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  4. Coenzyme Q10 reduces ethanol-induced apoptosis in corneal fibroblasts
 
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Coenzyme Q10 reduces ethanol-induced apoptosis in corneal fibroblasts

Journal
PLoS ONE
Journal Volume
6
Journal Issue
4
Pages
e19111
Date Issued
2011
Author(s)
Chen C.-C.
Liou S.-W.
Chen C.-C.
Chen W.-C.
FUNG-RONG HU  
I-JONG WANG  
Lin S.-J.
DOI
10.1371/journal.pone.0019111
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-79955682893&doi=10.1371%2fjournal.pone.0019111&partnerID=40&md5=f8158e45d722203e428e17aaae623890
https://scholars.lib.ntu.edu.tw/handle/123456789/567297
Abstract
Dilute ethanol (EtOH) is a widely used agent to remove the corneal epithelium during the modern refractive surgery. The application of EtOH may cause the underlying corneal fibroblasts to undergo apoptosis. This study was designed to investigate the protective effect and potential mechanism of the respiratory chain coenzyme Q(10) (CoQ(10)), an electron transporter of the mitochondrial respiratory chain and a ubiquitous free radical scavenger, against EtOH-induced apoptosis of corneal fibroblasts. Corneal fibroblasts were pretreated with CoQ(10) (10 µM) for 2 h, followed by exposure to different concentrations of EtOH (0.4, 2, 4, and 20%) for 20 s. After indicated incubation period (2-12 h), MTT assay was used to examine cell viability. Treated cells were further assessed by flow cytometry to identify apoptosis. Reactive oxygen species (ROS) and the change in mitochondrial membrane potential were assessed using dichlorodihydrofluorescein diacetate/2',7'-dichlorofluorescein (DCFH-DA/DCF) assays and flow-cytometric analysis of JC-1 staining, respectively. The activity and expression of caspases 2, 3, 8, and 9 were evaluated with a colorimetric assay and western blot analysis. We found that EtOH treatment significantly decreased the viability of corneal fibroblasts characterized by a higher percentage of apoptotic cells. CoQ(10) could antagonize the apoptosis inducing effect of EtOH. The inhibition of cell apoptosis by CoQ(10) was significant at 8 and 12 h after EtOH exposure. In EtOH-exposed corneal fibroblasts, CoQ(10) pretreatment significantly reduced mitochondrial depolarization and ROS production at 30, 60, 90, and 120 min and inhibited the activation and expression of caspases 2 and 3 at 2 h after EtOH exposure. In summary, pretreatment with CoQ(10) can inhibit mitochondrial depolarization, caspase activation, and cell apoptosis. These findings support the proposition that CoQ(10) plays an antiapoptotic role in corneal fibroblasts after ethanol exposure.
Type
journal article

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