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naltrexone targets OPRM1

Subject
naltrexone
Relation
targets
Object
OPRM1
p-value
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
Diagnosis and Pharmacotherapy of Alcohol Use Disorder: A Review. (2018) PMID:30167705 cited
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
Pharmacogenetics of OPRM1. (2014) PMID:24201053 cited
Naltrexone, a MOR antagonist
confidence: 0.96
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
Pharmacological treatment of cannabis dependence. (2011) PMID:21524266 cited
Naltrexone acts as an antagonist of the mu‑opioid receptor (mOR), the protein product of OPRM1.
confidence: 0.90