Department of Rehabilitation Medicine, Nanfang Hospital, Southern Medical University, 1838 Guangzhou North Road, Guangzhou, Guangdong Province 510515, China.
Department of Nuclear Medicine, Nanfang Hospital, Southern Medical University, 1838 Guangzhou North Road, Guangzhou, Guangdong Province 510515, China.
Mol Pharm. 2021 Mar 1;18(3):1277-1284. doi: 10.1021/acs.molpharmaceut.0c01133. Epub 2021 Jan 25.
Glycogen synthase kinase-3β (GSK-3β), a cytoplasmic serine/threonine protein kinase, is involved in several human pathologies including Alzheimer's disease, bipolar disorder, diabetes, and cancer. Positron emission tomography (PET) imaging of GSK-3β could aid in investigating GSK-3β levels under normal and pathological conditions. In this study, we designed and synthesized fluorinated PET radioligands starting with recently identified isonicotinamide derivatives that showed potent affinity to GSK-3β. After extensive inhibitory activity assays and analyzing U87 cell uptake, we identified [F] as potential tracers with good specificity and high affinity. They were then subjected to further evaluation in rodent brain comprising PET imaging and metabolism studies. The radioligands [F] penetrated the blood-brain barrier and accumulated in GSK-3β-rich regions, including amygdala, cerebellum, and hippocampus. Also, it could be specifically blocked using the corresponding standard compounds. With these results, this work sets the basis for further development of novel F-labeled GSK-3β PET probes.
糖原合酶激酶-3β(GSK-3β)是一种细胞质丝氨酸/苏氨酸蛋白激酶,涉及多种人类疾病,包括阿尔茨海默病、双相情感障碍、糖尿病和癌症。GSK-3β 的正电子发射断层扫描(PET)成像可以帮助研究正常和病理条件下的 GSK-3β 水平。在这项研究中,我们从最近鉴定出的对 GSK-3β 具有高亲和力的异烟酰胺衍生物开始设计和合成了氟化的 PET 放射性配体。经过广泛的抑制活性测定和 U87 细胞摄取分析,我们鉴定出 [F] 是具有良好特异性和高亲和力的潜在示踪剂。然后,它们在包括 PET 成像和代谢研究的啮齿动物大脑中进行了进一步评估。放射性配体 [F] 穿透血脑屏障并在富含 GSK-3β 的区域积聚,包括杏仁核、小脑和海马体。此外,它可以使用相应的标准化合物进行特异性阻断。有了这些结果,这项工作为进一步开发新型 F 标记的 GSK-3β PET 探针奠定了基础。