Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:1566917rdf:typepubmed:Citationlld:pubmed
pubmed-article:1566917lifeskim:mentionsumls-concept:C0242692lld:lifeskim
pubmed-article:1566917lifeskim:mentionsumls-concept:C0003765lld:lifeskim
pubmed-article:1566917lifeskim:mentionsumls-concept:C1704632lld:lifeskim
pubmed-article:1566917lifeskim:mentionsumls-concept:C0871261lld:lifeskim
pubmed-article:1566917lifeskim:mentionsumls-concept:C2911692lld:lifeskim
pubmed-article:1566917lifeskim:mentionsumls-concept:C1706817lld:lifeskim
pubmed-article:1566917lifeskim:mentionsumls-concept:C1704259lld:lifeskim
pubmed-article:1566917lifeskim:mentionsumls-concept:C1705987lld:lifeskim
pubmed-article:1566917lifeskim:mentionsumls-concept:C0851285lld:lifeskim
pubmed-article:1566917pubmed:issue4 Pt 2lld:pubmed
pubmed-article:1566917pubmed:dateCreated1992-5-21lld:pubmed
pubmed-article:1566917pubmed:abstractTextWith in vivo television microscopy, changes in arteriolar diameter to topical administration of various vasoactive agents were examined in the absence or in the presence of NG-monomethyl-L-arginine (L-NMMA, topical 100 microM) or NG-nitro-L-arginine (L-NNA, 2.5 microM, 20 microliters/min ia), specific inhibitors of endothelium-derived relaxing factor (EDRF) biosynthesis. In cremaster muscle arterioles (15-22 microns) of rats (n = 6-11), dilations to acetylcholine (1-100 ng) were significantly inhibited (60-70%) by either of the arginine analogues. This inhibition was reversed by subsequent administration of 1 mM L-arginine. Dose-dependent constriction to norepinephrine was enhanced by L-NMMA. Indomethacin treatment reduced arteriolar dilation to bradykinin (BK, 1-100 ng), which was significantly inhibited by additional administration of L-NNA. Application of L-NNA first, followed by additional indomethacin, elicited similar results. Dilations to sodium nitroprusside and adenosine were not reduced in the presence of the inhibitors. L-NMMA or L-NNA caused no change in systemic blood pressure but elicited a significant reduction in arteriolar diameter; this effect was not reversed by 1 mM L-arginine. These data demonstrate the presence of an L-arginine pathway to produce EDRF (nitric oxide) in skeletal muscle microcirculation that mediates and/or modulates arteriolar responses to vasoactive agents and could contribute to the regulation of basal vascular tone.lld:pubmed
pubmed-article:1566917pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1566917pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1566917pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1566917pubmed:languageenglld:pubmed
pubmed-article:1566917pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1566917pubmed:citationSubsetIMlld:pubmed
pubmed-article:1566917pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1566917pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1566917pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1566917pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1566917pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1566917pubmed:statusMEDLINElld:pubmed
pubmed-article:1566917pubmed:monthAprlld:pubmed
pubmed-article:1566917pubmed:issn0002-9513lld:pubmed
pubmed-article:1566917pubmed:authorpubmed-author:KollerAAlld:pubmed
pubmed-article:1566917pubmed:authorpubmed-author:KaleyGGlld:pubmed
pubmed-article:1566917pubmed:authorpubmed-author:MessinaE JEJlld:pubmed
pubmed-article:1566917pubmed:authorpubmed-author:WolinM SMSlld:pubmed
pubmed-article:1566917pubmed:authorpubmed-author:RodenburgJ...lld:pubmed
pubmed-article:1566917pubmed:issnTypePrintlld:pubmed
pubmed-article:1566917pubmed:volume262lld:pubmed
pubmed-article:1566917pubmed:ownerNLMlld:pubmed
pubmed-article:1566917pubmed:authorsCompleteYlld:pubmed
pubmed-article:1566917pubmed:paginationH987-92lld:pubmed
pubmed-article:1566917pubmed:dateRevised2007-11-14lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:meshHeadingpubmed-meshheading:1566917-...lld:pubmed
pubmed-article:1566917pubmed:year1992lld:pubmed
pubmed-article:1566917pubmed:articleTitleRegulation of arteriolar tone and responses via L-arginine pathway in skeletal muscle.lld:pubmed
pubmed-article:1566917pubmed:affiliationDepartment of Physiology, New York Medical College, Valhalla 10595.lld:pubmed
pubmed-article:1566917pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1566917pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:1566917pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1566917lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1566917lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1566917lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1566917lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1566917lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1566917lld:pubmed