Mitochondria, Oxygen and Reperfusion Damage

References

• Manning A S. Reperfusion induced arrhythmias: Do free radicals play a critical role?. Free Radic Biol Med 1988; 4: 305–16
   PubMed Web of Science ®Google Scholar
• Ganote C E, Kaltenbach J P. Oxygen induced enzyme release: early events and a proposed mechanism. J Mol Cell Cardiol 1979; 11: 389–406
   PubMed Web of Science ®Google Scholar
• Lucchesi B R, Mullane K M. Leukocytes and ischaemia-induced myocardial injury. Ann Rev Pharmacol Toxicol 1986; 26: 201–24
   PubMed Web of Science ®Google Scholar
• Hearse D J, Humphrey S M, Bullock G R. The oxygen paradox and the calcium paradox: two facets of the same problem. J Mol Cell Cardiol 1978; 10: 641–68
   PubMed Web of Science ®Google Scholar
• Shen A C, Jennings R B. Kinetics of calcium accumulation in acute myocardial ischemic injury. Am J Pathol 1972; 67: 441–52
   PubMed Web of Science ®Google Scholar
• McCord J M. Superoxide radical: A likely link between reperfusion injury and inflammation. Free Radic Biol Med 1986; 2: 325–45
   Web of Science ®Google Scholar
• Blaustein A S, Schine L, Brooks W W, Fanburg B L, Bing O HL. Influence of exogenously generated oxidant species on myocardial function. Am J Physiol 1986; 250: H595–9
   PubMedGoogle Scholar
• Darley-Usmar V M, O'Leary V J, Stone D. The glutathione status of perfused rat hearts subjected to hypoxia and reoxygenation: the oxygen paradox. Free Radic Res Comm 1989; 5: 283–9
   Web of Science ®Google Scholar
• Curello S, Ceconi C, Bigoli C, Ferrari R, Albertini A, Guarnieri C. Changes in the cardiac glutathione status after ischaemia and reperfusion. Experientia 1985; 41: 42–3
   PubMedGoogle Scholar
• Vander Heide R S, Sabotka P A, Ganote C E. Effects of the free radical scavenger DMTU and Mannitol on the oxygen paradox in perfused hearts. J Mol Cell Cardiol 1987; 19: 615–25
   PubMed Web of Science ®Google Scholar
• Darley-Usmar V M, Stone D, Smith D R. Oxygen and reperfusion damage: an overview. Free Radic Res Comm 1989; 7: 247–54
   PubMed Web of Science ®Google Scholar
• Grum C M, Ketai L H, Myers C L, Shlafer M. Purine efflux after cardiac ischaemia: relevance to allopurinol protection. Am J Physiol 1987; 252: H368–73
   PubMedGoogle Scholar
• Kehrer J P, Piper H M, Sies H. Xanthine oxidase is not responsible for reoxygenation injury in isolated perfused rat heart. Free Radic Res Comm 1987; 3: 69–78
   PubMedGoogle Scholar
• Nohl H, Hegner D. Do mitochondria produce oxygen radicals in vivo?. Eur J Biochem 1978; 82: 563–7
   PubMedGoogle Scholar
• Boveris A, Chance B. The mitochondrial generation of hydrogen peroxide. Biochem J 1973; 134: 707–16
   PubMed Web of Science ®Google Scholar
• Bhatnagar A, Srivastava S K, Szabo G. Oxidative stress alters specific membrane currents in isolated cardiac myocytes. Circ Res 1990; 67: 535–49
   PubMedGoogle Scholar
• Ganote C E, Worstell J, Kaltenbach J P. Oxygen induced enzyme release after irreversible myocardial injury: effects of cyanide in perfused rat hearts. Am J Pathol 1976; 84: 327–50
   PubMed Web of Science ®Google Scholar
• Stone D, Darley-Usmar V M, Smith D R, O'Leary V J. Hypoxia-reoxygenation induced increase in cellular Ca2+ in myocytes and perfused hearts: the role of mitochondria. J Mol Cell Cardiol 1989; 21: 963–73
   PubMed Web of Science ®Google Scholar
• Hardy L, Clark J B, Darley-Usmar V M, Smith D R, Stone D. Reoxygenation dependent decrease in mitochondrial NADH: CoQ reductase (complex I) activity in the hypoxic/reoxygenated rat heart. Biochem J 1991; 274: 133–7
   PubMed Web of Science ®Google Scholar
• Rouslin W, Millard R W. Mitochondrial inner membrane enzyme defects in porcine myocardial ischaemia. Am J Physiol 1981; 240: H308–13
   PubMedGoogle Scholar
• Denton R M, McCormack J G. Calcium as the second messenger within mitochondria of the heart and other tissues. Ann Rev Physiol 1990; 52: 451–66
   PubMedGoogle Scholar
• Crompton M. The regulation of mitochondrial calcium transport in heart. Curr Top Memb Trans 1985; 25: 231–76
   Web of Science ®Google Scholar
• Crompton M, Ellinger H, Costi A. Inhibition by cyclosporin A of a Ca2+-dependent pore in heart mitochondria activated by inorganic phosphate and oxidative stress. Biochem J 1988; 255: 357–60
   PubMed Web of Science ®Google Scholar
• Richter C, Frei B. Ca2+ release from mitochondria induced by pro-oxidants. Free Radic Biol Med 1988; 4: 365–75
   PubMed Web of Science ®Google Scholar
• Crompton M, Costi A. A heart mitochondrial Ca2+ dependent pore of possible relevance to reperfusion injury. Biochem J 1990; 266: 33–9
   PubMed Web of Science ®Google Scholar
• Griffiths E J, Halestrap A P. Further evidence that cyclosporin A protects mitochondria from calcium overload by inhibiting a matrix peptidyl-prolyl cis-trans isomerase. Biochem J 1991; 274: 611–14
   PubMedGoogle Scholar
• Broekemeier K M, Pfeiffer D R. Cyclosporin A-sensitive and insensitive mechanisms produce the permeability transition in mitochondria. Biochem Biophys Res Comm 1989; 163: 561–6
   PubMed Web of Science ®Google Scholar
• Fisher G, Wittman-Liebold B, Lang K, Kiefhaber T, Schmid F X. Cyclophilin and peptidyl-prolyl cistrans isomerase are probably identical proteins. Nature 1989; 337: 476–8
   PubMedGoogle Scholar
• Khauli R B, Strzelecki T, Stoff J, Menon M. Cyclosporine ischaemia effects in the rat kidney: further biochemical observations with emphasis on calcium handling. Transplant Proc 1988; 20: 551–5
   PubMedGoogle Scholar
• Bereiter-Hahn J, Seipel K H, Voth M, Ploem J S. Fluorimetry of mitochondria in cells vitally stained with DASPMI or rhodamine 6GO. Cell Biochem Funct 1983; 1: 147–55
   PubMedGoogle Scholar
• Allshire A, Piper H M, Cuthbertson K SR, Cobbold P H. Cytosolic free calcium in single rat heart cells during anoxia and reoxygenation. Biochem J 1987; 244: 331–4
   PubMedGoogle Scholar
• Pesaturo J A, Gwathmey J K. The role of mitochondria and sarcoplasmic reticulum calcium handling upon reoxygenation of hypoxic myocardium. Circ Res 1990; 66: 696–709
   PubMedGoogle Scholar
• Grinwald P M, Brosnahan C. Sodium imbalance as a cause of calcium overload in post hypoxic reoxygenation injury. J Mol Cell Cardiol 1987; 19: 487–95
   PubMedGoogle Scholar
• Steenbergen C, Murphy E, Levy L, London R E. Elevation in cytosolic free calcium concentration early in myocardial ischaemia in perfused rat heart. Circ Res 1987; 60: 700–7
   PubMedGoogle Scholar
• Bourdillon P D, Poole-Wilson A. The effects of verapamil, quiescence and cardioplegia on calcium exchange and mechanical function in ischemic rabbit myocardium. Circ Res 1982; 50: 360–8
   PubMed Web of Science ®Google Scholar
• Lochner A, Van der Merwe N, de Villiers M, Stelnmann C, Kotze J CN. Mitochondrial calcium fluxes and levels during ischaemia and reperfusion: possible mechanisms. Biochim Biophys Acta 1987; 927: 8–17
   PubMedGoogle Scholar
• Kehrer J P, Park Y, Sies H. Energy dependence of enzyme release from hypoxic isolated perfused rat heart tissue. J Appl Physiol 1988; 65: 1855–60
   PubMedGoogle Scholar