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dc.contributor.authorAshton, Kevinen_US
dc.contributor.authorWillems, Lauraen_US
dc.contributor.authorHolmgren, Kirstyen_US
dc.contributor.authorFerreira, Lindaen_US
dc.contributor.authorHeadrick, Johnen_US
dc.contributor.editorGeorg Wick and Beatrix Grubeck-Loebensteinen_US
dc.date.accessioned2017-05-03T11:16:42Z
dc.date.available2017-05-03T11:16:42Z
dc.date.issued2006en_US
dc.date.modified2007-08-07T04:47:28Z
dc.identifier.issn05315565en_US
dc.identifier.urihttp://hdl.handle.net/10072/14269
dc.description.abstractAged hearts exhibit reduced tolerance to ischemia-reperfusion, together with altered structure and post-ischemic remodelling. The molecular bases of such changes are unclear. Using cDNA microarrays and quantitative RT-PCR we characterized shifts in gene expression patterns with aging in normoxic and post-ischemic (20 min global ischemia, 60 min reperfusion) murine hearts (young: 2-4 months; aged: 16-18 months). We identified an age-associated up-regulation of transcripts involved in cell death, oxygen transport and metabolism in normoxic hearts. Down-regulated transcripts were involved in transporter activity, protein binding and hydrolase activity, changes in MAPK, WNT and TGF-beta signalling with aging were also observed. Ischemic stress generated a much greater degree of contractile impairment and cellular damage in aged vs. young hearts. This was associated with a substantially modified transcriptional response, with selective changes in Ca2+, WNT, NOTCH and G-protein coupled receptor signalling paths in aged vs. young hearts. Despite some common responses to ischemia in young and aged hearts (induction of heat shock protein transcripts), aging selectively modified ischemic responses of immediate early genes, and genes involved in modulating apoptosis and remodelling/angiogenesis. In summary, aging is associated with shifts in cardiovascular gene expression consistent with the phenotypic features of older hearts. Reduced tolerance with age may be related to modification of signalling (particularly WNT and TGF-beta), and shifts in expression of immediate early genes, and genes important in control of cell death/survival, angiogenesis, and cardiac remodelling.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherElsevier Incen_US
dc.publisher.placeNew York, NYen_US
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefrom189en_US
dc.relation.ispartofpageto204en_US
dc.relation.ispartofedition2006en_US
dc.relation.ispartofissue2en_US
dc.relation.ispartofjournalExperimental Gerontologyen_US
dc.relation.ispartofvolume41en_US
dc.rights.retentionNen_AU
dc.subject.fieldofresearchcode329999en_US
dc.subject.fieldofresearchcode270201en_US
dc.titleAge-associated shifts in cardiac gene transcription and transcriptional responses to ischemic stressen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.facultyGriffith Health, School of Medical Scienceen_US
gro.date.issued2006
gro.hasfulltextNo Full Text


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