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Divergent effects of different oxidants on glutathione homeostasis and protein damage in erythrocytes from diabetic patients: Effects of high glucose

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Abstract

Long‐term complications of diabetes mellitus have been ascribed to both the effects of prolonged hyperglycemia and to increased oxidative stress. In an attempt to identify the mechanisms underlying the acute effects of hyperglycemia on oxidative stress, we investigated the hypothesis that high glucose might lead to an insufficiency in reducing equivalents (such as NADPH) and thus to a disruption in the glutathione‐dependent antioxidant defences and to an incapacity to deal with oxidant attack. For this purpose, erythrocytes from diabetic patients were incubated for 0–90 min in 5.55 or 33.3 mM D‐glucose containing tert‐butyl hydroperoxide 0.5 and 1 mM, Menadione 100 μM, or glucose oxidase. The time course of the changes in non‐protein bound glutathione (reduced and oxidised), lactate and pyruvate, alanine and fluorescent products of oxidative proteolysis, hemolysis and methemoglobin was monitored. The results show that although glucose utilisation was unaffected, all oxidants caused a persistent decrease in total non‐protein‐bound glutathione suggesting binding to proteins. However, changes in glutathione and redox status differed between the various oxidants and were not directly related to the extent of oxidative cellular damage. In these experimental conditions, with short incubations and using the erythrocyte as the simplest cellular model of glucose metabolism, neither high glucose nor the diabetic condition worsened the susceptibility of erythrocytes to acute in vitro oxidative damage.

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References

  1. The DCCT Research Group: The effect of intensive diabetes treatment on the development and progression of long-term complications in insulin-dependent diabetes mellitus: The Diabetes Control and Complications Trial. N Engl J Med 329: 977–986, 1993

    Google Scholar 

  2. Griesmacher A, Kindhauser M, Andert SE, Schreiner W, Toma C, Knoebl P, Pietschmann P, Prager R, Schnack C, Schernthaner G, Mueller MM: Enhanced serum levels of thiobarbituric-acid reactive substances in diabetes mellitus. Am J Med 98: 469–475, 1995

    Google Scholar 

  3. Sell DR, Lapolla A, Odetti P, Fogarty J, Monnier VM: Pentosidine formation in skin correlates with severity of complications in individuals with long-standing IDDM. Diabetes 41: 1286–1292, 1992

    Google Scholar 

  4. McCance DR, Dyer DG, Dunn JA, Bailie KE, Thorpe SR, Baynes JW, Lyons TJ: Maillard reaction products and their relation to complications in insulin-dependent diabetes mellitus. J Clin Invest 91: 2470–2478, 1993

    Google Scholar 

  5. Dandona P, Thusu K, Cook S, Snyder B, Makowski J, Armstrong D, Nicotera T: Oxidative damage to DNA in diabetes mellitus. Lancet 347: 444–445, 1996

    Google Scholar 

  6. Oberley LW: Free radicals and diabetes. Free Rad Biol Med 5: 113–124, 1988

    Google Scholar 

  7. Wolff SP: Diabetes mellitus and free radicals. Br Med Bull 49: 642–652, 1993

    Google Scholar 

  8. Baynes JW: Role of oxidative stress in development of complications in diabetes. Diabetes 40: 405–412, 1991

    Google Scholar 

  9. Wolff SP, Dean RT: Glucose autoxidation and protein modification: The potential role of autooxidative glycosylation in diabetes. Biochem J 245: 243–250, 1987

    Google Scholar 

  10. Mullarkey CJ, Edelstein D, Brownlee M: Free radical generation by early glycation products: A mechanism for accelerated atherogenesis in diabetes. Biochem Biophys Res Commun 173: 932–939, 1990

    Google Scholar 

  11. Arai K, Iizuka S, Tada Y, Oikawa K, Taniguchi N: Increase in the glucosylated form of erythrocyte Cu-Zn superoxide dismutase in diabetes and close association of the nonenzymatic glucosylation with the enzyme activity. Biochem Biophys Acta 924: 292–296, 1987

    Google Scholar 

  12. Godin DV, Wohaieb SA, Garnett ME, Goumeniouk AD: Antioxidant enzyme alterations in experimental and clinical diabetes. Mol Cell Biochem 84: 223–231, 1988

    Google Scholar 

  13. Sinclair AJ, Girling AJ, Gray L, LeGuen C, Lunec J, Barnett AH: Disturbed handling of ascorbic acid in diabetic patients with and without microangiopathy during high dose ascorbate supplementation. Diabetologia 34: 171–175, 1991

    Google Scholar 

  14. Murakami K, Kondo T, Ohtsuka Y, Fujiwara Y, Shimada M, Kawakami Y: Impairment of glutathione metabolism in erythrocytes from patients with diabetes mellitus. Metabolism 38: 753–758, 1989

    Google Scholar 

  15. Jain SK, McVie R: Effect of glycemic control, race (white vs. black), and duration of diabetes on reduced glutathione content in erythrocytes of diabetic patients. Metabolism 43: 306–309, 1994

    Google Scholar 

  16. Thornalley PJ, McLellan AC, Lo TWC, Benn J, Sönksen PH: Negative association between erythrocyte reduced glutathione concentration and diabetic complications. Clin Sci 91: 575–582, 1996

    Google Scholar 

  17. Kosower NS, Kosower EM: The glutathione-glutathione disulphide system. In: W.A. Pryor (ed). Free Radicals in Biology, vol. II. Academic Press, New York, 1976, pp 55–84

    Google Scholar 

  18. Gillbert HF: Redox control of enzyme activities by thiol/disulphide exchange. Meth Enzymol 107: 330–351, 1984

    Google Scholar 

  19. May JM, Qu ZC, Whitesell RR, Cobb CE: Ascorbate recycling in human erythrocytes: role of GSH in reducing dehydroascorbate. Free Rad Biol Med 20: 543–551, 1996

    Google Scholar 

  20. Kashiwagi A, Asahina T, Ikebuchi M, Tanaka Y, Takagi Y, Nishio Y, Kikkawa R, Shigeta Y: Abnormal glutathione metabolism and increased cytotoxicity caused by H2O2 in human umbilical vein endothelial cells cultured in high glucose medium. Diabetologia 37: 264–269, 1994

    Google Scholar 

  21. Manuel y Keenoy B, Malaisse-Lagae F, Malaisse WJ: Metabolism of tritiated D-glucose by rat erythrocytes. Metabolism 40: 978–985, 1991

    Google Scholar 

  22. Davies KJA, Goldberg AL: Oxygen radicals stimulate intracellular proteolysis and lipid peroxidation by independent mechanisms in erythrocytes. J Biol Chem 262: 8220–8226, 1987

    Google Scholar 

  23. Passonneau JV: Fluorometric methods. In: H.A. Bergmeyer (ed). Methods of Enzymatic Analysis. Academic Press, San Diego, CA, 1974, pp 1468–1501

    Google Scholar 

  24. Giulivi C, Davies KJA: Dityrosine and tyrosine oxidation products are endogenous markers for the selective proteolysis of oxidatively modified red blood cell hemoglobin (the 19S) proteasome. J Biol Chem 268: 8752–8759, 1993

    Google Scholar 

  25. Goldberg B, Stern A: Superoxide anion as a mediator of drug-induced oxidative hemolysis. J Biol Chem 251: 6468–6470, 1976

    Google Scholar 

  26. Fairbanks VF: In: N.W. Tietz (ed). Fundamentals of Clinical Chemistry. W.B. Saunders Company, Philadelphia/London/Toronto, 1976, pp 414–415

    Google Scholar 

  27. Wolff SP: Ferrous ion oxidation in presence of ferric ion indicator Xylenol Orange for measurement of hydroperoxides. Meth Enzymol 233: 182–189, 1994

    Google Scholar 

  28. Boveris A, Martino E, Stoppani AOM: Evaluation of the horseradish peroxidase-scopoletin method for the measurement of hydrogen peroxide formation in biological systems. Anal Biochem 80: 145–158, 1977

    Google Scholar 

  29. Sedlak J, Lindsay RH: Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent. Anal Biochem 25: 192–205, 1968

    Google Scholar 

  30. Hu ML: Measurement of protein thiol groups and glutathione in plasma. Meth Enzymol 233: 380–385, 1994

    Google Scholar 

  31. Redegeld FAM, Van Opstal MAJ, Houdkamp E, Van Bennekom WP: Determination of glutathione in biological material by flow-injection analysis using an enzymatic recycling reaction. Anal Biochem 174: 489–495, 1988

    Google Scholar 

  32. Sacchetta P, Di Cola D, Federici G: Alkaline hydrolysis of N-ethylmaleimide allows a rapid assay of glutathione disulfide in biological systems. Anal Biochem 154: 205–208, 1986

    Google Scholar 

  33. Beutler E: In: Red Cell Metabolism. A Manual of Biochemical Methods. Grune & Stratton, Orlando, FL, 1984, pp 74–75

    Google Scholar 

  34. Authors ?: In: D. Schomburg, D. Stephan (eds). Enzyme Handbook 8. Springer-Verlag, Berlin/Heidelberg 1994, p 3

    Google Scholar 

  35. Veech RL, Eggleston LV, Krebs HA: The redox state of free nicotinamide-adenine dinucleotide phosphate in the cytoplasm of rat liver. Biochem J 115: 609–619, 1969

    Google Scholar 

  36. Di Simplicio P, Rossi R: The time-course of mixed disulfide formation between GSH and proteins in rat blood after oxidative stress with tert-butyl hydroperoxide. Biochim Biophys Acta 1199: 245–252, 1994

    Google Scholar 

  37. Freeman BA, Mudd JB: Reaction of ozone with sulfhydryls of human erythrocytes. Arch Biochem Biophys 208: 212–220, 1981

    Google Scholar 

  38. Huisman THJ, Dozy AM: Studies on the heterogeneity of hemoglobins. V. Binding of hemoglobins to oxidized glutathione. J Lab Clin Med 60: 302–319, 1962

    Google Scholar 

  39. Srivastava SK, Beutler E: Glutathione metabolism of the erythrocyte. The enzymatic cleavage of glutathione-haemoglobin preparations by glutathione reductase. Biochem J 119: 353–357, 1970

    Google Scholar 

  40. Schöneich C: Thiyl radicals, perthiyl radicals, and oxidative reactions. In L. Packer, E. Cadenas (eds). Biothiols in Health and Disease. Marcel Dekker, New York/Basel/Hong Kong, 1995, pp 21–48

    Google Scholar 

  41. Gaetani GF, Kirkman HN, Mangerini R, Ferraris AM: Importance of catalase in the disposal of hydrogen peroxide within the human erythrocyte. Blood 84: 325–330, 1994

    Google Scholar 

  42. Nicholls P: Activity of catalase in the red cell. Biochim Biophys Acta 99: 286–297, 1965

    Google Scholar 

  43. Gaetani GF, Galiano S, Canepa L, Ferraris AM, Kirkman HN: Catalase and glutathione peroxidase are equally active in detoxification of hydrogen peroxide in human erythrocytes. Blood 73: 334–339, 1989

    Google Scholar 

  44. Winterbourn CC: Superoxide as an intracellular radical sink. Free Rad Biol Med 14: 85–90, 1993

    Google Scholar 

  45. Di Monte D, Ross D, Bellomo G, Eklöw L, Orreniuls S: Alterations in cellular thiol homeostasis during the metabolism of Menadione by isolated rat hepatocytes. Arch Biochem Biophys 235: 334–342, 1984

    Google Scholar 

  46. Francis GS, Mendez AJ, Bierman EL, Heinecke JW: Oxidative tyrosylation of high density lipoprotein by peroxidase enhances cholesterol removal from cultured fibroblasts and macrophage foam cells. Proc Natl Acad Sci 90: 6631–3365, 1993

    Google Scholar 

  47. Kikugawa K, Kato T, Hayasaka A: Formation of dityrosine and other fluorescent amino acids by reaction of amino acids with lipid hydroperoxides. Lipids 26: 922–929, 1991

    Google Scholar 

  48. Guptasarma P, Balasubramanian D: Hydroxyl radical mediated damage to proteins, with special reference to the crystallins. Biochemistry 31: 4296–4303, 1992

    Google Scholar 

  49. Vanderyse L, Devreese AM, Baert J, Vanloo B, Lins L, Ruysschaert JM, Rosseneu M: Structural and functional properties of apolipoprotein B in chemically modified low density proteins. Atherosclerosis 97: 187–199, 1992

    Google Scholar 

  50. Halliwell B, Gutteridge JMC: The definition and measurement of antioxidants in biological systems. Free Rad Biol Med 18: 125, 1995

    Google Scholar 

  51. Mazzanti L, Rabini R, Staffolani R, Faloia E, De Pirro R, Pugnaloni A, Littarru GP, Biagini G: Diabetes mellitus and red blood cell aging: A structural and functional study. In: L. Magnani, A. De Flora (eds). Advances in Experimental Medicine and Biology, vol. 307: Red Blood Cell Aging. Plenum Press, New York/London, 1991

    Google Scholar 

  52. Szergold BS, Lal S, Taylor AH, Kappler F, Su B, Brown TR: 31Nuclear magnetic resonance evidence of an activate hexose-monophosphate shunt in hyerglycemic rat lenses in vivo. Diabetes 44: 810–815, 1995

    Google Scholar 

  53. Nishikawa T, Edelstein D, Du XL, Yamagishi S, Matsumura T, Kaneda Y, Yorek MA, Beebe D, Oates PJ, Hammes HP, Giardino I, Brownlee M: Normalizing mitochondiral superoxide production blocks three pathways of hyperglycaemic damage. Nature 404: 787–790, 2000

    Google Scholar 

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Correspondence to Begoña Manuel y Keenoy.

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Keenoy, B.M.y., Vertommen, J. & De Leeuw, I. Divergent effects of different oxidants on glutathione homeostasis and protein damage in erythrocytes from diabetic patients: Effects of high glucose. Mol Cell Biochem 225, 59–73 (2001). https://doi.org/10.1023/A:1012268807728

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