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Byproducts of oxidative protein damage and antioxidant enzyme activities in plasma of patients with different degrees of essential hypertension

Abstract

Despite evidence that essential hypertension (EH) is a state of increased oxidative stress, the data on oxidative protein modifications is lacking. Besides, the role of extracellular antioxidant enzymes in EH has not been systematically studied. Study was performed in 45 subjects with EH and 25 normotensive controls. Patients were divided into three groups according to the 2003 ESH/ESC guidelines (grade 1–3). Plasma protein reactive carbonyl derivatives (RCD) and SH-groups (as byproducts of oxidative protein damage) as well as antioxidant enzyme activities superoxide dismutase (SOD), glutathione peroxidase (GPX) and catalase were studied spectrophotometrically and correlated with blood pressure (BP). RCD levels were increased in EH patients compared to controls and correlated significantly with both systolic blood pressure (SBP) (r=0.495, P<0.01) and diastolic blood pressure (DBP) (r=0.534, P<0.01). Plasma SH-groups content was significantly lower in all patients with EH, with no correlation with BP. SOD and catalase activity in patients with grade 1 EH were similar to that of controls. Patients with grade 2 and 3 of EH had lower SOD and catalase activity. However, significant correlation with SBP and DBP was observed for catalase only (r=−0.331; P<0.05 and r=−0.365; P<0.05, respectively). EH patients exhibited higher plasma GPX activity compared to those in controls, and it correlated with SBP (r=0.328; P<0.05). The results presented show that increased oxidative protein damage is present in all grades of EH. In mild hypertension extracellular antioxidant enzyme activities are not decreased, suggesting they are probably not critical in early EH, but could be important in moderate to severe EH.

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References

  1. Touyz RM . Reactive oxygen species, vascular oxidative stress, and redox signaling in hypertension. What is the clinical significance? Hypertension 2004; 44: 248–252.

    Article  CAS  Google Scholar 

  2. Higashi Y, Sasaki S, Nakagawa K, Matsuura H, Oshima T, Chayama K . Endothelial function and oxidative stress in renovascular hypertension. N Engl J Med 2002; 346: 1954–1962.

    Article  CAS  Google Scholar 

  3. Lip GY, Edmunds E, Nuttall SL, Landray MJ, Blann AD, Beevers DG . Oxidative stress in malignant and non-malignant phase hypertension. J Hum Hypertens 2002; 16: 333–336.

    Article  CAS  Google Scholar 

  4. Lee VM, Quinn PA, Jennings SC, Ng LL . Neutrophil activation and production of reactive oxygen species in pre-eclampsia. J Hypertens 2003; 21: 395–402.

    Article  CAS  Google Scholar 

  5. Parik T, Allikmets K, Teesalu R, Zilmer M . Oxidative stress and hyperinsulinaemia in essential hypertension: different factors of increased risk. J Hypertens 1996; 14: 407–410.

    Article  CAS  Google Scholar 

  6. Redon J, Oliva MR, Tormos C, Giner V, Chaves J, Iradi A et al. Antioxidant activities and oxidative stress byproducts in human hypertension. Hypertension 2003; 41: 1096–1101.

    Article  CAS  Google Scholar 

  7. Ward NC, Hodgson JM, Puddey IB, Mori TA, Beilin LJ, Croft KD . Oxidative stress in human hypertension: association with antihypertensive treatment, gender, nutrition and lifestyle. Free Radic Biol Med 2004; 36: 226–232.

    Article  CAS  Google Scholar 

  8. Davies KJA . Protein damage and degradation by oxygen free radicals. II Modification of amino acids. J Biol Chem 1987; 262: 9902–9907.

    CAS  PubMed  Google Scholar 

  9. Levine RL, Williams JA, Stadtman ER, Shacter E . Carbonyl assays for determination of oxidatively modified proteins. Methods Enzymol 1994; 233: 346–357.

    Article  CAS  Google Scholar 

  10. Miao-Lin Hu . Measurement of protein thiol groups and glutathione in plasma. Methods Enzymol 1994; 233: 380–385.

    Article  Google Scholar 

  11. Halliwell B . Reactive oxygen species in living systems. Source, biochemistry and role. Am J Med 1991; 9: 114–122.

    Google Scholar 

  12. Inagi R, Miyata T . Oxidative protein damage with carbohydrates and lipids in uremia: ‘Carbonyl stress’. Blood Purif 1999; 17: 95–98.

    Article  CAS  Google Scholar 

  13. Himmelfarb J, McMonagle E, McMenamin E . Plasma protein thiol oxidation and carbonyl formation in chronic renal failure. Kidney Int 2000; 58: 2571–2578.

    Article  CAS  Google Scholar 

  14. Mimic-Oka J, Simic T, Pljesa M, Stupar N, Turkovic S . Oxidative modifications of plasma proteins in different stages of chronic renal failure. Facta Universitatis 2001; 8: 1–5.

    Google Scholar 

  15. Wassmann S, Wassmann K, Nickenig G . Modulation of oxidant and antioxidant enzyme expression and function in vascular cells. Hypertension 2004; 44: 381–386.

    Article  CAS  Google Scholar 

  16. Russo C, Olivieri O, Girelli D, Faccini G, Zenari ML, Lombardi S et al. Anti-oxidant status and lipid peroxidation in patients with essential hypertension. J Hypertens 1998; 16: 1267–1271.

    Article  CAS  Google Scholar 

  17. Guidelines Committee. 2003 European Society of Hypertension-European Society of Cardiology Guidelines for the Management of Arterial Hypertension. J Hypertens 2003; 21: 1011–1053.

  18. Lowry OH, Rosebrough NJ, Farr AL, Randall TD . Protein measurement with the Folin phenol reagent. J Biol Chem 1951; 193: 265–275.

    CAS  Google Scholar 

  19. Jocelyn PC . Spectrophotometric assay of thiols. Methods Enzymol 1987; 143: 44–67.

    Article  CAS  Google Scholar 

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

    CAS  PubMed  Google Scholar 

  21. Goth L . A simple method for determination of serum catalase activity and revision of reference range. Clin Chim Acta 1991; 196: 143–152.

    Article  CAS  Google Scholar 

  22. Gunzler WA, Kremers H, Flohe L . An improved coupled test procedure for glutathione peroxidase in blood. Z Klin Chem Klin Biochem 1974; 12: 444–448.

    CAS  PubMed  Google Scholar 

  23. Bland JM, Altmann DG . Statistical method for assessing agreement between two methods of clinical measurement. Lancet 1986; 1: 307–310.

    Article  CAS  Google Scholar 

  24. Vaziri ND . Roles of oxidative stress and antioxidant therapy in chronic kidney disease and hypertension. Curr Opin Nephrol Hypertens 2004; 13: 93–99.

    Article  CAS  Google Scholar 

  25. Turi S, Friedman A, Bereczki C, Papp F, Kovacs J, Karg E et al. Oxidative stress in juvenile essential hypertension. J Hypertens 2003; 21: 145–152.

    Article  CAS  Google Scholar 

  26. Sowers JR . Hypertension, angiotensin II and oxidative stress. N Engl J Med 2002; 346: 1999–2001.

    Article  Google Scholar 

  27. Uchida K, Kawakishi S . Identification of oxidized histidine generated at the active site of Cu,Zn-superoxide dismutase exposed to H2O2. Selective generation of 2-oxo-histidine at the histidine 118. J Biol Chem 1994; 269: 2405–2410.

    CAS  PubMed  Google Scholar 

  28. Baykal Y, Yilmaz MI, Celik T, Gok F, Rehber H, Akay C et al. Effects of antihypertensive agents, alpha receptor blockers, beta blockers, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers and calcium channel blockers, on oxidative stress. J Hypertens 2003; 21: 1207–1211.

    Article  CAS  Google Scholar 

  29. Taddei S, Virdis A, Ghiadoni L, Salvetti G, Bernini G, Magagna A et al. Age-related reduction of NO availability and oxidative stress in humans. Hypertension 2001; 38: 274–279.

    Article  CAS  Google Scholar 

  30. Lacy F, Kailasam MT, O’Connor DT, Schmid-Schonbein GW, Parmer RJ . Plasma hydrogen peroxide production in human essential hypertension: role of heredity, gender, and ethnicity. Hypertension 2000; 36: 878–884.

    Article  CAS  Google Scholar 

  31. Whitin JC, Bhamre S, Tham DM, Cohen HJ . Extracellular glutathione peroxidase is secreted basolaterlaly by human renal proximal tubule cells. Am J Physiol Renal Physiol 2002; 283: F20–F28.

    Article  CAS  Google Scholar 

  32. Takakhashi K, Avissar N, Whitin J, Cohen H . Purification and characterization of human plasma glutathione peroxidase: a selenoglycoprotein distinct from the known cellular enzyme. Arch Biochem Biophys 1987; 256: 677–686.

    Article  Google Scholar 

  33. Maser RL, Margenheimer BS, Calvet JP . Mouse plasma glutathione peroxidase. cDNA sequence analysis and renal proximal tubular expression and secretion. J Biol Chem 1994; 269: 27066–27073.

    CAS  PubMed  Google Scholar 

  34. Touyz RM, Tabet F, Schiffrin EL . Redox-dependent signaling by angiotensin II and vascular remodeling in hypertension. Clin Exp Pharmacol Physiol 2003; 30: 860–866.

    Article  CAS  Google Scholar 

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Acknowledgements

This work was supported by a Grant 1919 from the Serbian Ministry of Science and Technology.

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Correspondence to T Simic.

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Supplementary Information accompanies the paper on Journal of Human Hypertension (http://www.nature.com/jhh)

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Simic, D., Mimic-Oka, J., Pljesa-Ercegovac, M. et al. Byproducts of oxidative protein damage and antioxidant enzyme activities in plasma of patients with different degrees of essential hypertension. J Hum Hypertens 20, 149–155 (2006). https://doi.org/10.1038/sj.jhh.1001945

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