Wolfson Molecular Imaging Center, Institute of Brain, Behaviour and Mental Health, The University of Manchester, 27 Palatine Road, Withington, Manchester, M20 3LJ, UK,
Curr Neurol Neurosci Rep. 2013 Dec;13(12):405. doi: 10.1007/s11910-013-0405-9.
Microglial activation is a key aspect of the neuroinflammatory process in neurodegenerative disorders including idiopathic and atypical parkinsonian disorders. Using positron emission tomography, it has become possible to image this phenomenon in vivo and over the last years patterns of microglia activation corresponding well known distribution of neuropathologic changes in these disorders have successfully been demonstrated using this technique. It has also been possible to measure the effects of interventions aimed at suppressing microglia activation as part interventional trials. Current research aims at evaluating positron emission tomography tracers for microglial activation with more favorable properties than the prototypical [(11)C]-(R)-PK11195, as well as developing tracers targeting additional parameters of the neuroinflammatory process like astroglial function or the cannabinoid receptor type 2.
小胶质细胞激活是神经退行性疾病(包括特发性和非典型帕金森病)神经炎症过程的一个关键方面。正电子发射断层扫描(PET)的应用使得能够在体内对这一现象进行成像,在过去的几年中,使用该技术已经成功地证明了与这些疾病中已知的神经病理学变化分布相对应的小胶质细胞激活模式。也有可能测量旨在抑制小胶质细胞激活的干预措施的效果,作为干预试验的一部分。目前的研究旨在评估具有比原型 [(11)C]-(R)-PK11195 更有利特性的正电子发射断层扫描(PET)示踪剂,以及开发针对神经炎症过程的其他参数(如星形胶质细胞功能或大麻素受体 2)的示踪剂。