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Arg-Phe-酰胺肽 26RFa/谷氨酰胺 RF-酰胺肽及其受体:IUPHAR 评论 24。

The Arg-Phe-amide peptide 26RFa/glutamine RF-amide peptide and its receptor: IUPHAR Review 24.

机构信息

INSERM U1239, Laboratory of Neuronal and Neuroendocrine Differentiation and Communication, Normandy University, Rouen, France.

CNS Drug Discovery, Arena Pharmaceuticals Inc., San Diego, CA, USA.

出版信息

Br J Pharmacol. 2017 Oct;174(20):3573-3607. doi: 10.1111/bph.13907. Epub 2017 Sep 8.

Abstract

The RFamide neuropeptide 26RFa was first isolated from the brain of the European green frog on the basis of cross-reactivity with antibodies raised against bovine neuropeptide FF (NPFF). 26RFa and its N-terminally extended form glutamine RF-amide peptide (QRFP) have been identified as cognate ligands of the former orphan receptor GPR103, now renamed glutamine RF-amide peptide receptor (QRFP receptor). The 26RFa/QRFP precursor has been characterized in various mammalian and non-mammalian species. In the brain of mammals, including humans, 26RFa/QRFP mRNA is almost exclusively expressed in hypothalamic nuclei. The 26RFa/QRFP transcript is also present in various organs especially in endocrine glands. While humans express only one QRFP receptor, two isoforms are present in rodents. The QRFP receptor genes are widely expressed in the CNS and in peripheral tissues, notably in bone, heart, kidney, pancreas and testis. Structure-activity relationship studies have led to the identification of low MW peptidergic agonists and antagonists of QRFP receptor. Concurrently, several selective non-peptidic antagonists have been designed from high-throughput screening hit optimization. Consistent with the widespread distribution of QRFP receptor mRNA and 26RFa binding sites, 26RFa/QRFP exerts a large range of biological activities, notably in the control of energy homeostasis, bone formation and nociception that are mediated by QRFP receptor or NPFF2. The present report reviews the current knowledge concerning the 26RFa/QRFP-QRFP receptor system and discusses the potential use of selective QRFP receptor ligands for therapeutic applications.

摘要

RFamide 神经肽 26RFa 最初是根据与牛神经肽 FF (NPFF) 抗体的交叉反应性从欧洲绿蛙脑中分离出来的。26RFa 和其 N 端延伸形式谷氨酸 RF-酰胺肽 (QRFP) 已被鉴定为前孤儿受体 GPR103 的同源配体,现在该受体被重新命名为谷氨酸 RF-酰胺肽受体 (QRFP 受体)。在各种哺乳动物和非哺乳动物物种中,已经对 26RFa/QRFP 前体进行了表征。在哺乳动物的大脑中,包括人类,26RFa/QRFP mRNA 几乎仅在下丘脑核中表达。26RFa/QRFP 转录本也存在于各种器官中,特别是在内分泌腺中。虽然人类只表达一种 QRFP 受体,但在啮齿动物中存在两种同工型。QRFP 受体基因在中枢神经系统和外周组织中广泛表达,特别是在骨骼、心脏、肾脏、胰腺和睾丸中。结构-活性关系研究导致了 QRFP 受体的低分子量肽激动剂和拮抗剂的鉴定。同时,从高通量筛选命中优化设计了几种选择性非肽拮抗剂。与 QRFP 受体 mRNA 和 26RFa 结合位点的广泛分布一致,26RFa/QRFP 发挥了广泛的生物学活性,特别是在能量平衡、骨形成和伤害感受的控制中,这些活性由 QRFP 受体或 NPFF2 介导。本报告回顾了关于 26RFa/QRFP-QRFP 受体系统的当前知识,并讨论了选择性 QRFP 受体配体在治疗应用中的潜在用途。

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