Department of Medicinal Chemistry, Jiangsu Key Laboratory of Neuropsychiatric Diseases and College of Pharmaceutical Sciences , Soochow University , Suzhou , Jiangsu 215123 , China.
Department of Pharmacology and Toxicology, Center for Addiction Research , University of Texas Medical Branch , Galveston , Texas 77555 , United States.
ACS Chem Neurosci. 2019 Jan 16;10(1):190-200. doi: 10.1021/acschemneuro.8b00572. Epub 2018 Dec 20.
Although G protein-coupled receptors (GPCRs) are recognized as pivotal drug targets involved in multiple physiological and pathological processes, the majority of GPCRs including orphan GPCRs (oGPCRs) are unexploited. GPR88, a brain-specific oGPCR with particularly robust expression in the striatum, regulates diverse brain and behavioral functions, including cognition, mood, movement control, and reward-based learning, and is thus emerging as a novel drug target for central nervous system disorders including schizophrenia, Parkinson's disease, anxiety, and addiction. Nevertheless, no effective GPR88 synthetic ligands have yet entered into clinical trials, and GPR88 endogenous ligands remain unknown. Despite the recent discovery and early stage study of several GPR88 agonists, such as 2-PCCA, RTI-13951-33, and phenylglycinol derivatives, further research into GPR88 pharmacology, medicinal chemistry, and chemical biology is urgently needed to yield structurally diversified GPR88-specific ligands. Drug-like pharmacological tool function and relevant signaling elucidation will also accelerate the evaluation of this receptor as a viable neurotherapeutic target.
尽管 G 蛋白偶联受体 (GPCRs) 被认为是参与多种生理和病理过程的关键药物靶点,但包括孤儿 GPCRs (oGPCRs) 在内的大多数 GPCRs 尚未得到开发。GPR88 是一种大脑特异性的 oGPCR,在纹状体中表达特别丰富,调节多种大脑和行为功能,包括认知、情绪、运动控制和基于奖励的学习,因此作为治疗包括精神分裂症、帕金森病、焦虑和成瘾在内的中枢神经系统疾病的新型药物靶点而备受关注。然而,目前尚无有效的 GPR88 合成配体进入临床试验,GPR88 的内源性配体也尚未被发现。尽管最近发现并初步研究了几种 GPR88 激动剂,如 2-PCCA、RTI-13951-33 和苯甘氨酸衍生物,但仍迫切需要进一步研究 GPR88 的药理学、药物化学和化学生物学,以产生结构多样化的 GPR88 特异性配体。具有类似药物性质的药理学工具功能和相关信号转导的阐明也将加速评估该受体作为可行的神经治疗靶点的进程。