TY - JOUR T1 - PET of Glial Metabolism Using 2-<sup>18</sup>F-Fluoroacetate JF - Journal of Nuclear Medicine JO - J Nucl Med SP - 982 LP - 990 DO - 10.2967/jnumed.108.057356 VL - 50 IS - 6 AU - Jan Marik AU - Annie Ogasawara AU - Baby Martin-McNulty AU - Jed Ross AU - Judith E. Flores AU - Herman S. Gill AU - Jeff N. Tinianow AU - Alexander N. Vanderbilt AU - Merry Nishimura AU - Franklin Peale AU - Cinthia Pastuskovas AU - Joan M. Greve AU - Nicholas van Bruggen AU - Simon P. Williams Y1 - 2009/06/01 UR - http://jnm.snmjournals.org/content/50/6/982.abstract N2 - Imaging of the glial activation that occurs in response to central nervous system trauma and inflammation could become a powerful technique for the assessment of several neuropathologies. The selective uptake and metabolism of 2-18F-fluoroacetate (18F-FAC) in glia may represent an attractive strategy for imaging glial metabolism. Methods: We have evaluated the use of 18F-FAC as a specific PET tracer of glial cell metabolism in rodent models of glioblastoma, stroke, and ischemia–hypoxia. Results: Enhanced uptake of 18F-FAC was observed (6.98 ± 0.43 percentage injected dose per gram [%ID/g]; tumor-to-normal ratio, 1.40) in orthotopic U87 xenografts, compared with healthy brain tissue. The lesion extent determined by 18F-FAC PET correlated with that determined by MRI (R2 = 0.934, P = 0.007). After transient middle cerebral artery occlusion in the rat brain, elevated uptake of 18F-FAC (1.00 ± 0.03 %ID/g; lesion-to-normal ratio, 1.90) depicted the ischemic territory and correlated with infarct volumes as determined by 2,3,5-triphenyltetrazolium chloride staining (R2 = 0.692, P = 0.010) and with the presence of activated astrocytes detected by anti–glial fibrillary acidic protein. Ischemia–hypoxia, induced by permanent ligation of the common carotid artery with transient hypoxia, resulted in persistent elevation of 18F-FAC uptake within 30 min of the induction of hypoxia. Conclusion: Our data support the further evaluation of 18F-FAC PET for the assessment of glial cell metabolism associated with neuroinflammation. ER -