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Epigallocatechin gallate eye drops protect against ultraviolet B–induced corneal oxidative damage in mice
PURPOSE: Ultraviolet B (UVB) radiation from sunlight is a known risk factor for human corneal injury. The aim of the present study was to investigate the protective effects of green tea polyphenol epigallocatechin gallate (EGCG) on UVB radiation–induced corneal oxidative damage in male imprinting co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919670/ https://www.ncbi.nlm.nih.gov/pubmed/24520184 |
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author | Chen, Mu-Hsin Tsai, Chia-Fang Hsu, Yu-Wen Lu, Fung-Jou |
author_facet | Chen, Mu-Hsin Tsai, Chia-Fang Hsu, Yu-Wen Lu, Fung-Jou |
author_sort | Chen, Mu-Hsin |
collection | PubMed |
description | PURPOSE: Ultraviolet B (UVB) radiation from sunlight is a known risk factor for human corneal injury. The aim of the present study was to investigate the protective effects of green tea polyphenol epigallocatechin gallate (EGCG) on UVB radiation–induced corneal oxidative damage in male imprinting control region (ICR) mice. METHODS: Corneal oxidative damage was induced by exposure to UVB radiation at 560 μW/cm(2). The animals received 0%, 0.1%, and 0.01% EGCG eye drops at a 5 mg/ml dose, twice daily for 8 days. Corneal surface damage was graded according to smoothness and the extent of lissamine green staining. Corneal glutathione (GSH), thiobarbituric acid-reactive substances (TBARS), and protein carbonyl levels, as well as superoxide dismutase (SOD), catalase, glutathione peroxidase (GSH-Px), and glutathione reductase (GSH-Rd) activity in the cornea, were measured to monitor corneal injury. RESULTS: UVB radiation caused significant damage to the corneas, including apparent corneal ulceration and severe epithelial exfoliation, leading to a decrease in SOD, catalase, GSH-Px, GSH-Rd, and GSH activity in the cornea. However, the corneal TBARS and protein carbonyls increased compared with the control group. Treatment with EGCG eye drops significantly (p<0.05) ameliorated corneal damage, increased SOD, catalase, GSH-Px, GSH-Rd, and GSH activity, and decreased the TBARS and protein carbonyls in the corneas compared with the UVB-treated group. CONCLUSIONS: EGCG eye drops exhibit potent protective effects on UVB radiation–induced corneal oxidative damage in mice, likely due to the increase in antioxidant defense system activity and the inhibition of lipid peroxidation and protein oxidation. |
format | Online Article Text |
id | pubmed-3919670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Molecular Vision |
record_format | MEDLINE/PubMed |
spelling | pubmed-39196702014-02-11 Epigallocatechin gallate eye drops protect against ultraviolet B–induced corneal oxidative damage in mice Chen, Mu-Hsin Tsai, Chia-Fang Hsu, Yu-Wen Lu, Fung-Jou Mol Vis Research Article PURPOSE: Ultraviolet B (UVB) radiation from sunlight is a known risk factor for human corneal injury. The aim of the present study was to investigate the protective effects of green tea polyphenol epigallocatechin gallate (EGCG) on UVB radiation–induced corneal oxidative damage in male imprinting control region (ICR) mice. METHODS: Corneal oxidative damage was induced by exposure to UVB radiation at 560 μW/cm(2). The animals received 0%, 0.1%, and 0.01% EGCG eye drops at a 5 mg/ml dose, twice daily for 8 days. Corneal surface damage was graded according to smoothness and the extent of lissamine green staining. Corneal glutathione (GSH), thiobarbituric acid-reactive substances (TBARS), and protein carbonyl levels, as well as superoxide dismutase (SOD), catalase, glutathione peroxidase (GSH-Px), and glutathione reductase (GSH-Rd) activity in the cornea, were measured to monitor corneal injury. RESULTS: UVB radiation caused significant damage to the corneas, including apparent corneal ulceration and severe epithelial exfoliation, leading to a decrease in SOD, catalase, GSH-Px, GSH-Rd, and GSH activity in the cornea. However, the corneal TBARS and protein carbonyls increased compared with the control group. Treatment with EGCG eye drops significantly (p<0.05) ameliorated corneal damage, increased SOD, catalase, GSH-Px, GSH-Rd, and GSH activity, and decreased the TBARS and protein carbonyls in the corneas compared with the UVB-treated group. CONCLUSIONS: EGCG eye drops exhibit potent protective effects on UVB radiation–induced corneal oxidative damage in mice, likely due to the increase in antioxidant defense system activity and the inhibition of lipid peroxidation and protein oxidation. Molecular Vision 2014-02-07 /pmc/articles/PMC3919670/ /pubmed/24520184 Text en Copyright © 2014 Molecular Vision. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited, used for non-commercial purposes, and is not altered or transformed. |
spellingShingle | Research Article Chen, Mu-Hsin Tsai, Chia-Fang Hsu, Yu-Wen Lu, Fung-Jou Epigallocatechin gallate eye drops protect against ultraviolet B–induced corneal oxidative damage in mice |
title | Epigallocatechin gallate eye drops protect against ultraviolet B–induced corneal oxidative damage in mice |
title_full | Epigallocatechin gallate eye drops protect against ultraviolet B–induced corneal oxidative damage in mice |
title_fullStr | Epigallocatechin gallate eye drops protect against ultraviolet B–induced corneal oxidative damage in mice |
title_full_unstemmed | Epigallocatechin gallate eye drops protect against ultraviolet B–induced corneal oxidative damage in mice |
title_short | Epigallocatechin gallate eye drops protect against ultraviolet B–induced corneal oxidative damage in mice |
title_sort | epigallocatechin gallate eye drops protect against ultraviolet b–induced corneal oxidative damage in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919670/ https://www.ncbi.nlm.nih.gov/pubmed/24520184 |
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