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Grape seed proanthocyanidin extract protects human lens epithelial cells from oxidative stress via reducing NF-кB and MAPK protein expression

PURPOSE: Oxidative damage induced by H(2)O(2) treatment can irreversibly damage the lens epithelium, resulting in cell death and cataract. Grape seed extract (GSE) is a widely consumed dietary supplement that has the capability to scavenge oxidants and free radicals. GSE contain 70%–95% standardized...

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Detalles Bibliográficos
Autores principales: Jia, Zhiyan, Song, Zhen, Zhao, Yuhui, Wang, Xiurong, Liu, Ping
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025097/
https://www.ncbi.nlm.nih.gov/pubmed/21264233
Descripción
Sumario:PURPOSE: Oxidative damage induced by H(2)O(2) treatment can irreversibly damage the lens epithelium, resulting in cell death and cataract. Grape seed extract (GSE) is a widely consumed dietary supplement that has the capability to scavenge oxidants and free radicals. GSE contain 70%–95% standardized proanthocyanidins. The study described herein investigated the protective effect of Grape seed proanthocyanidin extract (GSPE) on H(2)O(2)-induced oxidative stress in human lens epithelial B-3 (HLEB-3) cells and the possible molecular mechanism involved. METHODS: HLE-B3 cells exposed to different doses of H(2)O(2) were cultured with various concentrations of GSPE and subsequently monitored for cell viability by the 4,5-dimethylthiazol-2-yl-2,5-diphenyltetrazolium bromide (MTT) assay. The apoptosis rate and ROS generation were detected by flow cytometric analysis. Expression of NF-кB/P65 and mitogen activated protein kinase (MAPK) proteins were measured by western blot. RESULTS: GSPE clearly reduced H(2)O(2) induced cell apoptosis and reactive oxygen species (ROS) generation and protected HLEB-3 cells from H(2)O(2) induced oxidative damage. GSPE depressed H(2)O(2)-induced activation and translocation of NF-кB/p65. GSPE also depressed H(2)O(2)-induced phosphorylation of the p38 and c-Jun N-terminal kinase (JNK) proteins of the MAPK family at various time points studied. CONCLUSIONS: GSPE could be useful in attenuation of H(2)O(2)-induced oxidative stress and the activation of NF-кB and MAPK signaling in HLE-B3 cells, which suggests that GSPE has a potential protective effect against cataractogenesis.