Suppr超能文献

孤儿受体 GPR88 作为一种新兴的神经治疗靶点。

Orphan Receptor GPR88 as an Emerging Neurotherapeutic Target.

机构信息

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.

出版信息

ACS Chem Neurosci. 2019 Jan 16;10(1):190-200. doi: 10.1021/acschemneuro.8b00572. Epub 2018 Dec 20.

Abstract

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.

摘要

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。

相似文献

1
Orphan Receptor GPR88 as an Emerging Neurotherapeutic Target.
ACS Chem Neurosci. 2019 Jan 16;10(1):190-200. doi: 10.1021/acschemneuro.8b00572. Epub 2018 Dec 20.
4
Effect of Substitution on the Aniline Moiety of the GPR88 Agonist 2-PCCA: Synthesis, Structure-Activity Relationships, and Molecular Modeling Studies.
ACS Chem Neurosci. 2016 Oct 19;7(10):1418-1432. doi: 10.1021/acschemneuro.6b00182. Epub 2016 Aug 16.
5
The GPR88 receptor agonist 2-PCCA does not alter the behavioral effects of methamphetamine in rats.
Eur J Pharmacol. 2013 Jan 5;698(1-3):272-7. doi: 10.1016/j.ejphar.2012.10.037. Epub 2012 Nov 2.
6
Orphan receptor GPR88 as a potential therapeutic target for CNS disorders - an approach.
J Biomol Struct Dyn. 2024 Jun;42(9):4745-4758. doi: 10.1080/07391102.2023.2222820. Epub 2023 Jun 12.
7
Activation and allosteric regulation of the orphan GPR88-Gi1 signaling complex.
Nat Commun. 2022 May 2;13(1):2375. doi: 10.1038/s41467-022-30081-5.
8
Orphan peptide and G protein-coupled receptor signalling in alcohol use disorder.
Br J Pharmacol. 2024 Mar;181(5):595-609. doi: 10.1111/bph.16301. Epub 2024 Jan 8.
10
Discovery of a Potent, Selective, and Brain-Penetrant Small Molecule that Activates the Orphan Receptor GPR88 and Reduces Alcohol Intake.
J Med Chem. 2018 Aug 9;61(15):6748-6758. doi: 10.1021/acs.jmedchem.8b00566. Epub 2018 Jul 30.

引用本文的文献

1
Perinatal fentanyl exposure drives enduring addiction risk and central amygdala gene dysregulation.
Neuropharmacology. 2025 Nov 1;278:110581. doi: 10.1016/j.neuropharm.2025.110581. Epub 2025 Jun 27.
2
Perinatal Fentanyl Exposure Drives Enduring Addiction Risk and Central Amygdala Gene Dysregulation.
bioRxiv. 2025 May 25:2025.05.20.655167. doi: 10.1101/2025.05.20.655167.
3
4
Persistent changes in nociceptor translatomes govern hyperalgesic priming in mouse models.
bioRxiv. 2024 Aug 8:2024.08.07.606891. doi: 10.1101/2024.08.07.606891.
5
Exploring orphan GPCRs in neurodegenerative diseases.
Front Pharmacol. 2024 Jun 4;15:1394516. doi: 10.3389/fphar.2024.1394516. eCollection 2024.
6
Discovery of 3-((4-Benzylpyridin-2-yl)amino)benzamides as Potent GPR52 G Protein-Biased Agonists.
J Med Chem. 2024 Jun 13;67(11):9709-9730. doi: 10.1021/acs.jmedchem.4c00856. Epub 2024 May 24.
7
Orphan GPR52 as an emerging neurotherapeutic target.
Drug Discov Today. 2024 Apr;29(4):103922. doi: 10.1016/j.drudis.2024.103922. Epub 2024 Feb 20.
9
Orphan G Protein-Coupled Receptor GPR37 as an Emerging Therapeutic Target.
ACS Chem Neurosci. 2023 Sep 20;14(18):3318-3334. doi: 10.1021/acschemneuro.3c00479. Epub 2023 Sep 7.
10
Improvement of the Metabolic Stability of GPR88 Agonist RTI-13951-33: Design, Synthesis, and Biological Evaluation.
J Med Chem. 2023 Feb 23;66(4):2964-2978. doi: 10.1021/acs.jmedchem.2c01983. Epub 2023 Feb 7.

本文引用的文献

1
Allosteric Modulation of Class A GPCRs: Targets, Agents, and Emerging Concepts.
J Med Chem. 2019 Jan 10;62(1):88-127. doi: 10.1021/acs.jmedchem.8b00875. Epub 2018 Aug 28.
2
Discovery of a Potent, Selective, and Brain-Penetrant Small Molecule that Activates the Orphan Receptor GPR88 and Reduces Alcohol Intake.
J Med Chem. 2018 Aug 9;61(15):6748-6758. doi: 10.1021/acs.jmedchem.8b00566. Epub 2018 Jul 30.
3
Increased Alcohol Seeking in Mice Lacking Gpr88 Involves Dysfunctional Mesocorticolimbic Networks.
Biol Psychiatry. 2018 Aug 1;84(3):202-212. doi: 10.1016/j.biopsych.2018.01.026. Epub 2018 Feb 9.
4
Small Molecule Allosteric Modulators of G-Protein-Coupled Receptors: Drug-Target Interactions.
J Med Chem. 2019 Jan 10;62(1):24-45. doi: 10.1021/acs.jmedchem.7b01844. Epub 2018 Feb 26.
5
Current and Future Challenges in GPCR Drug Discovery.
Methods Mol Biol. 2018;1705:1-21. doi: 10.1007/978-1-4939-7465-8_1.
6
Trends in GPCR drug discovery: new agents, targets and indications.
Nat Rev Drug Discov. 2017 Dec;16(12):829-842. doi: 10.1038/nrd.2017.178. Epub 2017 Oct 27.
7
How Ligands Illuminate GPCR Molecular Pharmacology.
Cell. 2017 Jul 27;170(3):414-427. doi: 10.1016/j.cell.2017.07.009.
8
Striatal GPR88 Modulates Foraging Efficiency.
J Neurosci. 2017 Aug 16;37(33):7939-7947. doi: 10.1523/JNEUROSCI.2439-16.2017. Epub 2017 Jul 20.
10
Design, synthesis and pharmacological evaluation of 4-hydroxyphenylglycine and 4-hydroxyphenylglycinol derivatives as GPR88 agonists.
Bioorg Med Chem. 2017 Jan 15;25(2):805-812. doi: 10.1016/j.bmc.2016.11.058. Epub 2016 Dec 1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验