Volume 65, Issue 1 pp. 295-303
Full Papers

Mapping of redox status in a brain-disease mouse model by three-dimensional EPR imaging

Hirotada Fujii

Corresponding Author

Hirotada Fujii

Department of Liberal Arts and Sciences, Center for Medical Education, Sapporo Medical University, Sapporo, Hokkaido, Japan

Department of Liberal Arts and Sciences, Center for Medical Education, Sapporo Medical University, Sapporo, Hokkaido 060-8556, Japan===Search for more papers by this author
Hideo Sato-Akaba

Hideo Sato-Akaba

Department of Systems Innovation, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka, Japan

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Katsuya Kawanishi

Katsuya Kawanishi

Division of Occlusion and Removable Prosthodontics, Department of Oral Rehabilitation, Health Sciences University of Hokkaido School of Dentistry, Ishikari-Tobetsu, Hokkaido, Japan

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Hiroshi Hirata

Hiroshi Hirata

Division of Bioengineering and Bioinformatics, Graduate School of Information Science and Technology, Hokkaido University, Sapporo, Hokkaido, Japan

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First published: 21 September 2010
Citations: 36

Abstract

Electron paramagnetic resonance imaging using nitroxides is a powerful method for visualizing the redox status modulated by oxidative stress in vivo. Typically, however, data acquisition times have been too slow to obtain a sufficient number of projections for three-dimensional images, when using continuous wave-electron paramagnetic resonance imager in small rodents, using nitroxides with comparatively short T2 and a half-life values. Because of improvements in imagers that enable rapid data-acquisition, the feasibility of three-dimensional electron paramagnetic resonance imaging with good quality in mice was tested with nitroxides. Three-dimensional images of mice were obtained at an interval of 15 sec under field scanning of 0.3 sec and with 46 projections in the case of strong electron paramagnetic resonance signals. Three-dimensional electron paramagnetic resonance images of a blood brain barrier-permeable nitroxide, 3-hydroxymethyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl, in the mouse head clearly showed that 3-hydroxymethyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl was distributed within brain tissues, and this was confirmed by MRI observations. Based on the pharmacokinetics of nitroxides in mice, half-life mapping was demonstrated in an ischemia-reperfusion model mouse brain. Inhomogeneous half-lives were clearly mapped pixel-by-pixel in mouse head under oxidative stress by the improved continuous wave-electron paramagnetic resonance imager noninvasively. Magn Reson Med, 2010. © 2010 Wiley-Liss, Inc.

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