L. Vantoledoeppinga et al., LEUCINE AND GLUCOSE KINETICS DURING GROWTH-HORMONE TREATMENT IN INTRAUTERINE GROWTH-RETARDED PRETERM INFANTS, American journal of physiology: endocrinology and metabolism, 33(3), 1996, pp. 451-455
The present study was performed with the objective to investigate the
possible effects of recombinant human growth hormone (rhGH) supplement
ation on protein and glucose metabolism during the early postnatal per
iod in seven intrauterine growth-retarded (IUGR) preterm infants. Eigh
t infants were studied as controls. The metabolic rate was measured by
indirect calorimetry, and whole body protein and glucose kinetics wer
e measured using constant-rate infusions of [1-C-13]leucine and [U-C-1
3]glucose during continuous adequate oral feeding. Energy expenditure
was similar in both groups. In the rhGH-treated group of infants, leuc
ine turnover (470 +/- 76 vs. 409 +/- 47 mu mol . kg(-1). day(-1)), leu
cine used for protein synthesis (402 +/- 72 vs. 337 +/- 36 mu mol . kg
(-1). day(-1)), and leucine derived from protein breakdown (365 +/- 71
vs. 304 +/- 41 mu mol . kg(-1). day(-1)) were increased. However, net
leucine balance was not increased (37 +/- 17 vs. 34 +/- 13 mu mol . k
g(-1). day(-1)). The total rate of appearance of glucose was 10.1 +/-
1.2 vs. 10.0 +/- 1.3 mg . kg(-1). min(-1). We suggest that immediate p
ostnatal treatment with rhGH is not effective in stimulating protein g
ain and has no effect on glucose kinetics in IUGR preterm infants.