Effects of 1,25 Dihydroxyvitamin D on Human Retinal Pigment Epithelial Cell Lines.

Int Ophthalmol

Department of Ophthalmology, Faculty of Medicine, Bezmialem Vakif University, Adnan Menderes (Vatan) Avenue, 34093, Fatih, Istanbul, Turkey.

Published: October 2021

Purpose: To assess the effects of 1,25 dihydroxyvitamin D (vitamin D) either alone or under oxidative damage on human retinal pigment epithelium cell lines.

Methods: The human retinal pigment epithelial cell lines were pretreated with hydrogen peroxide with different concentrations (100-1000 μM) and durations (4, 12 and 24 h) to determine the appropriate dose. A group of cells were treated with vitamin D alone, and another group of cells were co-treated with different concentrations of (10-100 nM) vitamin D and hydrogen peroxide. Anti-cytotoxic, anti-apoptotic and anti-genotoxic effects of vitamin D on the hydrogen peroxide treated cell line were evaluated. In addition, mitochondrial membrane potentials of treated cell lines were measured.

Results: Vitamin D showed statistically significant anti-cytotoxic effects and increased cell viability in all concentrations (p < 0.001). It has also significantly decreased the intracellular ROS generation at concentrations between 10-60 nM and increased intracellular reactive oxygen species in high doses over 90 nM (p < 0.01). When apoptosis was evaluated, vitamin D caused statistically significant decrease in a dose-dependent manner (p < 0.001). In terms of DNA damage which was caused by oxidative stress, it was observed that vitamin D significantly reduced the damage in a dose-dependent manner (p < 0.001). At the doses of 10-50 nM, vitamin D significantly decreased the mitochondrial membrane potential (p < 0.01).

Conclusion: Our study suggests that 1,25 (OH) D3 is capable for alleviating the oxidative damage in ARPE cell lines. With these results, vitamin D is thought to be a therapeutic alternative for the prevention of age-related macular degeneration. This warrants further investigations.

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http://dx.doi.org/10.1007/s10792-021-01895-xDOI Listing

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