naltrexone targets OPRM1
Evidence from:
primary |
all sources
Evidence (7 sources)
Differential sensitivity of human neurons carrying μ opioid receptor (MOR) N40D variants in response to ethanol.
(2020)
PMID:32561311
primary
opioid antagonist naltrexone ... found no effect
confidence: 0.80
Naltrexone is a non-selective antagonist of mu, kappa, and delta opioid receptors
confidence: 0.98
Review: Pharmacogenetics of alcoholism treatment: Implications of ethnic diversity.
(2017)
PMID:28134463
cited
Variations in the μ-opioid receptor (OPRM1) gene and response to NTX are among the most commonly investigated pharmacogenetic effects in research on AUDs.
confidence: 0.90
Delta and kappa opioid receptor polymorphisms influence the effects of naltrexone on subjective responses to alcohol.
(2012)
PMID:22954510
cited
naltrexone dose (50mg) blocked nearly all (about 94%) of mu opioid receptors
confidence: 0.96
Delta and kappa opioid receptor polymorphisms influence the effects of naltrexone on subjective responses to alcohol.
(2012)
PMID:22954510
cited
naltrexone has highest binding affinity for mu‑opioid receptors encoded by the OPRM1 gene
confidence: 0.90
Naltrexone acts as an antagonist of the mu‑opioid receptor (mOR), the protein product of OPRM1.
confidence: 0.90