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Permanent link (DOI): https://doi.org/10.7939/R3K64B185

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Protracted Vascular Retinopathy in a Novel Model of Spontaneous Type 2 Diabetes Open Access

Descriptions

Other title
Subject/Keyword
retinal pericytes
Nile grass rat
Diabetic retinopathy
Type of item
Thesis
Degree grantor
University of Alberta
Author or creator
Gotzmann, Jonathan D.
Supervisor and department
Sauve, Yves (Ophthalmology and Visual Sciences)
Examining committee member and department
Allison, William (Biological Sciences)
Nguyen, Peter (Physiology)
Chan, Catherine (Physiology)
Sauve, Yves (Ophthalmology and Visual Sciences)
MacDonald, Patrick (Pharmacology)
Department
Department of Physiology
Specialization

Date accepted
2015-12-23T11:56:30Z
Graduation date
2016-06
Degree
Master of Science
Degree level
Master's
Abstract
Diabetic retinopathy (DR) is the leading cause of blindness in working aged adults, however lack of a suitable animal model has limited our understanding of the disease. The Nile grass rat (NR) is a cone-rich crepuscular rodent that spontaneously develops hyperglycemia (HG) when fed standard lab chow, making them a candidate to study the effects of HG on the retina. Vascular integrity was assessed in two groups of NRs at 6, 12 and 18 months of age: 1) standard lab chow: fed Prolab 2000 (HG); 2) low calorie, high fiber diet: fed Mazuri Chinchilla (control). Results revealed many classic hallmarks of human DR, such as pericyte loss, degeneration of capillaries and microaneurysm formation. Furthermore, early cataract development was seen in hyperglycemic NRs, as early as 12 months of age. In addition to the classic vascular changes associated with DR, differences in inner retinal circuitry were investigated. Hyperglycemic NRs showed a decreased ability for age-related dendritic sprouting specific to dopaminergic amacrine cells and also a marked reduction of connexin 36 (Cx36) expression in the outer plexiform layer (OPL) and inner plexiform layer (IPL). Together, our results demonstrate that NRs recapitulate the key pathological features and slow time course of early human DR. Therefore, NRs provide a unique opportunity to study the pathogenesis of DR as well as providing new understanding to the changes of the diabetic retina.
Language
English
DOI
doi:10.7939/R3K64B185
Rights
This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for the purpose of private, scholarly or scientific research. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
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