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Metabolism of Cysteine Is Modified During the Acute Phase of Sepsis in Rats

Manuscript received 16 April 1997. Initial reviews completed 16 May 1997. Revision accepted 18 August 1997.

Thierry Malmezat, Denis Breuillé*, Corinne Pouyet*, Philippe Patureau Mirand, and Christiane Obled

Laboratoire d'Etude du Métabolisme Azoté, INRA Clermont-Ferrand Theix, 63122 Saint Genès Champanelle, France and * Clintec Technologie, 92352 Le Plessis Robinson, France

In vivo cysteine metabolism during the inflammatory state has been studied minimally. We investigated cysteine metabolism (i.e. taurine, sulfate and glutathione formation) using a single dose of [35S] cysteine in septic rats that had been injected with live Escherichia coli into the tail vein and in control, pair-fed rats. Cysteine metabolites were separated by ion exchange chromatography, and radioactivity was counted in the different fractions. Radioactivity incorporated in tissue proteins was also measured after protein precipitation. [35S]Sulfate production was significantly lower in septic rats than in pair-fed rats. [35S]Taurine contents were significantly lower only in kidneys, spleen and gastrointestinal tract of septic rats. The higher production of [35S] taurine in the livers (the major site of taurine production) of septic rats could have a protective effect against oxidation. Glutathione concentrations were also significantly greater in liver, spleen, kidneys and gastrocnemius muscle of septic rats, presumably in order to combat oxidative stress induced by sepsis. [35S]Cysteine incorporation in glutathione was significantly higher in spleen and kidneys but not in liver of septic rats compared to pair-fed rats. This could be explained by the fact that, in liver, a greater amount of labeled glutathione had been utilized for host defense, or by a high level in glutathione turnover. Finally, [35S]cysteine incorporation into protein, in septic rats, was significantly greater than in pair-fed rats in spleen, lung and particulary in whole plasma proteins other than albumin, which mainly represent the acute-phase proteins. These data suggest an increased requirement for cysteine during sepsis in rats.

Key words: cysteine, glutathione, rats, sulfate, taurine.

The Journal of Nutrition Vol. 128 No. 1 January 1998, pp. 97-105
Copyright ©1998 by the American Society for Nutritional Sciences




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