Is There an Optimal Combination of AREDS2 Antioxidants Zeaxanthin, Vitamin E and Vitamin C on Light-Induced Toxicity of Vitamin A Aldehyde to the Retina?

Vitamins C and E and zeaxanthin are components of a supplement tested in a large clinical trial-Age-Related Eye Disease Study 2 (AREDS2)-and it has been demonstrated that they can inhibit the progression of age-related macular degeneration. The aim of this study was to determine the optimal combinat...

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Main Authors: Małgorzata B. Różanowska (Author), Barbara Czuba-Pełech (Author), Bartosz Różanowski (Author)
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Published: MDPI AG, 2022-06-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Małgorzata B. Różanowska  |e author 
700 1 0 |a Barbara Czuba-Pełech  |e author 
700 1 0 |a Bartosz Różanowski  |e author 
245 0 0 |a Is There an Optimal Combination of AREDS2 Antioxidants Zeaxanthin, Vitamin E and Vitamin C on Light-Induced Toxicity of Vitamin A Aldehyde to the Retina? 
260 |b MDPI AG,   |c 2022-06-01T00:00:00Z. 
500 |a 10.3390/antiox11061132 
500 |a 2076-3921 
520 |a Vitamins C and E and zeaxanthin are components of a supplement tested in a large clinical trial-Age-Related Eye Disease Study 2 (AREDS2)-and it has been demonstrated that they can inhibit the progression of age-related macular degeneration. The aim of this study was to determine the optimal combinations of these antioxidants to prevent the phototoxicity mediated by vitamin A aldehyde (ATR), which can accumulate in photoreceptor outer segments (POS) upon exposure to light. We used cultured retinal pigment epithelial cells ARPE-19 and liposomes containing unsaturated lipids and ATR as a model of POS. Cells and/or liposomes were enriched with lipophilic antioxidants, whereas ascorbate was added just before the exposure to light. Supplementing the cells and/or liposomes with single lipophilic antioxidants had only a minor effect on phototoxicity, but the protection substantially increased in the presence of both ways of supplementation. Combinations of zeaxanthin with α-tocopherol in liposomes and cells provided substantial protection, enhancing cell viability from ~26% in the absence of antioxidants to ~63% in the presence of 4 µM zeaxanthin and 80 µM α-tocopherol, and this protective effect was further increased to ~69% in the presence of 0.5 mM ascorbate. The protective effect of ascorbate disappeared at a concentration of 1 mM, whereas 2 mM of ascorbate exacerbated the phototoxicity. Zeaxanthin or α-tocopherol partly ameliorated the cytotoxic effects. Altogether, our results suggest that the optimal combination includes upper levels of zeaxanthin and α-tocopherol achievable by diet and/or supplementations, whereas ascorbate needs to be at a four-fold smaller concentration than that in the vitreous. The physiological relevance of the results is discussed. 
546 |a EN 
690 |a carotenoid 
690 |a xanthophyll 
690 |a zeaxanthin 
690 |a α-tocopherol 
690 |a ascorbate 
690 |a retina 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antioxidants, Vol 11, Iss 6, p 1132 (2022) 
787 0 |n https://www.mdpi.com/2076-3921/11/6/1132 
787 0 |n https://doaj.org/toc/2076-3921 
856 4 1 |u https://doaj.org/article/40ae1188b4b04b3e842a25b87e66ded4  |z Connect to this object online.