Literature DB >> 23663971

Disease-specific heteromerization of G-protein-coupled receptors that target drugs of abuse.

Ivone Gomes1, Wakako Fujita, Moraje V Chandrakala, Lakshmi A Devi.   

Abstract

Drugs of abuse such as morphine or marijuana exert their effects through the activation of G-protein-coupled receptors (GPCRs), the opioid and cannabinoid receptors, respectively. Moreover, interactions between either of these receptors have been shown to be involved in the rewarding effects of drugs of abuse. Recent advances in the field, using a variety of approaches, have demonstrated that many GPCRs, including opioid, cannabinoid, and dopamine receptors, can form associations between different receptor subtypes or with other GPCRs to form heteromeric complexes. The formation of these complexes, in turn, leads to the modulation of the properties of individual protomers. The development of tools that can selectively disrupt GPCR heteromers as well as monoclonal antibodies that can selectively block signaling by specific heteromer pairs has indicated that heteromers involving opioid, cannabinoid, or dopamine receptors may play a role in various disease states. In this review, we describe evidence for opioid, cannabinoid, and dopamine receptor heteromerization and the potential role of GPCR heteromers in pathophysiological conditions.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23663971      PMCID: PMC3973131          DOI: 10.1016/B978-0-12-386931-9.00009-X

Source DB:  PubMed          Journal:  Prog Mol Biol Transl Sci        ISSN: 1877-1173            Impact factor:   3.622


  294 in total

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3.  Heterodimerization of human apelin and kappa opioid receptors: roles in signal transduction.

Authors:  Yalin Li; Jing Chen; Bo Bai; Hui Du; Youwang Liu; Haiqing Liu
Journal:  Cell Signal       Date:  2011-12-20       Impact factor: 4.315

4.  Effects of D1 and D2 dopamine receptor antagonists on cocaine-induced self-stimulation and locomotor activity in rats.

Authors:  K Kita; T Shiratani; K Takenouchi; H Fukuzako; M Takigawa
Journal:  Eur Neuropsychopharmacol       Date:  1999-01       Impact factor: 4.600

5.  Antiparkinsonian effect of a new selective adenosine A2A receptor antagonist in MPTP-treated monkeys.

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Journal:  Neurology       Date:  1999-05-12       Impact factor: 9.910

6.  Catalepsy induced by a blockade of dopamine D1 or D2 receptors was reversed by a concomitant blockade of adenosine A(2A) receptors in the caudate-putamen of rats.

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Journal:  Eur J Neurosci       Date:  2001-10       Impact factor: 3.386

Review 7.  The peripheral cannabinoid receptor knockout mice: an update.

Authors:  N E Buckley
Journal:  Br J Pharmacol       Date:  2007-10-29       Impact factor: 8.739

8.  Neurokinin 1 receptors regulate morphine-induced endocytosis and desensitization of mu-opioid receptors in CNS neurons.

Authors:  Y Joy Yu; Seksiri Arttamangkul; Christopher J Evans; John T Williams; Mark von Zastrow
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9.  Dopamine D1 and D2 receptor Co-activation generates a novel phospholipase C-mediated calcium signal.

Authors:  Samuel P Lee; Christopher H So; Asim J Rashid; George Varghese; Regina Cheng; A José Lança; Brian F O'Dowd; Susan R George
Journal:  J Biol Chem       Date:  2004-05-24       Impact factor: 5.157

10.  The interaction between dopamine D2-like and beta-adrenergic receptors in the prefrontal cortex is altered by mood-stabilizing agents.

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  17 in total

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Review 2.  Heteromers of μ-δ opioid receptors: new pharmacology and novel therapeutic possibilities.

Authors:  Wakako Fujita; Ivone Gomes; Lakshmi A Devi
Journal:  Br J Pharmacol       Date:  2014-07-01       Impact factor: 8.739

Review 3.  G protein-coupled receptor oligomerization revisited: functional and pharmacological perspectives.

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Review 4.  Revolution in GPCR signalling: opioid receptor heteromers as novel therapeutic targets: IUPHAR review 10.

Authors:  Wakako Fujita; Ivone Gomes; Lakshmi A Devi
Journal:  Br J Pharmacol       Date:  2014-09       Impact factor: 8.739

5.  The bivalent ligand MCC22 potently attenuates hyperalgesia in a mouse model of cisplatin-evoked neuropathic pain without tolerance or reward.

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6.  Targeting MOR-mGluR5 heteromers reduces bone cancer pain by activating MOR and inhibiting mGluR5.

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7.  Detection of Receptor Heteromerization Using In Situ Proximity Ligation Assay.

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Journal:  Curr Protoc Pharmacol       Date:  2016-12-13

8.  Bivalent ligand MCC22 potently attenuates nociception in a murine model of sickle cell disease.

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9.  The bivalent ligand, MMG22, reduces neuropathic pain after nerve injury without the side effects of traditional opioids.

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Review 10.  Cannabinoid-hypocretin cross-talk in the central nervous system: what we know so far.

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