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Cannabinoid CB(1) and CB(2) Receptor Signaling and Bias

An agonist that acts through a single receptor can activate numerous signaling pathways. Recent studies have suggested that different ligands can differentially activate these pathways by stabilizing a limited range of receptor conformations, which in turn preferentially drive different downstream s...

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Detalles Bibliográficos
Autores principales: Ibsen, Mikkel Søes, Connor, Mark, Glass, Michelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436336/
https://www.ncbi.nlm.nih.gov/pubmed/28861504
http://dx.doi.org/10.1089/can.2016.0037
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author Ibsen, Mikkel Søes
Connor, Mark
Glass, Michelle
author_facet Ibsen, Mikkel Søes
Connor, Mark
Glass, Michelle
author_sort Ibsen, Mikkel Søes
collection PubMed
description An agonist that acts through a single receptor can activate numerous signaling pathways. Recent studies have suggested that different ligands can differentially activate these pathways by stabilizing a limited range of receptor conformations, which in turn preferentially drive different downstream signaling cascades. This concept, termed “biased signaling” represents an exciting therapeutic opportunity to target specific pathways that elicit only desired effects, while avoiding undesired effects mediated by different signaling cascades. The cannabinoid receptors CB(1) and CB(2) each activate multiple pathways, and evidence is emerging for bias within these pathways. This review will summarize the current evidence for biased signaling through cannabinoid receptor subtypes CB(1) and CB(2).
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spelling pubmed-54363362017-08-31 Cannabinoid CB(1) and CB(2) Receptor Signaling and Bias Ibsen, Mikkel Søes Connor, Mark Glass, Michelle Cannabis Cannabinoid Res Mini-Review An agonist that acts through a single receptor can activate numerous signaling pathways. Recent studies have suggested that different ligands can differentially activate these pathways by stabilizing a limited range of receptor conformations, which in turn preferentially drive different downstream signaling cascades. This concept, termed “biased signaling” represents an exciting therapeutic opportunity to target specific pathways that elicit only desired effects, while avoiding undesired effects mediated by different signaling cascades. The cannabinoid receptors CB(1) and CB(2) each activate multiple pathways, and evidence is emerging for bias within these pathways. This review will summarize the current evidence for biased signaling through cannabinoid receptor subtypes CB(1) and CB(2). Mary Ann Liebert, Inc. 2017-03-01 /pmc/articles/PMC5436336/ /pubmed/28861504 http://dx.doi.org/10.1089/can.2016.0037 Text en © Mikkel Søes Ibsen et al. 2017; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Mini-Review
Ibsen, Mikkel Søes
Connor, Mark
Glass, Michelle
Cannabinoid CB(1) and CB(2) Receptor Signaling and Bias
title Cannabinoid CB(1) and CB(2) Receptor Signaling and Bias
title_full Cannabinoid CB(1) and CB(2) Receptor Signaling and Bias
title_fullStr Cannabinoid CB(1) and CB(2) Receptor Signaling and Bias
title_full_unstemmed Cannabinoid CB(1) and CB(2) Receptor Signaling and Bias
title_short Cannabinoid CB(1) and CB(2) Receptor Signaling and Bias
title_sort cannabinoid cb(1) and cb(2) receptor signaling and bias
topic Mini-Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436336/
https://www.ncbi.nlm.nih.gov/pubmed/28861504
http://dx.doi.org/10.1089/can.2016.0037
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