Delta Opioid Receptor-Mediated Antidepressant-Like Effects of Diprenorphine in Mice.
Animals
Mice
Analgesics, Opioid
/ pharmacology
Antidepressive Agents
/ pharmacology
Depressive Disorder, Major
Diprenorphine
/ pharmacology
Mice, Inbred C57BL
Receptors, Opioid
Receptors, Opioid, delta
/ metabolism
Receptors, Opioid, kappa
/ metabolism
Receptors, Opioid, mu
/ metabolism
Seizures
/ chemically induced
Journal
The Journal of pharmacology and experimental therapeutics
ISSN: 1521-0103
Titre abrégé: J Pharmacol Exp Ther
Pays: United States
ID NLM: 0376362
Informations de publication
Date de publication:
03 2023
03 2023
Historique:
received:
01
03
2022
accepted:
22
11
2022
pubmed:
2
12
2022
medline:
3
3
2023
entrez:
1
12
2022
Statut:
ppublish
Résumé
Major depressive disorder is a highly common disorder, with a lifetime prevalence in the United States of approximately 21%. Traditional antidepressant treatments are limited by a delayed onset of action and minimal efficacy in some patients. Ketamine is effective and fast-acting, but there are concerns over its abuse liability. Thus, there is a need for safe, fast-acting antidepressant drugs. The opioid buprenorphine shows promise but also has abuse liability due to its mu-agonist component. Preclinical evidence indicates that the delta-opioid system contributes to mood disorders, and delta-opioid agonists are effective in preclinical models of depression- and anxiety-like states. In this study, we test the hypothesis that the mu-opioid antagonist diprenorphine by virtue of its partial delta opioid agonist activity may offer a beneficial profile for an antidepressant medication without abuse liability. Diprenorphine was confirmed to bind with high affinity to all three opioid receptors, and functional experiments for G protein activation verified diprenorphine to be a partial agonist at delta- and kappa-opioid receptors and a mu-antagonist. Studies in C57BL/6 mice demonstrated that an acute dose of diprenorphine produced antidepressant-like effects in the tail suspension test and the novelty-induced hypophagia test that were inhibited in the presence of the delta-selective antagonist, naltrindole. Diprenorphine did not produce convulsions, a side effect of many delta agonists but rather inhibited convulsions caused by the full delta agonist SNC80; however, diprenorphine did potentiate pentylenetetrazole-induced convulsions. Diprenorphine, and compounds with a similar pharmacological profile, may provide efficient and safe rapidly acting antidepressants. SIGNIFICANCE STATEMENT: The management of major depressive disorder, particularly treatment-resistant depression, is a significant unmet medical need. Here we show that the opioid diprenorphine, a compound with mu-opioid receptor antagonist activity and delta- and kappa-opioid receptor partial agonist activities, has rapid onset antidepressant-like activity in animal models. Diprenorphine and compounds with a similar pharmacological profile to diprenorphine should be explored as novel antidepressant drugs.
Identifiants
pubmed: 36456196
pii: jpet.122.001182
doi: 10.1124/jpet.122.001182
pmc: PMC9976798
doi:
Substances chimiques
Analgesics, Opioid
0
Antidepressive Agents
0
Diprenorphine
1F0L5N25ZZ
Receptors, Opioid
0
Receptors, Opioid, delta
0
Receptors, Opioid, kappa
0
Receptors, Opioid, mu
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, N.I.H., Intramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
343-352Subventions
Organisme : NIDA NIH HHS
ID : R21 DA041565
Pays : United States
Organisme : NIDA NIH HHS
ID : R37 DA039997
Pays : United States
Organisme : NIDA NIH HHS
ID : T32 DA007268
Pays : United States
Organisme : NIDA NIH HHS
ID : T32 DA007281
Pays : United States
Informations de copyright
U.S. Government work not protected by U.S. copyright.
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