Orphan peptide and G protein-coupled receptor signalling in alcohol use disorder

被引:1
|
作者
Anversa, Roberta Goncalves [1 ,2 ]
Maddern, Xavier J. [1 ,2 ]
Lawrence, Andrew J. [1 ,2 ]
Walker, Leigh C. [1 ,2 ,3 ]
机构
[1] Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia
[2] Univ Melbourne, Florey Dept Neurosci & Mental Hlth, Melbourne, Vic, Australia
[3] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne Brain Ctr, 30 Royal Parade, Melbourne, Vic 3052, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
alcohol use disorder; CART; GPCR; GPR135; GPR158; GPR26; GPR6; GPR88; neuropeptide; orphan; AMPHETAMINE-REGULATED TRANSCRIPT; CONTEXT-INDUCED REINSTATEMENT; CONCISE GUIDE; MOLECULAR-CLONING; COCAINE; CART; EXPRESSION; GPR139; GENE; IDENTIFICATION;
D O I
10.1111/bph.16301
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Neuropeptides and G protein-coupled receptors (GPCRs) have long been, and continue to be, one of the most popular target classes for drug discovery in CNS disorders, including alcohol use disorder (AUD). Yet, orphaned neuropeptide systems and receptors (oGPCR), which have no known cognate receptor or ligand, remain understudied in drug discovery and development. Orphan neuropeptides and oGPCRs are abundantly expressed within the brain and represent an unprecedented opportunity to address brain function and may hold potential as novel treatments for disease. Here, we describe the current literature regarding orphaned neuropeptides and oGPCRs implicated in AUD. Specifically, in this review, we focus on the orphaned neuropeptide cocaine- and amphetamine-regulated transcript (CART), and several oGPCRs that have been directly implicated in AUD (GPR6, GPR26, GPR88, GPR139, GPR158) and discuss their potential and pitfalls as novel treatments, and progress in identifying their cognate receptors or ligands.
引用
收藏
页码:595 / 609
页数:15
相关论文
共 50 条
  • [1] G protein-coupled receptor signalling in the kidney
    Weiss, RH
    CELLULAR SIGNALLING, 1998, 10 (05) : 313 - 320
  • [2] G protein-coupled receptor signalling mechanisms
    Hill, S. J.
    CALCIFIED TISSUE INTERNATIONAL, 2007, 80 : S19 - S20
  • [3] Targeting G protein-coupled receptor signalling by blocking G proteins
    Campbell, Adrian P.
    Smrcka, Alan V.
    NATURE REVIEWS DRUG DISCOVERY, 2018, 17 (11) : 789 - 803
  • [4] Targeting G protein-coupled receptor signalling by blocking G proteins
    Adrian P. Campbell
    Alan V. Smrcka
    Nature Reviews Drug Discovery, 2018, 17 : 789 - 803
  • [5] Peptide inhibitors of G protein-coupled receptor kinases
    Winstel, R
    Ihlenfeldt, HG
    Jung, G
    Krasel, C
    Lohse, MJ
    BIOCHEMICAL PHARMACOLOGY, 2005, 70 (07) : 1001 - 1008
  • [6] Peptide inhibitors of G protein-coupled receptor kinases
    Winstel, R
    Ihlenfeldt, HG
    Jung, G
    Lohse, MJ
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1998, 357 (04) : R52 - R52
  • [7] The Orphan G Protein-Coupled Receptor 3 Modulates Amyloid-Beta Peptide Generation in Neurons
    Thathiah, Amantha
    Spittaels, Kurt
    Hoffmann, Marcel
    Staes, Mik
    Cohen, Adrian
    Horre, Katrien
    Vanbrabant, Mieke
    Coun, Frea
    Baekelandt, Veerle
    Delacourte, Andre
    Fischer, David F.
    Pollet, Dirk
    De Strooper, Bart
    Merchiers, Pascal
    SCIENCE, 2009, 323 (5916) : 946 - 951
  • [8] G protein-coupled receptor signalling in in vivo cardiac overload
    Rapacciuolo, A
    Esposito, G
    Prasad, SVN
    Rockman, HA
    ACTA PHYSIOLOGICA SCANDINAVICA, 2001, 173 (01): : 51 - 57
  • [9] Novel inverse agonists for the orphan G protein-coupled receptor 6
    Laun, Alyssa S.
    Shrader, Sarah H.
    Song, Zhao-Hui
    HELIYON, 2018, 4 (11):
  • [10] The physiological response to cardiovascular 'orphan' G protein-coupled receptor agonists
    Joshua M. Hare
    David A. Kass
    Jonathan S. Stamler
    Nature Medicine, 1999, 5 : 1241 - 1242