Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:8880221rdf:typepubmed:Citationlld:pubmed
pubmed-article:8880221lifeskim:mentionsumls-concept:C0026809lld:lifeskim
pubmed-article:8880221lifeskim:mentionsumls-concept:C0037993lld:lifeskim
pubmed-article:8880221lifeskim:mentionsumls-concept:C0441655lld:lifeskim
pubmed-article:8880221lifeskim:mentionsumls-concept:C0128561lld:lifeskim
pubmed-article:8880221lifeskim:mentionsumls-concept:C0301625lld:lifeskim
pubmed-article:8880221pubmed:issue1lld:pubmed
pubmed-article:8880221pubmed:dateCreated1997-3-14lld:pubmed
pubmed-article:8880221pubmed:abstractTextMirfentanil [N-(2-pyrazinyl)-N-(1-phenethyl-4-piperidinyl)-2-furamide] was studied for its antinociceptive and immunomodulatory effects in mice Mirfentanil (1.0-32.0 mg/kg) increased tail-flick latency to a thermal stimulus and this effect was antagonized (94 +/- 2%) by naltrexone (10.0 mg/kg). Unlike naltrexone, the delta opioid selective antagonist naltrindole (20.0 mg/kg) had no effect on mirfentanil-induced analgesia. In a dose-dependent fashion, the mu-selective antagonists beta-funaltrexamine (1.0-40.0 mg/kg) and naloxonazine (1.0-35.0 mg/kg) blocked mirfentanil (10.0 mg/kg)-induced analgesia up to 75% of the maximum analgesic effect. Norbinaltorphimine (10.0 mg/kg) partially blocked (35%) the maximum analgesic effect following mirfentanil (10.0 mg/kg) administration. Single doses of mirfentanil (0.1-32.0 mg/kg) had no effect on splenic NK activity. However, preadministration of mirfentanil (1.0-10.0 mg/kg) blocked morphine-induced suppression of splenic NK activity. Collectively, the results suggest that mirfentanil is a novel opioid that induces antinociception predominately through mu opioid receptors but, unlike morphine or fentanyl, does not suppress splenic NK activity.lld:pubmed
pubmed-article:8880221pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8880221pubmed:languageenglld:pubmed
pubmed-article:8880221pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8880221pubmed:citationSubsetIMlld:pubmed
pubmed-article:8880221pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8880221pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8880221pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8880221pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8880221pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8880221pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8880221pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8880221pubmed:statusMEDLINElld:pubmed
pubmed-article:8880221pubmed:monthAuglld:pubmed
pubmed-article:8880221pubmed:issn0162-3109lld:pubmed
pubmed-article:8880221pubmed:authorpubmed-author:ScottMMlld:pubmed
pubmed-article:8880221pubmed:authorpubmed-author:FranceC PCPlld:pubmed
pubmed-article:8880221pubmed:authorpubmed-author:BagleyJ RJRlld:pubmed
pubmed-article:8880221pubmed:authorpubmed-author:CarrD JDJlld:pubmed
pubmed-article:8880221pubmed:authorpubmed-author:BrockunierL...lld:pubmed
pubmed-article:8880221pubmed:issnTypePrintlld:pubmed
pubmed-article:8880221pubmed:volume34lld:pubmed
pubmed-article:8880221pubmed:ownerNLMlld:pubmed
pubmed-article:8880221pubmed:authorsCompleteYlld:pubmed
pubmed-article:8880221pubmed:pagination9-16lld:pubmed
pubmed-article:8880221pubmed:dateRevised2007-11-14lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:meshHeadingpubmed-meshheading:8880221-...lld:pubmed
pubmed-article:8880221pubmed:year1996lld:pubmed
pubmed-article:8880221pubmed:articleTitleMirfentanil antagonizes morphine-induced suppression of splenic NK activity in mice.lld:pubmed
pubmed-article:8880221pubmed:affiliationDepartment of Microbiology, Immunology, Parasitology, Louisiana State University Medical Center, New Orleans 70112-1393, USA. dcarr@pop3.lsumc.edulld:pubmed
pubmed-article:8880221pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8880221pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:8880221pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed