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dc.contributor.authorSlusar, Joanna
dc.date.accessioned2010-12-06T14:59:33Z
dc.date.available2010-12-06T14:59:33Z
dc.date.issued2010-12-06
dc.identifier.urihttp://hdl.handle.net/10222/13126
dc.description.abstractAnandamide (AEA), a well characterized endocannabinoid that has actions at multiple targets in the eye, may have potential as a novel therapeutic in the treatment of retinal disease. However, AEA is rapidly degraded by fatty acid amide hydrolase (FAAH). Therefore this study examined the drug URB597, that inhibits FAAH degradation of AEA, to assess AEA effects in experimental models of retinal damage. The objectives were to: 1) evaluate changes present in the aging retina, 2) determine whether the aging retina is more susceptible to tissue damage, and 3) investigate whether increasing AEA can provide retinal neurovascular protection in young and aged retina following damage. The results from this study showed that URB597 had protective effects on retinal ganglion cells and retinal capillaries and inhibited phagocytotic MG in models of retinal damage in young, but not the aged retina.en_US
dc.language.isoenen_US
dc.subjectagingen_US
dc.subjectendocannabinoidsen_US
dc.subjectretinal vasculatureen_US
dc.subjectoptic nerve injuryen_US
dc.subjectneuroprotectionen_US
dc.subjectischemiaen_US
dc.titleExamination of the Neuroprotective Effects of URB597 in Young and Aged Rat Retinaen_US
dc.date.defence2010-09-23
dc.contributor.departmentDepartment of Pharmacology with Neuroscienceen_US
dc.contributor.degreeMaster of Scienceen_US
dc.contributor.external-examinerN/Aen_US
dc.contributor.graduate-coordinatorDr. Eileen Denovan-Wrighten_US
dc.contributor.thesis-readerDr. Christian Lehmannen_US
dc.contributor.thesis-readerDr. William Baldridgeen_US
dc.contributor.thesis-supervisorDr. Melanie Kellyen_US
dc.contributor.ethics-approvalNot Applicableen_US
dc.contributor.manuscriptsNot Applicableen_US
dc.contributor.copyright-releaseNot Applicableen_US
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