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Inhibitory effect of intravenous lysine infusion on urea cycle metabolism

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Abstract

Intravenous infusion of 0.5 mmol/kgl-lysine monohydrochloride was performed in six normal volunteer subjects aged 10–14 years to study the inhibitory effect of lysine on urea cycle metabolism. The lysine infusion resulted in a significant increase in plasma levels of arginine and ornithine, and in urinary homocitrulline, putrescine, and orotic acid, accompanied by a significant increase in blood ammonia. There was little change in plasma urea and citrulline. The increase in plasma arginine appears to reflect an inhibited arginase activity although the plasma urea level did not change. The increased homocitrulline excretion suggests that ornithine conversion to citrulline via ornithine transcarbamylase (OTC) was inhibited. The simultaneous increase in plasma ornithine and urinary putrescine may reflect an inhibition of mitochondrial ornithine transport. In addition to the direct ammoniagenic property of lysine, impaired ornithine conversion to citrulline resulting from the inhibition of both OTC activity and mitochondrial ornithine uptake by lysine may be responsible for the increase in blood ammonia and urinary orotic acid. Despite the retarded citrulline formation, a promoted efflux of citrulline from mitochondria may have kept the plasma citrulline level unchanged.

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Abbreviations

OTC:

ornithine transcarbamylase

References

  1. Batshaw ML, Walser M, Brusilow SW (1980) Plasma α-ketoglutarate in urea cycle enzymopathies and its role as a harbinger of hyperammonemic coma. Pediatr Res 14:1316–1319

    Google Scholar 

  2. Bradford NM, McGivan JD (1980) Evidence for the existence of an ornithine/citrulline antiporter in rat liver mitochondria. FEBS Lett 113:294–298

    Google Scholar 

  3. Cederbaum SD, Shaw KNF, Spector EB, Verity MA, Snodgrass PJ, Sugarman GI (1979) Hyperargininemia with arginase deficiency. Pediatr Res 13:827–833

    Google Scholar 

  4. Cittadini D, Pietropaolo C, de Cristofaro D, D'Ayjello-Caracciolo M (1964) In vivo effect ofL-lysine on rat liver arginase. Nature 203:643–644

    Google Scholar 

  5. de Vrese M, Barth CA (1985) Influence of lysine on urea cycle activity and orotate formation in the isolated perfused rat liver. Biol Chem Hoppe-Seyler 366:455–461

    Google Scholar 

  6. Fico ME, Hassan AS, Milner JA (1982) The influence of excess lysine on urea cycle operation and pyrimidine biosynthesis. J Nutr 112:1854–1861

    Google Scholar 

  7. Freedland RA, Crozier GL, Hicks BL, Meijer AJ (1984) Arginine uptake by isolated rat liver mitochondria. Biochim Biophys Acta 802:407–412

    Google Scholar 

  8. Hallett CJ, Cook JGH (1971) Reduced nicotinamide adenine dinucleotide-coupled reaction for emergency blood urea estimation. Clin Chim Acta 35:33–37

    Google Scholar 

  9. Hommes FA, Kitchings L, Eller AG (1983) The uptake of ornithine and lysine by rat liver mitochondria. Biochem Med 30: 313–321

    Google Scholar 

  10. Lusty CJ, Jilka RL, Nietsch EH (1979) Ornithine transcarbamylase of rat liver. Kinetic, physical, and chemical properties. J Biol Chem 254:10030–10036

    Google Scholar 

  11. Marton LJ, Russell DH, Levy CC (1973) Measurement of putrescine, spermidine, and spermine in physiological fluids by use of an amino acid analyzer. Clin Chem 19:923–926

    Google Scholar 

  12. Persson LO (1981) Decarboxylation of ornithine and lysine by ornithine decarboxylase from kidneys of testosterone treated mice. Acta Chem Scand [B] 35:451–459

    Google Scholar 

  13. Ratnaike RN, Buttery JE, Hoffmann S (1984) Blood ammonia measurement using a simple reflectometer. J Clin Chem Clin Biochem 22:105–108

    Google Scholar 

  14. Rogers LE, Porter FS (1968) Hereditary orotic aciduria. 11. A urinary screening test. Pediatrics 42:423–428

    Google Scholar 

  15. Segal S, Thier SO (1983) Cystinuria. In: Stanbury JB, Wyngaarden JB, Fredrickson DS, Brown MS (eds) The metabolic basis of inherited disease. McGraw-Hill, New York, pp 1774–1791

    Google Scholar 

  16. Shih VE (1978) Urea cycle disorders and other congenital hyperammonemic syndromes. In: Stanbury JB, Wyngaarden JB, Fredrickson DS (eds) The metabolic basis of inherited disease. McGraw-Hill, New York, pp 362–386

    Google Scholar 

  17. Simell O, Luukkainen P, Sipilä I (1985) Alanine-induced hyper-ammonemia in hyperlysinemia and in saccharopinuria. Pediatr Res 19:320A

    Google Scholar 

  18. Statter M, Russell A (1978) Competitive interrelationships between lysine and arginine in rat liver under normal conditions and in experimental hyperammonemia. Life Sci 22:2097–2102

    Google Scholar 

  19. Ulman EA, Kari FW, Hevia P, Visek WJ (1981) Orotic aciduria caused by feeding excess lysine to growing rats. J Nutr 111:1772–1779

    Google Scholar 

  20. Valle D, Simell O (1983) The hyperornithinemias. In: Stanbury JB, Wyngaarden JB, Fredrickson DS, Brown MS (eds) The metabolic basis of inherited disease. McGraw-Hill, New York, pp 382–401

    Google Scholar 

  21. Zweig JI (1973) Effects of lysine on ammonia formation, hydrogen ion, and potassium ion balance: A review and an hypothesis. Clin Chem 19:943–949

    Google Scholar 

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Kato, T., Sano, M. & Mizutani, N. Inhibitory effect of intravenous lysine infusion on urea cycle metabolism. Eur J Pediatr 146, 56–58 (1987). https://doi.org/10.1007/BF00647285

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  • DOI: https://doi.org/10.1007/BF00647285

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