Majority of dietary glutamine is utilized in first pass in preterm infants
Glutamine is a conditionally essential amino acid for very low-birth weight infants by virtue of its ability to play an important role in several key metabolic processes of immune cells and enterocytes. Although glutamine is known to be used to a great extend, the exact splanchnic metabolism in enterally fed preterm infants is unknown. We hypothesized that preterm infants show a high splanchnic first-pass glutamine metabolism and the primary metabolic fate of glutamine is oxidation. Five preterm infants (mean ± SD birth weight 1.07 ± 0.22 kg and GA 29 ± 2 wk) were studied by dual tracer ([U-C]glutamine and [N2]glutamine) cross-over techniques on two study days (at postnatal week 3 ± 1 wk). Splanchnic and whole-body glutamine kinetics were assessed by plasma isotopic enrichment of [U-C]glutamine and [N2]glutamine and breath CO2 enrichments. Mean fractional first-pass glutamine uptake was 73 ± 6% and 57 ± 17% on the study days. The splanchnic tissues contributed for a large part (57 ± 6%) to the total amount of labeled carbon from glutamine retrieved in expiratory air. Dietary glutamine is used to a great extent by the splanchnic tissues in preterm infants and its carbon skeleton has an important role as fuel source.
|Keywords||article, birth weight, blood, breath analysis, carbon, carbon dioxide, clinical trial, controlled study, crossover procedure, diet, dietary intake, energy metabolism, enteric feeding, exhalation, expired air, glutamine, human, infant, kinetics, metabolism, newborn, oxidation, oxidation reduction reaction, prematurity, priority journal, skeleton, splanchnic blood flow, very low birth weight|
|Persistent URL||dx.doi.org/10.1203/PDR.0b013e3181c34609, hdl.handle.net/1765/19293|
van der Schoor, S.R.D., Schierbeek, H., Bet, P.M., Vermeulen, M., Lafeber, H.N., van Goudoever, J.B., & van Elburg, R.M.. (2010). Majority of dietary glutamine is utilized in first pass in preterm infants. Pediatric Research: international journal of human developmental biology, 67(2), 194–199. doi:10.1203/PDR.0b013e3181c34609