Rimonabant, a potent CB1 cannabinoid receptor antagonist, is a Gαi/o protein inhibitor

Content Provider	Scilit
Author	Porcu, Alessandra Melis, Miriam Turecek, Rostislav Ullrich, Celine Mocci, Ignazia Bettler, Bernhard Gessa, Gian Luigi Castelli, M. Paola
Copyright Year	2018
Description	Journal: Neuropharmacology Rimonabant is a potent and selective cannabinoid CB1 receptor antagonist widely used in animal and clinical studies. Besides its antagonistic properties, numerous studies have shown that, at micromolar concentrations rimonabant behaves as an inverse agonist at CB1 receptors. The mechanism underpinning this activity is unclear. Here we show that micromolar concentrations of rimonabant inhibited Gα-type G proteins, resulting in a receptor-independent block of G protein signaling. Accordingly, rimonabant decreased basal and agonist stimulated [S]GTPγS binding to cortical membranes of CB1- and GABA-receptor KO mice and Chinese Hamster Ovary (CHO) cell membranes stably transfected with GABA or D2 dopamine receptors. The structural analog of rimonabant, AM251, decreased basal and baclofen-stimulated GTPγS binding to rat cortical and CHO cell membranes expressing GABA receptors. Rimonabant prevented G protein-mediated GABA and D2 dopamine receptor signaling to adenylyl cyclase in Human Embryonic Kidney 293 cells and to G protein-coupled inwardly rectifying K channels (GIRK) in midbrain dopamine neurons of CB1 KO mice. Rimonabant suppressed GIRK gating induced by GTPγS in CHO cells transfected with GIRK, consistent with a receptor-independent action. Bioluminescent resonance energy transfer (BRET) measurements in living CHO cells showed that, in presence or absence of co-expressed GABA receptors, rimonabant stabilized the heterotrimeric Gαi/o-protein complex and prevented conformational rearrangements induced by GABA receptor activation. Rimonabant failed to inhibit Gαs-mediated signaling, supporting its specificity for Gα-type G proteins. The inhibition of Gα protein provides a new site of rimonabant action that may help to understand its pharmacological and toxicological effects occurring at high concentrations.
Related Links	https://edoc.unibas.ch/76138/1/20200327102017_5e7dc55116042.pdf
Ending Page	120
Page Count	14
Starting Page	107
ISSN	00283908
e-ISSN	18737064
DOI	10.1016/j.neuropharm.2018.01.024
Journal	Neuropharmacology
Volume Number	133
Language	English
Publisher	Elsevier BV
Publisher Date	2018-05-01
Access Restriction	Open
Subject Keyword	Journal: Neuropharmacology Biochemistry and Molecular Biology Bioluminescence Resonance Energy Transfer (bret) Cb1-receptor Antagonist Cannabinoid Receptor Type 1 (cb1) G Protein G Protein-coupled Receptor (gpcr) Inverse Agonist
Content Type	Text
Resource Type	Article
Subject	Pharmacology Cellular and Molecular Neuroscience