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Pain Rep. 2018 Apr 06;3(3):e650. doi: 10.1097/PR9.0000000000000650. eCollection 2018 May.

Biased agonism: the quest for the analgesic holy grail.

Pain reports

M Alexander Stanczyk, Ram Kandasamy

Affiliations

  1. Department of Pharmacology and Edward F. Domino Research Center, University of Michigan Medical School, Ann Arbor, MI, USA.

PMID: 29922742 PMCID: PMC5999417 DOI: 10.1097/PR9.0000000000000650

Abstract

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.

Keywords: Bias; Functional selectivity; Opioid; Signaling

Conflict of interest statement

Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.

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