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dc.contributor.authorM. Prele, Ceciliaen_US
dc.contributor.authorE. Reichelt, Melissaen_US
dc.contributor.authorE. Mutsaers, Stevenen_US
dc.contributor.authorDavies, Marilynen_US
dc.contributor.authorM. Delbridge, Leaen_US
dc.contributor.authorHeadrick, Johnen_US
dc.contributor.authorRosenthal, Nadiaen_US
dc.contributor.authorA. Bogoyevitch, Marieen_US
dc.contributor.authorD. Grounds, Mirandaen_US
dc.date.accessioned2017-05-03T11:16:48Z
dc.date.available2017-05-03T11:16:48Z
dc.date.issued2012en_US
dc.date.modified2012-08-08T23:34:11Z
dc.identifier.issn10548807en_US
dc.identifier.doi10.1016/j.carpath.2010.11.008en_US
dc.identifier.urihttp://hdl.handle.net/10072/46101
dc.description.abstractBACKGROUND: Acute insulin-like growth factor-1 administration has been shown to have beneficial effects in cardiac pathological conditions. The aim of the present study was to assess the structural and ex vivo functional impacts of long-term cardiomyocyte-specific insulin-like growth factor-1 overexpression in hearts of transgenic aMHC-IGF-1 Ea mice. METHODS: Performance of isolated transgenic aMHC-IGF-1 Ea and littermate wild-type control hearts was compared under baseline conditions and in response to 20-min ischemic insult. Cardiac desmin and laminin expression patterns were determined histologically, and myocardial hydroxyproline was measured to assess collagen content. RESULTS: Overexpression of insulin-like growth factor-1 did not modify expression patterns of desmin or laminin but was associated with a pronounced increase (~30%) in cardiac collagen content (from ~3.7 to 4.8 姯mg). Baseline myocardial contractile function and coronary flow were unaltered by insulin-like growth factor-1 overexpression. In contrast to prior evidence of acute cardiac protection, insulin-like growth factor-1 overexpression was associated with significant impairment of acute functional response to ischemia-reperfusion. Insulin-like growth factor-1 overexpression did not modify ischemic contracture development, but postischemic diastolic dysfunction was aggravated (51ᵠvs. 22ᶠmmHg in nontransgenic littermates). Compared with wild-type control, recovery of pressure development and relaxation indices relative to baseline performance were significantly reduced in transgenic aMHC-IGF-1 Ea after 60-min reperfusion (34ᷥ vs. 62ᷥ recovery of +dP/dt; 35ᱱ% vs. 57ḥ recovery of -dP/dt). CONCLUSIONS: Chronic insulin-like growth factor-1 overexpression is associated with reduced functional recovery after acute ischemic insult. Collagen deposition is elevated in transgenic aMHC-IGF-1 Ea hearts, but there is no change in expression of the myocardial structural proteins desmin and laminin. These findings suggest that sustained cardiac elevation of insulin-like growth factor-1 may not be beneficial in the setting of an acute ischemic insult.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_US
dc.languageEnglishen_US
dc.publisherElsevieren_US
dc.publisher.placeUnited Statesen_US
dc.relation.ispartofstudentpublicationNen_US
dc.relation.ispartofpagefrom17en_US
dc.relation.ispartofpageto27en_US
dc.relation.ispartofissue1en_US
dc.relation.ispartofjournalCardiovascular Pathologyen_US
dc.relation.ispartofvolume21en_US
dc.rights.retentionYen_US
dc.subject.fieldofresearchCardiology (incl. Cardiovascular Diseases)en_US
dc.subject.fieldofresearchcode110201en_US
dc.titleInsulin-like growth factor-1 overexpression in cardiomyocytes diminishes ex vivo heart functional recovery after acute ischemiaen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.date.issued2012
gro.hasfulltextNo Full Text


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