The role of orphan G protein-coupled receptors in pain

• Published in: Heliyon Vol. 10; no. 7; p. e28818
• Main Authors: Xu, Chengfei, Wang, Yahui, Ni, Huadong, Yao, Ming, Cheng, Liang, Lin, Xuewu
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 15.04.2024; Elsevier
• Subjects: Endogenous ligand; G protein-coupled receptor; Monoclonal antibody; Orphan G protein-coupled receptor; Pain; Review; Rodents; G protein-coupled receptor; Orphan G protein-coupled receptor; Pain; Monoclonal antibody; Endogenous ligand; Rodents
• ISSN: 2405-8440; 2405-8440
• DOI: 10.1016/j.heliyon.2024.e28818

G protein-coupled receptors (GPCRs), which form the largest family of membrane protein receptors in humans, are highly complex signaling systems with intricate structures and dynamic conformations and locations. Among these receptors, a specific subset is referred to as orphan GPCRs (oGPCRs) and has garnered significant interest in pain research due to their role in both central and peripheral nervous system function. The diversity of GPCR functions is attributed to multiple factors, including allosteric modulators, signaling bias, oligomerization, constitutive signaling, and compartmentalized signaling. This review primarily focuses on the recent advances in oGPCR research on pain mechanisms, discussing the role of specific oGPCRs including GPR34, GPR37, GPR65, GPR83, GPR84, GPR85, GPR132, GPR151, GPR160, GPR171, GPR177, and GPR183. The orphan receptors among these receptors associated with central nervous system diseases are also briefly described. Understanding the functions of these oGPCRs can contribute not only to a deeper understanding of pain mechanisms but also offer a reference for discovering new targets for pain treatment.