Sanabria-Bohórquez Sandra M, Biver Francoise, Damhaut Philippe, Wikler David, Veraart Claude, Goldman Serge
Present address: Merck Research Laboratories, 770 Sumneytown Pike, P.O. Box 4 WP44C-2, West Point, PA 19486, USA.
Eur J Nucl Med Mol Imaging. 2002 Jan;29(1):76-81. doi: 10.1007/s00259-001-0684-2. Epub 2001 Nov 22.
Serotonin-1A (5-HT(1A)) receptors are implicated in neurochemical mechanisms underlying anxiety and depression and their treatment. Animal studies have suggested that 4-(2'-methoxyphenyl)-1-[2'-[ N-(2"-pyridinyl)- p-[(18)F]fluorobenzamido] ethyl] piperazine ( p-MPPF) may be a suitable positron emission tomography (PET) tracer of 5-HT(1A) receptors. To test p-MPPF in humans, we performed 60-min dynamic PET scans in 13 healthy volunteers after single bolus injection. Metabolite quantification revealed a fast decrease in tracer plasma concentration, such that at 5 min post injection about 25% of the total radioactivity in plasma corresponded to p-MPPF. Radioactivity concentration was highest in hippocampus, intermediate in neocortex and lowest in basal ganglia and cerebellum. The interactions between p-MPPF and 5-HT(1A) receptors were described using linear compartmental models with plasma input and reference tissue approaches. The two quantification methods provided similar results which are in agreement with previous reports on 5-HT(1A) receptor brain distribution. In conclusion, our results show that p-MPPF is a suitable PET radioligand for 5-HT(1A) receptor human studies.
5-羟色胺-1A(5-HT(1A))受体与焦虑症、抑郁症及其治疗所涉及的神经化学机制有关。动物研究表明,4-(2'-甲氧基苯基)-1-[2'-[N-(2"-吡啶基)-p-[(18)F]氟苯甲酰胺基]乙基]哌嗪(p-MPPF)可能是一种适用于5-HT(1A)受体的正电子发射断层扫描(PET)示踪剂。为了在人体中测试p-MPPF,我们对13名健康志愿者进行了单次推注注射后的60分钟动态PET扫描。代谢物定量分析显示示踪剂血浆浓度迅速下降,以至于在注射后5分钟时,血浆中约25%的总放射性对应于p-MPPF。放射性浓度在海马体中最高,在新皮质中居中,在基底神经节和小脑中最低。使用具有血浆输入和参考组织方法的线性房室模型描述了p-MPPF与5-HT(1A)受体之间的相互作用。两种定量方法提供了相似的结果,这与先前关于5-HT(1A)受体脑部分布的报告一致。总之,我们的结果表明p-MPPF是一种适用于5-HT(1A)受体人体研究的PET放射性配体。