Horti Andrew G
Department of Radiology, The Johns Hopkins School of Medicine, 600 North Wolfe Street, Baltimore, MD 21287-0816, USA.
Biochem Pharmacol. 2015 Oct 15;97(4):566-575. doi: 10.1016/j.bcp.2015.07.030. Epub 2015 Jul 29.
The alpha-7 subtype of the nicotinic acetylcholine receptor (α7-nAChR) is fundamental to physiology; it mediates various brain functions and represents an important target for drug discovery. Exploration of the brain nicotinic acetylcholine receptors (nAChRs) using positron-emission tomography (PET) will make it possible to better understand the important role of this receptor and to study its involvement in schizophrenia, bipolar disorder, Alzheimer's and Parkinson's diseases, drug dependence, inflammation and many other disorders and simplify the development of nicotinic drugs for treatment of these disorders. Until recently, PET imaging of α7-nAChRs has been impeded by the absence of good radiotracers. This review describes various endeavors to develop α7-nAChR PET tracers by several research groups including the author's group. Most initial PET tracers for imaging α7-nAChRs did not exhibit suitable imaging properties due to their low specific binding. Newly discovered [(18)F]ASEM is the first highly specific α7-nAChR radioligand and in 2014 it was translated to human PET imaging.
烟碱型乙酰胆碱受体的α7亚型(α7-nAChR)对生理学至关重要;它介导多种脑功能,是药物研发的重要靶点。利用正电子发射断层扫描(PET)对脑烟碱型乙酰胆碱受体(nAChRs)进行研究,将有助于更好地理解该受体的重要作用,并研究其在精神分裂症、双相情感障碍、阿尔茨海默病和帕金森病、药物依赖、炎症及许多其他疾病中的作用,还能简化用于治疗这些疾病的烟碱类药物的研发。直到最近,由于缺乏合适的放射性示踪剂,α7-nAChRs的PET成像一直受到阻碍。这篇综述描述了包括作者所在团队在内的几个研究小组为开发α7-nAChR PET示踪剂所做的各种努力。大多数最初用于α7-nAChRs成像的PET示踪剂由于特异性结合低而未表现出合适的成像特性。新发现的[(18)F]ASEM是首个高特异性的α7-nAChR放射性配体,并于2014年应用于人体PET成像。