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评估 [¹⁸F]MK-0911,一种正电子发射断层扫描(PET)示踪剂,用于阿片受体样 1(ORL1),在恒河猴和人类中的应用。

Evaluation of [¹⁸F]MK-0911, a positron emission tomography (PET) tracer for opioid receptor-like 1 (ORL1), in rhesus monkey and human.

机构信息

Imaging, Merck Research Laboratories, West Point, PA 19486, USA.

出版信息

Neuroimage. 2013 Mar;68:1-10. doi: 10.1016/j.neuroimage.2012.11.053. Epub 2012 Dec 11.

Abstract

Antagonism of the central opioid receptor like-1 receptor (ORL1) has been implicated in cognition, and has been a focus of drug discovery efforts to ameliorate the cognitive deficits that remain during the stable treatment of schizophrenia with current antipsychotics. In order to facilitate dose selection for phase II clinical testing an ORL1-specific PET tracer was developed to determine drug plasma concentration versus occupancy relationships in order to ensure that the doses selected and the degree of target engagement were sufficient to ensure adequate proof of concept testing. MK-0911 is a selective, high affinity antagonist for the ORL1 receptor radiolabeled with high specific activity (18)F for positron emission tomography (PET) studies. Evaluation of [(18)F]MK-0911 in rhesus monkey PET studies showed a pattern of brain uptake which was consistent with the known distribution of ORL1. In vitro autoradiography with [(18)F]MK-0911 in rhesus monkey and human brain tissue slices showed a regional distribution that was consistent with in vivo imaging results in monkey. Pre-treatment of rhesus monkeys with high doses of structurally diverse ORL1 antagonists MK-0584, MK-0337, or MK-5757 achieved blockade of [(18)F]MK-0911 in all gray matter regions. Baseline PET studies with [(18)F]MK-0911 in healthy human subjects showed tracer distribution and kinetics similar to that observed in rhesus monkey. Quantification of [(18)F]MK-0911 uptake in repeat human baseline PET studies showed a test-retest variability in volume of distribution (V(T)) averaging 3% across brain regions. Humans dosed orally with MK-5757 showed reduced [(18)F]MK-0911 tracer concentration in brain proportional with MK-5757 dose and plasma level. [(18)F]MK-0911 was useful for determining MK-5757-induced receptor occupancy of ORL1 to guide MK-5757 dose-selection for clinical proof-of-concept studies. Additionally, [(18)F]MK-0911 may be a useful tool for studying the pharmacology of ORL1 in various human populations and disease states.

摘要

拮抗中枢阿片受体样 1 受体 (ORL1) 已被认为与认知有关,并且一直是药物发现工作的重点,旨在改善当前抗精神病药物稳定治疗期间仍存在的认知缺陷。为了便于进行 II 期临床测试的剂量选择,开发了一种 ORL1 特异性 PET 示踪剂,以确定药物血浆浓度与占有率之间的关系,以确保选择的剂量和目标占有率足以确保充分的概念验证测试。MK-0911 是一种选择性、高亲和力的 ORL1 受体拮抗剂,用高比活度 (18)F 放射性标记,用于正电子发射断层扫描 (PET) 研究。在恒河猴 PET 研究中评估 [(18)F]MK-0911 表明,脑摄取模式与 ORL1 的已知分布一致。在恒河猴和人脑组织切片中用 [(18)F]MK-0911 进行的体外放射自显影显示,区域分布与猴体内成像结果一致。用高剂量结构多样的 ORL1 拮抗剂 MK-0584、MK-0337 或 MK-5757 预处理恒河猴可实现所有灰质区域 [(18)F]MK-0911 的阻断。在健康人类受试者中进行的 [(18)F]MK-0911 基线 PET 研究显示,示踪剂分布和动力学与在恒河猴中观察到的相似。在重复的人类基线 PET 研究中对 [(18)F]MK-0911 摄取进行定量,显示脑内分布容积 (V(T)) 的测试-再测试变异性平均为 3%,分布于各个脑区。口服给予 MK-5757 的人类显示,[(18)F]MK-0911 示踪剂在脑中的浓度与 MK-5757 剂量和血浆水平成比例降低。[(18)F]MK-0911 可用于确定 MK-5757 诱导的 ORL1 受体占有率,以指导用于临床概念验证研究的 MK-5757 剂量选择。此外,[(18)F]MK-0911 可能是研究各种人类人群和疾病状态下 ORL1 药理学的有用工具。

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