Turku PET Centre, University of Turku, Turku, Finland.
Medicity Research Laboratory, University of Turku, Turku, Finland.
Sci Rep. 2019 Dec 31;9(1):20412. doi: 10.1038/s41598-019-56848-3.
There is a substantial interest in the development of NK1 substance P antagonists as potential treatments for various neuropsychiatric and somatic disorders. The aim of this study was to determine whether [F]SPA-RQ can be utilized as a tool for studying the whole body distribution and function of NK1 receptors in preclinical settings. The compound was injected into guinea pigs with or without premedication with a NK1 receptor antagonist (NK1A-2). For comparison, we included two rats in the study, as the affinity of antagonists for NK1 receptors is known to vary between species. The whole body biodistribution of the tracer was determined at several time points. The tracer showed specific binding in organs compatible with the known location of NK1-receptors. Premedication with a NK1 antagonist led to an inhibited uptake of [F]SPA-RQ in several organs of guinea pigs, notably intestine, pancreas, urinary bladder, uterus, skin and lung. Specific binding was also seen in both cortex and striatum. In contrast, negligible specific binding was observed in the rat brain with [F]SPA-RQ, whereas the tracer uptake in peripheral tissues was similar to that seen in guinea pigs. We conclude that [F]SPA-RQ/PET is a useful tool to study the distribution and function of peripherally located NK1 receptors e.g. in different disease models.
人们对开发 NK1 物质 P 拮抗剂作为治疗各种神经精神和躯体疾病的潜在方法有着浓厚的兴趣。本研究旨在确定 [F]SPA-RQ 是否可以作为研究 NK1 受体在临床前环境中的全身分布和功能的工具。将该化合物注射到豚鼠体内,同时或不预先给予 NK1 受体拮抗剂(NK1A-2)。为了进行比较,我们在研究中还包括了两只大鼠,因为已知拮抗剂对 NK1 受体的亲和力在不同物种之间存在差异。在几个时间点测定示踪剂的全身生物分布。该示踪剂在与 NK1 受体已知位置相匹配的器官中显示出特异性结合。预先给予 NK1 拮抗剂会导致豚鼠的几个器官(特别是肠、胰腺、膀胱、子宫、皮肤和肺)中 [F]SPA-RQ 的摄取受到抑制。在大脑皮层和纹状体也观察到特异性结合。相比之下,[F]SPA-RQ 在大鼠大脑中几乎没有观察到特异性结合,而外周组织中的示踪剂摄取与在豚鼠中观察到的相似。我们得出结论,[F]SPA-RQ/PET 是研究外周 NK1 受体分布和功能的有用工具,例如在不同疾病模型中。