[18F]MPPF as a tool fot the in vivo imaging of 5-HT1A receptors in animal and human brain

被引:74
|
作者
Aznavour, Nicolas
Zimmer, Luc
机构
[1] Univ Lyon 1, Lab Neuropharmacol, F-69365 Lyon, France
[2] CERMEP, Lyon, France
关键词
PET; serotonin; brain imaging; 5-HT1A receptors; MPPF;
D O I
10.1016/j.neuropharm.2006.09.023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Serotonin (5-hydroxytryptamine, 5-HT) and its various receptors are involved in numerous CNS functions and psychiatric disorders. 5-HT1A, the best-characterized subtype of currently known 5-HT receptors, is tightly implicated in the pathogenesis of depression, anxiety, epilepsy and eating disorders. It thus represents an important target for drug therapy. Specific radioligands and positron emission tomography (PET) allow for a quantitative imaging of brain 5-HT1A receptor distribution in living animals and humans. Recently, the selective 5-HT1A receptor antagonist, MPPF, has been successfully labeled with [F-18]fluorine ([F-18]MPPF), and an increasing number of academic and industry centres have used this radiotracer in preclinical and clinical studies. After a brief account of some of the structural, distributional and electrophysiological characteristics of brain 5-HT1A receptors, this review focuses on studies conducted with [F-18]MPPF, with emphasis on preclinical results illustrating the actual and potential value of this PET radioligand for clinical research and drug development. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:695 / 707
页数:13
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