Title:
The Selective Benefits of Acute Dosing with Dopamine Receptor Agonists on the Visual Function, Cognitive Function, and Blood Glucose Levels in a Rat Model of Type I Diabetes

dc.contributor.advisor Pardue, Machelle
dc.contributor.author Cardelle, Lidia
dc.contributor.committeeMember Ethier, Ross
dc.contributor.department Biomedical Engineering (Joint GT/Emory Department)
dc.date.accessioned 2021-06-30T17:37:46Z
dc.date.available 2021-06-30T17:37:46Z
dc.date.created 2021-05
dc.date.issued 2021-05
dc.date.submitted May 2021
dc.date.updated 2021-06-30T17:37:47Z
dc.description.abstract Purpose: Previous studies have demonstrated that dopamine D1 and D4 receptor (D1R, D4R) agonists selectively improve spatial frequency and contrast sensitivity thresholds, respectively, in healthy and diabetic mice (Jackson et al., 2012; Aung et al., 2014). The purpose of this experiment was to investigate the selective benefits of three dopamine receptor agonists (D1R, D2R, D4R) on visual function, cognitive function, and blood glucose in a rat model of Type I diabetes with progression of diabetes. Methods: Streptozotocin (STZ) was used to induce hyperglycemia in 2-month-old male Long–Evans rats (n=17). Outcome measures were acquired before and 30 minutes after an intraperitoneal injection of a single dose of a dopamine receptor agonist. Each agonist was injected 2-3 days apart. After 8, 16 and 20 weeks post-STZ, optomotor response (OMR) assessments were conducted. After 10 weeks post-STZ, blood glucose and Y-maze performance were measured on a subset of animals (n=4 diabetics; 6 controls). The spatial frequency, contrast sensitivity, Y-maze performance, and blood glucose for the diabetic rats and control rats post injection were compared to the baseline values to determine the effect of the acute dosing of each dopamine receptor agonist. Results: At the 8, 16, and 20 week timepoints, spatial frequency and contrast sensitivity thresholds were impaired in diabetic animals compared to controls (p<0.0001). At 8 weeks post-STZ, D1R agonist selectively restored spatial frequency thresholds for diabetic rats (p<0.0001), but did not alter thresholds in control rats. At 8 weeks post-STZ, the D4R agonist selectively restored contrast sensitivity thresholds for diabetic rats (p<0.0001) but did not alter thresholds for control rats. The improvements that we observed at 8 weeks in the diabetic animals with the D1R and D4R agonists were no longer observed at 16 or 20 weeks. The D2R agonist did not demonstrate any effects at any timepoint. There was no significant differences in Y-maze and blood glucose values with agonist treatment. Conclusions: Based on these findings, acute dosing of dopamine receptor agonists selectively benefits visual acuity (D1R) and contrast sensitivity (D4R) at early stages of diabetic retinopathy. Thus, dopamine receptor agonists may provide protective treatment options for early stage visual deficits characteristic of Type I diabetes.
dc.description.degree Undergraduate
dc.format.mimetype application/pdf
dc.identifier.uri http://hdl.handle.net/1853/64872
dc.language.iso en_US
dc.publisher Georgia Institute of Technology
dc.subject Diabetic retinopathy
dc.subject Visual function
dc.subject Cognitive function
dc.subject Type I diabetes
dc.subject Dopamine
dc.subject Dopamine receptor agonists
dc.title The Selective Benefits of Acute Dosing with Dopamine Receptor Agonists on the Visual Function, Cognitive Function, and Blood Glucose Levels in a Rat Model of Type I Diabetes
dc.type Text
dc.type.genre Undergraduate Thesis
dspace.entity.type Publication
local.contributor.corporatename Wallace H. Coulter Department of Biomedical Engineering
local.contributor.corporatename Undergraduate Research Opportunities Program
local.contributor.corporatename College of Engineering
local.relation.ispartofseries Undergraduate Research Option Theses
relation.isOrgUnitOfPublication da59be3c-3d0a-41da-91b9-ebe2ecc83b66
relation.isOrgUnitOfPublication 0db885f5-939b-4de1-807b-f2ec73714200
relation.isOrgUnitOfPublication 7c022d60-21d5-497c-b552-95e489a06569
relation.isSeriesOfPublication e1a827bd-cf25-4b83-ba24-70848b7036ac
thesis.degree.level Undergraduate
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