Nociceptin/Orphanin FQ Peptide Receptor-Related Ligands as Novel Analgesics.


Journal

Current topics in medicinal chemistry
ISSN: 1873-4294
Titre abrégé: Curr Top Med Chem
Pays: United Arab Emirates
ID NLM: 101119673

Informations de publication

Date de publication:
2020
Historique:
received: 03 01 2020
revised: 10 04 2020
accepted: 14 04 2020
pubmed: 10 5 2020
medline: 2 7 2021
entrez: 9 5 2020
Statut: ppublish

Résumé

Despite similar distribution patterns and intracellular events observed in the nociceptin/ orphanin FQ peptide (NOP) receptor and other opioid receptors, NOP receptor activation displays unique pharmacological profiles. Several researchers have identified a variety of peptide and nonpeptide ligands to determine the functional roles of NOP receptor activation and observed that NOP receptor- related ligands exhibit pain modality-dependent pain processing. Importantly, NOP receptor activation results in anti-nociception and anti-hypersensitivity at the spinal and supraspinal levels regardless of the experimental settings in non-human primates (NHPs). Given that the NOP receptor agonists synergistically enhance mu-opioid peptide (MOP) receptor agonist-induced anti-nociception, it has been hypothesized that dual NOP and MOP receptor agonists may display promising functional properties as analgesics. Accumulating evidence indicates that the mixed NOP/opioid receptor agonists demonstrate favorable functional profiles. In NHP studies, bifunctional NOP/MOP partial agonists (e.g., AT-121, BU08028, and BU10038) exerted potent anti-nociception via NOP and MOP receptor activation; however, dose-limiting adverse effects associated with the MOP receptor activation, including respiratory depression, itch sensation, physical dependence, and abuse liability, were not observed. Moreover, a mixed NOP/opioid receptor agonist, cebranopadol, presented promising outcomes in clinical trials as a novel analgesic. Collectively, the dual agonistic actions on NOP and MOP receptors, with appropriate binding affinities and efficacies, may be a viable strategy to develop innovative and safe analgesics.

Identifiants

pubmed: 32384033
pii: CTMC-EPUB-106452
doi: 10.2174/1568026620666200508082615
pmc: PMC7720806
mid: NIHMS1649230
doi:

Substances chimiques

Analgesics, Opioid 0
BU10038 0
Isoquinolines 0
Ligands 0
Phenylpropionates 0
Receptors, Opioid 0
Naltrexone 5S6W795CQM

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2878-2888

Subventions

Organisme : NIDA NIH HHS
ID : R01 DA032568
Pays : United States
Organisme : NIAMS NIH HHS
ID : R21 AR069861
Pays : United States
Organisme : NIDA NIH HHS
ID : R21 DA044450
Pays : United States

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

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Auteurs

Norikazu Kiguchi (N)

Department of Pharmacology, Wakayama Medical University, Wakayama, Japan.

Huiping Ding (H)

Department of Physiology & Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27101, United States.

Shiroh Kishioka (S)

Department of Pharmacology, Wakayama Medical University, Wakayama, Japan.

Mei-Chuan Ko (MC)

Department of Physiology & Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27101, United States.

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Classifications MeSH