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The Single Administration of a Chromophore Alleviates Neural Defects in Diabetic Retinopathy. | LitMetric

AI Article Synopsis

  • Diabetic retinopathy (DR) is a serious complication of diabetes that leads to blindness, and can affect vision before any observable eye damage occurs.
  • In a study with Akita mice, which are a type 1 diabetic model, treatment with the visual pigment 9-cis-retinal improved visual function and restored electrical responses in the eye.
  • The treatment also reduced oxidative stress and retinal cell death, indicating that lack of chromophore contributes to early visual problems in diabetic retinopathy.

Article Abstract

Diabetic retinopathy (DR) is a common complication of diabetes and a leading cause of blindness among the working-age population. Diabetic patients often experience functional deficits in dark adaptation, contrast sensitivity, and color perception before any microvascular pathologies on the fundus become detectable. Previous studies showed that the regeneration of 11-cis-retinal and visual pigment is impaired in a type 1 diabetes animal model, which negatively affects visual function at the early stage of DR. Here, Akita mice, type 1 diabetic model, were treated with the visual pigment chromophore, 9-cis-retinal. This treatment rescued a- and b-wave amplitudes of scotopic electroretinography responses, compared with vehicle-treated Akita mice. In addition, the administration of 9-cis-retinal alleviated oxidative stress significantly as shown by reduced 3-nitrotyrosine levels in the retina of Akita mice. Furthermore, the 9-cis-retinal treatment decreased retinal apoptosis as shown by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling and DNA fragment enzyme-linked immunosorbent assay. Overall, these findings showed that 9-cis-retinal administration restored visual pigment formation and decreased oxidative stress and retinal degeneration, which resulted in improved visual function in diabetic mice, suggesting that chromophore deficiency plays a causative role in visual defects in early DR.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369574PMC
http://dx.doi.org/10.1016/j.ajpath.2020.03.009DOI Listing

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