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Schwartz Center for Metabolism and Nutrition; and Department of Pediatrics, Case Western Reserve University School of Medicine at MetroHealth Medical Center, Cleveland, Ohio
Submitted 23 March 2005 ; accepted in final form 14 July 2005
Threonine kinetics, threonine oxidative pathway, and the relationship between threonine and whole body protein turnover were quantified in 10 healthy term infants during the first 48 h after birth. The kinetic data were obtained 6 h after the last feed (fasting) and in response to formula feeding, using [U-13C4,15N]threonine, [2H5]phenylalanine, and [15N]glycine tracers. The rate of carbon dioxide production (
CO2) and 13C enrichment of the expired CO2 were measured to quantify the rate of oxidation of threonine. The rate of appearance (Ra) of threonine (136 ± 37 µmol·kg1·h1) was higher in newborn infants than that reported in adults. Formula feeding resulted in a significant decrease in threonine Ra (P < 0.05). A significant positive correlation was seen between phenylalanine Ra and threonine Ra, both during fasting and after formula feeding (r2 = 0.65). In contrast to a 1:1 ratio of threonine and phenylalanine in mixed muscle protein, threonine Ra relative to phenylalanine Ra was 2.2 ± 0.4. The fractional rate of threonine flux oxidized was 20% during fasting and 26% (P < 0.05) in response to nutrient administration. There was a significant correlation between plasma threonine concentration and threonine oxidation (r2 = 0.75). No measurable incorporation of threonine in plasma glycine was seen. These data suggest that threonine is exclusively degraded by the glycine-independent serine/threonine dehydratase pathway. A higher flux of threonine relative to phenylalanine indicates higher turnover of threonine enriched proteins.
glycine; phenylalanine; stable isotopes; threonine oxidation
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