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Am J Physiol Endocrinol Metab 282: E247-E258, 2002; doi:10.1152/ajpendo.00206.2001
0193-1849/02 $5.00
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Vol. 282, Issue 2, E247-E258, February 2002

Plasma L-5-oxoproline kinetics and whole blood glutathione synthesis rates in severely burned adult humans

Yong-Ming Yu, Colleen M. Ryan, Zhe-Wei Fei, Xiao-Ming Lu, Leticia Castillo, John T. Schultz, Ronald G. Tompkins, and Vernon R. Young

Shriners Burns Hospital and Trauma Services, Massachusetts General Hospital, Boston 02114; and Laboratory of Human Nutrition and Clinical Research Center, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142

Compromised glutathione homeostasis is associated with increased morbidity in various disease states. We evaluated the kinetics of L-5-oxoproline, an intermediate in the gamma -glutamyl cycle of glutathione production, in fourteen severely burned adults by use of a primed, constant intravenous infusion of L-5-[1-13C]oxoproline. In nine of these patients, whole blood glutathione synthesis and plasma kinetics of glycine and leucine were also measured with [15N]glycine and L-[2H3]leucine tracers. Patients were studied under a "basal" condition that provided a low dose of glucose and total parenteral nutrition. For comparison with control subjects, whole blood glutathione synthesis was estimated in six healthy adults. Burn patients in a basal condition showed significantly higher rates of plasma oxoproline clearance and urinary D- and L-oxoproline excretion compared with fasting healthy control subjects. Whole blood glutathione concentration and absolute synthesis rate in the basal state were lower than for control subjects. Total parenteral feeding without cysteine but with generous methionine did not affect oxoproline kinetics or whole blood glutathione synthesis. The estimated rate of glycine de novo synthesis was also lower in burn patients, suggesting a possible change in glycine availability for glutathione synthesis. The roles of precursor amino acid availability, as well as alterations in metabolic capacity, in modulating whole blood glutathione production in burns now require investigation.

flux; glycine; de novo synthesis; clearance; urinary excretion





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