EGCG-S Impacts Oxidative Stress and Infection of Enterovirus 69 in Lung Cells

Hager S. G. Mohamed, Lee H. Lee, Sandra D. Adams
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Abstract

Enteroviruses are responsible for emerging diseases which cause diverse symptoms and may result in neurological complications. An antiviral with multiple mechanisms of action can help prevent enterovirus mediated disease despite differences in the pathogenesis between enteroviruses, including the recently identified enterovirus 69 (EV-69) for which pathogenesis is not well understood. This study investigated the efficacy of epigallocatechin-3-gallate stearate (EGCG-S), a modified form of the antioxidant green tea catechin epigallocatechin-3-gallate (EGCG), in inhibiting EV-69 infection of lung fibroblast cells in vitro. Treatment with EGCG-S resulted in moderate protection from EV-69 mediated cytotoxicity as demonstrated by increased metabolic activity as well as maintenance of cell morphology and mitochondrial function. These effects were correlated with reduced hydrogen peroxide production in infected cells following EGCG-S treatment with concentrations less than 100 μM, suggesting a role for inhibition of EV-69 mediated oxidative stress. This study provides insight into characteristics of EV-69 infection as well as the efficacy of EGCG-S mediated inhibition of EV-69 infection.
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EGCG-S对肺细胞氧化应激和肠道病毒69感染的影响
肠道病毒是新出现的疾病的罪魁祸首,这些疾病会引起多种症状,并可能导致神经系统并发症。具有多种作用机制的抗病毒药物可以帮助预防肠道病毒介导的疾病,尽管肠道病毒之间的发病机制存在差异,包括最近发现的肠道病毒69(EV-69),其发病机制尚不清楚。本研究研究了抗氧化剂绿茶儿茶素-表没食子儿茶素-3-没食子酸盐(EGCG)的改性形式-表没食子儿茶素-3-硬脂酸酯(EGCG-S)在体外抑制肺成纤维细胞EV-69感染的效果。用EGCG-S处理导致对EV-69介导的细胞毒性的适度保护,如代谢活性增加以及细胞形态和线粒体功能的维持所证明的。这些作用与浓度低于100μM的EGCG-S处理后感染细胞中过氧化氢产生减少有关,表明其对EV-69介导的氧化应激具有抑制作用。本研究深入了解了EV-69感染的特征以及EGCG-S介导的EV-69抑制感染的功效。
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