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Section of Neonatal-Perinatal Medicine, Department of Pediatrics, Indiana University School of Medicine, James Whitcomb Riley Hospital for Children, Indianapolis, Indiana 46202
To determine whether increased amino acid availability can
reduce proteolysis in premature neonates and to assess the capacity of
infants born prematurely to acutely increase the irreversible catabolism of the essential amino acids leucine (via oxidation) and
phenylalanine (via hydroxylation to form tyrosine), leucine and
phenylalanine kinetics were measured under basal conditions and in
response to a graded infusion of intravenous amino acids (1.2 and 2.4 g · kg
1 · day
1) in
clinically stable premature (~32 wk gestation) infants in the 1st wk
of life. In contrast to the dose-dependent suppression of proteolysis
seen in healthy full-term neonates, the endogenous rates of appearance
of leucine and phenylalanine (reflecting proteolysis) were unchanged in
response to amino acids (297 ± 21, 283 ± 19, and 284 ± 31 µmol · kg
1 · h
1 for
leucine and 92 ± 6, 92 ± 4, and 84 ± 7 µmol · kg
1 · h
1 for
phenylalanine). Similar to full-term neonates, leucine oxidation (40 ± 5, 65 ± 6, and 99 ± 7 µmol · kg
1 · h
1) and
phenylalanine hydroxylation (12 ± 1, 16 ± 1, and 20 ± 2 µmol · kg
1 · h
1)
increased in a stepwise fashion in response to graded amino acids. This
capacity to increase phenylalanine hydroxylation may be crucial to meet
tyrosine needs when exogenous supply is limited. Finally, to determine
whether amino acids stimulate glucose production in premature neonates,
glucose rate of appearance was measured during each study period. In
response to amino acid infusion, rates of endogenous glucose production
were unchanged (and near zero).
premature newborns; leucine; phenylalanine; protein turnover; stable isotope tracers
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