Yousef K A, Volkow N D, Schlyer D J, Fowler J S, Wolf A P, Wang G J, Smith M R, Brodie J D, Warner D
Medical Department, Brookhaven National Laboratory, Upton, New York 11973, USA.
Synapse. 1995 Jan;19(1):14-7. doi: 10.1002/syn.890190103.
We had previously demonstrated extrastriatal uptake of [18F]N-methylspiroperidol (18F-NMS) in the human brain. This study evaluates the effect of haloperidol on 18F-NMS binding in extrastriatal brain regions. Six schizophrenic patients on haloperidol underwent two PET scans with 18F-NMS at 12 h and at 6 days after haloperidol withdrawal. There was a significant increase in 18F-NMS uptake in striatal, thalamic, and temporal regions but not in frontal, occipital, or cerebellar regions, following drug withdrawal. Haloperidol's ability to block the uptake of 18F-NMS is an indication of the specificity of the radioligand's binding in these regions and supports the postmortem data demonstrating the presence of dopamine D2 receptors in the thalamus and temporal cortex of the human brain.
我们之前已经证明了[18F]N-甲基螺哌啶醇(18F-NMS)在人脑纹状体以外区域的摄取。本研究评估了氟哌啶醇对纹状体以外脑区18F-NMS结合的影响。六名服用氟哌啶醇的精神分裂症患者在停用氟哌啶醇12小时和6天后接受了两次18F-NMS的PET扫描。停药后,纹状体、丘脑和颞叶区域的18F-NMS摄取显著增加,但额叶、枕叶或小脑区域没有增加。氟哌啶醇阻断18F-NMS摄取的能力表明放射性配体在这些区域结合的特异性,并支持尸检数据,证明人脑丘脑和颞叶皮质中存在多巴胺D2受体。