Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:1929619rdf:typepubmed:Citationlld:pubmed
pubmed-article:1929619lifeskim:mentionsumls-concept:C0041740lld:lifeskim
pubmed-article:1929619lifeskim:mentionsumls-concept:C0033085lld:lifeskim
pubmed-article:1929619lifeskim:mentionsumls-concept:C0018787lld:lifeskim
pubmed-article:1929619lifeskim:mentionsumls-concept:C0037633lld:lifeskim
pubmed-article:1929619lifeskim:mentionsumls-concept:C1382100lld:lifeskim
pubmed-article:1929619lifeskim:mentionsumls-concept:C2349209lld:lifeskim
pubmed-article:1929619lifeskim:mentionsumls-concept:C1549649lld:lifeskim
pubmed-article:1929619lifeskim:mentionsumls-concept:C0043193lld:lifeskim
pubmed-article:1929619pubmed:issue4lld:pubmed
pubmed-article:1929619pubmed:dateCreated1991-11-13lld:pubmed
pubmed-article:1929619pubmed:abstractTextPrevious studies from this institution have suggested that University of Wisconsin solution is preferred for prolonged cardiac storage and preserves high-energy phosphates better than other storage fluids. University of Wisconsin solution contains adenosine (5 mmol/L), which may maintain the concentration of myocardial adenine nucleotides. Cultures of human adult myocytes were grown from left ventricular biopsy specimens obtained from patients undergoing coronary bypass procedures. Cells (seven to nine dishes per group) were rinsed of culture medium and stored at 0 degrees C in University of Wisconsin solution. Cells were analyzed for adenine nucleotide content after 1, 6, 12, and 24 hours of storage by high-performance liquid chromatography (units = nmol/microgram DNA) and compared with control samples (0 hour). Adenosine concentration increased from 0.03 +/- 0.02 (mean +/- standard deviation) to 1.77 +/- 1.03 by 1 hour (p less than 0.0001, analysis of variance) and remained increased thereafter. Adenosine was largely degraded to inosine (0 hours, 0.03 +/- 0.03; 6 hours, 0.88 +/- 0.56; p less than 0.001) and hypoxanthine (0 hours, 0.01 +/- 0.01; 6 hours, 0.15 +/- 0.09; p = 0.004). Measured levels of xanthine and uric acid were extremely low at all time intervals. Adenosine triphosphate levels were maintained at 1 hour (0 hours, 0.64 +/- 0.38; 1 hour, 0.67 +/- 0.45) but declined thereafter (6 hours, 0.21 +/- 0.21; 12 hours, 0.11 +/- 0.09; 24 hours, 0.04 +/- 0.03; p less than 0.0001). Levels of adenosine diphosphate (p = 0.007) and adenosine monophosphate (p less than 0.05) decreased to approximately 25% of original values by 24 hours.(ABSTRACT TRUNCATED AT 250 WORDS)lld:pubmed
pubmed-article:1929619pubmed:languageenglld:pubmed
pubmed-article:1929619pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1929619pubmed:citationSubsetAIMlld:pubmed
pubmed-article:1929619pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1929619pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1929619pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1929619pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1929619pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1929619pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1929619pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1929619pubmed:statusMEDLINElld:pubmed
pubmed-article:1929619pubmed:monthOctlld:pubmed
pubmed-article:1929619pubmed:issn0003-4975lld:pubmed
pubmed-article:1929619pubmed:authorpubmed-author:WeiselR DRDlld:pubmed
pubmed-article:1929619pubmed:authorpubmed-author:MickleD ADAlld:pubmed
pubmed-article:1929619pubmed:authorpubmed-author:TumiatiL CLClld:pubmed
pubmed-article:1929619pubmed:authorpubmed-author:FremesS ESElld:pubmed
pubmed-article:1929619pubmed:authorpubmed-author:LiR KRKlld:pubmed
pubmed-article:1929619pubmed:authorpubmed-author:FurukawaR DRDlld:pubmed
pubmed-article:1929619pubmed:issnTypePrintlld:pubmed
pubmed-article:1929619pubmed:volume52lld:pubmed
pubmed-article:1929619pubmed:ownerNLMlld:pubmed
pubmed-article:1929619pubmed:authorsCompleteYlld:pubmed
pubmed-article:1929619pubmed:pagination1021-5lld:pubmed
pubmed-article:1929619pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:meshHeadingpubmed-meshheading:1929619-...lld:pubmed
pubmed-article:1929619pubmed:year1991lld:pubmed
pubmed-article:1929619pubmed:articleTitleThe limits of cardiac preservation with University of Wisconsin solution.lld:pubmed
pubmed-article:1929619pubmed:affiliationDivision of Cardiovascular Surgery, University of Toronto, Ontario, Canada.lld:pubmed
pubmed-article:1929619pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1929619pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed