TY - JOUR T1 - Characteristic Brain Distribution of 1-<sup>14</sup>C-Octanoate in a Rat Model of Focal Cerebral Ischemia in Comparison with Those of <sup>123</sup>I-IMP and <sup>123</sup>I-Iomazenil JF - Journal of Nuclear Medicine JO - J Nucl Med SP - 1168 LP - 1175 VL - 44 IS - 7 AU - Yuji Kuge AU - Kenji Hikosaka AU - Koh-ichi Seki AU - Kazue Ohkura AU - Ken-ichi Nishijima AU - Tomohito Kaji AU - Satoshi Ueno AU - Eriko Tsukamoto AU - Nagara Tamaki Y1 - 2003/07/01 UR - http://jnm.snmjournals.org/content/44/7/1168.abstract N2 - 1-11C-Octanoate is a potential tracer for studying astroglial function in PET. To evaluate the usefulness of 1-11C-octanoate for studying ischemic stroke, we investigated the brain distribution of 1-14C-octanoate and compared it with N-isopropyl-p-123I-iodoamphetamine (123I-IMP) distribution (cerebral blood flow), 123I-iomazenil (123I-IMZ) distribution (neuronal viability based on 123I-IMZ binding to benzodiazepine receptors), and hematoxylin-eosin stain (morphologic changes) in a rat model of focal cerebral ischemia. Methods: The right middle cerebral artery of each rat was occluded intraluminally. The brain distribution of 1-14C-octanoate and 123I-IMP (or 123I-IMZ) was determined 4 and 24 h after the insult using a dual-tracer autoradiographic technique (n = 4–7 in each group). Coronal brain sections adjacent to those used for autoradiography were stained with hematoxylin and eosin. Regions of interest (ROIs) were determined for 3 coronal slices, and asymmetry indices (AIs, lesion/normal hemisphere) of the tracer uptake were calculated. ROIs on the hemisphere with the lesion were classified into 4 groups: In region A, widespread necrotic cells were observed; in region B, necrotic cells were occasionally observed; in region C1, no morphologic changes were observed and the AIs for 123I-IMP (or 123I-IMZ) were ≤0.8; and in region C2, no morphologic changes were observed and the AIs for 123I-IMP (or 123I-IMZ) were &gt;0.8. Results: 1-14C-Octanoate uptake decreased in the regions where morphologic changes were observed (regions A and B) but was relatively preserved in the surrounding region without morphologic changes despite reduced 123I-IMP and 123I-IMZ uptake (region C1). In the region without morphologic changes (region C1), AIs for 1-14C-octanoate were significantly higher than those for 123I-IMP (4 h, 0.73 ± 0.23 for 1-14C-octanoate and 0.37 ± 0.20 for 123I-IMP, P &lt; 0.0001; 24 h, 0.84 ± 0.11 for 1-14C-octanoate and 0.44 ± 0.15 for 123I-IMP, P &lt; 0.0001) and those for 123I-IMZ (4 h, 0.83 ± 0.19 for 1-14C-octanoate and 0.57 ± 0.13 for 123I-IMZ, P &lt; 0.0001; 24 h, 0.91 ± 0.13 for 1-14C-octanoate and 0.73 ± 0.06 for 123I-IMZ, P &lt; 0.0001). Conclusion: 1-14C-Octanoate uptake was relatively preserved in the regions without morphologic changes despite reduced 123I-IMP and 123I-IMZ uptake. 1-11C-Octanoate may provide further functional information on the pathophysiology of ischemic stroke, reflecting astroglial function based on fatty acid metabolism. ER -