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Effects of Tea Polyphenols on Ni_2O_3-Induced Lipid Peroxidation in Rat Alveolar Macrophage and DNA Damage of HLF Cells

机译:茶多酚对大鼠肺泡巨噬细胞脂质过氧化的茶多酚对HLF细胞DNA损伤的影响

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摘要

To study the effects of tea polyphenols (TP) on the injury of rat alveolar macrophages treated with Ni_2O_3. The alveolar macrophages were cultured in vitro with exposure to Ni_2O_3 (5mg/L). Meanwhile, TP (125, 250 and 500mg/L) were added in the media, respectively. The detection of malondialdehyde and activity of antioxidant enzyme in alveolar macrophages were carried out. The protective effects of TP against DNA damage of human lung fibroblasts (HLF) cells induced by Ni_2O_3 were also investigated. HLF cells were cultured in vitro and treated with Ni_2O_3 (5mg/L) and Ni_2O_3+TP (250mg/L), respectively. The single cell gel electrophoresis (SCGE) was used to detect the DNA breaks. The results showed that TP could increase the activity of superoxide dismutase in rat alveolar macrophages in a dose-dependent manner and inhibit significantly the production of malondialdehyde at dose of 250mg/L and 500mg/L compared with Ni_2O_3 group (p < 0.05). The level of DNA breaks induced by Ni_2O_3 was higher than the control group (P < 0.01). But the level of DNA breaks induced by Ni_2O_3+TP was lower than the Ni_2O_3 treated group (P < 0.01), which demonstrated that TP could prevent cells from DNA damage induced by Ni_2O_3.
机译:为了研究大鼠肺泡与Ni_2O_3的巨噬细胞的伤害茶多酚(TP)的影响。肺泡巨噬细胞在体外培养,暴露于Ni_2O_3(5mg / L)。同时,分别在培养基中加入TP(125,250和500mg / L)。进行了肺泡巨噬细胞中丙二醛的检测和抗氧化酶的活性。还研究了TP对Ni_2O_3诱导的人肺成纤维细胞(HLF)细胞DNA损伤的保护作用。在体外培养HLF细胞,并分别用Ni_2O_3(5mg / L)和Ni_2O_3 + TP(250mg / L)处理。单细胞凝胶电泳(SCGE)用于检测DNA断裂。结果表明,TP以剂量依赖性方式增加大鼠肺泡巨噬细胞中超氧化物歧化酶的活性,并抑制与Ni_2O_3组(P <0.05)相比为250mg / L和500mg / L的剂量的丙二醛的生产。 Ni_2O_3诱导的DNA断裂水平高于对照组(P <0.01)。但是,Ni_2O_3 + TP诱导的DNA断裂水平低于Ni_2O_3处理基团(P <0.01),这证明TP可以防止Ni_2O_3诱导的DNA损伤的细胞。

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