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Light deprivation reduces the severity of experimental diabetic retinopathy.

Citation
Thebeau, C., et al. “Light Deprivation Reduces The Severity Of Experimental Diabetic Retinopathy.”. Neurobiology Of Disease, p. 104754.
Center Washington University in St Louis
Author Christina Thebeau, Sheng Zhang, Alexander Kolesnikov V, Vladimir J Kefalov, Clay F Semenkovich, Rithwick Rajagopal
Keywords Db/db, Diabetic retinopathy, Electroretinography, Gnat1, Light deprivation, Rpe65, Streptozotocin, transducin1
Abstract

Illumination of the retina is a major determinant of energy expenditure by its neurons. However, it remains unclear whether light exposure significantly contributes to the pathophysiology of common retinal disease. Driven by the premise that light exposure reduces the metabolic demand of the retina, recent clinical trials failed to demonstrate a benefit for constant illumination in the treatment of diabetic retinopathy. Here, we instead ask whether light deprivation or blockade of visual transduction could modulate the severity of this common cause of blindness. We randomized adult mice with two different models of diabetic retinopathy to 1-3 months of complete dark housing. Unexpectedly, we find that diabetic mice exposed to short or prolonged light deprivation have reduced diabetes-induced retinal pathology, using measures of visual function, compared to control animals in standard lighting conditions. To corroborate these results, we performed assays of retinal vascular health in diabetic Gnat1 and Rpe65 mice, which lack phototransduction. Both mutants displayed less diabetes-associated retinal vascular disease compared to respective wild-type controls. Collectively, these results suggest that light-induced visual transduction promotes the development of diabetic retinopathy and implicate photoreceptors as an early source of visual pathology in diabetes.

Year of Publication
2020
Journal
Neurobiology of disease
Volume
137
Number of Pages
104754
Date Published
12/2020
ISSN Number
1095-953X
DOI
10.1016/j.nbd.2020.104754
Alternate Journal
Neurobiol. Dis.
PMID
31978605
PMCID
PMC7055708
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