Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:10463434rdf:typepubmed:Citationlld:pubmed
pubmed-article:10463434lifeskim:mentionsumls-concept:C0026809lld:lifeskim
pubmed-article:10463434lifeskim:mentionsumls-concept:C0038838lld:lifeskim
pubmed-article:10463434lifeskim:mentionsumls-concept:C1704632lld:lifeskim
pubmed-article:10463434lifeskim:mentionsumls-concept:C1280500lld:lifeskim
pubmed-article:10463434lifeskim:mentionsumls-concept:C0871261lld:lifeskim
pubmed-article:10463434lifeskim:mentionsumls-concept:C0035028lld:lifeskim
pubmed-article:10463434lifeskim:mentionsumls-concept:C2911692lld:lifeskim
pubmed-article:10463434lifeskim:mentionsumls-concept:C1706817lld:lifeskim
pubmed-article:10463434pubmed:issue2lld:pubmed
pubmed-article:10463434pubmed:dateCreated1999-9-30lld:pubmed
pubmed-article:10463434pubmed:abstractTextHigh concentration of acetylcholine (ACh) caused a rapid and long lasting relaxation response in age-matched controls, whereas this response was significantly weaker in streptozotocin (STZ)-diabetic and cholesterol fed mice. The levels of basal and ACh-stimulated cyclic GMP in the aorta was also significantly smaller in STZ-diabetic and cholesterol-fed mice. The attenuated relaxation responses to ACh in both STZ-diabetic and cholesterol-fed mice were ameliorated by the chronic administration of cholestyramine. A prior incubation of aortic strips with superoxide dismutase (SOD, 60 U/ml) improved the recovery phase of the relaxation of diabetic aorta after single administration of ACh, whereas SOD had no effects on ACh-induced relaxation of aortic strips from cholesterol fed mice. These results suggest that superoxide anion may be responsible for an impairment of endothelium-dependent relaxation of aorta from STZ induced diabetic mice. It is further suggested that impairment of endothelium-dependent relaxation in STZ-diabetic and cholesterol fed mice may be caused by different mechanisms.lld:pubmed
pubmed-article:10463434pubmed:languageenglld:pubmed
pubmed-article:10463434pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:citationSubsetIMlld:pubmed
pubmed-article:10463434pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10463434pubmed:statusMEDLINElld:pubmed
pubmed-article:10463434pubmed:monthAprlld:pubmed
pubmed-article:10463434pubmed:issn0916-8737lld:pubmed
pubmed-article:10463434pubmed:authorpubmed-author:SugiuraMMlld:pubmed
pubmed-article:10463434pubmed:authorpubmed-author:KamataKKlld:pubmed
pubmed-article:10463434pubmed:authorpubmed-author:NakajimaMMlld:pubmed
pubmed-article:10463434pubmed:issnTypePrintlld:pubmed
pubmed-article:10463434pubmed:volume35lld:pubmed
pubmed-article:10463434pubmed:ownerNLMlld:pubmed
pubmed-article:10463434pubmed:authorsCompleteYlld:pubmed
pubmed-article:10463434pubmed:pagination33-46lld:pubmed
pubmed-article:10463434pubmed:dateRevised2009-11-19lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:meshHeadingpubmed-meshheading:10463434...lld:pubmed
pubmed-article:10463434pubmed:year1999lld:pubmed
pubmed-article:10463434pubmed:articleTitleEffects of superoxide dismutase on the acetylcholine-induced relaxation response in cholesterol-fed and streptozotocin-induced diabetic mice.lld:pubmed
pubmed-article:10463434pubmed:affiliationDepartment of Physiology and Morphology, Institute of Medicinal Chemistry, Hoshi University, Tokyo, Japan. kamata@hoshi.ac.jplld:pubmed
pubmed-article:10463434pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10463434pubmed:publicationTypeIn Vitrolld:pubmed
pubmed-article:10463434pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:10463434lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:10463434lld:pubmed