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GPR139,一种古老的受体,也是神经精神和行为障碍的新兴靶点。

GPR139, an Ancient Receptor and an Emerging Target for Neuropsychiatric and Behavioral Disorders.

作者信息

Chan Minyu, Ogawa Satoshi

机构信息

Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Jalan Lagoon Selatan, Bandar Sunway, 47500, Subang Jaya, Selangor, Malaysia.

出版信息

Mol Neurobiol. 2025 Mar 18. doi: 10.1007/s12035-025-04828-2.

Abstract

GPR139 is an orphan G-protein-coupled receptor that is predominantly expressed in several midbrain regions, e.g., the habenula, striatum, and hypothalamus. GPR139 gene is highly conserved across vertebrate phylogenetic taxa, suggesting its fundamental importance in neurophysiology. Evidence from both animal studies and human genetic association studies has demonstrated that dysregulation of GPR139 expression and function is linked to aberrant behaviors, cognitive deficits, alterations in sleep and alertness, and substance abuse and withdrawal. Animal knockout models suggest that GPR139 plays an anti-opioid role by modulating the signaling activity of the μ-opioid receptor (MOR), as well as the intensity of withdrawal symptoms and nociception in behavioral paradigms. Modulation of GPR139 activity by surrogate agonists such as TAK-041 and JNJ-63533054 has shown promising results in experimental models; however, the use of TAK-041 in clinical trials has produced heterogeneous effects and has not met the intended primary endpoint. Here, we highlight current in vitro and in vivo studies of GPR139, its potential physiological roles, and therapeutic potential in the pathophysiology of neuropsychiatric and behavioral disorders. This review aims to focus on the current knowledge gaps to facilitate future studies that will contribute to the understanding of GPR139 as a therapeutic target for neuropsychiatric and behavioral disorders.

摘要

GPR139是一种孤儿G蛋白偶联受体,主要在几个中脑区域表达,例如缰核、纹状体和下丘脑。GPR139基因在脊椎动物系统发育类群中高度保守,表明其在神经生理学中具有根本重要性。动物研究和人类基因关联研究的证据均表明,GPR139表达和功能的失调与异常行为、认知缺陷、睡眠和警觉性改变以及药物滥用和戒断有关。动物基因敲除模型表明,GPR139通过调节μ阿片受体(MOR)的信号活性以及行为范式中戒断症状和痛觉的强度发挥抗阿片作用。在实验模型中,使用TAK - 041和JNJ - 63533054等替代激动剂调节GPR139活性已显示出有前景的结果;然而,TAK - 041在临床试验中的使用产生了异质性影响,且未达到预期的主要终点。在此,我们重点介绍目前关于GPR139的体外和体内研究、其潜在的生理作用以及在神经精神和行为障碍病理生理学中的治疗潜力。本综述旨在关注当前的知识空白,以促进未来的研究,这些研究将有助于将GPR139理解为神经精神和行为障碍的治疗靶点。

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