Kuikka J T, Akerman K K, Hiltunen J, Bergström K A, Räsänen P, Vanninen E, Halldin C, Tiihonen J
Department of Clinical Physiology, Kuopio University Hospital, FIN-70210 Kuopio, Finland.
Eur J Nucl Med. 1997 May;24(5):483-7. doi: 10.1007/BF01267678.
The iodine-123 labelled ligand benzamide epidepride was evaluated as a probe for in vivo imaging of striatal and extrastriatal dopamine D2 receptor sites in the human brain. Four healthy males were imaged with a high-resolution single-photon emission tomography scanner. Striatal radioactivity peaked at 3 h after injection. The specific binding in the striatum was 0.91+/-0.03 at 3 h and this ratio steadily increased with time. Extrastriatal radioactivity was highest in the thalamus, in the midbrain and in the temporal cortex, and peaked at 45-60 min after injection of tracer. A smaller amount of radioactivity was found in the parietal, frontal and occipital cortices. Two radioactive metabolites were observed, of which one was more lipophilic than the parent compound. The radiation burden to the patient was 0.035 mSv/MBq (effective dose equivalent). The preliminary results showed that [123I]epidepride can be used for imaging striatal and extrastriatal dopamine D2 receptor sites in the living human brain.
对碘 - 123标记的配体苯甲酰胺表哌立得进行了评估,作为人脑纹状体和纹状体外多巴胺D2受体位点体内成像的探针。使用高分辨率单光子发射断层扫描仪对4名健康男性进行成像。纹状体放射性在注射后3小时达到峰值。3小时时纹状体中的特异性结合为0.91±0.03,且该比值随时间稳步增加。纹状体外放射性在丘脑、中脑和颞叶皮质中最高,在注射示踪剂后45 - 60分钟达到峰值。在顶叶、额叶和枕叶皮质中发现的放射性较少。观察到两种放射性代谢物,其中一种比母体化合物更具亲脂性。患者的辐射负担为0.035 mSv/MBq(有效剂量当量)初步结果表明,[123I]表哌立得可用于活体人脑纹状体和纹状体外多巴胺D2受体位点的成像。