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Biased agonism: the quest for the analgesic holy grail

Opioids alleviate pain, but adverse effects severely limit their usefulness. To solve this problem, biased ligands favoring 1 signaling pathway downstream of the μ-opioid receptor over another are being developed. In the target article, the authors synthesize compounds that preferentially activate G...

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Detalles Bibliográficos
Autores principales: Stanczyk, M. Alexander, Kandasamy, Ram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999417/
https://www.ncbi.nlm.nih.gov/pubmed/29922742
http://dx.doi.org/10.1097/PR9.0000000000000650
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author Stanczyk, M. Alexander
Kandasamy, Ram
author_facet Stanczyk, M. Alexander
Kandasamy, Ram
author_sort Stanczyk, M. Alexander
collection PubMed
description Opioids alleviate pain, but adverse effects severely limit their usefulness. To solve this problem, biased ligands favoring 1 signaling pathway downstream of the μ-opioid receptor over another are being developed. In the target article, the authors synthesize compounds that preferentially activate G-protein or β-arrestin signaling. They find that increased bias towards G-protein signaling produces better antinociception with minimal side effects in mice models. G-protein–biased opioids may provide a safer treatment strategy.
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spelling pubmed-59994172018-06-19 Biased agonism: the quest for the analgesic holy grail Stanczyk, M. Alexander Kandasamy, Ram Pain Rep Journal Club Opioids alleviate pain, but adverse effects severely limit their usefulness. To solve this problem, biased ligands favoring 1 signaling pathway downstream of the μ-opioid receptor over another are being developed. In the target article, the authors synthesize compounds that preferentially activate G-protein or β-arrestin signaling. They find that increased bias towards G-protein signaling produces better antinociception with minimal side effects in mice models. G-protein–biased opioids may provide a safer treatment strategy. Wolters Kluwer 2018-04-06 /pmc/articles/PMC5999417/ /pubmed/29922742 http://dx.doi.org/10.1097/PR9.0000000000000650 Text en Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The International Association for the Study of Pain. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Journal Club
Stanczyk, M. Alexander
Kandasamy, Ram
Biased agonism: the quest for the analgesic holy grail
title Biased agonism: the quest for the analgesic holy grail
title_full Biased agonism: the quest for the analgesic holy grail
title_fullStr Biased agonism: the quest for the analgesic holy grail
title_full_unstemmed Biased agonism: the quest for the analgesic holy grail
title_short Biased agonism: the quest for the analgesic holy grail
title_sort biased agonism: the quest for the analgesic holy grail
topic Journal Club
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999417/
https://www.ncbi.nlm.nih.gov/pubmed/29922742
http://dx.doi.org/10.1097/PR9.0000000000000650
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