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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/11442
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dc.contributor.advisorWerstuck, Geoff H.en_US
dc.contributor.advisorPeter Gross, Bernardo Trigattien_US
dc.contributor.advisorPeter Gross, Bernardo Trigattien_US
dc.contributor.authorVeerman, Kaley J.en_US
dc.date.accessioned2014-06-18T16:54:40Z-
dc.date.available2014-06-18T16:54:40Z-
dc.date.created2011-09-10en_US
dc.date.issued2011-10en_US
dc.identifier.otheropendissertations/6407en_US
dc.identifier.other7156en_US
dc.identifier.other2229530en_US
dc.identifier.urihttp://hdl.handle.net/11375/11442-
dc.description<p>Please remove prior submission under the same title</p>en_US
dc.description.abstract<p>Diabetes mellitus (DM) is associated with a significantly increased risk of microvascular complications, such as retinopathy, nephropathy, and neuropathy, as well as macrovascular disorders, including cerebro- and cardiovascular disease. Traditionally, the micro- and macro- vascular complications of DM have been considered distinct and independent disorders; however, data from several epidemiological and pathophysiological studies suggest they may be linked. It has been suggested that the <em>vasa vasorum</em>, a microvascular network which nourishes the walls of large muscular arteries, may play a role in macrovascular atherosclerosis. The effect of hyperglycemia on the microvessels of the vasa vasorum, and the potential impact of these effects on macrovascular atherosclerosis are not known.</p> <p>Here, we use a multiple-low-dose streptozotocin (STZ) injected apolipoprotein-E deficient mouse model to investigate the effects of hyperglycemia on the vasa vasorum, and to correlate such effects to atherosclerotic plaque progression. Hyperglycemia significantly increased plaque size and necrotic area (3- and 4-fold, respectively) relative to controls by 15 weeks of age. However, the density of vasa vasorum microvessels in the aortic wall of hyperglycemic mice was reduced at each time point examined. A similar vasa vasorum deficiency was also seen in STZ-induced hyperglycemic C57Bl/6J mice and hyperglycemic Ins2<sup>Akita</sup> mice, and microvessel density could be corrected by insulin-mediated glucose normalization, suggesting a hyperglycema-specific effect. A localized deficiency in VEGF appears to be responsible for the reduced neovascularisation. Lastly, hyperglycemic mice fed standard chow supplemented with benfotiamine, a drug used to treat microvascular disorders in DM, appear to have reduced atherosclerosis.</p> <p>These findings provide the first indication that, in addition to retinal and glomerular capillary beds, hyperglycemia alters the microvessel structure of the vasa vasorum. Such microvascular changes directly correlate to the development and progression of atherosclerosis in hyperglycemic ApoE-deficient mice.</p>en_US
dc.subjectDiabetesen_US
dc.subjectHyperglycemiaen_US
dc.subjectAtherosclerosisen_US
dc.subjectMicrovascular Diseaseen_US
dc.subjectAngiogenesisen_US
dc.subjectMouse Modelen_US
dc.subjectCardiovascular Diseasesen_US
dc.subjectCardiovascular Diseasesen_US
dc.titleInvestigating the Pro-Atherogenic Potential of Chronic Hyperglycemia: Is Diabetic Atherosclerosis a Microvascular Complication?en_US
dc.typethesisen_US
dc.contributor.departmentMedicineen_US
dc.description.degreeMaster of Science (MSc)en_US
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