• Taketoshi Asanuma, Sabrina Doblas, Yasvir A Tesiram, Debra Saunders, Rebecca Cranford, Hironobu Yasui, Osamu Inanami, Nataliya Smith, Robert A Floyd, Yashige Kotake, and Rheal A Towner.
• Small Animal MRI Facility, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104, USA.
• J Magn Reson Imaging. 2008 Sep 1; 28 (3): 574-87.

PurposeTo apply fiber tractography to assess the effect of a possible antiglioma drug, phenyl N-tert-butyl nitrone (PBN), on glioma-affected neuronal fibers. The fiber tractography method was able to differentiate between different tumor types, such as the C6 and F98 rat glioma models.Materials And MethodsC6 or F98 cells were intracranially injected into the cortex of male Fischer 344 rats. PBN treatment was initiated before or after cell implantation. Tumor growth was monitored with diffusion tensor imaging (DTI) and fiber tractography using diffusion-weighting gradients in 30 noncolinear directions.ResultsAlthough proton density-weighted (PDw) and T2-weighted (T2w) images did not show any difference between C6 and F98 gliomas without edema, the apparent diffusion coefficient (ADC) and fractional anisotropy (FA) maps were able to discriminate between these two tumor models. Fiber tractography was used to visualize C6 glioma-induced ischemia of tumor-surrounding tissues, whereas F98 glioma was found to infiltrate and penetrate into the corpus callosum (CC). During glioma growth, neuronal fibers were found to disappear at the border regions between the tumor and surrounding tissues. PBN treatment was shown to inhibit glioma growth with accompanying changes in the surrounding tissue.ConclusionBy noninvasively monitoring the degree of neuronal fiber integrity and connectivity with the use of neuronal fiber tractography, we were able to evaluate the protective effect of PBN against invasive glioma growth in rat brains. PBN provided protection of the neuronal fibers against tumor-induced ischemia and tumor invasion.Copyright (c) 2008 Wiley-Liss, Inc.

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