Vasoconstrictor Effects in Isolated Rabbit Heart Perfused with Bis(3,5-Dibromosalicyl) Fumarate Cross-Linked Hemoglobin (ααhb)

References

• Gilroy D., Shaw C., Odling-Party E., Smee W. Detection of a vasoconstrictor factor in stroma-free haemoglobin solutions. J. Trauma. 1989; 28: 1312–16
   Google Scholar
• Toda N., Shimizu K., Ohta T. Mechanism of cerebral arterial contraction induced by blood constituents. J. Neurosurg. 1980; 53: 312–322
   PubMed Web of Science ®Google Scholar
• White C. T., Murray A. J., Greene J. R., Smith D. J., Medina F., Makovec G. T.E.J., Bolin R. B. Toxicity of human hemoglobin solution infused into rabbits. J. Lab. Clin. Med. 1986; 108: 121–131
   PubMed Web of Science ®Google Scholar
• Macdonald V. W., Winslow R. M., Marini M. A., Klinker M. T. Coronary vasoconstriction activity of purified and modified human hemoglobin. Biomat. Art. Cells Art. Org. 1990; 18: 263–282
   PubMed Web of Science ®Google Scholar
• Vogel W. M., Dennis R. C., Cassidy G., Apstein C. S., Valeri C. R. Coronary constrictor effect of stroma-free hemoglobin solutions. Am. J. Physiol. 1986; 251: H413–H420
   PubMed Web of Science ®Google Scholar
• Martin W., Smith J. A., White D. G. The mechanism by which hemoglobin inhibits the relaxation of rabbit aorta induced by nitrovasodilators, nitric oxide, or bovine retractor penis inhibitory factor. Br. J. Pharmacol. 1986; 89: 563–571
   PubMed Web of Science ®Google Scholar
• Palmer R. M.J., Ferrige A. G., Monacada S. Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor. Nature 1987; 327: 524–526
   PubMed Web of Science ®Google Scholar
• Simoni J., Feola M., Canizaro P. C. Generation of free oxygen radicals and the toxicity of hemoglobin solutions. Biomat. An. Cells Art. Org. 1990; 18(2)189–202
   PubMed Web of Science ®Google Scholar
• Sadrzadeh S. M.H., Graf E., Panter S. S., Hallaway P. E., Eaton J. W. Hemoglobin: A biological Fenton reagent. J. Biol. Chem. 1984; 259: 14354–56
   PubMed Web of Science ®Google Scholar
• Rubanyi G. M., Vanhoutte P. M. Superoxide anions and hyperoxia inactivate endothelium-derived relaxing factor. Am. J. Physiol. 1986; 250: H822–H827
   PubMed Web of Science ®Google Scholar
• Macdonald V. M., Winslow R. M. Oxygen delivery and myocardial function in rabbit hearts perfused with cell-free hemoglobin. J. Appl. Physiol. 1992; 72(2)476–483
   PubMedGoogle Scholar
• Snyder S. R., Welty E. V., Walder R. Y., Williams L. A., Walder J. A. 88HbXL99α: a hemoglobin derivative that is crosslinked between the α subunits is useful as a blood substitute. Proc. Natl. Acad. Sci. USA 1987; 84: 7280–7284
   PubMed Web of Science ®Google Scholar
• Amezcua J. L., Palmer R. M.J., de Souza B. M., Moncada S. Nitric oxide synthesized from L-arginine regulates vascular tone in the coronary circulation of the rabbit. Br. J. Pharmacol. 1989; 97: 1119–1124
   PubMed Web of Science ®Google Scholar
• Kelm M., Schrader J. Control of coronary vascular tone by nitric oxide. Cir. Res. 1990; 66: 1561–1575
   PubMed Web of Science ®Google Scholar
• Kelm M., Schrader J. Nitric oxide release from the isolated guinea pig heart. Eur. J. Pharmacol. 1988; 155: 313–316
   PubMedGoogle Scholar
• Lamontagne D., Pohl U., Busse R. N G-Nitro-L-arginine antagonizes endothelium-dependent dilator responses by inhibiting endothelium-derived relaxing factor. Pflugers Arch. 1991; 418: 226–270
   Google Scholar
• Martin W., Villani G. M., Jothianandan D., Furchgott F. Selective blockade of endothelium-dependent and glyceryl trinitrate-induced relaxation by hemoglobin and by methylene blue in the rabbit aorta. J. Pharmacol. Exp. Ther. 1985; 232: 708–716
   PubMed Web of Science ®Google Scholar
• Amezcua J. L., Dusting G. J., Palmer R. M.J., Moncada S. Acetylcholine induces vasodilation in the rabbit isolated heart through the release of nitric oxide, the endogenous nitrovasodilator. 1988; 95: 830–834
   Google Scholar
• Furchgott R. F., Zawadski J. V. The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine. Nature 1980; 288: 373–376
   PubMed Web of Science ®Google Scholar
• Misra H. P., Fridovich I. The generation of superoxide radical during the autoxidation of hemoglobin. J. Biol. Chem. 1972; 247: 6960–62
   PubMed Web of Science ®Google Scholar
• Halliwell B., Gutteridge J. M.C. Oxygen toxicity, oxygen radicals, transition metals and disease. Biochem. J. 1984; 219: 1–14
   PubMed Web of Science ®Google Scholar
• Stewart D. J., Pohl U., Bassenge E. Free radicals inhibit endothelium-dependent dilation in the coronary resistance bed. Am. J. Physiol. 1988; 255: H765–H769
   Google Scholar