作者: Nadja Van Camp , Raphael Boisgard , Bertrand Kuhnast , Benoit Thézé , Thomas Viel
DOI: 10.1007/S00259-009-1353-0
关键词: Pathology 、 Preclinical imaging 、 Benzodiazepine 、 Pharmacology 、 Central nervous system 、 Receptor 、 Inflammation 、 Neuroinflammation 、 Translocator protein 、 Positron emission tomography 、 Medicine
摘要: Purpose The key role of neuroinflammation in acute and chronic neurological disorders has stimulated the search for specific radiotracers targeting peripheral benzodiazepine receptor (PBR)/18 kDa translocator protein (TSPO), a hallmark neuroinflammation. Here we evaluate new radiotracer positron emission tomography (PET) [18F]PBR111 rodent model inflammation compare it with [11C]CLINME, an 11C-labelled tracer same chemical family, isoquinolinic carboxamide [11C]PK11195.