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Lipid peroxidation and scavenger mechanism in experimentally induced heart infarcts

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Summary

Dog experiments were performed to describe the time course of lipid peroxidation after various ischemic influences of the heart measured by formation of malondialdehyde (MDA), and the scavenger action determined by reduced glutathione (GSH) content and superoxide dismutase (SOD) activity. Experimental groups consisted of control dogs having intact hearts and dogs with acute ramus descendens anterior ligature (LAD) having ischemic areas through 15, 30, 45 minutes and 1, 2, 3, 24 hours. Heart tissue for biochemical assays was excised from both the ischemic areas and from nonischemic left ventricle. The acute ischemia caused characteristic alterations in the biochemical parameters: MDA level gradually increased with its peak value being found at the end of 3 hours ligature. GSH levels decreased moderately, whereas SOD levels reduced sharply. As incrcased MDA formation indicates breakdown of the polyunsaturated fatty acids (PUFA) in the membranes and decreaased GSH and SOD levels indicate impairment of the natural scavengering, the observed changes clearly outline the extent of disintegration of membrane structure and function.

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References

  1. Burlakova EB (1980) Molecular mechanisms of the anti-oxidant effect in the treatment of cardiovascular diseases. Kardiologia 8:48–52

    Google Scholar 

  2. Burton KM, McCord JM, Ghai G (1984) Myocardial alterations due to free-radical generation. Am J Physiol 246 (Heart Circ Physiol 15) H776-H783

    PubMed  Google Scholar 

  3. Dianzani MU, Ugazio G (1978) Lipid peroxidation. In: Slater FF (ed) Biochemical mechanisms of liver injury. Acad Press, London New York 669–700

    Google Scholar 

  4. Ellman GL (1959) Tissue sulphydryl groups. Arch Biochem Biophys 82:70–77

    PubMed  Google Scholar 

  5. Farber JL (1982) Biology of disease. Membrane injury and calcium homeostasis in the pathogenesis of coagulative necrosis. Lab Invest 47:114–123

    PubMed  Google Scholar 

  6. Fong KL, McKay PB, Poyer JL (1973) Evidence that lipid peroxidation of lysosomal membranes is initiated by hydroxyl free radicals produced during flavin enzyme activity. J Biol Chem 248:7792–7797

    PubMed  Google Scholar 

  7. Fridovich I (1974) Superoxide dismutase. Advances in enzymology 41:35–97

    Google Scholar 

  8. Fridovich I (1975) Superoxide dismutases. Ann Rev Biochem 44:147–159

    PubMed  Google Scholar 

  9. Fridovich I (1979) Hypoxia and oxygen toxicity. Advances Neur 26:256–259

    Google Scholar 

  10. Gauduel Y, Duvelleroy MA (1984) Role of oxygen radicals in cardiac injury due to reoxigenation. J Mol Cell Cardiol 16:459–470

    PubMed  Google Scholar 

  11. Guarnieri C, Flamingi F, Caldarera CM (1980) Role of oxygen in the cellular damage induced by re-oxygenation of hypoxic heart. J Mol Cell Cardiol 12:797–808

    PubMed  Google Scholar 

  12. Hess ML, Okabe E, Kontos HA (1981) Rapid communication. Proton and free oxygen radical interaction with the calcium transport system of cardiac sarcoplasmic reticulum. J Mol Cell Cardiol 13:767–772

    PubMed  Google Scholar 

  13. Jennings RB, Ganote ChE, Reimer KA (1975) Ischemic tissue injury. Am J Pathol 81:179–198

    PubMed  Google Scholar 

  14. Jennings RB, Reimer KA (1981) Lethal myocardial ischemic injury. Am J Path 102:241–255

    PubMed  Google Scholar 

  15. Katz AM, Messineo FC (1981) Lipid membrane interactions and the pathogenesis of ischemic damage in the myocardium. Circ Res 48:1–16

    PubMed  Google Scholar 

  16. Klein HH, Schaper J, Puschmann St, Mienaber Ch, Kreuzer H, Schaper W (1981) Loss of canine myocardial nicotinamide adenine dinucleotides determines the transition from reversible to irreversible ischemic damage of myocardial cells. Basic Res Cardiol 76:612–621

    PubMed  Google Scholar 

  17. Kosower EM (1978) The glutathione status of cells. Academic Press International review of cytology 54:109–160

    Google Scholar 

  18. Loschen G, Azzi A (1976) On the formation of hydrogen peroxide and oxygen radicals in heart mitochondria. In: Recent advances in studies on cardiac structure and metabolism. University Park Press Baltimore 7:3–12

    Google Scholar 

  19. Matkovics B, Szöllösiné Varga I (1976) Biological role of radicals arising from molecular oxygen (in Hungarian). In: Csaba Gy (ed) Current problems of biology. Vol 7. Medicina Budapest, p 203–267

    Google Scholar 

  20. Meerson FZ, Belkina LM, Ugolev AA, Golubeva LYu, Abdikaliev NA, Solomatina ES (1980) The use of free radical scavengers for prevention of experimental myocardial infarction and reoxygenation damages of heart function. Kardiologia 20:81–86

    Google Scholar 

  21. Meerson FZ, Kagan VE, Arkhipenko YuV, Belkina LM, Rozhitskaya II (1981) Prevention of activation lipid peroxidation and myocardial antioxidant system damages in stress and experimental myocardial infarction. Kardiologia 12:55–60

    Google Scholar 

  22. Meerson FZ, Kagan VE, Kozlov YuP, Belkina LM, Arkhipenko YuV (1982) The role of lipid peroxidation in pathogenesis of ischemic damage and the antioxidant protection of the heart. Basic Res cardiol 77:465–485

    PubMed  Google Scholar 

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

    PubMed  Google Scholar 

  24. Neely JR, Feuvray D (1981) Metabolic products and myocardial ischemia. Am J Path 102:282–291

    PubMed  Google Scholar 

  25. Parks DA, Granger DN (1983) Oxygen-derived radicals and ischemia-induced tissue injury. In: Greenwald RA, Cohen G (eds) Oxyradicals and their scavenger systems. Vol II. Cellular and medical aspects, 135–144

  26. Rao PS, Cohen MV, Mueller HS (1983) Rapid communication. Production of free radicals and lipid peroxides in early experimental myocardial ischemia. J Mol Cell Cardiol 15:713–716

    PubMed  Google Scholar 

  27. Rao PS, Cohen MV, Mueller HS (1983) Sequential transcardiac changes in free radicals, catecholamines and lipid peroxides in early experimental myocardial ischemia. In: Greenwald R, Cohen G (eds) Oxyradicals and their scavenger systems. Vol 2. Elsevier New York p 357–360

    Google Scholar 

  28. Sedlak J, Lindsay RH (1968) Estimation of total protein-bound and non-protein sulphydryl groups in tissue with Ellman's reagent. Anal Biochem 25:192–205

    PubMed  Google Scholar 

  29. Schaper J, Schwarz F, Kittstein H, Kreisel E, Winkler B, Hehrlein FW (1980) Ultrastructural evaluation of the effects of global ischemia and reperfusion on human myocardium. Thorac Cardiovasc Surg 28:377–381

    Google Scholar 

  30. Shlafer M, Kane PF, Kirsh MM (1982) Possible role for cytotoxic oxygen metabolites in the pathogenesis of cardiac ischemic injury. Circulation 66, Suppl I:85–92

    Google Scholar 

  31. Shlafer M, Kane PF, Kirsh MM (1982) Superoxide dismutase plus catalase enhances the efficacy of hypothermic cardioplegia to protect the globally ischemic, reperfused heart. Thorac Cardiovasc Surg 83:830–839

    PubMed  Google Scholar 

  32. Silver EH, Szabó S (1983) Role of lipid peroxidation in tissue injury after hepatic ischaemia. Exp Mol Path 38:69–76

    Google Scholar 

  33. Slater FF (1979) Mechanisms of protection against the damage produced in biological systems by oxygen-derived animals. In: Oxygen free radicals and tissue damage. (Ed). Ciba Found Symp 65, Amsterdam, Exp Med 143–176

    Google Scholar 

  34. Smith DS, Rehncrona S, Sjiesjo BK (1980) Barbiturates as protective agents in brain ischemia and as free radical scavengers in vitro. Acta Physiol Scnad 492:129–132

    Google Scholar 

  35. Takayanagi R, Takeshige K, Minakami S (1980) NADH-and NADPH-dependent lipid peroxidation in bovine heart submitochondrial particles. Biochem J 192:853–860

    PubMed  Google Scholar 

  36. Tappel AL, Dillard J (1981) In vivo lipid peroxidation measurement via exhaled pentane and protection by vitamin E. Fed Proc 40:174–178

    PubMed  Google Scholar 

  37. Tien M, Svingen BA, Aust SD (1981) Superoxide dependent lipid peroxidation. Fed Proc 40:179–182

    PubMed  Google Scholar 

  38. Török B, Röth E, Trombitás K (1982) Ultrastructural changes of the subendocardium in ischemic and cardioplegic states before and after reperfusion. Eur Surg Res 14:17–26

    Google Scholar 

  39. Török B, Trombitás K, Röth E (1983) Ultrastructural consequences of reperfusion of the ischemic myocardium. Acta morph Acad Sci Hung 31:315–326

    Google Scholar 

  40. Török B, Röth E, Matkovics B (1984) Oxygen free radicals mediated injuries in myocardial tissue Acta Physiol Hung (to be published)

  41. Vladimirov YuA, Olenev VI, Suslova TB, Cheremisina ZP (1980) Lipid peroxidation in mitochondrial membrane. Advances in lipid research 17:173–249

    PubMed  Google Scholar 

  42. Zimmermann R, Flohé L, Weser U, Hartmann HJ (1973) Inhibition of lipid peroxidation in isolated inner membrane of rat liver mitochondria by superoxide dismutase. FEBS Letter 29:117–120

    Google Scholar 

  43. Zsoldos T, Tigyi A, Montskó T, Puppi A (1983) Lipid peroxidation in the membrane damaging effect of silica-containing dust on rat lungs. Exp Path 23:73–77

    Google Scholar 

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Röth, E., Török, B., Zsoldos, T. et al. Lipid peroxidation and scavenger mechanism in experimentally induced heart infarcts. Basic Res Cardiol 80, 530–536 (1985). https://doi.org/10.1007/BF01907916

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  • DOI: https://doi.org/10.1007/BF01907916

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