DePasquale Olivia, O'Brien Chris, Gordon Baila, Barker David J
Department of Psychology, Rutgers, The State University of New Jersey, 152 Frelinghuysen Road, Piscataway, New Jersey 08854, United States.
Brain Health Institute, Rutgers University, Piscataway, New Jersey 08854, United States.
ACS Chem Neurosci. 2025 May 7;16(9):1639-1646. doi: 10.1021/acschemneuro.4c00780. Epub 2025 Apr 28.
G protein-coupled receptors (GPCRs) are among the most prominent druggable targets in the human genome, accounting for approximately 40% of marketed drugs. Despite this, current GPCR-targeted therapies address only about 10% of the GPCRs encoded in the genome. Expanding our knowledge of the remaining "orphan" GPCRs represents a critical frontier in drug discovery. GPR151 emerges as a compelling target due to its distinct expression in the habenula complex, spinal cord neurons, and dorsal root ganglia. This receptor is highly conserved across mammals and possesses orthologs in species such as zebrafish and chickens, underscoring its evolutionarily conserved role in fundamental mammalian processes. Although the precise function of GPR151 remains unknown, it has been strongly implicated in pain modulation and reward-seeking behavior. These attributes position GPR151 as a promising candidate for the development of targeted and specialized pharmacological therapies. This review summarizes the current literature on GPR151, including its discovery, structure, mechanisms, anatomical distribution, and functional roles, while also exploring potential directions for future research.
G蛋白偶联受体(GPCRs)是人类基因组中最主要的可成药靶点之一,约占已上市药物的40%。尽管如此,目前针对GPCR的疗法仅针对基因组中约10%的GPCR编码基因。拓展我们对其余“孤儿”GPCR的认识是药物研发的一个关键前沿领域。GPR151因其在缰核复合体、脊髓神经元和背根神经节中的独特表达而成为一个引人注目的靶点。该受体在哺乳动物中高度保守,在斑马鱼和鸡等物种中也有直系同源物,这突出了其在基本哺乳动物过程中进化保守的作用。尽管GPR151的确切功能尚不清楚,但它与疼痛调节和奖赏寻求行为密切相关。这些特性使GPR151成为开发靶向和特殊药物疗法的一个有前景的候选靶点。本综述总结了目前关于GPR151的文献,包括其发现、结构、机制、解剖分布和功能作用,同时也探讨了未来研究的潜在方向。