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Endogenous glutamine production in critically ill patients: the effect of exogenous glutamine supplementation

INTRODUCTION: Glutamine rate of appearance (R(a)) may be used as an estimate of endogenous glutamine production. Recently a technique employing a bolus injection of isotopically labeled glutamine was introduced, with the potential to allow for multiple assessments of the glutamine R(a) over time in...

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Detalles Bibliográficos
Autores principales: Mori, Maiko, Rooyackers, Olav, Smedberg, Marie, Tjäder, Inga, Norberg, Åke, Wernerman, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056090/
https://www.ncbi.nlm.nih.gov/pubmed/24731231
http://dx.doi.org/10.1186/cc13829
Descripción
Sumario:INTRODUCTION: Glutamine rate of appearance (R(a)) may be used as an estimate of endogenous glutamine production. Recently a technique employing a bolus injection of isotopically labeled glutamine was introduced, with the potential to allow for multiple assessments of the glutamine R(a) over time in critically ill patients, who may not be as metabolically stable as healthy individuals. Here the technique was used to evaluate the endogenous glutamine production in critically ill patients in the fed state with and without exogenous glutamine supplementation intravenously. METHODS: Mechanically ventilated patients (n = 11) in the intensive care unit (ICU) were studied on two consecutive days during continuous parenteral feeding. To allow the patients to be used as their own controls, they were randomized for the reference measurement during basal feeding without supplementation, before or after the supplementation period. Glutamine R(a) was determined by a bolus injection of (13)C-glutamine followed by a period of frequent sampling to establish the decay-curve for the glutamine tracer. Exogenous glutamine supplementation was given by intravenous infusion of a glutamine containing dipeptide, L-alanyl-L-glutamine, 0.28 g/kg during 20 hours. RESULTS: A 14% increase of endogenous glutamine R(a) was seen at the end of the intravenous supplementation period as compared to the basal measurements (P = 0.009). CONCLUSIONS: The bolus injection technique to measure glutamine R(a) to estimate the endogenous production of glutamine in critically ill patients was demonstrated to be useful for repetitive measurements. The hypothesized attenuation of endogenous glutamine production during L-alanyl-L-glutamine infusion given as a part of full nutrition was not seen.