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In Vitro Safety/Protection Assessment of Resveratrol and Pterostilbene in a Human Hepatoma Cell Line (HepG2)

机译:人肝癌细胞系(HepG2)中白藜芦醇和萜烯的体外安全性/保护性评估

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The aim of this work was to evaluate in vitro the genotoxic and/or antigenotoxic effects of resveratrol (RESV) and pterostilbene (PTER) on HepG2 cells. Moreover, additional tests were performed to evaluate early and late apoptosis events induced by the tested stilbenes. RESV and PTER did not show any genotoxic activity. As regards antigenotoxicity testing, RESV and PTER showed a typical, U-shaped hormetic dose-response relationship characterized by a biphasic trend with small quantities having opposite effects to large ones. HepG2 cells treated with PTER exhibited a marked increase in early apoptosis (40.1 %) at 250 mu M; whereas, the highest concentration tested for both RESV and PTER significantly increased the proportion of HepG2 cells undergoing late apoptosis (32.5 and 51.2 %, respectively). The observed pro-apoptotic activity could, at least in part, explain the hormetic response observed when the compounds were tested for antigenotoxicity (i.e., in the presence of induced DNA damage).
机译:这项工作的目的是在体外评估白藜芦醇(RESV)和紫檀萜(PTER)对HepG2细胞的遗传毒性和/或抗原毒性作用。此外,还进行了其他测试,以评估由测试的斯蒂芬苯酯诱导的早期和晚期凋亡事件。 RESV和PTER没有显示任何遗传毒性活性。关于抗原毒性测试,RESV和PTER显示出典型的U形荷尔蒙剂量-反应关系,其特征是呈两相趋势,少量与大剂量相反。用PTER处理的HepG2细胞在250μM时显示出早期凋亡的显着增加(40.1%)。而RESV和PTER的最高测试浓度则显着增加了晚期凋亡的HepG2细胞的比例(分别为32.5%和51.2%)。所观察到的促凋亡活性至少可以部分解释当测试化合物的抗原毒性时(即在存在诱导的DNA损伤的情况下)观察到的激素反应。

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