Disulphide reduction in glutathione-deficient erythrocytes from a patient with pyroglutamic acidemia

References

• Boivin P., Galand C., Schaison G. Deficit en glutathion synthetase avec 5-oxoprolinurie. Deux nouveaux cas et revue de la litterature. Nouv. Presse. Med 1978; 7: 1531
   PubMedGoogle Scholar
• Boivin P., Saudubray J. M., Pousset J. L., Galand C. Glutathione synthetase deficiency and pyroglutamic aciduria. Int. Soc. Haematol. London 1975; 20, Third Meeting of European African Division Abstract 1
   Google Scholar
• Boxer L. A., Oliver J. M., Spielberg S. P., Allen J. M., Schulman J. D. Protection of granulocytes by vitamin E in glutathione synthetase deficiency. N. Engl. J. Med 1979; 301: 901
   PubMed Web of Science ®Google Scholar
• Beutler E. p. Red Cell Metabolism. Grune & Stratton, New York 1975; 69
   Google Scholar
• Eldjarn L., Bremer J. The inhibitory effect at the hexokinase level of disulphides on glucose metabolism in human erythrocytes. Biochem. J 1962; 84: 286
   PubMedGoogle Scholar
• Eldjam L., Bremer J., Berrresen H. C. The reduction of disulphides by human erythrocytes. Biochem. J 1962; 82: 192
   PubMedGoogle Scholar
• Eldjarn L., Pihl A. The equilibrium constants and oxidation-reduction potentials of some thioldisulphide systems. J. Am. Chem. Soc 1957; 79: 4589
   Web of Science ®Google Scholar
• Ellman G. L. Tissue sulfhydryl groups. Arch. Biochem. Biophys 1959; 82: 70
   PubMed Web of Science ®Google Scholar
• Hagenfeldt N., Larsson A., Zetterstrøm R. Pyroglutamic aciduria: studies in an infant with chronic metabolic acidosis. Acta paediatr. scund 1974; 63: 1
   PubMedGoogle Scholar
• Harris J. W., Kellermeyer R. W. The Red Cell. Harvard University Press, Cambridge, Massachusetts 1970; 159
   Google Scholar
• Hartter P., Weber U. The thiol-disulphide exchange reactions of assymetric disulphides of cysteine and cyclic cystine peptides with G-SH. Glutathione. Proceedings of the 16th Conference of the German Society of Biological Chemistry, Tübingen, L. Flohk, H. C. Benøhr, H. Sies, H. D. Waller, A. Wendel. Georg Thieme, Stuttgart March, 1973; 29, 1974
   Google Scholar
• Jellum E., Kluge T., Bsrresen H. C., Stokke O., E'djarn L. Pyroglutamic aciduria: a new inborn error of metabolism. Scand. J. clin. Lab. Invest 1970; 264: 327
   Google Scholar
• Kosower N. S., Kosower E. M. Functional aspects of glutathione disulphide and hidden forms of glutathione. Glutathione: Metabolism and Function, I. M. Arias, W. B. Jacoby. Raven Press, New York 1976; 159
   Google Scholar
• Kosower N. S., Kosower E. M. Protection of membranes by glutathione. Glutathione. Proceedings of the 16th Conference of the German Society of Biological Chemistry., L. Flohé, H.C. Benerhr, H. Sies, H.D. Waller, A. Wendel. Tübingen, Georg Thieme, Stuttgart March, 1973; 216, 1974
   Google Scholar
• Larsson A., Zetterstrøm R., Hagenfeldt L., Anderson R., Dreborg S., Hørnell H. Pyroglutamic aciduria (5-oxoprolinuria), an inborn error in glutathione metabolism. Pediat. Res 1974; 8: 852
   PubMedGoogle Scholar
• Mannervik B., Eriksson A. Enzymatic reduction of mixed disulphides and thiosulfate esters. Glutathione. Proceedings of the 16th Conference of the German Society of Biological Chemistry, Tübingen., L. Flohé, H. C. Benøhr, H. Sies, H. D. Waller, A. Wendel. Georg Thieme, Stuttgart March, 1973; 120, 1974
   Google Scholar
• Marstein S., Jellum E., Halpern B., Eldjarn L., Perry T. L. Biochemical studies of erythrocytes in a patient with pyroglutamic acidemia (5-oxopro-linemia). N. Engl. J. Med 1976; 295: 405
   Google Scholar
• Marstein S., Perry T. L. Studies on amino acid composition and transport in glutathione deficient erythrocytes from a patient with pyroglutamic acidemia (5-oxoprolinemia). Clin. Chim. Acta 1981; 109: 13
   PubMedGoogle Scholar
• Mendelson I. S., Zaleski W. A., Casey R. E., Christie E. J., Wellner V. P., Meister A. Ataxia in 5-oxoprolinuria: is there a connection between the γ-glutamyl cycle and GABA-function ?. Abstract XI:th International Congress of Biochemistry, TorontoCanada July, 1979
   Google Scholar
• Mohler D. M., Majerus P. W., Minnich V., Hess C. E., Garrick M. D. Glutathione synthetase deficiency as a cause of hereditary hemolytic disease. N. Engl. J. Med 1970; 283: 1253
   PubMedGoogle Scholar
• Porath U., Schreier K. Eine Familie mit Pyroglutaminacidurie. Dtsch. Med. Wschr 1978; 103: 939
   PubMedGoogle Scholar
• Prins H. K., Oort M., Loos J. A., Zürcher C., Beckers T. Congenital nonspherocytic hemolytic anemia, associated with glutathione deficiency of the erythrocytes; hematologic, biochemical and genetic studies. Blood 1966; 27: 145
   PubMedGoogle Scholar
• Spielberg S. P., Kramer L. I., Goodman S. I., Butler J., Tietze F., Quinn P., Schulman J. D. 5-Oxoprolinuria: biochemical observations and case report. J. Pediat 1917; 91: 237
   Google Scholar
• Tietze F. Disulphide reduction in rat liver. 1. Evidence for the presence of non-specific nucleotide-dependent disulphide reductase and GSH-disulphide transhydrogenase activities in the high-speed supernatant fraction. Arch. Biochem. Biophys 1970; 138: 177
   PubMed Web of Science ®Google Scholar
• Tietze F. Enzymatic method for quantitative determination of nanograms amounts of total and oxidized glutahione: application to mammalian blood and other tissues. Anal. Biochem 1969; 27: 502
   PubMed Web of Science ®Google Scholar
• Wellner W. P., Sekura R., Meister A., Larsson A. Glutathione synthetase deficiency, an inborn error of metabolism involving the γ-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria). Proc. natn. Acad. Sci. USA 1974; 71: 2505
   PubMed Web of Science ®Google Scholar