Wang S, Mateos R, Goya L, Amigo-Benavent M, Sarriá B, Bravo L
Department of Metabolism and Nutrition, Institute of Food Science, Technology and Nutrition (ICTAN-CSIC), C/ José Antonio Novais, 10, 28040, Madrid, Spain.
Department of Metabolism and Nutrition, Institute of Food Science, Technology and Nutrition (ICTAN-CSIC), C/ José Antonio Novais, 10, 28040, Madrid, Spain.
Food Chem Toxicol. 2016 Feb;88:65-74. doi: 10.1016/j.fct.2015.12.005. Epub 2015 Dec 17.
Grape/wine industry produces large amounts of by-products, however knowledge on their health-promoting qualities is limited. This study investigated the effects of a grape phenolic extract (GPE) and its phenolic compounds, gallic acid (GA) and syringic acid (SA) on human intestinal Caco-2 cells, directly or after cytotoxicity induced by tert-butylhydroperoxide (t-BOOH). Direct treatment with 0.1-10 μg/mL GPE, or 0.1-10 μM GA and SA produced no major cytotoxic effect, either changes in antioxidant defences (glutathione content, glutathione peroxidase and reductase activities) or protein damage (carbonyl groups). However, 10 μg/mL GPE, 1 and 10 μM GA and 10 μM SA decreased reactive oxygen species (ROS) production. Pre-treatment with GPE, SA and GA at the same concentrations for 20 h showed that 10 μg/mL GPE and 10 μM GA or SA significantly counteracted ROS increase induced by t-BOOH. 10 μg/mL GPE and 1-10 μM GA or 10 μM of SA significantly reduced pro-oxidant-induced cytotoxicity. 1-10 μg/mL GPE, 1-10 μM GA and 10 μM SA significantly recovered both depleted glutathione and enhanced glutathione reductase and peroxidase activities, and reduced protein oxidative damage. Therefore, treatment with realistic concentrations of GPE and its main hydroxybenzoic acids protected Caco-2 cells against induced oxidative stress.
葡萄/葡萄酒产业会产生大量副产品,然而,关于这些副产品促进健康特性的知识却很有限。本研究调查了葡萄酚类提取物(GPE)及其酚类化合物没食子酸(GA)和丁香酸(SA)对人肠道Caco-2细胞的影响,包括直接作用以及在叔丁基过氧化氢(t-BOOH)诱导细胞毒性后的作用。用0.1 - 10μg/mL的GPE、或0.1 - 10μM的GA和SA直接处理,未产生主要的细胞毒性作用,抗氧化防御(谷胱甘肽含量、谷胱甘肽过氧化物酶和还原酶活性)或蛋白质损伤(羰基)也没有变化。然而,10μg/mL的GPE、1和10μM的GA以及l0μM的SA可降低活性氧(ROS)的产生。用相同浓度的GPE、SA和GA预处理20小时表明,10μg/mL GPE和10μM GA或SA可显著对抗t-BOOH诱导的ROS增加。10μg/mL GPE和1 - 10μM GA或10μM SA可显著降低促氧化剂诱导的细胞毒性。1 - 10μg/mL GPE、1 - 10μM GA和10μM SA可显著恢复耗尽的谷胱甘肽、增强谷胱甘肽还原酶和过氧化物酶活性,并减少蛋白质氧化损伤。因此,用实际浓度的GPE及其主要羟基苯甲酸处理可保护Caco-2细胞免受诱导的氧化应激。