Subtype-Selective Dopamine Receptor Radioligands for PET Imaging: Current Status and Recent Developments

被引:9
作者
Banerjee, A. [1 ]
Prante, O. [1 ]
机构
[1] Univ Erlangen Nurnberg, Nucl Med Clin, Lab Mol Imaging & Radiochem, D-91054 Erlangen, Germany
关键词
Dopamine; D2; D3; D4; dopamine receptor; selectivity; subtype-selectivity; positron emission tomography; PET; radioligand; PET ligand; radiopharmaceutical; F-18; C-11; POSITRON-EMISSION-TOMOGRAPHY; IN-VITRO EVALUATION; HIGH-AFFINITY STATE; D-4; RECEPTOR; HUMAN-BRAIN; PRIMATE BRAIN; RAT-BRAIN; POTENTIAL RADIOTRACER; CELLULAR-DISTRIBUTION; NONHUMAN-PRIMATES;
D O I
10.2174/092986712802002518
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review presents a general overview of the subtype-selective dopamine receptor radioligands for in vivo imaging of dopamine receptor expression by positron emission tomography (PET). Besides the C-11- and F-18-labeled radioligands which are already in clinical use, a summary of subtype-selective radioligands which had been studied in vitro and in vivo is provided, which shines light onto the current status and recent developments in this field of radiopharmaceutical research.
引用
收藏
页码:3957 / 3966
页数:10
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