Prevention of reoxygenation injury by sodium salicylate in isolated- perfused rat liver

Free Radical Biology and Medicine

Volumn 25, Issue 1, 1998, Pages 87-94

  Colantoni, Alessandra ^a,b   De Maria, Nicola ^a   Caraceni, Paolo ^b   Bernardi, Mauro ^b   Floyd, Robert A ^c   Van Thiel, David H ^a  

^a LOYOLA UNIVERSITY CHICAGO   (United States)

^b UNIVERSITY OF BOLOGNA   (Italy)

^c OKLAHOMA MEDICAL RESEARCH FOUNDATION   (United States)

Author keywords

Free radical; Hydroxyl radical; Liver; Oxidative stress; Reoxygenation; Salicylate; Trapping agent

Indexed keywords

CARBONYL DERIVATIVE; FREE RADICAL; HYDROXYL RADICAL; LACTATE DEHYDROGENASE; MALONALDEHYDE; REACTIVE OXYGEN METABOLITE; SALICYLATE SODIUM;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DAMAGE; CONTROLLED STUDY; ENZYME RELEASE; ISOLATED LIVER; LIPID PEROXIDATION; LIVER ISCHEMIA; MALE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; RAT; REPERFUSION INJURY;

ANIMALS; CELL SURVIVAL; FREE RADICALS; HYDROXYL RADICAL; LIPID METABOLISM; LIPID PEROXIDATION; LIVER; MALE; OXIDATION-REDUCTION; PERFUSION; PROTEINS; RATS; RATS, WISTAR; SODIUM SALICYLATE; TIME FACTORS;

ANIMALIA;

EID: 0032125460     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0891-5849(98)00033-1     Document Type: Article

References (42)

1. McCord J. M. Oxygen derived free radicals in postischemic tissue injury. N. Engl. J. Med. 312:1985;159-164.
2. Land W., Messmer K. The impact of ischemia/reperfusion injury on specific and nonspecific, early and late chronic events after organ transplantation. Early events. Transplant. Rev. 10:1996;108-121.
3. Connor H. D., Gao W., Nukina S., Lemasters J. J., Mason R. P., Thurman R. G. Evidence that free radicals are involved in graft failure following orthotopic liver transplantation in the rat - An electron paramagnetic resonance spin trapping study. Transplantation. 54:1992;199-204.
4. Kalid M. A., Ashraf M. Direct detection of endogenous hydroxyl radical production in cultured adult cardiomyocytes during anoxia and reoxygenation. Is the hydroxyl radical really the most damaging radical species? Circ. Res. 72:1993;725-736.
5. Yu B. P. Cellular defenses against damage from reactive oxygen species. Physiol. Rev. 74:1994;139-162.
6. Bzeizi K. I., Jalan R., Plevris J. N., Hayes P. C. Primary graft dysfunction after liver transplantation from pathogenesis to prevention . Liver Transplant. Surg. 3:1997;137-148.
7. Clavein P. A., Harvey P. R., Strasberg S. M. Preservation and reperfusion injuries in liver allografts. An overview and synthesis of current studies. Transplantation. 53:1992;957-978.
8. Lemasters J. J., Thurman R. G. The many facets of reperfusion injury (editorial). Gastroenterology. 108:1995;1317-1320.
9. Caraceni P., Gasbarrini A., Van Thiel D. H., Borle A. B. Oxygen free radical formation by hepatocytes during post-anoxic reoxygenation scavenging effect of albumin . Am. J. Physiol. 266:1994;G451-G458.
10. Sies H. Oxidative stress Oxidants and antioxidants . Exp. Physiol. 82:1997;291-295.
11. Powell S. R. Salicylate trapping of OH• as a tool for studying post-ischemic oxidative injury in the isolated rat heart. Free Radic. Res. 21:1994;355-370.
12. Das D. K., George A., Liu X. K., Rao P. S. Detection of hydroxyl radical in the mitochondria of ischemic-reperfused myocardium by trapping with salicylate. Biochem. Biophys. Res. Commun. 165:1989;1004-1009.
13. Delbarre B., Floyd R. A., Delbarre G., Calinon F. Glutamate accumulation and increased hydroxyl free radical formation in the abdominal aorta and heart of gerbil after ischemia/reperfusion injury. Free Radic. Biol. Med. 13:1992;31-34.
14. Kadkhodaee M., Endre Z. H., Towner R. A., Cross M. Hydroxyl radical generation following ischaemia-reperfusion in cell-free perfused rat kidney. Biochem. Biophys. Acta. 1243:1995;169-174.
15. Liu X., Tosaki A., Engelman R. M., Das D. K. Salicylate reduces ventricular dysfunction and arrythmias during reperfusion in isolated rat hearts. J. Cardiovasc. Pharmacol. 19:1992;209-215.
16. Van Jaarsveld H., Kuyl J. M., Van Zyl G. F., Barnard H. C. Salicylate in the perfusate during ischemia/reperfusion prevented mitochondrial injury. Res. Commun. Mol. Path. Pharmacol. 86:1994;287-295.
17. Marotto M. E., Thurman R. G., Lemasters J. J. Early midzonal cell death during low-flow hypoxia in the isolated, perfused rat liver Protection by allopurinol . Hepatology. 8:1988;585-590.
18. Ingelman-Sundberg M., Kaur H., Terelius Y., Persson J. O., Halliwell B. Hydroxylation of salicylate by microsomal fractions and cytochrome P-450. Biochem. J. 276:1991;753-757.
19. Floyd R. A., Watson J. J., Wong P. K. Sensitive assay of hydroxyl radical formation utilizing high pressure liquid chromatography with electrochemical detection of pheol and salicylate hydroxylation products. J. Biochem. Biophys. Methods. 10:1984;221-235.
20. Levine R. L., Williams J. A., Stadtman E. R., Shachter E. Carbonyl assays for determination of oxydatively modified proteins. Methods Enzymol. 223:1994;334-339.
21. Esterbauer H. Determination of aldehydic lipid peroxidation products malonaldehyde and 4-hydoxynonenal . Methods Enzymol. 186:1990;407-421.
22. Belinsky S. A., Popp J. A., Kauffman F. C., Thurman R. G. Trypan blue uptake as a new method to investigate hepatotoxicity in periportal and pericentral regions of liver lobule. Studies with allyl alcohol in the perfused liver. J. Pharmacol. Exp. Ther. 230:1984;755-760.
23. Holley A. E., Cheeseman G. C. Measurement free radical reactions in vivo. Br. Med. Bull. 49:1993;494-505.
24. Pryor W. A., Godber S. S. Non invasive measures of oxidative stress status in humans. Free Radic. Biol. Med. 10:1991;177-184.
25. Coudray C., Talla M., Martin S., Fatome M., Favier A. High-performance liquid chromatography-electrochemical determination of salicylate hydroxylation products as an in vivo marker of oxidative stress. Anal. Biochem. 227:1995;101-111.
26. Grammas P., Liu G. J., Wood K., Floyd R. A. Anoxia/reoxygenation induces hydroxyl free radical formation in brain microvessels. Free Radic. Biol. Med. 14:1994;553-557.
27. 2-dependent hydroxyl radical production during ischemia-reperfusion lung injury. Am. J. Physiol. 265:1993;L279-L285.
28. Kil H. Y., Zhang J., Piantadosi C. A. Brain temperature alters hydroxyl radical production during cerebral ischemia/reperfusion in rats. J. Cereb. Blood Flow Metab. 16:1996;100-106.
29. Togashi H., Shinzawa H., Yong H., Takahashi T., Noda H., Oikawa K., Kamada H. Ascorbic acid radical, superoxide and hydroxyl radical are detected in reperfusion injury of rat liver using electron spin resonance spectroscopy. Arch. Biochem. Biophys. 308:1994;1-7.
30. Kehrer J. Free radicals as mediators of tissue injury and disease. Crit. Rev. Toxicol. 23:1993;21-48.
31. Stadtman E. R. Metal ion-catalyzed oxidation of proteins biochemical mechanism and biological consequences . Free Radic. Biol. Med. 9:1990;315-325.
32. Tribble D. L., Aw T. Y., Jones D. P. The pathophysiological significance of lipid peroxidation in oxidative cell injury. Hepatology. 7:1987;377-387.
33. Chazouilleres O., Calmus Y., Vaubourdolle M., Ballet F. Preservation-induced liver injury. Clinical aspects, mechanisms and therapeutic approaches. J. Hepatol. 18:1993;123-134.
34. Matthews W. R., Guido D. M., Fisher M. A., Jaeschke H. Lipid peroxidation as molecular mechanism of liver cell injury during reperfusion after ischemia. Free Radic. Biol. Med. 16:1994;763-770.
35. Zhong Z., Qu W., Connor H. D., Thurman R. G. Role of Kupffer cells in the pathogenesis of hepatic reperfusion injury. Am. J. Physiol. 267:1994;G630-G636.
36. Fiegen R. J., Rauen U., Hartmann M., Decking U. K., deGroot H. Decrease of ischemic injury to the isolated perfused rat liver by loop diuretics. Hepatology. 25:1997;1425-1431.
37. Kaur H., Halliwell B. Detection of hydroxyl radicals by aromatic hydroxylation. Methods Enzymol. 233:1994;67-82.
38. Takemura G., Onodera T., Millard R. W., Ashraf M. Demonstration of hydroxyl radical and its role in hydrogen peroxide-induced myocardial injury Hydroxyl radical dependent and independent mechanisms . Free Radic. Biol. Med. 15:1993;13-25.
39. Graziano J. H., Grady R. W., Cerami A. The identification of 2,3-dihydroxybenzoic acid as a potentially useful iron-chelating agent. J. Pharmacol. Exp. Ther. 109:1974;570-575.
40. Schreck R., Rieber P., Bauerle P. A. Reactive oxygen intermediates as apparently widely used messengers in the activation of NF-κB trascription factor and HIV-1. EMBO J. 10:1991;2247-2258.
41. Kopp E., Ghosh S. Inhibition of NF-κB by sodium salicylate and aspirin. Science. 265:1994;956-959.
42. Colletti L., Kunkel S. L., Walz A., Burdick M. D., Kunkel R. G., Wilke C. A., Strieter R. M. The role of cytokine networks in the local liver injury following hepatic ischemia/reperfusion in the rat. Hepatology. 23:1996;506-514.