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Recent Progress in the Development of TSPO PET Ligands for Neuroinflammation Imaging in Neurological Diseases

机译:用于神经疾病的神经炎症成像的TSPO PET配体的最新进展

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摘要

Neuroinflammation is heavily associated with various neurological diseases including Alzheimer’s disease, Parkinson’s disease, multiple sclerosis, and stroke. It is strongly characterized by the activation of microglia which can be visualized using position emission tomography (PET). Traditionally, translocator protein 18 kDa (TSPO) has been the preferred target for imaging the inflammatory progression of the microglial component. TSPO is expressed in the outer mitochondrial membrane and present in very low concentrations in the healthy human brain, but is markedly upregulated in response to brain injury and inflammation. Due to its value as a marker of microglial activation and subsequent utility for evaluating neuroinflammation in CNS disorders, several classes of TSPO radioligands have been developed and evaluated. However, the application of these second-generation TSPO radiotracers has been subject to several limiting factors, including a polymorphism that affects TSPO binding. This review focuses on recent developments in TSPO imaging, as well as current limitations and suggestions for future directions from a medical imaging perspective.
机译:神经炎症与多种神经系统疾病密切相关,包括阿尔茨海默氏病,帕金森氏病,多发性硬化症和中风。它的显着特征是小胶质细胞的激活,可以使用位置发射断层扫描(PET)进行可视化。传统上,易位蛋白18 kDa(TSPO)是成像小胶质细胞组分炎症过程的首选靶标。 TSPO在线粒体外膜中表达,在健康的人脑中浓度很低,但在对脑损伤和炎症的反应中明显上调。由于其作为小胶质细胞激活的标志物的价值以及随后用于评估CNS疾病中神经炎症的价值,已经开发和评估了几类TSPO放射性配体。但是,这些第二代TSPO放射性示踪剂的应用受到一些限制因素的影响,包括影响TSPO结合的多态性。这篇综述着重于TSPO成像的最新发展,以及从医学成像的角度来看当前的局限性和对未来方向的建议。

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