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Paraoxonase, total antioxidant response, and peroxide levels in children with steroid-sensitive nephrotic syndrome

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Abstract

Reactive oxygen species (ROS) are reported to play a role in inducing the proteinuria of nephrotic syndrome (NS). This study investigated paraoxonase (PON), total antioxidant response (TAR), and oxidant total peroxide together with serum proteins and lipoproteins in children with steroid-sensitive NS. The study included 40 children with steroid-sensitive NS (21 with acute-period NS in group I, 19 nonproteinuric while receiving steroids in group II) and 22 sex- and age-matched formerly nephrotic children in remission weaned from steroids (group III). The following parameters were determined: total peroxide, oxidative stress index (OSI), PON and TAR. Serum proteins and lipoproteins were also determined. Patients in the active phase of NS had significantly lower PON and TAR levels and higher OSI and total peroxide values than those in full remission; no differences were found in PON, TAR, or OSI values of groups I and II. Significant correlations were found between PON, TAR, and total peroxide. Serum total protein had a significantly positive correlation with PON and negative correlation with total peroxide in acute-period NS patients. Our results demonstrate greater oxidative stress and decreased antioxidants in the active phase of steroid-sensitive NS and while patients receive steroids than during full remission. Low-dose alternate-day steroids do not seem to decrease oxidative stress even while proteinuria ceases. Despite some conflicting data increased oxidation and/or decreased antioxidant response may be related to the pathogenesis of steroid-sensitive NS.

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References

  1. International study of Kidney Disease in Children (1981) The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. J Pediatr 98:561–564

    PubMed  Google Scholar 

  2. Kemper MJ, Meyer-Jark T, Lilova M, Muller-Wiefel DE (2003) Combined T- and B-cell activation in childhood steroid-sensitive nephrotic syndrome. Clin Nephrol 60:242–247

    CAS  PubMed  Google Scholar 

  3. Diamond JR, Bonventre JV, Karnovsky MJ (1986) A role for oxygen free radicals in aminonucleoside nephrosis. Kidney Int 29:478–483

    CAS  PubMed  Google Scholar 

  4. Zima T, Tesar V, Stipek S, Crkovska J, Poledne R, Teminova J, Platenik J, Rychlik I, Merta M, Nemecek K (1997) The influence of cyclosporin on lipid peroxidation and superoxide dismutase in adriamycin nephropathy in rats. Nephron 75:464–469

    CAS  PubMed  Google Scholar 

  5. Ece A, Atamer Y, Gürkan F, Bilici M, Koçyiğit Y (2004) Anti-oxidant status in relation to lipoproteins, leptin and pro-inflammatory cytokines in children with steroid-sensitive nephrotic syndrome. Nephrology 9:366–373

    Article  CAS  PubMed  Google Scholar 

  6. Keane WF, Kasiske BL, O’Donnel MP (1998) Lipids and progressive glomerulo-sclerosis: a model analogous to atherosclerosis. Am J Nephrol 8:261–271

    Article  Google Scholar 

  7. Solin ML, Ahola H, Haltia A, Ursini F, Montine T, Roveri A, Kerjaschki D, Holthofer H (2001) Lipid peroxidation in human proteinuric disease. Kidney Int 59:481–487

    Article  CAS  PubMed  Google Scholar 

  8. Orzechowski A, Ostaszewski P, Wilczak J, Jank M, Balasinska B, Wareski P, Fuller J Jr (2002) Rats with a glucocorticoid-induced catabolic state show symptoms of oxidative stress and spleen atrophy: the effects of age and recovery. J Vet Med A Physiol Pathol Clin Med 49:256–263

    Google Scholar 

  9. Iuchi T, Akaike M, Mitsui T, Ohshima Y, Shintani Y, Azuma H, Matsumoto T (2003) Glucorticoid excess induces superoxide production in vascular endothelial cells and elicits vascular endothelial dysfunction. Circ Res 92:81–87

    Article  CAS  PubMed  Google Scholar 

  10. Mackness MI, Mackness B, Durrington PN, Connely PW, Hegele RA (1996) Paraoxonase: biochemistry, genetics and relationship to plasma proteins. Curr Opin Lipidol 7:69–76

    CAS  PubMed  Google Scholar 

  11. Furlong CE, Richter RJ, Seidel SL, Costa LG, Matulsky AG (1989) Spectrophotometric assays for the enzymatic hydrolysis of the active metabolites of chlorpyrifos and parathion by plasma paraoxonase/arylesterase. Anal Biochem 180:242–247

    Article  CAS  PubMed  Google Scholar 

  12. Erel O (2004) A novel automated method to measure total antioxidant response against potent free radical reactions. Clin Biochem 37:112–119

    Google Scholar 

  13. Miyazawa T (1989) Determination of phospholipids hydroperoxides in human blood plasma by a chemiluminesence’s-HPLC assay. Free Radic Biol Med 7:209–217

    Article  CAS  PubMed  Google Scholar 

  14. Mackness MI, Harty D, Bahtnagar D, Winocour PH, Arrol S, Ishola M, Durrington PN (1991) Serum paraoxonase activity in familial hypercholesterolaemia and insulin-dependent diabetes mellitus. Atherosclerosis 86:193–199

    CAS  PubMed  Google Scholar 

  15. Turi S, Nemeth I, Torkos A, Saghy L, Varga I, Matkovics B, Nagy J (1997) Oxidative stress and antioxidant defense mechanism in glomerular diseases. Free Radic Biol Med 22:161–168

    Article  CAS  PubMed  Google Scholar 

  16. Yoshioka T, Ichikawa J, Fogo A (1991) Reactive oxygen metabolites cause massive, reversible proteinuria and glomerular sieving defect without apparent ultrastructural abnormality. J Am Soc Nephrol 2:902–912

    CAS  PubMed  Google Scholar 

  17. Alfrey AC (1994) Role of iron and oxygen radicals in the progression of chronic renal failure. Am J Kidney Dis 23:183–187

    CAS  PubMed  Google Scholar 

  18. Kawaguchi M, Yamada M, Wada H, Okigaki T (1992) Roles of active oxygen species in glomerular epithelial cell injury in vitro caused by puromycin aminonucleoside. Toxicology 72:329–340

    Article  CAS  PubMed  Google Scholar 

  19. Gwinner W, Landmesser U, Brandes RP, Kubat B, Plasger J, Eberhard O, Koch KM, Olbricht CJ (1997) Reactive oxygen species and antioxidant defense in puromycin aminonucleoside glomerulopathy. J Am Soc Nephrol 8:1722–1731

    CAS  PubMed  Google Scholar 

  20. Ghiselli A, Serafini M, Natella F, Scaccini C (2000) Total antioxidant capacity as a tool to assess redox status: critical view and experimental data. Free Radic Biol Med 29:1106–1114

    Article  CAS  PubMed  Google Scholar 

  21. Moran EC, Kamiguti AS, Cawley JC, Pettitt AR (2002) Cytoprotective antioxidant activity of serum albumin and autocrine catalase in chronic lymphocytic leukemia. Br J Haematol 116:316–328

    CAS  PubMed  Google Scholar 

  22. Fydryk J, Jacobson E, Kurzawska O, Malecka G, Gonet B, Urasinski T, Brodkiewicz A, Bukowska H (1998) Antioxidant status of children with steroid-sensitive nephrotic syndrome. Pediatr Nephrol 12:751–754

    Article  CAS  PubMed  Google Scholar 

  23. Koracevic D, Koracevic G, Djordjevic V, Andrejevic S, Cosic V (2001) Method for the measurement of antioxidant activity in human fluids. J Clin Pathol 54:356–362

    Article  CAS  PubMed  Google Scholar 

  24. Iscan A, Yigitoglu R, Vurgun N, Uyanik BS, Akyildiz M (1998) Low levels of high density lipoprotein cholesterol in Turkish children: an important risk factor. Acta Paediatr Jpn 40:41–46

    CAS  PubMed  Google Scholar 

  25. Kinra S, Rath B, Kabi BC (2000) Indirect quantification of lipid peroxidation in steroid responsive nephrotic syndrome. Arch Dis Child 82:76–78

    Article  CAS  PubMed  Google Scholar 

  26. bin Ali A, Zhang Q, Lim YK, Fang D, Retnam L, Lim SK (2003) Expression of major HDL-associated antioxidant PON-1 is gender dependent and regulated during inflammation. Free Radic Biol Med 34:824–829

    Article  PubMed  Google Scholar 

  27. Frishberg Y, Toledano H, Becker-Cohen R, Feigin E, Halle D (2000) Genetic polymorphism in paraoxonase is a risk factor childhood focal segmental glomerulosclerosis. Am J Kidney Dis 36:1253–1261

    CAS  PubMed  Google Scholar 

  28. Mackness B, Durrington P, McElduff P, Yarnell J, Azam N, Watt M, Mackness M (2003) Low paraoxonase activity predict coronary events in the Caerphylly Prospective Study. Circulation 107:2775–2779

    Article  CAS  PubMed  Google Scholar 

  29. Volk T, Schmutzler M, Engelhardt L, Pantke U, Laule M, Stangl K, Grune T, Wernecke KD, Konertz W, Kox WJ (2003) Effects of different steroid treatment on reperfusion-associated production of reactive oxygen species and arrhythmias during coronary surgery. Acta Anaesthesiol Scand 47:667–674

    Google Scholar 

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Correspondence to Aydın Ece.

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Ece, A., Atamer, Y., Gürkan, F. et al. Paraoxonase, total antioxidant response, and peroxide levels in children with steroid-sensitive nephrotic syndrome. Pediatr Nephrol 20, 1279–1284 (2005). https://doi.org/10.1007/s00467-005-1956-z

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  • DOI: https://doi.org/10.1007/s00467-005-1956-z

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