32
Views
38
CrossRef citations to date
0
Altmetric
Original Article

In vivo Nitric Oxide Detection in the Septic Rat Brain by Electron Paramagnetic Resonince

, , , , &
Pages 293-299 | Received 08 Dec 1997, Published online: 07 Jul 2009

References

  • Baniere S. L., Lowry S. F. An overview of mortality risk prediction in sepsis. Critical Care Medicine 1995; 23: 376–393
  • St. John R. C., Dorinsky P. M. Immunologic therapy for ARDS, septic shock, and multipleorgan failure. Chest 1993; 103: 932–943
  • Kilbourn R. G., Griffith O. W. Overproduction of nitric oxide in cytokine-mediated and septic shock. Journal of the National Cancer Institute 1992; 84: 827–831
  • Moncada S., Palmer R. M. J., Higgs E. A. Nitric oxide: physiology, pathophysiology and pharmacology. Pharmacological Reviews 1991; 43: 109–142
  • Parratt J. R. Myocardial and circulatory effects of E. coli endotoxin; modification of responses to catecho-lamines. British Journal of Pharmacology 1973; 47: 12–25
  • Suffredini A. F., Fromm R. E., Parker M. M., Brenner M., Kovacs J. A., Wesley R. A., Parrillo J. The cardiovascular responses of normal humans to the administration of endotoxin. The New England Journal of Medicine 1989; 321: 280–287
  • Schuman E. M., Madison D. V. A requirement for the intercellular messenger nitric oxide in long-term potentiation. Science 1991; 254: 1503–1506
  • Rettori V., Belova N., Dees W. L., Nyberg C. L., Gimeno M., McCann S. M. Role of nitric oxide in the control of luteinizing hormone-releasing hormone release in vivo and in vitro. Proceedings of the National Academy of Sciences of the USA 1993; 90: 10130–10134
  • Janigro D., West G. A., Nguyen T.-S., Winn H. R. Regulation of blood-brain barrier endothelial cells by nitric oxide. Circulation Research 1994; 75: 528–538
  • Iadecola C., Pligrino D. A., Moskowitz M. A., Lassen N. A. Nitric oxide synthase inhibition and cerebrovascular regulation. Journal of Cerebral Blood Flow and Metabolism 1994; 14: 175–192
  • Huang Z., Huang P. L., Panahian N., Dalkara T., Fishman M. C., Moskowitz M. A. Effects of cerebral ischemia in mice deficient in neuronal nitric oxide synthase. Science 1994; 256: 1883–1885
  • Iadecola C., Xu X., Zhang F., El-Fakahany E. E., Ross M. E. Marked induction of calcium-independent nitric oxide synthase activity after focal cerebral ischemia. Journal of Cerebral Blood Flow and Metabolisim 1995; 15: 52–59
  • Koprowski H., Zheng Y. M., Heber-Katz E., Fraser N., Rorke L., Fu Z. F., Hanlon C., Dietzschold B. In vivo expression of nitric oxide synthase in experimentally induced neurologic diseases. Proceedings of the National Academy of Sciences of the USA 1993; 90: 3024–3027
  • Van Dam A.-M., Baubr J., Man-A-Hing W. K. H., Marquette C., Tilders F. J. H., Berkenbosch F. Appearance of inducible nitric oxide synthase in the rat central nervous system after rabies virus infection and during experimental allergic encephalomyelitis but nor after peripheral administration of endotoxin. Journal of Neuroscience Research 1995; 40: 251–260
  • Tabatabaie T., Stewart C., Pye Q., Kotake Y., Floyd R. A. In vivo trapping of nitric oxide in the brain of neonatal rats treated with the HW-1 envelope protein gp 120: Protective effects of cu-phenyl-tert-butyl-nitrone. Biochemical and Biophysical Research Communications 1996; 221: 386–390
  • Wong M.-L., Rettori V., Al-Sheklee A., Bongiorno P. B., Canteros G., McCann S. M., Gold P. W., Licinio J. Inducible nitric oxide synthase gene expression in the brain during systemic inflammation. Nature Medicine 1996; 2: 581–584
  • Mordvintcev P., Miilsch A., Busse R., Vanin A. On-line detection of nitric oxide formation in liquid aqueous phase by electron paramagnetic resonance spectroscopy. Analytical Biochemistry 1991; 199: 142–146
  • Mulsch A., Busse R., Mordvintcev P. I., Vanin A., Nielsen E. O., Scheel-Kriiger J. S., Olesen S.-P. Nitric oxide promotes seizure activity in kainate-treated rats. Neuropharmacology and Toxicology 1994; 5: 2325–2328
  • 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 Research 1994; 647: 91–96
  • Tominaga T., Sato S., Ohnishi T., Ohnishi S. T. Electron paramagnetic resonance detection of nitric oxide produced during forebrain ischemia of the rat. Journal of Cerebral Blood Flow and Metabolism 1994; 14: 715–722
  • Lai C.-S., Komarov M. Spin trapping of nitric oxide produced in vivo in septic-shock mice. FEBS. Letters 1994; 345: 120–124
  • Yoshimura T., Yokoyama H., Fujii S., Takayama F., Oikawa K., Karnada H. In vivo EPR detection and imaging of endogenous nitric oxide in lipopolysac-charide-treated mice. Nature Biotechnology 1996; 14: 992–994
  • Fujii S., Yoshimura T., Kamada H. Nitric oxide trapping efficiency of water-soluble iron(III) complexes with dithiocarbamate derivatives. Chemistry Letters 1996; 1996: 785–786
  • Yoshimura T. Endogenous nitric oxide, its chemical characterization and the high affinity for metal ions and metalloproteins. CVD Ground Round Series, T. Yoshimoto. Neuron Publ., Tokyo 1996; Vol. 3: 1–26
  • Vedernikov Y. P., Mordvintcev P. I., Maleckova I. V., Vanin A. F. Effect of diethyldithiocarbamate on the activity of nitric oxide-releasing vasodilators. European Journal of Pharmacology 1992; 212: 125–128
  • Suzuki Y., Fujii S., Tominaga T., Yoshimoto T., Yoshimura T., Karnada H. The origin of an EPR signal observed in dithiocarbamate-loaded tissues: Copper(II)-dithiocarbamate complexes account for the narrow hy-perfine lines. Biochimica et Biophysica Acta 1997; 1335: 242–245
  • Yoshimura T., Fujii S., Yokoyama H., Kamada H. In vivo electron paramagnetic resonance imaging of NO-bound iron complex in a rat head. Chemistry Letters 1995; 1995: 309–310
  • Kubrina L. N., Mikoyan V. D., Mordvintcev P. I., Vanin A. F. Iron potentiates bacterial lipopolysac-charide-induced nitric oxide formation in animal organs. Biochimica et Biophysica Acta 1993; 1176: 240–244
  • Westenberger U., Thanner S., Ruf H. H., Gersonde K., Sutter G., Trenz O. Formation of free radicals and nitric oxide derivative of hemoglobin in rats during shock syndrome. Free Radical Research Communications 1990; 11: 167–178
  • Fujimura M., Tominaga T., Kato I., Takasaka S., Kawase M., Taniguchi T., Okamoto H., Yoshimoto T. Attenuation of nitric oxide synthase induction in IRF-1-deficient glial cells. Brain Research 1997; 759: 247–250
  • Kosaka H., Sakaguchi H., Sawai Y., Kumura E., Seiyama A., Chen S.-S., Shiga T. Effect of interferon-γ on nitric oxide hemoglobin production in endotoxin-treated rats and its synergism with interleukin 1 or tumor necrosis factor. Life Sciences 1994; 54: 1523–1529
  • Forstermann U., Gath I., Schwarz P., Closs E. I., Kleinert H. Isoform of nitric oxide synthase. Biochemical Pharmacology 1995; 50: 7321–1332
  • Murphy S., Grzybicki D. Glial NO Normal and pathological roles. Neuroscientist 1996; 2: 90–99
  • Nomura Y., Kitamura Y. Inducible nitric oxide synthase in glial cells. The Neuroscience Research 1993; 18: 103–107

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.