Skip to main content
Log in

Lipid peroxidation and antioxidant enzymes in children with chronic renal failure

  • Original Article
  • Published:
Pediatric Nephrology Aims and scope Submit manuscript

Abstract

Increased lipid peroxidation (LP) has been observed in dialysis patients and in predialysis adults with advanced chronic renal failure (CRF). The aim of this study was to investigate whether predialysis CRF children have increased LP in plasma and red blood cells (RBC) and to evaluate the activity of the antioxidant enzymes [superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-Px)] in RBC. Concentrations of selenium (Se), copper (Cu), and zinc (Zn)—cofactors of these enzymes—were determined both in erythrocytes and in plasma. LP was monitored by plasma and erythrocyte malonyldialdehyde (MDA) and by plasma organic hydroperoxide (OHP) concentrations. Forty-six predialysis children, aged 5–18 years, divided into two groups according to their serum creatinine levels [group I (n=14, mean serum creatinine 421.61±141.08 μmol/l), group II (n=32, mean serum creatinine 174.94±45.50 μmol/l)] and 27 age-matched healthy subjects were enrolled in the study. Significantly higher concentrations of plasma and erythrocyte MDA and plasma OHP, significantly lower activities of GSH-Px and CAT, and significantly lower concentrations of erythrocyte Se, Cu, and Zn and plasma Se and Cu were found in both groups of renal patients compared with controls. The SOD activity was reduced in both groups of CRF children. In group I the activity of SOD and GSH-Px was significantly lower than in group II. In summary, there is increased LP in plasma and RBC in children with predialysis CRF, even those patients with moderate renal insufficiency. The activity of the enzymatic antioxidant defense system is reduced in the RBC of predialysis patients. The antioxidant capacity is related to the severity of renal failure.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Marx ER, Wicckens DG, Griffin JFK, Kyle P, Curtis JR, Dormandy TL (1987) Oxygen free radicals linked to many diseases. Science 2:529–531

    Google Scholar 

  2. Vaziri ND, Dicus M, Ho ND, Boroujerdi-Rad L, Sindhu RK (2003) Oxidative stress and dysregulation of superoxide dismutase and NADPH oxidase in renal insufficiency. Kidney Int 63:179–185

    Article  CAS  PubMed  Google Scholar 

  3. Yawata Y, Jacob H (1975) Abnormal red cell metabolism causing hemolysis in uremia: nature of the defect and its persistence despite adequate hemodialysis. Blood 45:231–239

    CAS  PubMed  Google Scholar 

  4. Griendling KK, Sorecsu D, Ushio-Fukai M (2000) NAD(P)H oxidase: role in cardiovascular biology and disease. Cir Res 86:494–501

    CAS  Google Scholar 

  5. Galli F, Ronco C (2000) Oxidant stress in hemodialysis. Nephron 84:1–5

    Article  CAS  PubMed  Google Scholar 

  6. Taccone-Gallucci M, Giardini O, Lubrano R, Mazarella V (1986) Red blood cell membrane lipid peroxidation in continuous ambulatory peritoneal dialysis patients. Am Clin Nephrol 6:92–95

    CAS  Google Scholar 

  7. Zwolińska D (1998) Lipid peroxidation and antioxidant enzymes in patients with chronic renal failure. Adv Clin Exp Med 7:87–92

    Google Scholar 

  8. Durak I, Akyol O, Basesme E, Canbolat O, Kavutcu M (1994) Reduced erythrocyte defence mechanisms against free radical toxicity in patients with chronic renal failure. Nephron 66:76–80

    CAS  PubMed  Google Scholar 

  9. Mimic-Oka J, Simic T, Djukanovic L, Reljic Z, Davicevic Z (1999) Alteration in plasma antioxidant capacity in various degrees of chronic renal failure. Clin Nephrol 51:233–241

    CAS  PubMed  Google Scholar 

  10. Richard MJ, Arnaud J, Jurkovitz C, Hachache T, Meftahi H, Laporte F, Foret M, Favier A, Cordonnier D (1991) Trace elements and lipid peroxidation abnormalities in patients with chronic renal failure. Nephron 57:10–15

    CAS  PubMed  Google Scholar 

  11. Taccone-Gallucci M, Giardini O, Lubrano R, Bandino D, Mazzarella V, Mannarino O, Meloni C, Moroseti M, Elli M, Tozzo C, Strolighi L, Casciani CU (1987) Red blood cell lipid peroxidation in predialysis chronic renal failure. Clin Nephrol 27:238–241

    CAS  PubMed  Google Scholar 

  12. Ceballos-Picot I, Witko-Sarsat V, Merad-Boudia M, Nguyen AT, Thavenin M, Jaudon MC, Zingraff J, Verger C, Jungers P, Descamps-Latscha B (1996) Glutathione antioxidant system as a marker of oxidative stress in chronic renal failure. Free Radic Biol Med 21:845–853

    Article  CAS  PubMed  Google Scholar 

  13. Mimic-Oka J, Simic T, Ekmescic V, Dragicevic P (1995) Erythrocyte glutathione peroxidase and superoxide dismutase activities in different stages of chronic renal failure. Clin Nephrol 44:44–48

    CAS  PubMed  Google Scholar 

  14. Asoyama K, Shiki Y, Ito H, Hasegowa O, Miyao A, Hayashibe H, Dobashi K, Kato K (1990) Antioxidant enzymes and lipoperoxide in blood in uremic children and adolescents. Free Radic Biol Med 9:105–109

    Article  PubMed  Google Scholar 

  15. Sommerburg O, Grune T, Ehrich JH, Siemens WG (2002) Adaptation of glutation-peroxidase activity to oxidative stress occurs in children but not in adult patients with end-stage renal failure undergoing hemodialysis. Clin Nephrol 58 [Suppl 1]:S31–S36

  16. Turi S, Varga I, Matkovics B, Dobos E (1991) Erythrocyte defence mechanisms against free oxygen radicals in haemodialysed uraemic children. Pediatr Nephrol 5:179–183

    PubMed  Google Scholar 

  17. Otting VU, Hellmann C (1990) Malondialdehydkonzentration (MDA) im Serum chronisch niereninsuffizienter, chronisch hämodialysierter und nierentransplantierter Kinder. Z Urol Nephrol 83:141–148

    CAS  PubMed  Google Scholar 

  18. Chkawa H, Ohski N, Yagi K (1979) Assay for lipid peroxides in animal tissues by thiobarbituric reaction. Anal Biochem 95:351–358

    CAS  PubMed  Google Scholar 

  19. Nourooz-Zadeh J, Tajaddini Sarmadi J, Wolff S (1994) Measurement of plasma hydroperioxide concentration by ferrous oxidation xylenol orange assay in conjunction with triphenylphosphine. Anal Biochem 220:403–409

    Article  CAS  PubMed  Google Scholar 

  20. Paglia DE, Valentine WN (1967) Studies on the quantitative and qualitative characterisation of erythrocyte glutathione peroxidase. J Lab Clin Med 70:158–168

    CAS  PubMed  Google Scholar 

  21. Aebi H (1974) Catalase, vol 2. In: Bergmeyer HU (eds) Methods of enzymatic analysis. Weinheim Academic Press, New York, pp 673–678

  22. Misra HP, Fridovich I (1972) The role of superoxide anion in the autooxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 247:3170–3175

    PubMed  Google Scholar 

  23. Martin-Mateo MC, Sanchez-Portugal M, Iglesias S, Paula A de, Bustamante J (1999) Oxidative stress in chronic renal failure. Ren Fail 21:155–167

    CAS  PubMed  Google Scholar 

  24. Trznadel K, Pawlicki L, Kędziora J, Luciak M, Błaszczyk J, Buczyński A (1989) Aktywność dysmutazy ponadtlenkowej w erytrocytach oraz stężenie malonylodialdehydu w erytrocytach i osoczu w różnych okresach niewydolności nerek. Pol Arch Med Wewn 80:261–266

    Google Scholar 

  25. Annuk M, Fellström B, Åkerblom O, Zilmer K, Vihalemm T, Zilmer M (2001) Oxidative stress markers in pre-uremic patients. Clin Nephrol 56:308–314

    CAS  PubMed  Google Scholar 

  26. Zachara BA, Adamowicz A, Trafikowska U, Trafikowska A, Manitius J, Nartowicz E (2001) Selenium and glutathione levels and glutathione peroxidases and some other antioxidant parameters in blood of patients with chronic renal failure. J Trace Elem Med Biol 15:161–166

    CAS  PubMed  Google Scholar 

  27. Dasgupta A, Hussain S, Ahmad S (1992) Increased lipid peroxidation in patients on maintenance hemodialysis. Nephron 60:56–59

    CAS  PubMed  Google Scholar 

  28. Lucchi L, Banni S, Capelli B, Medici G, Melis MP, Tomasi A, Vannini V, Lusvarghi E (1993) Conjugated diene fatty acids in patients with chronic renal failure: evidence of increased lipid peroxidation? Nephron 65:401–409

    CAS  PubMed  Google Scholar 

  29. Dursun E, Ozben T, Suleymanlar G, Dursun B, Yakupoglu G (2002) Effect of hemodialysis on the oxidative stress and antioxidants. Clin Chem Lab Med 40:1009–1013

    CAS  PubMed  Google Scholar 

  30. Konukoglu D, Ercan M, Ayaz M, Onen S (2001) Plasma and erythrocytes antioxidant status and trace element levels in proteinuric patients with moderate glomerular function. J Trace Elem Med Biol 15:119–122

    CAS  PubMed  Google Scholar 

  31. Nagase S, Aoyagi K, Hirayama A, Gotoh M, Ueda A, Tomida C, Kamezaki T, Nagai Y, Kikuchi H, Koyama A (1997) Favorable effect of hemodialysis on decreased serum antioxidant activity in hemodialysis patients demonstrated by electron spin resonance. J Am Soc Nephrol 8:1157–1163

    CAS  PubMed  Google Scholar 

  32. Ozden M, Maral H, Akaydin D, Cetinalp P, Kalender B (2002) Erythrocyte glutathione peroxidase activity, plasma malonyldialdehyde and erythrocyte glutathione levels in hemodialysis and CAPD patients. Clin Biochem 35:269–273

    Article  CAS  PubMed  Google Scholar 

  33. Paul JL, Sall ND, Soni T, Poignet JL, Lindenbaum A, Man NK, Moatti N, Raichvarg D (1993) Lipid peroxidation abnormalities in hemodialyzed patients. Nephron 64:106–109

    CAS  PubMed  Google Scholar 

  34. Vanella A, Geremia E, Pinturo R, Triolo P, Liuzzo G, Triolo C, Custorella A, Condorelli G, Giglio A (1983) Superoxide dismutase activity and reduced glutathione content in erythrocytes of uremic patients on chronic dialysis. Acta Haematol 70:312–315

    CAS  PubMed  Google Scholar 

  35. Zachara BA, Adamowicz A, Trafikowska U, Trafikowska A, Manitius J, Nartowicz E (2001) Selenium and glutathione levels and glutathione peroxidase activities in blood component of uremic patients on hemodialysis supplemented with selenium and treated with erythropoietin. J Trace Elem Med Biol 15:201–208

    CAS  PubMed  Google Scholar 

  36. Van Den Branden C, Ceyssens B, De Craemer D, De Bleser P, Hellemans K, Geerts A, Verbeelen D (2000) Antioxidant enzyme gene expression in rats with remnant kidney induced chronic renal failure. Exp Nephrol 8:91–96

    PubMed  Google Scholar 

  37. Avissar N, Ornt DB, Yagil Y, Horovitz S, Watkins RH, Kerl EA, Takahashi K, Palmer IS, Cohen HJ (1994) Human kidney proximal tubules are the main source of plasma glutathione peroxidase. Am J Physiol 266: C367–C375

    CAS  PubMed  Google Scholar 

  38. Adamowicz A, Trafikowska U, Trafikowska A, Zachara BA, Manitius J (2002) Effect of erythropoietin on selected antioxidant parameters in blood of uremic patients on long-term hemodialysis. Med Sci Monit 8:CR202–205

    CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Danuta Zwolińska.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zwolińska, D., Grzeszczak, W., Kiliś-Pstrusińska, K. et al. Lipid peroxidation and antioxidant enzymes in children with chronic renal failure. Pediatr Nephrol 19, 888–892 (2004). https://doi.org/10.1007/s00467-004-1512-2

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00467-004-1512-2

Keywords

Navigation