正电子发射断层摄影术
断层摄影术
脑正电子发射断层扫描术
临床前影像学
核医学
医学
放射科
体内
生物
生物技术
作者
Xingrui Guo,Jie Xiang,Keqiang Ye,Zhentao Zhang
出处
期刊:Cells
[MDPI AG]
日期:2025-06-16
卷期号:14 (12): 907-907
被引量:2
标识
DOI:10.3390/cells14120907
摘要
Neurodegenerative diseases (NDDs) that are characterized by the accumulation of alpha-synuclein (α-syn) aggregates in both neurons and the non-neuronal cells of the brain are called synucleinopathies. The most common synucleinopathies includes Parkinson's disease (PD), Parkinson's disease dementia (PDD), multiple system atrophy (MSA), and dementia with Lewy bodies (DLB). Significant progress has been made in the development of positron emission tomography (PET) radiotracers for synucleinopathies, yielding several α-syn tracers that have entered clinical studies. However, selective α-syn imaging still faces inherent challenges. This review provides a comprehensive overview of the progress in α-syn PET radiotracers from three angles: Alzheimer's disease (AD)-derived scaffolds, representative compound scaffolds and analogs, and the identification of α-syn tracers through high-throughput screening (HTS). We discuss the characteristics, advantages, and limitations of the tracers for preclinical and clinical application. Finally, future directions in the development of radioligands for proteinopathies are discussed. There is no clinical available PET radiotracer for imaging α-syn aggregates, but these advances have laid a key foundation for non-invasive α-syn imaging and early diagnosis of synucleinopathies.
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