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. 1996 May 15;97(10):2260–2267. doi: 10.1172/JCI118667

Nitric oxide production and perivascular nitration in brain after carbon monoxide poisoning in the rat.

H Ischiropoulos 1, M F Beers 1, S T Ohnishi 1, D Fisher 1, S E Garner 1, S R Thom 1
PMCID: PMC507305  PMID: 8636405

Abstract

Nitric oxide is a short-lived free radical and physiological mediator which has the potential to cause cytotoxicity. Studies were conducted to investigate whether nitric oxide, and the potent oxidant peroxynitrite, were generated in brain during experimental carbon monoxide (CO) poisoning in the rat. Nitric oxide production was documented by electron paramagnetic resonance spectroscopy, and found to be increased by ninefold immediately after CO poisoning. Evidence that peroxynitrite was generated was sought by looking for nitrotyrosine in the brains of CO-poisoned rats. Nitrotyrosine was found deposited in vascular walls, and also diffusely throughout the parenchyma in inummocytochemical studies. The affinity and specificity of an anti-nitrotyrosine antibody was investigated and a solid phase immunoradiochemical assay was developed to quantity nitrotyrosine in brain homogenates. A 10-fold increase in nitrotyrosine was found in the brains of CO-poisoned rats. Platelets were involved with production of nitrotyrosine in the early phase of exposure to CO. However, nitrotyrosine formation and leukocyte sequestration were not decreased in thrombocytopenic rats poisoned with CO according to the standard model. When rats were pre-treated with the nitric oxide synthase inhibitor, L-nitroarginine methyl ester, formation of both nitric oxide and nitrotyrosine in response to CO poisoning were abolished, as well as leukocyte sequestration in the microvasculature, endothelial xanthine dehydrogenase conversion to xanthine oxidase, and brain lipid peroxidation. We conclude that perivascular reactions mediated by peroxynitrite are important in the cascade of events which lead to brain oxidative stress in CO poisoning.

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Selected References

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  1. Bath P. M., Hassall D. G., Gladwin A. M., Palmer R. M., Martin J. F. Nitric oxide and prostacyclin. Divergence of inhibitory effects on monocyte chemotaxis and adhesion to endothelium in vitro. Arterioscler Thromb. 1991 Mar-Apr;11(2):254–260. doi: 10.1161/01.atv.11.2.254. [DOI] [PubMed] [Google Scholar]
  2. Beckman J. S., Beckman T. W., Chen J., Marshall P. A., Freeman B. A. Apparent hydroxyl radical production by peroxynitrite: implications for endothelial injury from nitric oxide and superoxide. Proc Natl Acad Sci U S A. 1990 Feb;87(4):1620–1624. doi: 10.1073/pnas.87.4.1620. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Beckman J. S., Chen J., Ischiropoulos H., Crow J. P. Oxidative chemistry of peroxynitrite. Methods Enzymol. 1994;233:229–240. doi: 10.1016/s0076-6879(94)33026-3. [DOI] [PubMed] [Google Scholar]
  4. Beckmann J. S., Ye Y. Z., Anderson P. G., Chen J., Accavitti M. A., Tarpey M. M., White C. R. Extensive nitration of protein tyrosines in human atherosclerosis detected by immunohistochemistry. Biol Chem Hoppe Seyler. 1994 Feb;375(2):81–88. doi: 10.1515/bchm3.1994.375.2.81. [DOI] [PubMed] [Google Scholar]
  5. Bianco F., Floris R. Transient disappearance of bilateral low-density lesions of the globi pallidi in carbon monoxide intoxication and MRI. J Neuroradiol. 1988;15(4):381–385. [PubMed] [Google Scholar]
  6. Carreras M. C., Pargament G. A., Catz S. D., Poderoso J. J., Boveris A. Kinetics of nitric oxide and hydrogen peroxide production and formation of peroxynitrite during the respiratory burst of human neutrophils. FEBS Lett. 1994 Mar 14;341(1):65–68. doi: 10.1016/0014-5793(94)80241-6. [DOI] [PubMed] [Google Scholar]
  7. Haddad I. Y., Pataki G., Hu P., Galliani C., Beckman J. S., Matalon S. Quantitation of nitrotyrosine levels in lung sections of patients and animals with acute lung injury. J Clin Invest. 1994 Dec;94(6):2407–2413. doi: 10.1172/JCI117607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Heffner J. E., Katz S. A., Halushka P. V., Cook J. A. Human platelets attenuate oxidant injury in isolated rabbit lungs. J Appl Physiol (1985) 1988 Sep;65(3):1258–1266. doi: 10.1152/jappl.1988.65.3.1258. [DOI] [PubMed] [Google Scholar]
  9. Hogg N., Darley-Usmar V. M., Wilson M. T., Moncada S. Production of hydroxyl radicals from the simultaneous generation of superoxide and nitric oxide. Biochem J. 1992 Jan 15;281(Pt 2):419–424. doi: 10.1042/bj2810419. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Huie R. E., Padmaja S. The reaction of no with superoxide. Free Radic Res Commun. 1993;18(4):195–199. doi: 10.3109/10715769309145868. [DOI] [PubMed] [Google Scholar]
  11. Ischiropoulos H., Duran D., Horwitz J. Peroxynitrite-mediated inhibition of DOPA synthesis in PC12 cells. J Neurochem. 1995 Nov;65(5):2366–2372. doi: 10.1046/j.1471-4159.1995.65052366.x. [DOI] [PubMed] [Google Scholar]
  12. Ischiropoulos H., Zhu L., Chen J., Tsai M., Martin J. C., Smith C. D., Beckman J. S. Peroxynitrite-mediated tyrosine nitration catalyzed by superoxide dismutase. Arch Biochem Biophys. 1992 Nov 1;298(2):431–437. doi: 10.1016/0003-9861(92)90431-u. [DOI] [PubMed] [Google Scholar]
  13. Ishimaru H., Katoh A., Suzuki H., Fukuta T., Kameyama T., Nabeshima T. Effects of N-methyl-D-aspartate receptor antagonists on carbon monoxide-induced brain damage in mice. J Pharmacol Exp Ther. 1992 Apr;261(1):349–352. [PubMed] [Google Scholar]
  14. Kooy N. W., Royall J. A., Ye Y. Z., Kelly D. R., Beckman J. S. Evidence for in vivo peroxynitrite production in human acute lung injury. Am J Respir Crit Care Med. 1995 Apr;151(4):1250–1254. doi: 10.1164/ajrccm/151.4.1250. [DOI] [PubMed] [Google Scholar]
  15. Lipton S. A., Choi Y. B., Pan Z. H., Lei S. Z., Chen H. S., Sucher N. J., Loscalzo J., Singel D. J., Stamler J. S. A redox-based mechanism for the neuroprotective and neurodestructive effects of nitric oxide and related nitroso-compounds. Nature. 1993 Aug 12;364(6438):626–632. doi: 10.1038/364626a0. [DOI] [PubMed] [Google Scholar]
  16. Mayevsky A., Meilin S., Rogatsky G. G., Zarchin N., Thom S. R. Multiparametric monitoring of the awake brain exposed to carbon monoxide. J Appl Physiol (1985) 1995 Mar;78(3):1188–1196. doi: 10.1152/jappl.1995.78.3.1188. [DOI] [PubMed] [Google Scholar]
  17. Patel K. D., Zimmerman G. A., Prescott S. M., McEver R. P., McIntyre T. M. Oxygen radicals induce human endothelial cells to express GMP-140 and bind neutrophils. J Cell Biol. 1991 Feb;112(4):749–759. doi: 10.1083/jcb.112.4.749. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Radi R., Beckman J. S., Bush K. M., Freeman B. A. Peroxynitrite oxidation of sulfhydryls. The cytotoxic potential of superoxide and nitric oxide. J Biol Chem. 1991 Mar 5;266(7):4244–4250. [PubMed] [Google Scholar]
  19. Ródenas J., Mitjavila M. T., Carbonell T. Simultaneous generation of nitric oxide and superoxide by inflammatory cells in rats. Free Radic Biol Med. 1995 May;18(5):869–875. doi: 10.1016/0891-5849(94)00215-6. [DOI] [PubMed] [Google Scholar]
  20. Sato S., Tominaga T., Ohnishi T., Ohnishi S. T. Electron paramagnetic resonance study on nitric oxide production during brain focal ischemia and reperfusion in the rat. Brain Res. 1994 May 30;647(1):91–96. doi: 10.1016/0006-8993(94)91402-8. [DOI] [PubMed] [Google Scholar]
  21. Silverman C. S., Brenner J., Murtagh F. R. Hemorrhagic necrosis and vascular injury in carbon monoxide poisoning: MR demonstration. AJNR Am J Neuroradiol. 1993 Jan-Feb;14(1):168–170. [PMC free article] [PubMed] [Google Scholar]
  22. Stern F. B., Halperin W. E., Hornung R. W., Ringenburg V. L., McCammon C. S. Heart disease mortality among bridge and tunnel officers exposed to carbon monoxide. Am J Epidemiol. 1988 Dec;128(6):1276–1288. doi: 10.1093/oxfordjournals.aje.a115081. [DOI] [PubMed] [Google Scholar]
  23. Szabó C., Salzman A. L., Ischiropoulos H. Endotoxin triggers the expression of an inducible isoform of nitric oxide synthase and the formation of peroxynitrite in the rat aorta in vivo. FEBS Lett. 1995 Apr 24;363(3):235–238. doi: 10.1016/0014-5793(95)00322-z. [DOI] [PubMed] [Google Scholar]
  24. Thom S. R. Carbon monoxide-mediated brain lipid peroxidation in the rat. J Appl Physiol (1985) 1990 Mar;68(3):997–1003. doi: 10.1152/jappl.1990.68.3.997. [DOI] [PubMed] [Google Scholar]
  25. Thom S. R. Dehydrogenase conversion to oxidase and lipid peroxidation in brain after carbon monoxide poisoning. J Appl Physiol (1985) 1992 Oct;73(4):1584–1589. doi: 10.1152/jappl.1992.73.4.1584. [DOI] [PubMed] [Google Scholar]
  26. Thom S. R. Leukocytes in carbon monoxide-mediated brain oxidative injury. Toxicol Appl Pharmacol. 1993 Dec;123(2):234–247. doi: 10.1006/taap.1993.1242. [DOI] [PubMed] [Google Scholar]
  27. Thom S. R., Ohnishi S. T., Ischiropoulos H. Nitric oxide released by platelets inhibits neutrophil B2 integrin function following acute carbon monoxide poisoning. Toxicol Appl Pharmacol. 1994 Sep;128(1):105–110. doi: 10.1006/taap.1994.1186. [DOI] [PubMed] [Google Scholar]
  28. Tominaga T., Sato S., Ohnishi T., Ohnishi S. T. Electron paramagnetic resonance (EPR) detection of nitric oxide produced during forebrain ischemia of the rat. J Cereb Blood Flow Metab. 1994 Sep;14(5):715–722. doi: 10.1038/jcbfm.1994.92. [DOI] [PubMed] [Google Scholar]
  29. Vaporciyan A. A., DeLisser H. M., Yan H. C., Mendiguren I. I., Thom S. R., Jones M. L., Ward P. A., Albelda S. M. Involvement of platelet-endothelial cell adhesion molecule-1 in neutrophil recruitment in vivo. Science. 1993 Dec 3;262(5139):1580–1582. doi: 10.1126/science.8248808. [DOI] [PubMed] [Google Scholar]
  30. White C. R., Brock T. A., Chang L. Y., Crapo J., Briscoe P., Ku D., Bradley W. A., Gianturco S. H., Gore J., Freeman B. A. Superoxide and peroxynitrite in atherosclerosis. Proc Natl Acad Sci U S A. 1994 Feb 1;91(3):1044–1048. doi: 10.1073/pnas.91.3.1044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Wizemann T. M., Gardner C. R., Laskin J. D., Quinones S., Durham S. K., Goller N. L., Ohnishi S. T., Laskin D. L. Production of nitric oxide and peroxynitrite in the lung during acute endotoxemia. J Leukoc Biol. 1994 Dec;56(6):759–768. doi: 10.1002/jlb.56.6.759. [DOI] [PubMed] [Google Scholar]
  32. Zamora C. A., Baron D., Heffner J. E. Washed human platelets prevent ischemia-reperfusion edema in isolated rabbit lungs. J Appl Physiol (1985) 1991 Mar;70(3):1075–1084. doi: 10.1152/jappl.1991.70.3.1075. [DOI] [PubMed] [Google Scholar]
  33. Zhang J., Piantadosi C. A. Mitochondrial oxidative stress after carbon monoxide hypoxia in the rat brain. J Clin Invest. 1992 Oct;90(4):1193–1199. doi: 10.1172/JCI115980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Zimmerman G. A., McIntyre T. M., Mehra M., Prescott S. M. Endothelial cell-associated platelet-activating factor: a novel mechanism for signaling intercellular adhesion. J Cell Biol. 1990 Feb;110(2):529–540. doi: 10.1083/jcb.110.2.529. [DOI] [PMC free article] [PubMed] [Google Scholar]

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