The protective effect of simvastatin against ultraviolet B-induced corneal endothelial cell death

被引:2
|
作者
Ho, Yi-Ru [1 ]
Lin, Chih-Hung [2 ]
Kuo, Chan-Yen [3 ,4 ]
机构
[1] Chang Bing Show Chwan Mem Hosp, Dept Med Res & Dev, Changhua, Taiwan
[2] Cathay Gen Hosp, Dept Internal Med, Taipei, Taiwan
[3] Natl Cent Univ, Grad Inst Syst Biol & Bioinformat, Dept Biomed Sci & Engn, Chungli, Taiwan
[4] Hsin Sheng Jr Coll Med Care & Management, Dept Ophthalmol, Longtan, Taiwan
关键词
Apoptosis; caspase-3; activity; corneal endothelium cells; simvastatin; ultraviolet B; EPITHELIAL STEM-CELLS; NF-KAPPA-B; INDUCED PHOTOKERATITIS; REDUCTASE INHIBITORS; INDUCED APOPTOSIS; MOUSE MODEL; UV-B; MICE; INFLAMMATION; RADIATION;
D O I
10.4103/ijo.IJO_93_18
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: Excessive ultraviolet B (UVB) exposure causing corneal endothelium injury, including apoptosis, is a serious condition. Therefore, drugs that can inhibit apoptosis in corneal endothelial cells represent an effective strategy. Simvastatin is widely used as a specific inhibitor of 3-hydroxy-3-methyl-glutaryl-CoA reductase, can reduce levels of low density lipoprotein (LDL) cholesterol, and exerts anti-inflammatory effects. However, the protective effect of simvastatin on corneal endothelial cells remains unclear. Therefore, the aim of this study was to elucidate whether UVB promotes the initiation of apoptosis in corneal endothelial cells and injury reversible by simvastatin treatment. Methods: We detected the cell viability, subG1 population, and caspase-3 activity. Results: Results showed that simvastatin alleviates UVB-induced cell death, cell apoptosis, and caspase-3 activity. Conclusion: Our findings indicated that simvastatin alleviated UVB-induced corneal endothelial cell apoptosis via caspase-3 activity.
引用
收藏
页码:1080 / 1083
页数:4
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