Interaction Between Allopurinol and Copper: Possible Role in Myocardial Protection

References

• Guarnieri C., Flamigni F., Caldarera C. M. Role of oxygen in the cellular damage induced by re-oxygenation of hypoxic heart. Journal of Molecular anil Cellular Cardiology. 1980; 12: 797–808
   PubMed Web of Science ®Google Scholar
• Ferrari R., Ceconi C., Curello S., Guarnieri C., Caldarera C. M., Albertini A., Visioli O. Oxygen-mediated myocardial damage during ischemia and reperfusion: Role of the cellular defences against oxygen toxicity. Journal of Molecular and Cellular Cardiology 1985; 17: 937–945
   PubMed Web of Science ®Google Scholar
• McCord J. M. Oxygen-derived free radicals in postischemic tissue injury. New England Journal of Medicine 1985; 312: 159–163
   PubMed Web of Science ®Google Scholar
• Hammond B., Hess M. L. Oxygen free radical system: Potential mediator of myocardial injury. Journal of American Cellular Cardiology 1985; 6: 215–220
   PubMed Web of Science ®Google Scholar
• Appelbaum Y. J., Kuvin J., Borman J. B., Uretzky G., Chevion M. The protective role of neocuproine against cardiac damage in isolated perfused rat hearts. Free Radicals in Biology & Medicine 1990; 8: 133–143
   PubMed Web of Science ®Google Scholar
• Chevion M. A site specific mechanism for free radical induced biological damage: The essential role of redox-active transition metals. Free Radicals in Biology & Medicine 1988; 5: 27–37
   PubMed Web of Science ®Google Scholar
• Van der Kraaij A. M.M., Mostert L. J., Van Eijk H. G., Koster J. F. Iron-load increases the susceptibility of rat hearts to oxygen reperfusion damage. Protection by the antioxidant (+)-cyanidanol-3- and deferoxamine. Circulation 1988; 78: 442–449
   PubMed Web of Science ®Google Scholar
• Rowley D. A., Halliwell B. Formation of hydroxyl radicals from NADH and NADPH in the presence of copper salts. Journal of Inorganic Biochemistry 1985; 23: 103–108
   PubMed Web of Science ®Google Scholar
• Baker M. S., Gebicki J. M. The effect of pH on yields of hydroxyl radicals produced from superoxide by potential biological iron chelators. Archives of Biochemistry and Biophysics 1986; 246: 581–588
   PubMed Web of Science ®Google Scholar
• Halliwell B., Gutteridge J. M.C. Oxygen free radicals and iron in relation to biology and medicine: Some problems and concepts. Archives of Biochemistry and Biophysics 1986; 246: 501–514
   PubMed Web of Science ®Google Scholar
• Simpson J. A., Cheeseman K. H., Smith S. E., Dean R. T. Free radical generation by copper ions and hydrogen peroxide. Stimulation by HEPES buffer. Biochemical Journal 1988; 254: 519–523
   PubMed Web of Science ®Google Scholar
• Chambers D. E., Parks D. A., Patterson G., Roy R., McCord J. M., Yoshida S., Parmley L. F., Downey J. M. Xanthine oxidase as a source of free radical damage in myocardial ischemia. Journal of Molecular and Cellular Cardiology 1985; 17: 145–152
   PubMed Web of Science ®Google Scholar
• Hearse D. J., Manning A. S., Downey J. M., Yellon D. M. Xanthine oxidase: A critical mediator of myocardial injury during ischemia and reperfusion?. Acta Phvsiologica Scandanavia 1986; 548: 65–78
   Google Scholar
• Eddy L. J., Stewart J. R., Jones H. P., Engerson T. D., McCord J. M., Downey J. M. Free radical producing enzyme, xanthine oxidase is undetectable in human hearts. American Journal of Physiology 1987; 253: H709–H711
   Google Scholar
• Adachi H., Motomatsu K., Yaka I. Effect of allopurinol on patients undergoing open heart surgery. Japan Circulatory Journal 1979; 43: 395–401
   PubMedGoogle Scholar
• Yoshida S., Yamamoto F., Tanaka K., Takahashi A., Murashita T., Yamamoto H., Ichikawa H., Kawazoe K., Takaichi S., Fujita T. The effect of allopurinol on ischemia and reperfusion injury during open heart surgery (Abstract). Journal of Molecular and Cellular Cardiology 1988; 20(Suppl. V)S57, #116
   Google Scholar
• Nagano T., Hirano T., Hirobe M. Superoxide dismutase mimics based on iron in vivo. Journal of Biological Chemistry 1989; 264: 9243–9249
   PubMed Web of Science ®Google Scholar
• Yamauchi O., Hirano Y., Niakao Y., Nakahara A. Stability of fused rings in metal chelates. 6. Structures and stability constants of copper (2) chelates of dipeptides containing glycine and/or bcta-alanine. Canadian Journal of Chemistry 1969; 47: 3441–3447
   Web of Science ®Google Scholar
• Verdier E., Piro J. Determination of formation constants of metal ion complexes by polarography. Annates de Chimka 1969; 4: 213–216
   Google Scholar
• Keberle H. The biochemistry of desferrioxamine and its relation to iron metabolism. Annals of New York Academy of Sciences 1964; 119: 758–768
   PubMed Web of Science ®Google Scholar
• Perrin D. D. Stability Constant of Metal-Ion Complexes, Part B: Organic Ligands: IUPAC Chemical Data Series. Pergamon Press, Oxford 1979, No. 22
   Google Scholar
• Chevion M., Navok T. A novel method for quantitation of favism-inducing agents in legumes. Analytical Biochemistry 1983; 128: 152–158
   PubMed Web of Science ®Google Scholar
• Shreier P. H., Cortese R. A fast and simple method for sequencing DNA cloned in the single stranded bacteriophage M13. Journal of Molecular Biology 1979; 129: 169–172
   PubMed Web of Science ®Google Scholar
• Cotton F. A., Wilkinson G. Advanced Inorganic Chemistry: A Comprehensive Text. J. Wiley & Sons, Inc., New York 1972; 911–922
   Google Scholar
• Ko K. M., Godin D. V. Inhibition of transition metal ion-catalyzed ascorbate oxidation and lipid peroxidation by allopurinol and oxypurinol. Biochemical Pharmacology 1990; 40: 803–809
   PubMed Web of Science ®Google Scholar
• Tabayashi K., Suzuki Y., Nagamine S., Ito Y., Sekino Y., Mohri H. A clinical trial of allopurinol (zyloric) for myocardial protection. Journal of Thoracic and Cardiovascular Surgery 1991; 101: 713–718
   PubMed Web of Science ®Google Scholar
• Moorhouse P. C., Grootveld M., Halliwell B., Quinlan J. C., Gutteridge J. M.C. Allopurinol and oxypurinol arc hydroxyl radical scavengers. FEBS Letters 1987; 213P: 23–28
   Google Scholar
• Czapski G. On the use of OH scavengers in biological systems. Israel Journal of Chemistry 1984; 24: 29–32
   Web of Science ®Google Scholar
• Williams R. J.P. Free manganese(II) and iron(II) cations can act as intracellular cell controls. FEBS Letters 1982; 140: 3–10
   PubMed Web of Science ®Google Scholar
• Sorenson J. R.J. Copper complexes: A physiologic approach to treatment of chronic disease. Comprehensive Therapy 1985; 11: 49–64
   PubMedGoogle Scholar
• Hochstein P., Hatch L., Sevanian A. Uric acid: Functions and determination. Methods in Enzymology 1984; 105: 162–167
   PubMed Web of Science ®Google Scholar
• Sevanian A., Davies K. J.A., Hochstein P. Conservation of Vitamin C by uric acid in blood. Journal of Free Radicals in Biology & Medicine 1985; 1: 117–124
   PubMedGoogle Scholar
• Albert A. Quantitative studies of the avidity of naturally occurring substances for trace metals: 3. Pteridines, riboflavin and purines. Biochemical Journal 1953; 54: 646–654
   PubMed Web of Science ®Google Scholar
• Albert A. Quantitative studies of the avidity of naturally occurring substances for trace metals: 1. Amino acids having only two ionizing groups. Biochemistry Journal 1950; 47: 531–538
   PubMed Web of Science ®Google Scholar
• Czapski G., Aronovich J., Godinger D., Samuni A., Chevion M. On the mechanisms of cytotoxicity induced by superoxide. Oxygen Radicals in Chemistry and Biology, W. Bors, M. Saran, D. Tait. Walter de Gruyter and Co., Berlin 1984; 225–228
   Google Scholar
• Aronovich J., Godinger D., Samuni A., Czapski G. The effect of cell-bound copper on the toxicity of superoxide and Vitamin C. Oxygen Radicals in Chemistry and Biology, W. Bors, M. Saran, D. Tait. Walter de Gruyter and Co., Berlin 1984; 219–223
   Google Scholar
• Shinar E., Rachmilewitz E. A., Shifter A., Rahamin E., Saltman P. Oxidative damage to human red cells induced by copper and iron complexes in the presence of ascorbate. Biochimica Biophysica Acta 1989; 1014: 66–72
   PubMed Web of Science ®Google Scholar
• Walling C. The nature of the primary oxidants in oxidative mediated by metal ions. Oxidases and Related Redox Systems, T. E. King, H. S. Mason, M. Morrison. Pergamon Press, Oxford 1982; 85–97
   Google Scholar