Source:http://linkedlifedata.com/resource/pubmed/id/15956985
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2005-11-18
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pubmed:abstractText |
The opioid antagonist nalmefene offers an alternative to traditional pharmacological treatments for alcoholism. The present study was designed to investigate the relationship between nalmefene plasma concentration and central mu-opioid receptor occupancy after a clinically effective dose (20 mg, orally). Pharmacokinetics and mu-opioid receptor occupancy of nalmefene after single and repeated dosing over 7 days was studied in 12 healthy subjects. Serial blood samples were obtained after both dosings, and pharmacokinetic parameters for nalmefene and main metabolites were determined. Central mu-opioid receptor occupancy of nalmefene was measured with positron emission tomography (PET) and [(11)C]carfentanil at four time points (3, 26, 50, 74 h) after both dosings. Nalmefene was rapidly absorbed in all subjects. The mean t(1/2) of nalmefene was 13.4 h after single and repeated dosing. The accumulation of nalmefene and its main metabolites in plasma during the repeated dosing period was as expected for a drug with linear pharmacokinetics, and steady-state was reached for all analytes. Both nalmefene dosings resulted in a very high occupancy at mu-opioid receptors (87-100%), and the decline in the occupancy was similar after both dosings but clearly slower than the decline in the plasma concentration of nalmefene or metabolites. High nalmefene occupancy (83-100%) persisted at 26 h after the dosings. The prolonged mu-opioid receptor occupancy by nalmefene indicates slow dissociation of the drug from mu-opioid receptors. These results support the rational of administering nalmefene when needed before alcohol drinking, and they additionally suggest that a high mu-opioid receptor occupancy can be maintained when nalmefene is taken once daily.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Analgesics, Opioid,
http://linkedlifedata.com/resource/pubmed/chemical/Fentanyl,
http://linkedlifedata.com/resource/pubmed/chemical/Glucuronides,
http://linkedlifedata.com/resource/pubmed/chemical/Naltrexone,
http://linkedlifedata.com/resource/pubmed/chemical/Narcotic Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Opioid, mu,
http://linkedlifedata.com/resource/pubmed/chemical/carfentanil,
http://linkedlifedata.com/resource/pubmed/chemical/nalmefene
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0893-133X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2245-53
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pubmed:dateRevised |
2011-5-18
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pubmed:meshHeading |
pubmed-meshheading:15956985-Adolescent,
pubmed-meshheading:15956985-Adult,
pubmed-meshheading:15956985-Analgesics, Opioid,
pubmed-meshheading:15956985-Area Under Curve,
pubmed-meshheading:15956985-Caudate Nucleus,
pubmed-meshheading:15956985-Electrocardiography,
pubmed-meshheading:15956985-Fentanyl,
pubmed-meshheading:15956985-Glucuronides,
pubmed-meshheading:15956985-Humans,
pubmed-meshheading:15956985-Male,
pubmed-meshheading:15956985-Naltrexone,
pubmed-meshheading:15956985-Narcotic Antagonists,
pubmed-meshheading:15956985-Positron-Emission Tomography,
pubmed-meshheading:15956985-Prefrontal Cortex,
pubmed-meshheading:15956985-Receptors, Opioid, mu,
pubmed-meshheading:15956985-Thalamus
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pubmed:year |
2005
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pubmed:articleTitle |
Prolonged central mu-opioid receptor occupancy after single and repeated nalmefene dosing.
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pubmed:affiliation |
Clinical Research Services Turku (CRST), University of Turku, FIN-20521 Turku, Finland.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't
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