Sedvall G, Farde L, Barnett A, Hall H, Halldin C
Department of Psychiatry and Psychology, Karolinska Institute, Stockholm, Sweden.
Psychopharmacology (Berl). 1991;103(2):150-3. doi: 10.1007/BF02244195.
The new selective D1-dopamine receptor antagonist SCH 39166 was labelled with the positron emitting isotope 11C and used as ligand for visualization of dopamine-D1 receptor binding in Cynomolgus monkeys by PET. After intravenous administration of the ligand a marked uptake of radioactivity was recorded in the D1-dopamine receptor-rich striatum and neocortex but not in the dopamine receptor-poor cerebellum. The uptake of radioactivity in striatum and neocortex was markedly displaced after the intravenous injection of a high dose of the D1-dopamine receptor antagonist SCH 23390 but not after the 5-HT2 receptor antagonist ketanserine. 11C-SCH 39166 should be a useful tool to explore D1-dopamine receptor characteristics in the living human brain by PET.
新型选择性D1-多巴胺受体拮抗剂SCH 39166用发射正电子的同位素11C进行标记,并用作配体,通过正电子发射断层扫描(PET)在食蟹猴中可视化多巴胺D1受体结合情况。静脉注射该配体后,在富含D1-多巴胺受体的纹状体和新皮质中记录到明显的放射性摄取,但在多巴胺受体较少的小脑中未观察到。静脉注射高剂量的D1-多巴胺受体拮抗剂SCH 23390后,纹状体和新皮质中的放射性摄取明显被取代,但注射5-HT2受体拮抗剂酮色林后则没有这种现象。11C-SCH 39166应该是通过PET探索活体人脑中D1-多巴胺受体特征的有用工具。