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Oxidative stress in distant organs and the effects of allopurinol during experimental acute pancreatitis

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Summary

Background. The present study was aimed at an assessment of the role of oxygen-derived free radicals in the development of local and systemic manifestations of l-arginine (Arg)-induced acute pancreatitis and at an evaluation of the protective effect of the xanthine oxidase inhibitor allopurinol.

Methods. Acute pancreatitis was induced in male Wistar rats by injecting 2×250 mg/100 g body weight of Arg intraperitoneally at an interval of 1 h, as a 20% solution in 0.15 M NaCl. Control rats received the same quantity of glycine. In a third group, 200 mg/kg of allopurinol was administered subcutaneously 30 min before the first Arg injection. Rats were killed at 6, 12, 24, or 48 h following Arg administration. Acute pancreatitis was confirmed by a serum amylase level elevation and typical inflammatory features were observed microscopically. Tissue concentrations of malonyl dialdehyde (MDA), superoxide dismutase (Mn- and Cu,Zn-SOD), glutathione peroxidase (GPx), and catalase were measured in the pancreas, liver, and kidney.

Results. The tissue concentration of MDA was significantly elevated in each organ. The activities of Mn-SOD, Cu,Zn-SOD, GPx, and catalase were quickly depleted in the pancreas and kidney, whereas only the Mn-SOD and GPx activities were reduced in the liver after the onset of pancreatitis. Histologic examination revealed acinar cell necrosis in the pancreas, but only mild alterations in the liver and kidney. Allopurinol pretreatment prevented the generation of reactive oxygen metabolites in the pancreas and reduced their formation in the kidney.

Conclusion. Oxygen-derived free radicals are generated in the pancreas, liver, and kidney at an early stage of Arg-induced acute pancreatitis. The liver and the kidney, but not the pancreas, are able to defend against oxidative stress. The prophylactic application of allopurinol significantly restrains the generation of free radicals in pancreas and kidney.

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References

  1. Steinberg W, Tenner S. Acute pancreatitis. N Engl J Med 1994; 330: 1198–1220.

    Article  PubMed  CAS  Google Scholar 

  2. Renner IG, Savage WT, Pantoga JL, Renner VJ. Death due to acute pancreatitis. A retrospective analysis of 405 autopsy cases. Dig Dis Sci 1985; 10: 1005–1008.

    Article  Google Scholar 

  3. Schoenberg MH, Büchler M, Beger HG. Oxygen radicals in experimental acute pancreatitis. Hepato-Gastroenterology 1994; 41: 313–319.

    PubMed  CAS  Google Scholar 

  4. Chardavoyne R, Asher A, Bank S, Stein TA, Wise L. Role of reactive oxygen metabolites in early cardiopulmonary changes of acute hemorrhagic pancreatitis. Dig Dis Sci 1989; 34: 1581–1584.

    Article  PubMed  CAS  Google Scholar 

  5. Guice KS, Oldham KT, Caty MG, Johnson KJ, Ward PA. Neutrophil-dependent, oxygen-radical mediated lung injury associated with acute pancreatitis. Ann Surg 1989; 210: 740–747.

    Article  PubMed  CAS  Google Scholar 

  6. Sanfey H, Bulkley GB, Cameron JL. The pathogenesis of acute pancreatitis: The source and role of oxygen-derived free radicals in three different experimental models. Ann Surg 1985; 201: 633–639.

    Article  PubMed  CAS  Google Scholar 

  7. Wisner JR, Renner IG. Allopurinol attenuates caerulein induced acute pancreatitis in the rat. Gut 1988; 29: 926–929.

    Article  PubMed  CAS  Google Scholar 

  8. Sweiry JH, Mann GE. Role of oxidative stress in the pathogenesis of acute pancreatitis. Scan J Gastroenterol 1996; 31(Suppl. 219): 10–15.

    Article  CAS  Google Scholar 

  9. Fridovich I. The biology of oxygen radicals. Science 1978; 201: 875–880.

    Article  PubMed  CAS  Google Scholar 

  10. Sies H. Oxidative stress: from basic research to clinical application. Am J Med 1991; 91 (Suppl 3C): 31–38.

    Article  Google Scholar 

  11. Parks DA, Granger DN. Xanthine oxidase: biochemistry, distribution and physiology. Acta Physiol Scand 1986; 126(Suppl 548): 87–99.

    Google Scholar 

  12. Varga ISz, Matkovics B, Czakó L, Hai DQ, Kotormán M, Takács T, et al. Oxidative stress changes in L-Arginineinduced pancreatitis in rats. Pancreas 1997; 14: 355–359.

    Article  PubMed  CAS  Google Scholar 

  13. Ceska M, Birath K, Brown B. A new and rapid method for the clinical determination of amylase activities in human serum and urine. Clin Chem Acta 1969; 26: 437–444.

    Article  CAS  Google Scholar 

  14. Placer ZA, Cushman L, Johnson BC. Estimation of product of lipid peroxidation (malonyl dialdehydes) in biochemical systems. Anal Biochem 1966; 16: 359–364.

    Article  PubMed  CAS  Google Scholar 

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

    PubMed  CAS  Google Scholar 

  16. Beauchamp C, Fridovich I. Superoxide dismutase: Improved assay and an assay applicable to acrylamide gels. Anal Biochem 1971; 44: 276–287.

    Article  PubMed  CAS  Google Scholar 

  17. Beers RF Jr, Sizer IW. Spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem 1951; 195: 133–140.

    Google Scholar 

  18. Chiu DT, Stults FH, Tappel AL. Purification and properties of rat lung soluble glutathione peroxidase. Biochim Biophys Acta 1976; 445: 558–566.

    PubMed  CAS  Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  20. Tietze F. Enzymatic method for quantitative determination of nanogram amounts of total and oxidized glutathione: applications to mammalian blood and other tissues. Anal Biochem 1969; 27: 502–522.

    Article  PubMed  CAS  Google Scholar 

  21. Lowry OH, Rosenbrough NI, Farr AL, Randell RI. Protein measurements with the folinphenol reagent. J Biol Chem 1951; 193: 265–275.

    PubMed  CAS  Google Scholar 

  22. Takács T, Czakó L, Jármay K, Farkas Gy Jr, Mándi Y, Lonovics J. Cytokine level changes in L-arginine-induced acute pancreatitis in rat. Acta Physiol Hung 1996; 84: 147–156.

    PubMed  Google Scholar 

  23. Czakó L, Takács T, Varga IS, Tiszlavicz L, Hai DQ, Hegyi P, Matkovics B, Lonovics J. Involvement of oxygen-derived free radicals in L-Arginine-induced acute pancreatitis. Dig Dis Sci 1998; 43: 1770–1777.

    Article  PubMed  Google Scholar 

  24. Takeda Y, Tominaga T, Tei N, Kitamura M, Taga T, Murase J, et al. Inhibitory effect of L-arginine on growth of rat mammary tumors induced by 7,12-dimethyl-benz(α)anthracene. Cancer Res 1975; 35: 2390–2393.

    PubMed  CAS  Google Scholar 

  25. Norman JG. The role of cytokines in the pathogenesis of acute pancreatitis. Am J Surg 1998; 175: 76–83.

    Article  PubMed  CAS  Google Scholar 

  26. Stark ME, Szurszewski JH. Role of nitric oxide in gastrointestinal and hepatic function and disease. Gastroenterology 1992; 103: 1928–1949.

    PubMed  CAS  Google Scholar 

  27. Jorens PG, Vermeire PA, Herman AG. L-arginine-dependent nitric oxide synthase: a new metabolic pathway in the lung and airways. Eur Respir J 1993; 6: 258–266.

    PubMed  CAS  Google Scholar 

  28. Del Rio LA, Sandalio LM, Palma JM. A new cellular function for peroxisomes related to oxygen free radicals? Review. Experimentia 1990; 46: 989–992.

    Article  Google Scholar 

  29. Braganza JM. Experimental acute pancreatitis. Curr Opin Gastroenterol 1990; 6: 763–768.

    Article  Google Scholar 

  30. Björk J, Arfors KE. Oxygen radicals and lcucotrienes B4 induced increase in vascular leakage by PMN-leukocytes. Agents Actions 1984; 11: 1159–1163.

    Google Scholar 

  31. Lankisch PG, Pohl U, Otto J, Wereszczynska-Siemiatkowska U, Gröne HJ. Xanthine oxidase inhibitor in acute experimental pancreatitis in rats and mice. Pancreas 1989; 4: 436–440.

    Article  PubMed  CAS  Google Scholar 

  32. Niederau C, Niederau M, Borchard F, Ude K, Luthen R, Strohmeyer G, et al. Effects of antioxidants and free radical scavengers in three different models of acute pancreatitis. Pancreas 1992; 7: 486–496.

    Article  PubMed  CAS  Google Scholar 

  33. Klein AS, Joh JW, Rangan U, Wang D, Bulkley GB. Allo-purinol: discrimination of antioxidant from enzyme inhibitory activities. Free Rad Biol Med 1996; 21: 713–717.

    Article  PubMed  CAS  Google Scholar 

  34. Folch E, Gelpí E, Roselló-Catafau J, Closa D. Free radicals generated by xanthine oxidase mediate pancreatitis-associated organ failure. Dig Dis Sci 1998; 11: 2405–2410.

    Article  Google Scholar 

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Czakó, L., Takács, T., Varga, I.S. et al. Oxidative stress in distant organs and the effects of allopurinol during experimental acute pancreatitis. International Journal of Pancreatology 27, 209–216 (2000). https://doi.org/10.1385/IJGC:27:3:209

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  • DOI: https://doi.org/10.1385/IJGC:27:3:209

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