Department of Radiology, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Center for the Study of Itch and Sensory Disorders, Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Mol Imaging Biol. 2023 Apr;25(2):334-342. doi: 10.1007/s11307-022-01760-y. Epub 2022 Aug 11.
TRPC5 belongs to the mammalian superfamily of transient receptor potential (TRP) Ca-permeable cationic channels and it has been implicated in various CNS disorders. As part of our ongoing interest in the development of a PET radiotracer for imaging TRPC5, herein, we explored the radiosynthesis, and in vitro and in vivo evaluation of a new C-11 radiotracer [C]HC070 in rodents and nonhuman primates.
[C]HC070 was radiolabeled utilizing the corresponding precursor and [C]CHI via N-methylation protocol. Ex vivo biodistribution study of [C]HC070 was performed in Sprague-Dawley rats. In vitro autoradiography study was conducted for the rat brain sections to characterize the radiotracer distribution in the brain regionals. MicroPET brain imaging studies of [C]HC070 were done for 129S1/SvImJ wild-type mice and 129S1/SvImJ TRPC5 knockout mice for 0-60-min dynamic data acquisition after intravenous administration of the radiotracer. Dynamic PET scans (0-120 min) for the brain of cynomolgus male macaques were performed after the radiotracer injection.
[C]HC070 was efficiently prepared with good radiochemical yield (45 ± 5%, n = 15), high chemical and radiochemical purity (> 99%), and high molar activity (320.6 ± 7.4 GBq/μmol, 8.6 ± 0.2 Ci/μmol) at the end of bombardment (EOB). Radiotracer [C]HC070 has good solubility in the aqueous dose solution. The ex vivo biodistribution study showed that [C]HC070 had a quick rat brain clearance. Autoradiography demonstrated that [C]HC070 specifically binds to TRPC5-enriched regions in rat brain. MicroPET study showed the peak brain uptake (SUV value) was 0.63 in 129S1/SvImJ TRPC5 knockout mice compared to 1.13 in 129S1/SvImJ wild-type mice. PET study showed that [C]HC070 has good brain uptake with maximum SUV of ~ 2.2 in the macaque brain, followed by rapid clearance.
Our data showed that [C]HC070 is a TRPC5-specific radiotracer with high brain uptake and good brain washout pharmacokinetics in both rodents and nonhuman primates. The radiotracer is worth further investigating of its suitability to be a PET radiotracer for imaging TRPC5 in animals and human subjects in vivo.
TRPC5 属于哺乳动物瞬时受体电位 (TRP) 钙通透性阳离子通道超家族,它与各种中枢神经系统疾病有关。作为我们开发用于成像 TRPC5 的 PET 示踪剂的持续兴趣的一部分,在此,我们探索了新型 C-11 示踪剂 [C]HC070 在啮齿动物和非人类灵长类动物中的放射性合成、体外和体内评估。
利用相应的前体和 [C]CHI 通过 N-甲基化方案对 [C]HC070 进行放射性标记。在 Sprague-Dawley 大鼠中进行 [C]HC070 的离体生物分布研究。对大鼠脑切片进行体外放射自显影研究,以表征示踪剂在脑区域的分布。对 129S1/SvImJ 野生型小鼠和 129S1/SvImJ TRPC5 敲除小鼠进行 [C]HC070 的 microPET 脑成像研究,在静脉注射示踪剂后进行 0-60 分钟的动态数据采集。在放射性示踪剂注射后对食蟹猴雄性猕猴的大脑进行动态 PET 扫描(0-120 分钟)。
[C]HC070 的放射性合成效率高,放射化学产率为 45±5%(n=15),化学和放射化学纯度高(>99%),摩尔活度高(320.6±7.4GBq/μmol,8.6±0.2Ci/μmol)在终点(EOB)。示踪剂 [C]HC070 在水性剂量溶液中具有良好的溶解度。离体生物分布研究表明,[C]HC070 在大鼠脑中具有快速清除作用。放射自显影显示 [C]HC070 特异性结合大鼠脑中富含 TRPC5 的区域。microPET 研究表明,129S1/SvImJ TRPC5 敲除小鼠的脑摄取峰值(SUV 值)为 0.63,而 129S1/SvImJ 野生型小鼠为 1.13。PET 研究表明,[C]HC070 在猕猴大脑中具有良好的脑摄取,最大 SUV 值约为 2.2,随后清除迅速。
我们的数据表明,[C]HC070 是一种 TRPC5 特异性示踪剂,在啮齿动物和非人类灵长类动物中具有高脑摄取和良好的脑洗脱药代动力学。该示踪剂值得进一步研究,以确定其是否适合作为体内成像 TRPC5 的 PET 示踪剂在动物和人体中的适用性。