Year: 2018
Type: article
Abstract: The retinoid visual cycle is an ocular retinoid metabolism specifically dedicated to support vertebrate vision. The visual cycle serves not only to generate light-sensitive visual chromophore 11-cis-retinal, but also to clear toxic byproducts of normal visual cycle (i.e. all-trans-retinal and its condensation products) from the retina, ensuring both the visual function and the retinal health. Unfortunately, various conditions including genetic predisposition, environment and aging may attribute to a functional decline of the all-trans-retinal clearance. To combat all-trans-retinal mediated retinal degeneration, we sought to slow down the retinoid influx from the RPE by inhibiting the visual cycle with a small molecule. The present study describes identification of CU239, a novel non-retinoid inhibitor of RPE65, a key enzyme in the visual cycle. Our data demonstrated that CU239 selectively inhibited isomerase activity of RPE65, with IC50 of 6 μM. Further, our results indicated that CU239 inhibited RPE65 via competition with its substrate all-trans-retinyl ester. Mice with systemic injection of CU239 exhibited delayed chromophore regeneration after light bleach, and conferred a partial protection of the retina against injury from high intensity light. Taken together, CU239 is a potent visual cycle modulator and may have a therapeutic potential for retinal degeneration.
Language: English
Subfield: Ophthalmology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,010
Funders: Presbyterian Health Foundation, University of Oklahoma, Oklahoma Center for the Advancement of Science and Technology, Juvenile Diabetes Research Foundation United Kingdom, National Institutes of Health, University of Oklahoma Health Sciences Center, National Eye Institute, National Institute of General Medical Sciences
Awards: G3065872526, G4127644501, G4803274114, Mentoring Diabetes Research in Oklahoma, Studies of RPE65, G5393258158, Mentoring Diabetes Research in Oklahoma, G5943041002, G6068999854, G6665534447, G6680545722, Podocyte protective effect of neuropilin-1, The role of the Wnt signaling pathway in choroidal neovascularization, A Novel Pathogenic Pathway for Diabetic Keratopathy, A new pathogenic mechanism for diabetic retinopathy
OpenAlex ID: W2801578034
