Prolonged infusion of amino acids increases leucine oxidation in fetal sheep

Maternal high-protein supplements designed to increase birth weight have not been successful. We recently showed that maternal amino acid infusion into pregnant sheep resulted in competitive inhibition of amino acid transport across the placenta and did not increase fetal protein accretion rates. To bypass placental transport, singleton fetal sheep were intravenously infused with an amino acid mixture (AA, n = 8) or saline [control (Con), n = 10] for similar to 12 days during late gestation. Fetal leucine oxidation rate increased in the AA group (3.1 +/- 0.5 vs. 1.4 +/- 0.6 mu mol.min (-1) .kg(-1), P < 0.05). Fetal protein accretion (2.6 +/- 0.5 and 2.2 +/- 0.6 mu mol.min(-1).kg(-1) in AA and Con, respectively), synthesis (6.2 +/- 0.8 and 7.0 +/- 0.9 mu mol.min(-1).kg(-1) in AA and Con, respectively), and degradation (3.6 +/- 0.6 and 4.5 +/- 1.0 mu mol.min(-1).kg(-1) in AA and Con, respectively) rates were similar between groups. Net fetal glucose uptake decreased in the AA group (2.8 +/- 0.4 vs. 3.9 +/- 0.1 mg.kg(-1).min(-1), P < 0.05). The glucose-O-2 quotient also decreased over time in the AA group (P < 0.05). Fetal insulin and IGF-I concentrations did not change. Fetal glucagon increased in the AA group (119 +/- 24 vs. 59 +/- 9 pg/ml, P < 0.05), and norepinephrine (NE) also tended to increase in the AA group (785 +/- 181 vs. 419 +/- 76 pg/ml, P = 0.06). Net fetal glucose uptake rates were inversely proportional to fetal glucagon (r(2) = 0.38, P < 0.05), cortisol (r(2) = 0.31, P < 0.05), and NE (r(2) = 0.59, P < 0.05) concentrations. Expressions of components in the mammalian target of rapamycin signaling pathway in fetal skeletal muscle were similar between groups. In summary, prolonged infusion of amino acids directly into normally growing fetal sheep increased leucine oxidation. Amino acid-stimulated increases in fetal glucagon, cortisol, and NE may contribute to a shift in substrate oxidation by the fetus from glucose to amino acids.