Maintaining blood retinal barrier homeostasis to attenuate retinal ischemia-reperfusion injury by targeting the KEAP1/NRF2/ARE pathway with lycopene |
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| Affiliation: | 1. State Key laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China;2. Department of Ophthalmology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China;3. Biobank of Eye, State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China;1. School of Biological Sciences, Indian Association for the Cultivation of Science, Kolkata 700032, India;2. Department of Biochemistry, Centenary Campus, Bose Institute, P-1/12 C.I.T. Scheme VII-M, Kolkata 700054, India;1. Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR, USA;2. Department of Clinical Pharmacy, Faculty of Pharmacy, Cairo University, Cairo, Egypt;3. Vascular Biology Center, Augusta University, Augusta, GA, USA;4. Culver Vision Discovery Institute, Augusta University, Augusta, GA, USA;5. Department of Pharmacology and Toxicology, Augusta University, Augusta, GA, USA;6. Department of Cellular Biology & Anatomy, Augusta University, Augusta, GA, USA;7. Charlie Norwood VA Medical Center, Augusta, GA, USA;8. Bio-cancer Treatment International, 511-513, Bioinformatics Building, Hong Kong Science Park, Tai Po, Hong Kong, China;9. Department of Clinical and Administrative Pharmacy, University of Georgia, Augusta, GA, United States |
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| Abstract: | Retinal ischemia-reperfusion (I/R) often results in intractable visual impairments, where blood retinal barrier (BRB) homeostasis mediated by retinal pigment epithelium (RPE) and retinal microvascular endothelium (RME) is crucial. However, strategies targeting the BRB are limited. Thus, we investigated the inconclusive effect of lycopene (LYC) in retinal protection under I/R. LYC elevated cellular viability and reversed oxidative stress in aRPE-19 cells/hRME cells under I/R conditions based on oxygen-glucose deprivation (OGD) in vitro. Molecular analysis showed that LYC promoted NRF2 expression and enhanced the downstream factors of the KEAP1/NRF2/ARE pathway: LYC increased the activities of antioxidants, including SOD and CAT, whereas it enhanced the mRNA expression of HO-1 (ho-1) and NQO-1 (nqo-1). The activation resulted in restrained ROS and MDA. On the other hand, LYC ameliorated the damage to retinal function and morphology in a mouse I/R model, which was established by unilateral ligation of the left pterygopalatine artery/external carotid artery and reperfusion. LYC promoted the expression of NRF2 in both the neural retina and the RPE choroid in vivo. This evidence revealed the potential of LYC in retinal protection under I/R, uncovering the pharmacological effect of the KEAP1/NRF2/ARE pathway in BRB targeting. The study generates new insights into scientific practices in retinal research. |
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