Stimulation of Mitochondrial Oxygen Consumption in Isolated Cardiomyocytes After Hypoxia-Reoxygenation

References

• Ganote C. E., Worstell B. S., Kaltenbach J. P. Oxygen-induced enzyme release after irreversible myocardial injury. American Journal of Pathology 1976; 84: 327–350
   PubMed Web of Science ®Google Scholar
• Hearse D. J., Humphrey S. M., Bullock S. R. The oxygen paradox and the calcium paradox: two facts of the same problem?. Journal of Molecular and Cellular Cardiology 1978; 10: 641–668
   PubMed Web of Science ®Google Scholar
• Altschuld R., Hostetler B., Brierley G. P. Response of isolated ratheart cells to hypoxia-reoxygenation and acidosis. Circulation Research 1981; 49: 307–316
   PubMed Web of Science ®Google Scholar
• Hohl C., Ansel A., Altschuld R., Brierley G. P. Contracture of isolated rat heart cells on anaerobic to aerobic transition. American Journal of Physiology 1982; 242: H1022–H1030
   Google Scholar
• Stone D., Darley-Usmar V., Smith D. R., O'Leary V. Hypoxia-reoxygenation induced increase in cellular Ca2+ in myocytes and perfused hearts: the role of mitochondria. Journal of Molecular and Cellular Cardiology 1989; 21: 963–973
   PubMed Web of Science ®Google Scholar
• Peng C. F., Kane J. J., Straub K. D., Murphy M. L. Improvement of mitochondrial energy production in ischaemic myocardium by in vivo infusion of ruthenium red. Journal of Cardiovascular Pharmacology 1980; 2: 45–54
   PubMed Web of Science ®Google Scholar
• Stone D., Darley-Usmar V., Martin J. F. Calcium fluxes and reperf usion damage: the role of mitochondria. Myocardial Response to acute injury, J. R. Parratt. MacMillan Press, London 1992; 67–82
   Google Scholar
• Veitch K., Hombroeckx A., Caucheteux D., Pouler H., Hue L. Global ischemia induces a biphasic response of the mitochondrial respiratory chain. Biochemical Journal 1992; 281: 709–715
   PubMed Web of Science ®Google Scholar
• Rouslin W., Millard R. W. Mitochondrial inner membrane defects in porcine myocardial ischemia. American Journal of Physioliology 1981; 240: H308–H313
   PubMedGoogle Scholar
• Hardy D. L., Clark J. B., Darley-Usmar V., Smith D. R., Stone D. Reoxygenation dependent decrease in mitochondrial NADH CoQ reductase (Complex 1) activity in the hypoxic-reoxygenated rat heart. Biochemical Journal 1991; 274: 133–137
   PubMed Web of Science ®Google Scholar
• Powell T., Terrar D. A., Twist V. W. Electrical properties of individual cells isolated from adult rat ventricular myocardium. Journal of Physiology [Lond] 1980; 302: 131–153
   PubMed Web of Science ®Google Scholar
• Ingebretsen O. C., Bakken A. M., Sagadal L., Farstad M. Determination of adenine nucleotides and inosine in human myocardium by ion-pair reversed-phase high-performance liquid chromatrography. Journal of Chromatography 1982; 242: 119–126
   PubMed Web of Science ®Google Scholar
• Juengling E., Kammermeier H. Rapid assay of adenine nucleotides or creatine compounds in extracts of cardiac tissue by paired-ion reverse-phase high-performance liquid chromatography. Analytical Biochemistry 1980; 102: 358–361
   PubMed Web of Science ®Google Scholar
• Cheng J.-Y., Leaf A., Bonventre J. V. Mitochondrial function and intracellular calcium in anoxic cardiac myocytes. American Journal of Physiology 1986; 250: C18–C25
   Google Scholar
• Turrens J. F., Beconi M., Barilla J., Chavez U. B., McCord J. M. Mitochondrial generation of oxygen radicals during reoxygenation of ischemic tissues. Free Radical Research Communications 1991; 12: 681–689
   PubMedGoogle Scholar
• Piper H. M., Noll T., Siegmund B. Mitochondrial function in the oxygen depleted and reoxygenated myocardial cell. Cardiovascular Research 1994; 28: l–15
   Web of Science ®Google Scholar
• Grinwald P. M., Brosnahan C. Sodiurn inbalance as a cause of calcium overload in post-hypoxic reoxygenation injury. Journal of Molecular and Cellular Cardiology 1987; 19: 487–495
   PubMedGoogle Scholar
• Tani M., Neely J. R. Na+ accumulation increases Ca2+ overload and impairs function in anoxic rat heart. Journal of Molecular and Cellular Cardiology 1990; 22: 57–72
   PubMed Web of Science ®Google Scholar
• Poole-Wilson P. A. The nature of myocardial damage following reoxygenation. Control and Maniplation of calcium movement, J. R. Parratt. Raven Press, New York 1985; 325–340
   Google Scholar
• Smith G. L., Allen D. G. Effects of metabolic blockade on intracellular calcium concentration in isolated ferret ventricular muscle. Circulation Research 1988; 62: 1225–1236
   Web of Science ®Google Scholar
• Crompton M. The regulation of mitochondrial calcium transport in heart. Current Topics in Membrane Transport 1985a; 25: 231–276
   Web of Science ®Google Scholar
• Crompton M. The calcium carriers of mitochondria. Enzymes of biological membranes, A. Martonosi. Plenum Press, New York 1985b; 3: 249–286
   Google Scholar
• Shen A. C., Jennings R. B. Myocardial calcium and magnesium in acute myocardial injury. American Journal of Pathology 1972a; 67: 417–440
   PubMed Web of Science ®Google Scholar
• Shen A. C., Jenning R. B. Kinetics of calcium accumulation in acute myocardial ischaemic injury. American Journal of Pathology 1972b; 67: 441–452
   PubMed Web of Science ®Google Scholar
• Moreno-Sanchez R., Hansford R. G. Relation between cytosolic free calcium and respiratory rates in cardiac myocytes. American Journal of Physiology 1988; 255: H347–H357
   Google Scholar
• Allen S. P., Darley-Usmar V. M., McCormack J. G., Stone D.S. Changes in mitochondrial matrix free Calcium in perfused rat hearts subjected to hypoxia-reoxygenation. Journal of Molecular and Cellular Cardiology 1993; 25: 949–958
   PubMed Web of Science ®Google Scholar
• Darley-Usmar V. M., Stone D., Smith DR., Martin J. F. Mitochondria, oxygen and reperfusion damage. Annals of Medicine 1991; 23: 583–588
   PubMed Web of Science ®Google Scholar