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首页> 外文期刊>African Journal of Biotechnology >Assessment of MCF-7 cells as an in vitro model system for evaluation of chemical oxidative stressors
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Assessment of MCF-7 cells as an in vitro model system for evaluation of chemical oxidative stressors

机译:评估MCF-7细胞作为评价化学氧化胁迫源的体外模型系统

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Studies have been carried out to establish an experimental?in vitro?model system for routine testing of oxidative stress inducers through biochemical analysis using human breast carcinoma (MCF-7) cell line. Hydrogen peroxide (H2O-2) has been chosen as a test chemical oxidant to assess the level of induced glutathione (GSH), lipid peroxidation (LPO), superoxide dismutase (SOD), catalase, lactate dehydrogenase (LDH) release and cell viability using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) and neutral red uptake (NRU) assays in MCF-7 cells. Cells were exposed with H2O2?in the range of 0.1 to 1.6 mM in MEM culture medium up to 24 h. The sensitivity of the system was examined by determining the dose response curve for induction of mitochondrial activity and growth inhibition. The concentrations of H2O2?above 0.5 mM were found to be cytotoxic, whereas, lower concentrations did not cause any significant decrease in cell viability. Results of the study showed a decrease in GSH level at 12 and 24 h (39 and 44% of control) and maximum increase (60% of control) in LPO at 24 h. In case of catalase and SOD, a concentration of 0.5 mM of H2O2?was found instantly effective and caused reduction in activity within 2 h, with which decreases significantly up to 24 h. The results indicate that the H2O2?induced oxidative stress mediated cytotoxicity in MCF-7 cells and usefulness of these cell types as sensitive biological system for routine testing of chemical oxidative stressors.
机译:已经进行了研究以建立一个实验性的?在体外α模型系统,通过使用人乳腺癌(MCF-7)细胞通过生化分析进行氧化应激诱导剂的常规测试。已选择过氧化氢(H 2 O-2)作为测试化学氧化剂,以评估诱导的谷胱甘肽(GSH),脂质过氧化(LPO),超氧化物歧化酶(SOD),过氧化氢酶,乳酸脱氢酶(LDH)释放和电池活力的水平3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴(MTT)和MCF-7细胞中的中性红色吸收(NRU)测定。将细胞用H 2 O 2暴露在MEM培养基中的0.1至1.6mm的范围内,高达24小时。通过确定用于诱导线粒体活性和生长抑制的剂量响应曲线来检查系统的敏感性。发现H 2 O 2的浓度为0.5mm,是细胞毒性的,而较低浓度不会导致细胞活力的任何显着降低。该研究的结果表明,在12和24小时(39%和44%)下的GSH水平降低,24小时的LPO中最大增加(对照的60%)。在过氧化氢酶和SOD的情况下,浓度为0.5mm的H 2 O 2?发现瞬间有效并导致2小时内的活性降低,其显着降低至24小时。结果表明,H2O2?诱导氧化胁迫介导的MCF-7细胞中的细胞毒性,以及这些细胞类型作为敏感性生物系统的敏感性生物系统,用于常规检测化学氧化应激源。

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