, six randomized to receive r-hGH (0.067 mg/kg·d), and five to receive placebo. Whole body leucine turnover was measured at rest and during and after exercise, using a 5-h primed constant infusion of 1-[13C]leucine, from which rates of leucine appearance (an index of protein breakdown), leucine oxidation, and nonoxidative leucine disposal (an index of protein synthesis) were estimated. Under resting conditions, r-hGH administration increased rate of leucine appearance and nonoxidative leucine disposal, and reduced leucine oxidation (P < 0.01). This effect was apparent after 1 wk, and was accentuated after 4 wk, of r-hGH administration (P < 0.05). During and after exercise, GH attenuated the exercise-induced increase in leucine oxidation (P < 0.05). There were no changes observed in placebo-treated subjects compared with the baseline study. We conclude that GH administration to endurance-trained male athletes has a net anabolic effect on whole body protein metabolism at rest and during and after exercise.
Abbreviations: BCOADH, Branched chain 2-oxo acid dehydrogenase complex; CV, coefficient of variation; DEXA, dual energy x-ray absorptiometry; fT3, free T3; fT4, free T4; GHD, GH-deficient; HOMAIR, homeostasis model assessment of insulin resistance;
-KIC,
-ketoisocaproate; LBM, lean body mass; NOLD, nonoxidative leucine disposal; Ra, rate of appearance; r-GH, recombinant human GH; VO2max, maximal oxygen uptake.
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