Cargando…
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...
Autores principales: | , |
---|---|
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 |
_version_ | 1783331418351337472 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5999417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT stanczykmalexander biasedagonismthequestfortheanalgesicholygrail AT kandasamyram biasedagonismthequestfortheanalgesicholygrail |