The nociceptin/orphanin FQ receptor system as a target to alleviate cancer-induced bone pain in rats: Model validation and pharmacological evaluation.


Journal

British journal of pharmacology
ISSN: 1476-5381
Titre abrégé: Br J Pharmacol
Pays: England
ID NLM: 7502536

Informations de publication

Date de publication:
05 2021
Historique:
revised: 13 08 2019
received: 08 03 2019
accepted: 27 09 2019
pubmed: 15 11 2019
medline: 6 7 2021
entrez: 15 11 2019
Statut: ppublish

Résumé

Cancer-induced bone pain remains inadequately controlled, and current standard of care analgesics is accompanied by several side effects. Nociceptin/orphanin FQ peptide (NOP) receptor agonists have demonstrated broad analgesic properties in rodent neuropathic and inflammatory pain models. Here, we investigate the analgesic potential of NOP receptor activation in a rodent cancer-induced bone pain model. Model validation by intratibial inoculation in male Sprague Dawley rats was performed with varying MRMT-1/Luc2 cell quantities (0.5-1.5 × 10 Inoculation with 1.5 × 10 Nociceptin and Ro65-6570 selectively and dose-dependently reversed cancer-induced bone pain-like behaviour. The NOP receptor system may be a potential target for cancer-induced bone pain treatment. This article is part of a themed issue on The molecular pharmacology of bone and cancer-elated bone diseases. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v178.9/issuetoc.

Sections du résumé

BACKGROUND AND PURPOSE
Cancer-induced bone pain remains inadequately controlled, and current standard of care analgesics is accompanied by several side effects. Nociceptin/orphanin FQ peptide (NOP) receptor agonists have demonstrated broad analgesic properties in rodent neuropathic and inflammatory pain models. Here, we investigate the analgesic potential of NOP receptor activation in a rodent cancer-induced bone pain model.
EXPERIMENTAL APPROACH
Model validation by intratibial inoculation in male Sprague Dawley rats was performed with varying MRMT-1/Luc2 cell quantities (0.5-1.5 × 10
KEY RESULTS
Inoculation with 1.5 × 10
CONCLUSION AND IMPLICATIONS
Nociceptin and Ro65-6570 selectively and dose-dependently reversed cancer-induced bone pain-like behaviour. The NOP receptor system may be a potential target for cancer-induced bone pain treatment.
LINKED ARTICLES
This article is part of a themed issue on The molecular pharmacology of bone and cancer-elated bone diseases. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v178.9/issuetoc.

Identifiants

pubmed: 31724155
doi: 10.1111/bph.14899
pmc: PMC8246843
doi:

Substances chimiques

Opioid Peptides 0
Receptors, Opioid 0
Nociceptin Receptor 0
Oprl protein, rat 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1995-2007

Subventions

Organisme : H2020 Marie Skłodowska-Curie Actions
ID : 814244
Organisme : Marie Sklodowska-Curie
ID : 642720

Informations de copyright

© 2019 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

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Auteurs

Sonny H J Sliepen (SHJ)

Grünenthal Innovation, Grünenthal GmbH, Aachen, Germany.
Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Johanna Korioth (J)

Grünenthal Innovation, Grünenthal GmbH, Aachen, Germany.

Thomas Christoph (T)

Grünenthal Innovation, Grünenthal GmbH, Aachen, Germany.

Thomas M Tzschentke (TM)

Grünenthal Innovation, Grünenthal GmbH, Aachen, Germany.

Marta Diaz-delCastillo (M)

Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Anne-Marie Heegaard (AM)

Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Kris Rutten (K)

Grünenthal Innovation, Grünenthal GmbH, Aachen, Germany.

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Classifications MeSH