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Changes in cardiac electrophysiology, morphology, tissue biochemistry and vascular reactions in glutathione depleted animals

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The effects of acute and chronic glutathione depletion (single i.p. injection of 3 mmol/kg L-buthionine-S,R-sulphoximine and 2 mmol/kg for 4 days) on heart action potential (AP) characteristics, electronmicroscopy, cytochemistry and biochemistry and vascular contractility and nitric oxide-mediated relaxation were studied in rats and guinea pigs. In guinea pig cardiac preparations both acute and chronic glutathione depletion caused a significant decrease of maximum rate of rise of depolarization phase and duration of action potential AP(APD) at 25, 50, and 90% of repolarization but did not modify the other AP parameters. The contractile responses of helically cut aortic strips to norepinephrine were not altered by chronic glutathione depletion but the relaxing responses of precontracted preparations to acetylcholine were significantly reduced both in rats and guinea pigs. Morphologically there were indications of permeability changes, intracellular and interstitial edema and myofilament damage in the myocardium. There was also a decrease in cytochromoxydase and succinyl dehydrogenase activities both in rats and guinea pigs. The present data suggest that glutathione depletion may influence the Na+ and K+ channel activities, causes morphological and biochemical changes in cardiac preparations and may interfere with nitric oxide generation or its action in aortic strips.

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References

  1. Werns SW, Lucchesi BR: Free radical and myocardial injury: Pharmacologic implications. Circulation 75: 1–5, 1986

    Google Scholar 

  2. Thompson JA, Hess ML: The oxygen free radical system: A fundamental mechanism in the production of myocardial necrosis. Prog Cardiovasc Dis 28: 449–462, 1986

    Google Scholar 

  3. Chatham JC, Seymour AL, Harmsen E, Radda GK: Depletion of myocardial glutathione: Its effects on heart function and metabolism during ischemia and reperfusion. Cardiovasc Res 22: 833–839, 1988

    Google Scholar 

  4. Ceconi C, Curello S, Cargnoni A, Ferrari R, Albertini A, et al.: The role of glutathione status in the protection against ischaemic and reperfusion damage: Effects of N-acetylcysteine. J Mol Cell Cardiol 20: 5–13, 1987

    Google Scholar 

  5. Ferrari R, Ceconi C, Curello S, Guarneri C, Caldarela CM, Albertini A, Visioli O: Oxygen-mediated myocardial damage during ischemia and reperfusion: Role of cellular defenses against oxygen toxicity. J Mol Cell Cardiol 17: 937–945, 1985

    Google Scholar 

  6. Ferrari R, Ceconi C, Curello S, et al.: Oxygen free radicals and myocardial damage: protective role of thiol-containing agents. Am J Med 91(3C): 95S–105S, 1991

    Google Scholar 

  7. Ferrari R, Ceconi C, et al.: Myocardial damage during ischaemia and reperfusion. Eur Heart J 14: Suppl 25–30, 1993

    Google Scholar 

  8. Mezzetti A, et al.: Glutathione peroxidase, glutathione reductase and glutathione transferase activities in the human artery, vein and heart. J Mol Cell Cardiol 22: 935–938, 1990

    Google Scholar 

  9. Poot M, Teubert H, Rabinovitch PS, Kavanagh TJ: De novo synthesis of glutathione is required for both entry into and progression through the cell cycle. J Cell Physiol 163: 555–560, 1995

    Google Scholar 

  10. Blaustein A, Deneke SM, Stolz RI, Baxter D, Healey N, Fanburg BL: Myocardial glutathione depletion impairs recovery after short periods of ischemia. Circulation 80: 1449–1457, 1989

    Google Scholar 

  11. Yu BP: Cellular defense against damage from reactive oxygen species. Physiological Reviews 74(1): 139–162, 1994

    Google Scholar 

  12. Barsacchi R, Pelosi G, Camici P, Bonaldo L, Maiorino M, Ursini F: Glutathione depletion increases chemiluminescence emission and lipid peroxidation in the heart. Biochim Biophys Acta 804: 356–360, 1984

    Google Scholar 

  13. Kosower EM: A role of glutathione in muscle contraction. Experienta 26: 76–77, 1970

    Google Scholar 

  14. Blaustein AS, Deneke SM, Healey NA, Fanburg BL: Glutathione depletion impairs myocardial tolerance to hypoxia and ischemia. Circulation 74: 346, 1986

    Google Scholar 

  15. Griffith OW, Meister A: Potent and specific inhibition of glutathione synthesis by buthionine sulfoximine (S-n-butyl homocysteine sulfoximine). J Biol Chem 254: 7558–7560, 1979

    Google Scholar 

  16. Kecskemeti V, Pacher P, Nanasi P, Pankucsi Cs: Comparative study of cardiac electrophysiological effects of atrial natriuretic peptide. Molecular and Cellular Biochemistry 160/161: 53–59, 1996

    Google Scholar 

  17. Post J, Leunissen-Bijvelt J, Ruigrok TJC, et al.: Ultrastructural changes of sarcolemma and mitochondria in the isolated rabbit heart during ischemia and reperfusion. Biochim Biophys Acta 845: 119–123, 1985

    Google Scholar 

  18. Sotonyi P, Somogyi E, Balogh I et al.: The evaluation of electronmicroscopic cytochromoxydase reaction in experimental heart muscle hypoxia. J Cell Mol Biol 26: 9–15, 1980

    Google Scholar 

  19. Seligman SM, Karnovsy MJ, Wasserkrug KL, et al.: Nondroplet ultrastructural demonstration of cytochrome oxidase activity with polymerising osmiophilic reagent, diaminobenzidine (DAB). J Cell Biol 38: 1–14, 1986

    Google Scholar 

  20. Kerpel-Fronius S, Hajos F: The use of ferricyanide for the light and electronmicroscopic demonstration of succinic dehydrogenate activity. Histochem 14: 343–351, 1968

    Google Scholar 

  21. Furchgott RF, Bhadrakom S: Reactions of strips of rabbit aorta to epinephrine, isopropylarterenol, sodium nitrate and other drugs. J Pharmacol Exp Ther 108: 129–143, 1953

    Google Scholar 

  22. Snedecor GW, Cochran WG: Statistical methods. 8th ed. Iowa State University Press, Ames, 1994

    Google Scholar 

  23. Tallarida RJ, Jacobs LS: The dose-response relation in pharmacology. Springer-Verlag, New York, Heidelberg, Berlin, 1979

    Google Scholar 

  24. Griffith OW, Meister A: Origin and turnover of mitochondrial glutathione. Proc Natl Acad Sci USA 82: 4668–4672, 1985

    Google Scholar 

  25. Minchinton AI, Rojas A, Smith KA, Soranson JA, Shrieve DC, Jones NR, Bremner JC: Glutathione depletion in tissues after administration of buthionine sulfoximine. Int J Radial Oncol Biol Phys 10: 1261–1264, 1984

    Google Scholar 

  26. Mehendale HM, Svensson SA, Baldi C, et al.: Accumulation of Ca2+ induced by cytotoxic levels of menadione in the isolated perfused rat liver. Eur J Biochem 149: 201–206, 1985

    Google Scholar 

  27. Harlan JM, Levine JD, Callaham KS, Schwartz: Glutathione redox cycle protects cultured endothelial cells against lysis by extracellularly generated hydrogen peroxide. J Clin Invest 73: 706–713, 1984

    Google Scholar 

  28. Rubanyi GM, Vanhoutte PM: Superoxide anions and hyperoxia inactivate endothelium-derived relaxing factor. Am J Physiol 250 (Heart Circ Physiol 19): H822–H827, 1986

    Google Scholar 

  29. Ravingerova T, Slezak J, Tribulova N, Dzurba A, Uhrik B, Ziegelhoffer A: High arrythmogenesis during early reperfusion of ischemic myocardium: Participation of oxygen free radicals. Basic Clin Physiol Pharmacol 1: 335–346, 1993

    Google Scholar 

  30. Furchgott RF, Zawadzki JV: The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine. Nature 288: 373–376, 1980

    Google Scholar 

  31. Furchgott RF: The role of endothelium in the responses of vascular smooth muscle to drugs. Ann Rev Pharmacol Toxicol 24: 175–197, 1984

    Google Scholar 

  32. Igarashi T, Satoh T et al.: Species difference in glutathione level and glutathione related enzyme activities in rats, mice, guinea pigs and hamsters. J Pharmacobiodyn 6 (12): 941–949, 1983

    Google Scholar 

  33. Jennings RB, Reimer A, Steenbegen JR H: Total ischaemia III: Effect of inhibition of anaerobic glycolysis. J Mol Cell Cardiol 21 (Suppl): 37–74, 1989

    Google Scholar 

  34. Schwartz A, Wood JM, Allen JC, et al.: Biochemical and morphologic correlates of ischemia. I. Membranne systems. Am J Cardiol 32: 46–61, 1973

    Google Scholar 

  35. Ward BJ, McCarthy A: Endothelial cell 'swelling' in ischemia and reperfusion. J Mol Cell Cardiol 27: 1293–1300, 1995

    Google Scholar 

  36. Haddock PS, Woodward B, Hearse DJ: Cardiac Na/K ATPase activity and its relation to myocardial glutathione status: studies in the rats. J Mol Cell Cardiol 27(5): 1185–94, 1995

    Google Scholar 

  37. Haddock PS, Shattock MJ, Hearse DJ: Modulation of cardiac Na/K pump current: Role of protein and nonprotein sulfhydryl redox status. Am J Physiol 261: H297–H307, 1995

    Google Scholar 

  38. Reuter H: Ionic Channels in cardiac cell membranes. Ann Rev Physiol 46: 473–484, 1984

    Google Scholar 

  39. Matsuura H, Ehara T, Imoto Y: An analysis of the delayed outward current in single ventricular cells of the guinea-pig. Pflugers Arch 410: 596–603, 1987

    Google Scholar 

  40. Chinn K: Two delayed rectifiers in guinea pig ventricular myocytes distinguished by tail currrent kinetics. J Pharmacol Exp ther 264: 553–560, 1993

    Google Scholar 

  41. Sanguinetti MC, Jurkiewicz NK: Two components of cardiac delayed rectifier K+ currrent: Diffential sensitivity to block by class III antiarrhythmic agents. J Gen Physiol 96: 195–215, 1990

    Google Scholar 

  42. Zeng J, Lauritia KR, Rosenbaum DS, Rudy Y: Two components of the delayed rectifier K+ current in ventricular myocytes of the guinea pig type. Theoretical formulation and their role in repolarization. Circ Res 77: 140–152, 1995

    Google Scholar 

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Pacher, P., Kecskemeti, V., Ronai, A.Z. et al. Changes in cardiac electrophysiology, morphology, tissue biochemistry and vascular reactions in glutathione depleted animals. Mol Cell Biochem 185, 183–190 (1998). https://doi.org/10.1023/A:1006844012590

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