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Magnetic resonance imaging of organic contrast agents in mice: capturing the whole-body redox landscape

  1. Author:
    Davis, R. M.
    Matsumoto, S.
    Bernardo, M.
    Sowers, A.
    Matsumoto, K. I.
    Krishna, M. C.
    Mitchell, J. B.
  2. Author Address

    [Davis, Ryan M.; Matsumoto, Shingo; Sowers, Anastasia; Krishna, Murali C.; Mitchell, James B.] NIH, Radiat Biol Branch, Ctr Canc Res, Bethesda, MD 20892 USA. [Bernardo, Marcelino] NCI, Mol Imaging Program, NIH, Bethesda, MD 20892 USA. [Bernardo, Marcelino] NCI, SAIC Frederick, Frederick, MD 21702 USA. [Matsumoto, Ken-Ichiro] Natl Inst Radiol Sci, Mol Imaging Ctr, Chiba 260, Japan.;Davis, RM, NIH, Radiat Biol Branch, Ctr Canc Res, Bldg 10, Bethesda, MD 20892 USA.;davisrm2@mail.nih.gov
    1. Year: 2011
    2. Date: Feb
  1. Journal: Free Radical Biology and Medicine
    1. 50
    2. 3
    3. Pages: 459-468
  2. Type of Article: Article
  3. ISSN: 0891-5849
  1. Abstract:

    Nitroxides are a class of stable free radicals that have several biomedical applications including radioprotection and noninvasive assessment of tissue redox status. For both of these applications, it is necessary to understand the in vivo biodistribution and reduction of nitroxides. In this study, magnetic resonance imaging was used to compare tissue accumulation (concentration) and reduction of two commonly studied nitroxides: the piperidine nitroxide Tempol and the pyrrolidine nitroxide 3-CP. It was found that 3-CP was reduced 3 to 11 times slower (depending on the tissue) than Tempol in vivo and that maximum tissue concentration varies substantially between tissues (0.6-7.2 mM). For a given tissue, the maximum concentration usually did not vary between the two nitroxides. Furthermore, using electron paramagnetic resonance spectroscopy, we showed that the nitroxide reduction rate depends only weakly on cellular pO(2) in the oxygen range expected in vivo. These observations, taken with the marked variation in nitroxide reduction rates observed between tissues, suggest that tissue pO(2) is not a major determinant of the nitroxide reduction rate in vivo. For the purpose of redox imaging, 3-CP was shown to be an optimal choice based on the achievable concentrations and bioreduction observed in vivo. Published by Elsevier Inc.

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External Sources

  1. DOI: 10.1016/j.freeradbiomed.2010.11.028
  2. WOS: 000287429600006

Library Notes

  1. Fiscal Year: FY2010-2011
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