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dc.contributor.authorGhimire, Anjali
dc.date.accessioned2020-09-11T16:13:38Z
dc.date.available2020-09-11T16:13:38Z
dc.date.issued2020-09-11T16:13:38Z
dc.identifier.urihttp://hdl.handle.net/10222/79835
dc.description.abstractThis study investigated effects of G1, a G-protein estrogen receptor (GPER) agonist, in a Langendorff-perfused mouse heart model of cardioplegia in adult and aged mice of both sexes. The recovery of cardiac function using St. Thomas’ Hospital cardioplegic solution No. 2 (STH2), prior to ischemia/reperfusion insult was better in adult female hearts compared to adult males. By contrast, hearts from old mice of both sexes recovered similarly or recovery was even better in males. However, the extent of recovery with STH2 was sub-optimal. When G1 was incorporated in STH2 results showed enhanced cardiac recovery in adult female mouse hearts but not in males. This protection with G1 was, however, observed in old mouse hearts from both sexes. The effect of G1 was also blocked by the GPER antagonist, G15. Together these findings suggest that addition of G1 in STH2 is a useful strategy to improve outcomes of cardiac surgery.en_US
dc.language.isoenen_US
dc.subjectCardioplegic solutionen_US
dc.subjectGPER agonisten_US
dc.subjectcardioprotectionen_US
dc.subjectischemia/reperfusion injuryen_US
dc.titleSex- and age-specific acute beneficial effects of an estrogen receptor agonist added to a cardioplegic solution in adult and aging mouse heartsen_US
dc.typeThesisen_US
dc.date.defence2018-08-07
dc.contributor.departmentDepartment of Pharmacologyen_US
dc.contributor.degreeMaster of Scienceen_US
dc.contributor.external-examinern/aen_US
dc.contributor.graduate-coordinatorDr. Morgan Langilleen_US
dc.contributor.thesis-readerDr. George Robertsonen_US
dc.contributor.thesis-readerDr. T. Alexander Quinnen_US
dc.contributor.thesis-supervisorDr. Susan Howletten_US
dc.contributor.ethics-approvalReceiveden_US
dc.contributor.manuscriptsNot Applicableen_US
dc.contributor.copyright-releaseNot Applicableen_US
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