Purpose: To clarify the protective effect of astaxanthin (AST) against light-induced retinal damage in rats.
Methods: Albino rats were divided into three groups: a group treated orally with 1 mg/kg AST daily (group H), a group treated with 0.2 mg/kg AST (group L), and a control group (group C). Rats were administered AST in groups H and L and olive oil in group C followed by a 12-hour exposure to 3000-lux white light. After exposure for 7 days, the protective effect of AST was evaluated functionally by electroretinogram (ERG) and histologically by measuring outer nuclear layer (ONL) thickness and by counting rate of terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) stained cells.
Results: After exposure to light, the b-wave amplitudes were significantly preserved in the AST groups compared to group C, Further the rate of the residual amplitude was higher in group H than in group L. The ONL thicknesses were significantly thicker in AST-treated rats compared to group C. The rates of TUNEL stained cells were significantly lower in the following order: group H, L and C.
Conclusion: AST may have a protective effect against light-induced retinal damage in albino rats.
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Invest Ophthalmol Vis Sci
January 2025
Laboratory for Experimental Immunology of the Eye, Department of Ophthalmology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
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Department of Ophthalmology and Visual Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
Sunlight exposure is recognized as a risk factor for the development of age-related macular degeneration (AMD), a common neurodegenerative retinal disease in the elderly. Specifically, the blue light wavelengths within sunlight can negatively impact the physiology of light-sensitive retinal cells, including retinal pigmented epithelium (RPE) and photoreceptors. This review explores blue light-induced retinal degeneration, emphasizing the structural and functional impairments in RPE.
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Shenzhen Eye Hospital, Shenzhen Eye Institute, JinanUniversity, 18 Zetian Road, Shenzhen, 518040, Guangdong, China.
Microglia are highly specialized resident macrophages in the central nervous system that play a pivotal role in modulating neuroinflammation. Microglial plasticity is essential for their function, allowing them to polarize into proinflammatory M1-like or anti-inflammatory M2-like phenotypes. However, the mechanisms driving M1 and M2 microglial induction during retinal degeneration remain largely unexplored.
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