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Assessment of the potential of novel and classical opioids to induce respiratory depression in mice

Hill, Rob; Sanchez, Julie; Lemel, Laura; Antonijevic, Mirjana; Hosking, Yselkla; Mistry, Shailesh N.; Kruegel, Andrew C.; Javitch, Jonathan A.; Lane, J. Robert; Canals, Meritxell

Assessment of the potential of novel and classical opioids to induce respiratory depression in mice Thumbnail


Authors

Rob Hill

JULIE SANCHEZ JULIE.SANCHEZ@NOTTINGHAM.AC.UK
Research Fellow - Pharmacology Cell Biologist

Laura Lemel

Mirjana Antonijevic

Yselkla Hosking

Andrew C. Kruegel

Jonathan A. Javitch

ROB LANE ROB.LANE@NOTTINGHAM.AC.UK
Associate Professor



Abstract

Background and Purpose
Opioid-induced respiratory depression limits the use of μ-opioid receptor agonists in clinical settings and is the main cause of opioid overdose fatalities. The relative potential of different opioid agonists to induce respiratory depression at doses exceeding those producing analgesia is understudied despite its relevance to assessments of opioid safety. Here we evaluated the respiratory depressant and anti-nociceptive effects of three novel opioids and relate these measurements to their in vitro efficacy.

Experimental Approach
Respiration was measured in awake, freely moving male CD-1 mice using whole body plethysmography. Anti-nociception was measured using the hot plate test. Morphine, oliceridine and tianeptine were administered intraperitoneally, whereas methadone, oxycodone and SR-17018 were administered orally. Receptor activation and arrestin-3 recruitment were measured in HEK293 cells using BRET assays.

Key Results
Across the dose ranges examined, all opioids studied depressed respiration in a dose-dependent manner, with similar effects at the highest doses, and with tianeptine and oliceridine showing reduced duration of effect, when compared with morphine, oxycodone, methadone and SR-17018. When administered at doses that induced similar respiratory depression, all opioids induced similar anti-nociception, with tianeptine and oliceridine again showing reduced duration of effect. These data were consistent with the in vitro agonist activity of the tested compounds.

Conclusion and Implications
In addition to providing effective anti-nociception, the novel opioids, oliceridine, tianeptine and SR-17018 depress respiration in male mice. However, the different potencies and kinetics of effect between these novel opioids may be relevant to their therapeutic application in different clinical settings.

Journal Article Type Article
Acceptance Date Jul 15, 2023
Online Publication Date Jul 24, 2023
Publication Date 2023-12
Deposit Date Aug 1, 2023
Publicly Available Date Aug 1, 2023
Journal British Journal of Pharmacology
Print ISSN 0007-1188
Electronic ISSN 1476-5381
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 180
Issue 24
Pages 3160-3174
DOI https://doi.org/10.1111/bph.16199
Keywords Opioid; respiratory depression; anti-nociception; therapeutic window; opioid receptor
Public URL https://nottingham-repository.worktribe.com/output/23488593
Publisher URL https://bpspubs.onlinelibrary.wiley.com/doi/10.1111/bph.16199

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