Unique pharmacodynamic properties and low abuse liability of the μ-opioid receptor ligand (S)-methadone.

NMDAR computational model opioid

Journal

Research square
Titre abrégé: Res Sq
Pays: United States
ID NLM: 101768035

Informations de publication

Date de publication:
23 Mar 2023
Historique:
pubmed: 31 3 2023
medline: 31 3 2023
entrez: 30 3 2023
Statut: epublish

Résumé

(R,S)-methadone ((R,S)-MTD) is a racemic μ-opioid receptor (MOR) agonist comprised of (R)-MTD and (S)-MTD enantiomers used for the treatment of opioid use disorder (OUD) and pain. (R)-MTD is used as an OUD treatment, has high MOR potency, and is believed to mediate (R,S)-MTD's therapeutic efficacy. (S)-MTD is in clinical development as an antidepressant and is considered an N-methyl-D-aspartate receptor (NMDAR) antagonist. In opposition to this purported mechanism of action, we found that (S)-MTD does not occupy NMDARs in vivo in rats. Instead, (S)-MTD produced MOR occupancy and induced analgesia with similar efficacy as (R)-MTD. Unlike (R)-MTD, (S)-MTD was not self-administered and failed to increase locomotion or extracellular dopamine levels indicating low abuse liability. Moreover, (S)-MTD antagonized the effects of (R)-MTD in vivo and exhibited unique pharmacodynamic properties, distinct from those of (R)-MTD. Specifically, (S)-MTD acted as a MOR partial agonist with a specific loss of efficacy at the MOR-galanin 1 receptor (Gal1R) heteromer, a key mediator of the dopaminergic effects of opioids. In sum, we report novel and unique pharmacodynamic properties of (S)-MTD that are relevant to its potential mechanism of action and therapeutic use, as well as those of (R,S)-MTD.

Identifiants

pubmed: 36993715
doi: 10.21203/rs.3.rs-2644719/v1
pmc: PMC10055532
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIDA NIH HHS
ID : R01 DA049257
Pays : United States

Déclaration de conflit d'intérêts

MM has received research funding from AstraZeneca, Redpin Therapeutics, and Attune Neurosciences. Dr. Zarate is a full-time U.S government employee. He is listed as a coinventor on a patent for the use of ketamine in major depression and suicidal ideation. Dr. Zarate is listed as a coinventor on a patent for the use of (2R,6R)-hydroxynorketamine, (S)-dehydronorketamine and other stereoisomeric dehydro and hydroxylated metabolites of (R,S)-ketamine metabolites in the treatment of depression and neuropathic pain. Dr. Zarate is listed as co-inventor on a patent application for the use of (2R,6R)-hydroxynorketamine and (2S,6S)-hydroxynorketamine in the treatment of depression, anxiety, anhedonia, suicidal ideation and post-traumatic stress disorders. Dr. Zarate has assigned his patent rights to the U.S. government but will share a percentage of any royalties that may be received by the government.

Auteurs

Marjorie Levinstein (M)

National Institute on Drug Abuse.

Paulo De Oliveira (P)

National Institute on Drug Abuse.

Nil Casajuana-Martin (N)

Universitat Autònoma Barcelona.

Cesar Quiroz (C)

National Institute on Drug Abuse.

Reece Budinich (R)

National Institute on Drug Abuse.

Rana Rais (R)

Johns Hopkins School of Medicine.

William Rea (W)

National Institute on Drug Abuse.

Emilya Ventriglia (E)

National Institute on Drug Abuse.

Natàlia Llopart (N)

Universitat de Barcelona.

Verònica Casadó-Anguera (V)

Universitat de Barcelona.

Estefanía Moreno (E)

Department of Biochemistry and Molecular Biomedicine, Faculty of Biology, Institute of Biomedicine of the University of Barcelona, University of Barcelona.

Donna Walther (D)

National Institute on Drug Abuse.

Grant Glatfelter (G)

National Institute on Drug Abuse.

Michael Baumann (M)

National Institute on Drug Abuse.

Leonardo Pardo (L)

Universitat Autonoma de Barcelona.

Sergi Ferre (S)

National Institute on Drug Abuse.

Classifications MeSH