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Revista Brasileira de Terapia Intensiva

AMIB - Associação de Medicina Intensiva Brasileira

OFFICIAL JOURNAL OF THE ASSOCIAÇÃO BRASILEIRA DE MEDICINA INTENSIVA AND THE SOCIEDADE PORTUGUESA DE CUIDADOS INTENSIVOS

ISSN: 0103-507X
Online ISSN: 1982-4335

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Bernardi RM, Constantino L, Machado RA, Vuolo F, Budni P, Ritter C, et al. N-acetilcisteína e deferoxamina protegem contra insuficiência renal aguda induzida por isquemia/reperfusão em ratos. Rev Bras Ter Intensiva. 2012;24(3):219-223

 

 

2012;24(3):219-223
Original Article - Basic Research

http://dx.doi.org/10.1590/S0103-507X2012000300003

N-acetylcysteine and deferrioxamine protects against acute renal failure induced by ischemia/reperfusion in rats

N-acetilcisteína e deferoxamina protegem contra insuficiência renal aguda induzida por isquemia/reperfusão em ratos

Roberto Meister Bernardi, Larissa Constantino, Roberta Albino Machado, Francieli Vuolo, Patricia Budni, Cristiane Ritter, Felipe Dal-Pizzol

Experimental Physiopathology Laboratory, Health Sciences Postgraduate Program, Health Sciences Unit, Universidade do Extremo SulCatarinense - UNESC - Criciúma (SC), Brazil.

Conflict of interest: None.

Submitted on August 7, 2012
Accepted on September 10, 2012

Financial support: This research was supported by grants from Universidade do Extremo Sul Catarinense (UNESC), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Instituto Nacional de Ciência e Tecnologia Translacional em Medicina (INCT-TM).

Corresponding author:

Felipe Dal-Pizzol
Laboratório de Fisiopatologia Experimental Programa de Pós-Graduação em Ciências da Saúde Unidade Acadêmica Ciências da Saúde Universidade do Extremo Sul Catarinense
Avenida Universitária, 1.105
Zip Code: 88806-000 - Criciúma (SC), Brazil
E-mail: [email protected]

 

Abstract

OBJECTIVE: Antioxidants are widely used in animal models to prevent renal injury after ischemia/reperfusion, but it is unknown if the benefits of antioxidants are additive. In this study, we aimed to investigate the protective effects of N-acetylcysteine plus deferoxamine in an animal model of kidney ischemia/reperfusion injury.
METHODS: Bilateral kidney ischemia was mastintained for 45 minutes. N-acetylcysteine, deferoxamine or both were administered into the aorta above the renal arteries immediately prior to induction of ischemia. Five rats from each group were sacrificed 1, 6 or 12 hours after reperfusion for the determination of blood creatinine, kidney oxidative damage parameters and myeloperoxidase activity.
RESULTS: The combination of N-acetylcysteine and deferoxamine, but not their isolated use, prevented the increase in creatinine after ischemia/reperfusion. This prevention was followed by a consistent decrease in myeloperoxidase activity and oxidative damage parameters both in the kidney cortex and medulla.
CONCLUSION: Treatment with N-acetylcysteine and deferoxamine was superior to the isolated use of either compound in an animal model of kidney ischemia/reperfusion.

Keywords: Deferoxamine, Reperfusion injury, Renal insufficiency, Acetylcysteine, Reactive oxygen species, Rats

 

 

INTRODUCTION

Renal ischemia is observed in a variety of clinical situations, such as cardiac arrest with recovery, liver and kidney transplantation and partial nephrectomy. The acute renal failure (ARF) observed after ischemia is characterized by a decreased glomerular filtration rate, tubular necrosis and increased renal vascular resistance.(1,2)

The ischemia/reperfusion process (I/R) involves multiple pathophysiologic mechanisms, such as a disturbance in calcium homeostasis,(3) reactive oxygen species (ROS) production,(4) mitochondrial dysfunction,(5) and neutrophilic infiltration.(6) ROS have been implicated as a major pathophysiologic component of acute renal failure during I/R in the kidney,(4,7) and a component that may contribute to ROS generation is iron. Unbound iron can catalyze the conversion of H2O2 to OH or form reactive ferryl or perferryl species.(8) In addition, after I/R, activation of the endothelium and the recruitment of neutrophil cells were observed.(9) The migration of neutrophils into the injured kidney following reperfusion leads to increased renal myeloperoxidase (MPO) activity, suggesting that chlorinated species could play a role in kidney damage.(10)

In an effort to minimize these events, studies have used antioxidants, such as N-acetylcysteine(11) and deferoxamine.(12) N-acetylcysteine (NAC) is an antioxidant that acts by increasing intracellular levels of glutathione, enhancing glutathione-S-transferase activity, and scavenging ROS.(13-15) In addition, preloading animals with iron(16) could accelerate oxidative damage; the use of deferoxamine (DFX) prevents this effect,(17-21) suggesting that DFX could have clinical applications in preventing oxidative damage in ARF. Because NAC and DFX may confer protection by different mechanisms, their beneficial effects may be additive or synergistic.(22,23)

In this study, we hypothesized that NAC and DFX could have synergistic effects when administered in an animal model of kidney I/R injury.

 

METHODS

All experiments were performed in accordance with the National Institutes of Health (NIH) guidelines and with the approval of the Ethics Committee from the Universidade do Extremo Sul Catarinense.

General procedures

Male Wistar rats, 2-3 months old and weighing 300-350 g, were divided into five treatment groups containing 15 animals each: (1) sham operated animals, (2) I/R plus saline, (3) I/R plus NAC (20 mg/kg), (4) I/R plus DFX (20 mg/kg) and (5) I/R plus NAC and DFX (same doses as in groups 3 and 4). The drugs were administrated as a single dose immediately before the induction of ischemia. NAC and DFX doses were based on previous studies from our group.(24) For the I/R procedure, the rats were anaesthetized with ketamine (75 mg/kg). A midline incision was made, and the aorta and both renal arteries were identified. Drugs were administered into the aorta above the renal arteries, and then both pedicles were clamped with non-traumatic microvascular clamps. Ischemia was maintained for 45 min. After this time, fluid losses were replaced by the administration of 5 mL of warm isotonic saline solution, and the clamps were removed. Five rats from each group were sacrificed 1, 6 and 12 hours after reperfusion, and the blood and kidneys were removed and stored at -80ºC.

Plasma creatinine

Creatinine was determined using an enzymatic assay. In brief, serum was exposed to 2% naphthol and 0.05% diacetyl in a final volume of 1 mL and measured spectrophotometrically at 540 nm after 20 min. The results were expressed as milligrams per deciliter.

Myeloperoxidase activity

Myeloperoxidase (MPO) activity, an index of leukocyte infiltration, was measured 1, 6 and 12 hours after reperfusion, as previously described.(25) Briefly, the kidneys were homogenized in 0.5% hexadecyltrimethylammonium bromide and centrifuged at 15,000 g for 40 minutes. An aliquot of supernatant was mixed with a solution of 1.6 mM tetramethylbenzidine and 1 mM H2O2. The activity was measured spectrophotometrically as the change in absorbance at 650 nm and 37ºC.

Thiobarbituric acid reactive substances

The tissue TBARS levels were determined by a method based on the reaction with thiobarbituric acid (TBA) at 90-100ºC.(26) In the test, malondialdehyde (MDA) or MDA-like substances react with TBA to produce a pink pigment with a maximum absorption at 532 nm.

Protein oxidative damage

The oxidative damage to proteins was assessed by the determination of carbonyl group content based on the reaction with dinitrophenylhydrazine (DNPH), as previously described.(27) Briefly, proteins were precipitated by the addition of 20% trichloroacetic acid and redissolved in DNPH, and the absorbance was monitored at 370 nm.

Statistical analyses

The difference between groups was evaluated by a one-way analysis of variance (ANOVA). When the value of F was significant, post hoc comparisons were performed by an SNK test.

 

RESULTS

Creatinine levels did not differ among groups 1 h after reperfusion but increased from 6 to 12 h when compared to the sham group (Figure 1). The combination of NAC and DFX, but not their isolated use, prevented this increase (Figure 1).

The rats subjected to renal I/R exhibited a substantial increase in MPO activity in the kidney (Figure 2), both in the cortex and medulla. Treatment with NAC plus DFX produced a higher attenuation in MPO activity both in the cortex (Figure 2A) and medulla (Figure 2B) when compared to their isolated use. Oxidative damage to the kidney was assessed (Figures 3 and 4), and the TBARS levels were generally lower when NAC and DFX were administered in combination when compared to NAC or DFX use alone (Figure 3). This differential effect of NAC and DFX was less pronounced when oxidative damage was assessed using protein carbonyls (Figure 4).

 

DISCUSSION

In this study, we demonstrated that the combination of NAC and DFX was able to decrease kidney oxidative and inflammatory damage after I/R injury in an animal model. A differential response was expected in the renal cortex and medulla, secondary to the fact that the medulla is physiologically hypoxemic; however, we were unable to demonstrate this finding in the present study.

Hydrogen peroxide is present at high levels following kidney reperfusion and is associated with the generation of MPO-derived oxidants and the Fenton reaction. Superoxide anion radicals and hydrogen peroxide may be generated via membrane nicotinamide adenine dinucleotide phosphate (NADPH) oxidases or produced by the mitochondrial NADPH dehydrogenase complex in phagocytic (neutrophils) or nonphagocytic cells.(28-30) Hydrogen peroxide formation by the elevated activity of xanthine oxidase has not been proven to be relevant in human kidney reperfusion injury. However, in rodent kidneys, I/R induces the conversion of xanthine dehydrogenase, which uses oxidized nicotinamide adenine dinucleotide (NAD) as an electron acceptor, into xanthine oxidase, which, in contrast, uses oxygen as a substrate.(31-33) Because adenosine triphosphate (ATP) is consumed during ischemia, xanthine and hypoxanthine may accumulate; in the presence of oxygen, the superoxide anion radical and hydrogen peroxide could be generated during reperfusion.(34) Xanthine oxidase localized in renal endothelial cells could contribute in part to the microvascular oxidative injury that occurs following reperfusion.(35,36) In this context, antioxidants have been widely used in experimental models that attempt to prevent these alterations, but few studies have considered the role of antioxidant combinations. Shokeir et al. demonstrated that the combination of L-arginine and alpha-tocopherol has a more protective and synergistic antioxidant effect in an animal model of transplantation ischemia/reperfusion injury.(37) Furthermore, the combination of NAC and ebselen prevents kidney damage more extensively than when each drug is used alone,(38) and the same pattern of protection was observed using erdosteine and alpha-tocopherol.(39) In different models of inflammatory diseases, we had previously demonstrated that the combination of NAC and DFX is superior to the isolated use of the antioxidant.(24,40-42) Here we can confirm these previous results in a model of kidney ischemia/reperfusion. These synergistic actions are likely related to the ability to scavenge more than one radical species or to prevent the possible generation of antioxidant-derived free radicals. In fact, this finding is of major relevance to NAC, which can generate thiyl radicals in the presence of iron, thus the iron chelator effect of DFX can prevent NAC-induced oxidative stress.

 

CONCLUSION

Treatment with the combination of NAC and DFX was superior to the isolated use of these compounds in an animal model of kidney I/R, suggesting that the availability of iron can play a relevant role in the disease process or in the effectiveness of NAC.

 

REFERENCES

1. Biology of acute renal failure: therapeutic implications. Kidney Int. 1997;52(4):1102-15.

2. Thadhani R, Pascual M, Bonventre JV. Acute renal failure. N Engl J Med. 1996;334(22):1448-60. Review.

3. Meldrum DR, Cleveland JC Jr, Sheridan BC, Rowland RT, Banerjee A, Harken AH. Cardiac surgical implications of calcium dyshomeostasis in the heart. Ann Throrac Surg. 1996;61(4):1273-80.

4. Weight SC, Bell PR, Nicholson ML. Renal ischaemia--reperfusion injury. Br J Surg. 1996;83(2):162-70.

5. Rouslin W. Mitochondrial complexes I, II, III, IV, and V in myocardial ischemia and autolysis. Am J Physiol. 1983;244(6):H743-8.

6. Lauriat S, Linas SL. The role of neutrophils in acute renal failure. Semin Nephrol. 1998;18(5):498-504.

7. Paller MS, Jacob HS. Cytochrome P-450 mediates tissue-damaging hydroxyl radical formation during reoxygenation of the kidney. Proc Natl Acad Sci U S A. 1994;91(15):7002-6.

8. Halliwell B, Gutteridge JM. Role of free radicals and catalytic metal ions in human disease: an overview. Methods Enzymol. 1990;186:1-85. Review.

9. Witko-Sarsat V, Rieu P, Descamps-Latscha B, Lesavre P, Halbwachs-Mecarelli L. Neutrophils: molecules, functions and pathophysiological aspects. Lab Invest. 2000;80(5):617-53.

10. Klebanoff SJ. Myeloperoxidase: friend and foe. J Leukoc Biol. 2005;77(5):598-625.

11. Erbas H, Aydogdu N, Kaymak K. Effects of N-acetylcysteine on arginase, ornithine and nitric oxide in renal ischemia-reperfusion injury. Pharmacol Res. 2004;50(5):523-7.

12. Huang H, He Z, Roberts LJ 2nd, Salahudeen AK. Deferoxamine reduces cold-ischemic renal injury in a syngeneic kidney transplant model. Am J Transplant. 2003;3(12):1531-7.

13. Spapen H. N-acetylcysteine in clinical sepsis: a difficult marriage. Crit Care. 2004;8(4):229-30.

14. Hsu BG, Lee RP, Yang FL, Harn HJ, Chen HI. Post-treatment with N-acetylcysteine ameliorates endotoxin shock-induced organ damage in conscious rats. Life Sci. 2006;79(21):2010-6.

15. Paterson RL, Galley HF, Webster NR. The effect of N-acetylcysteine on nuclear factor-kappa B activation, interleukin-6, interleukin-8, and intercellular adhesion molecule-1 expression in patients with sepsis. Crit Care Med. 2003;31(11):2574-8.

16. Wu ZL, Paller MS. Iron loading enhances susceptibility to renal ischemia in rats. Ren Fail. 1994;16(4):471-80.

17. Paller MS, Hedlund BE. Extracellular iron chelators protect kidney cells from hypoxia/reoxygenation. Free Radic Biol Med. 1994;17(6):597-603.

18. Baliga R, Zhang Z, Baliga M, Ueda N, Shah SV. In vitro and in vivo evidence suggesting a role for iron in cisplatin-induced nephrotoxicity. Kidney Int. 1998;53(2):394-401.

19. de Vries B, Walter SJ, von Bonsdorff L, Wolfs TG, van Heurn LW, Parkkinen J, et al. Reduction of circulating redox-active iron by apotransferrin protects against renal ischemia-reperfusion injury. Transplantation.2004;77(5):669-75.

20. Shah SV, Walker PD. Evidence suggesting a role for hydroxyl radical in glycerol-induced acute renal failure. Am J Physiol. 1988;255(3 Pt 2):F438-43.

21. Paller MS. Hemoglobin- and myoglobin-induced acute renal failure in rats: role of iron in nephrotoxicity. Am J Physiol. 1988;255(3 Pt 2):F539-44.

22. Klebanoff SJ, Wallersdorph AM, Michel BR, Rosen H. Oxygen-based free radical generation by ferrous ions and deferoxamine. J Biol Chem. 1989;264(33):19765-71.

23. Zager RA, Foerder CA. Effects of inorganic iron and myoglobin on in vitro proximal tubular lipid peroxidation and cytotoxicity. J Clin Invest. 1992;89(3):989-95.

24. Ritter C, Andrades ME, Reinke A, Menna-Barreto S, Moreira JC, Dal-Pizzol F. Treatment with N-acetylcysteine plus deferoxamine protects rats against oxidative stress and improves survival in sepsis. Crit Care Med. 2004;32(2):342-9.

25. Liaudet L, Mabley JG, Soriano FG, Pacher P, Marton A, Haskó G, et al. Inosine reduces systemic inflammation and improves survival in septic shock induced by cecal ligation and puncture. Am J Respir Crit Care Med. 2001;164(7):1213-20.

26. Draper HH, Hadley M. Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol. 1990;186:421-31.

27. Levine RL, Williams JA, Stadtman ER, Shacter E. Carbonyl assays for determination of oxidatively modified proteins. Methods Enzymol. 1994;233:346-57.

28. Maruyama Y, Lindholm B, Stenvinkel P. Inflammation and oxidative stress in ESRD-- the role of myeloperoxidase. J Nephrol. 2004;17 Suppl 8:S72-6.

29. González-Flecha B, Boveris A. Mitochondrial sites of hydrogen peroxide production in reperfused rat kidney cortex. Biochim Biophys Acta. 1995;1243(3):361-6.

30. Zulueta JJ, Sawhney R, Yu FS, Cote CC, Hassoun PM. Intracellular generation of reactive oxygen species in endothelial cells exposed to anoxia-reoxygenation. Am J Physiol. 1997;272(5 Pt 1):L897-902.

31. McKelvey TG, Höllwarth ME, Granger DN, Engerson TD, Landler U, Jones HP. Mechanisms of conversion of xanthine dehydrogenase to xanthine oxidase in ischemic rat liver and kidney. Am J Physiol. 1988;254(5 Pt 1):G753-60.

32. Linas SL, Whittenburg D, Repine JE. Role of xanthine oxidase in ischemia/reperfusion injury. Am J Physiol. 1990;258(3 Pt 2):F711-6.

33. Greene EL, Paller MS. Xanthine oxidase produces O2-. in posthypoxic injury of renal epithelial cells. Am J Physiol. 1992;263(2 Pt 2):F251-5.

34. Granger DN. Role of xanthine oxidase and granulocytes in ischemia-reperfusion injury. Am J Physiol. 1988;255(6 Pt 2):H1269-75. Review.

35. Kooij A, Schijns M, Frederiks WM, Van Noorden CJ, James J. Distribution of xanthine oxidoreductase activity in human tissues--a histochemical and biochemical study. Virchows Arch B Cell Pathol Incl Mol Pathol. 1992;63(1):17-23.

36. Linder N, Rapola J, Raivio KO. Cellular expression of xanthine oxidoreductase protein in normal human tissues. Lab Invest. 1999;79(8):967-74.

37. Shokeir AA, Barakat N, Hussein AA, Awadalla A, Abdel-Aziz A, Abo-Elenin H. Role of combination of L-arginine and α-tocopherol in renal transplantation ischaemia/reperfusion injury: a randomized controlled experimental study in a rat model. BJU Int. 2011;108(4):612-8.

38. Kizilgun M, Poyrazoglu Y, Oztas Y, Yaman H, Cakir E, Cayci T, et al. Beneficial effects of N-acetylcysteine and ebselen on renal ischemia/reperfusion injury. Ren Fail. 2011;33(5):512-7.

39. Yurdakul T, Kulaksizoglu H, Pişkin MM, Avunduk MC, Ertemli E, Gokçe G, et al. Combination antioxidant effect of α-tocoferol and erdosteine in ischemia-reperfusion injury in rat model. Int Urol Nephrol. 2010;42(3):647-55. Erratum in Int Urol Nephrol. 2010;42(3):657. Gokçe, Gürhan [added].

40. Ritter C, Cunha AA, Echer IC, Andrades M, Reinke A, Lucchiari N, et al. Effects of N-acetylcysteine plus deferoxamine in lipopolysaccharide-induced acute lung injury in the rat. Crit Care Med. 2006;34(2):471-7.

41. Petronilho F, Constantino L, de Souza B, Reinke A, Martins MR, Fraga CM, et al. Efficacy of the combination of N- acetylcysteine and deferoxamine in the prevention and treatment of gentamicin-induced acute renal failure in male Wistar rats. Nephrol Dial Transplant. 2009;24(7):2077-82.

42. Fraga CM, Tomasi CD, Biff D, Topanotti MF, Felisberto F, Vuolo F, et al. The effects of N-acetylcysteine and deferoxamine on plasma cytokine and oxidative damage parameters in critically ill patients with prolonged hypotension: a randomized controlled trial. J Clin Pharmacol. 2012;52(9):1365-72.

 

 

This study was conducted at the Experimental Pathophysiology Laboratory, Universidade do Extremo Sul Catarinense - UNESC - Criciúma (SC), Brazil.

 

 

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