Characterization of a New Metabotropic Glutamate Receptor Subtype 5 PET Ligand

描述（由申请方提供）：拟定研究涉及表征新型正电子发射断层扫描（PET）放射性配体3-（6-甲基-吡啶-2-基乙炔基）-环己-2-烯酮-O-11 C-甲基-肟（[11 C] ABP 688），一种代谢型谷氨酸受体亚型5（mGluR 5）的拮抗剂。 大量不同的证据表明mGluR 5与抑郁症的病理生理学有关。 此外，mGluR 5功能障碍与焦虑、精神分裂症、成瘾、帕金森病和脆性X综合征等疾病有关。 随着对mGluR 5的关注的加强，建立可靠的成像这种受体的方法变得越来越重要。 PET提供了活体人脑中神经受体系统的可视化，使PET成为体内定量mGluR 5的理想模式。 为此，[11 C] ABP 688，一种在体外对mGluR 5具有高选择性的mGluR 5变构拮抗剂，最近被开发用于人体。 通过[11 C] ABP 688定量mGluR 5变异可以用于许多目的，从抑郁症或其他疾病的可能指标，到个体治疗有效性的潜在监测，再到在治疗前提供关于潜在治疗结果的个性化信息。 然而，与任何新开发的PET示踪剂一样，[11 C] ABP 688必须在人体中进行适当的表征，以提供其靶点的准确定量。 因此，我将定义和执行一个协议来表征[11 C] ABP 688，它可以推广到任何新的PET配体。 通过拟议的研究，与我的导师（精神病患者人群PET研究领域的领导者）的结构化会议，以及课程作业和与项目贡献者的定期会议，我将扩大我在神经生物学，放射化学，PET成像和分析，临床评估和情感障碍方面的专业知识。 在这样做的过程中，我不仅将提高[11 C] ABP 688和mGluR 5的现有知识，而且还将学习一套开发和使用PET示踪剂的程序，我可以作为一名独立的研究者。 具体而言，我计划：（1）确定[11 C] ABP 688的最佳建模技术和扫描时间，以确保可靠和准确的定量。 将使用这些最佳方法确定个体内结合变异。 (2)检查在没有动脉线的情况下计算完整血浆输入函数的方法，提高受试者舒适度并降低扫描成本。 使用数学方法，可以根据静脉样本或正弦图数据对动脉输入进行建模。 消除对动脉管路的需求可能会减少目前PET在解决公共卫生问题中广泛使用的障碍。 (3)研究[11 C] ABP 688对内源性谷氨酸的敏感性，以确定该配体是否可用于监测神经系统和精神疾病中的谷氨酸水平变化。 (4)比较mGluR 5在抑郁症和对照组中的分布和密度。 这将有助于深入了解抑郁症中mGluR 5功能障碍的机制。 这些研究的目的是增加对mGluR 5的了解，并开发急需的可靠mGluR 5 PET成像方法。

DESCRIPTION (provided by applicant): The proposed research involves characterizing the novel Positron Emission Tomography (PET) radioligand, 3- (6-Methyl-pyridin-2-ylethynyl)-cyclohex-2-enone-O-11C-methyl-oxime ([11C]ABP688), an antagonist of the metabotropic glutamate receptor subtype 5 (mGluR5), in humans. A large body of diverse evidence implicates mGluR5 in the pathophysiology of depression. In addition, mGluR5 dysfunction has been associated with disorders such as anxiety, schizophrenia, addiction, Parkinson's disease, and fragile X syndrome. As focus intensifies on mGluR5, it is becoming increasingly important to establish reliable methods of imaging this receptor. PET provides visualization of neuroreceptor systems in living human brain, making PET an ideal modality to quantify mGluR5 in vivo. To this end, [11C]ABP688, a highly selective allosteric antagonist of the mGluR5 in vitro with high selectivity for mGluR5 in vivo, has recently been developed for use in humans. Quantification of mGluR5 variation by [11C]ABP688 could serve many purposes, from a possible indicator of depression or other disorders, to a potential monitor of treatment effectiveness in an individual, to providing personalized information prior to treatment about potential therapeutic outcomes. However, as with any newly developed PET tracer, [11C]ABP688 must be properly characterized in humans in order to provide accurate quantification of its target. Therefore, I will define and perform a protocol to characterize [11C]ABP688, which can be generalized to any novel PET ligand. Through the proposed study, structured meetings with my mentors (leaders in the field of PET research of psychiatric patient populations), as well as coursework and regular meetings with project contributors, I will expand my expertise in neurobiology, radiochemistry, PET imaging and analysis, clinical assessment, and affective disorders. In doing so, I will not only enhance the current knowledge of [11C]ABP688 and mGluR5, but also learn a set procedures for developing and using PET tracers that I can employ as an independent investigator. Specifically, I plan to: (1) Determine the optimal modeling techniques and scanning time for [11C]ABP688, to ensure reliable and accurate quantification. Intra- individual binding variation will be established using these optimal methods. (2) Examine methods to calculate a full plasma input function without an arterial line, improving subject comfort and decreasing scan cost. Using mathematical approaches, it may be possible to model arterial input from either venous samples or sinogram data. Eliminating the need for arterial lines may reduce current barriers to widespread PET use in addressing public health issues. (3) Investigate sensitivity of [11C]ABP688 to endogenous glutamate to determine if this ligand can be used to monitor glutamate level variations in neurologic and psychiatric disorders. (4) Compare mGluR5 distribution and density in depressed and control subjects. This will provide insight into the mechanism of mGluR5 dysfunction in depression. The goal of these studies is an increased knowledge of mGluR5 and the development of much needed reliable mGluR5 PET imaging methods.