PET radiotracers for molecular imaging in the brain: Past, present and future

被引:71
作者
Zimmer, Luc [1 ,2 ]
Luxen, Andre [3 ]
机构
[1] Univ Lyon, CNRS, INSERM, Lyon Neurosci Res Ctr, Lyon, France
[2] Hosp Civils Lyon, CERMEP Imagerie Vivant, Lyon, France
[3] Univ Liege, Cyclotron Res Ctr, B-4000 Liege, Belgium
关键词
PET; Radiopharmaceuticals; Biomarker; Brain; Neurology; Psychiatry; Drug discovery; POSITRON-EMISSION-TOMOGRAPHY; IN-VIVO BINDING; PROTEIN-COUPLED RECEPTORS; P-GLYCOPROTEIN FUNCTION; CENTRAL-NERVOUS-SYSTEM; DORSAL RAPHE NUCLEUS; ALZHEIMERS-DISEASE; 5-HT1A RECEPTORS; TRANSLOCATOR PROTEIN; AGONIST RADIOLIGAND;
D O I
10.1016/j.neuroimage.2011.12.037
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuroimaging of brain receptors began in the early 1980s. Now, some thirty-five years later, PET imaging is still an expanding field of preclinical and clinical investigations. In addition to improvements in PET cameras and image analysis, the availability of suitable radiotracers is a crucial factor leading this expansion. Radiotracers have been developed to visualize and quantify a growing numbers of brain receptors, transporters, enzymes and other molecular targets. The development of adequate PET radiotracers represents an exciting challenge, given the large number of targets and neurochemical functions that have yet to be explored. In this article, we review the main evolutions led by preclinical radiotracers and clinical radiopharmaceuticals. The current main contributions of PET radiotracers are described in terms of imaging of neuronal metabolism, receptor and transporter quantification and neurodegenerative, neuroinflammatory and neurooncologic process imaging. In the last part, we highlight some applications presenting a potential for novel functional explorations of the brain. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:363 / 370
页数:8
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