Jagust W J, Eberling J L, Roberts J A, Brennan K M, Hanrahan S M, VanBrocklin H, Enas J D, Biegon A, Mathis C A
Center for Functional Imaging, Lawrence Berkeley Laboratory, University of California 94720.
Eur J Pharmacol. 1993 Sep 28;242(2):189-93. doi: 10.1016/0014-2999(93)90079-w.
Previous experiments have demonstrated that 5-iodo-6-nitro-2-piperazinylquinoline (5-I-6-NQP) is a potent and selective ligand for studying brain 5-hydroxytryptamine (5-HT) reuptake sites. We performed in vivo imaging in non-human primates using single photon emission computed tomography (SPECT) and the 123I-labeled compound [123I]5-I-6-NQP. These studies showed rapid brain uptake, with slow egress of the tracer from the brainstem, a region rich in 5-HT reuptake sites. Loss of the tracer from regions with a lower density of these sites, such as cerebellum, was relatively more rapid. Pretreatment of animals with paroxetine increased the washout of tracer from the brainstem to rates similar to that seen in cerebellum. Brainstem to cerebellar ratios of tracer accumulation were > 2 by 8 h after injection, and in paroxetine pretreated animals remained close to 1. These results indicate that the radiotracer has characteristics suitable for use as a SPECT imaging agent of serotonin reuptake sites.
先前的实验已证明,5-碘-6-硝基-2-哌嗪基喹啉(5-I-6-NQP)是用于研究脑5-羟色胺(5-HT)再摄取位点的一种强效且选择性的配体。我们使用单光子发射计算机断层扫描(SPECT)和123I标记的化合物[123I]5-I-6-NQP在非人类灵长类动物中进行了体内成像。这些研究显示,示踪剂在脑中摄取迅速,且从富含5-HT再摄取位点的脑干缓慢流出。示踪剂从小脑等这些位点密度较低的区域流失相对更快。用帕罗西汀对动物进行预处理会使示踪剂从脑干的清除率增加至与在小脑中观察到的相似的速率。注射后8小时,脑干与小脑的示踪剂积累比率>2,而在帕罗西汀预处理的动物中该比率保持接近1。这些结果表明,该放射性示踪剂具有适合用作5-羟色胺再摄取位点的SPECT成像剂的特性。