Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:2854856rdf:typepubmed:Citationlld:pubmed
pubmed-article:2854856lifeskim:mentionsumls-concept:C0022116lld:lifeskim
pubmed-article:2854856lifeskim:mentionsumls-concept:C0031381lld:lifeskim
pubmed-article:2854856lifeskim:mentionsumls-concept:C0036442lld:lifeskim
pubmed-article:2854856lifeskim:mentionsumls-concept:C0599946lld:lifeskim
pubmed-article:2854856lifeskim:mentionsumls-concept:C2346484lld:lifeskim
pubmed-article:2854856lifeskim:mentionsumls-concept:C1881189lld:lifeskim
pubmed-article:2854856lifeskim:mentionsumls-concept:C0205195lld:lifeskim
pubmed-article:2854856lifeskim:mentionsumls-concept:C0175668lld:lifeskim
pubmed-article:2854856lifeskim:mentionsumls-concept:C0205421lld:lifeskim
pubmed-article:2854856pubmed:issue4lld:pubmed
pubmed-article:2854856pubmed:dateCreated1989-7-7lld:pubmed
pubmed-article:2854856pubmed:abstractTextFasted Wistar rats were given a mild level of traumatic brain injury (TBI) and then subjected to 6 min of transient forebrain ischemia 24 h posttrauma. One group was given simultaneous 1 mg/kg scopolamine and 4 mg/kg phencyclidine intraperitoneally (IP) 15 min before trauma and another group an equal volume of plasmalyte A solution. After 7 days of postinjury survival, placebo-treated rats demonstrated increased posttraumatic vulnerability to secondary ischemic CA1 neuronal death even 24 h after trauma. This finding confirmed that increased posttraumatic ischemic vulnerability persists for at least 24 h even following mild trauma. Combined muscarinic receptor and N-methyl-D-aspartate (NMDA) receptor coupled ion channel blockade given and present during the mild TBI statistically attenuated this enhanced secondary ischemic CA1 neuronal death and thus posttraumatic increased ischemic vulnerability. Placebo-treated rats had 335.3 +/- 93.6 CA1 neurons/10(6) microns 2 and drug-treated rats had 844.8 +/- 184.9 CA1 neurons/10(6) microns 2. This result suggests that muscarinic and/or NMDA receptor-mediated events confined to TBI and the early posttraumatic period are in part responsible for the phenomenon of increased posttraumatic ischemic vulnerability.lld:pubmed
pubmed-article:2854856pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:languageenglld:pubmed
pubmed-article:2854856pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:citationSubsetIMlld:pubmed
pubmed-article:2854856pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2854856pubmed:statusMEDLINElld:pubmed
pubmed-article:2854856pubmed:issn0897-7151lld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:BalsterR LRLlld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:HayesR LRLlld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:MillerL PLPlld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:YoungH FHFlld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:LeweltWWlld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:JenkinsL WLWlld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:CliftonG LGLlld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:LyethB GBGlld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:MoszynskiKKlld:pubmed
pubmed-article:2854856pubmed:authorpubmed-author:DewittD SDSlld:pubmed
pubmed-article:2854856pubmed:issnTypePrintlld:pubmed
pubmed-article:2854856pubmed:volume5lld:pubmed
pubmed-article:2854856pubmed:ownerNLMlld:pubmed
pubmed-article:2854856pubmed:authorsCompleteYlld:pubmed
pubmed-article:2854856pubmed:pagination275-87lld:pubmed
pubmed-article:2854856pubmed:dateRevised2011-11-17lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:meshHeadingpubmed-meshheading:2854856-...lld:pubmed
pubmed-article:2854856pubmed:year1988lld:pubmed
pubmed-article:2854856pubmed:articleTitleCombined pretrauma scopolamine and phencyclidine attenuate posttraumatic increased sensitivity to delayed secondary ischemia.lld:pubmed
pubmed-article:2854856pubmed:affiliationDepartment of Anesthesiology, Medical College of Virginia, Richmond.lld:pubmed
pubmed-article:2854856pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2854856pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed