首页> 外文期刊>Neoplasma: Journal of Experimental and Clinical Oncology >Influence of different chemical agents (H2O2, t-BHP and MMS) on the activity of antioxidant enzymes in human HepG2 and hamster V79 cells: relationship to cytotoxicity and genotoxicity
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Influence of different chemical agents (H2O2, t-BHP and MMS) on the activity of antioxidant enzymes in human HepG2 and hamster V79 cells: relationship to cytotoxicity and genotoxicity

机译:不同化学试剂(H2O2,t-BHP和MMS)对人HepG2和仓鼠V79细胞中抗氧化酶活性的影响:与细胞毒性和基因毒性的关系

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摘要

We investigated activities of antioxidant enzymes (AEs), superoxide dismutase (SOD), glutathione peroxidase (GPx) and catalase (CAT) in human HepG2 and hamster V79 cells treated with a scale of concentrations of hydrogen peroxide (H2O2), tert-butyl hydroperoxide (t-BHP) and methyl methanesulfonate (MMS). Cytotmdcity and genotoxicity of these substances were evaluated simultaneously. We have found out that H2O2, t-BHP and MMS predictably induce significant concentration-dependent increase of DNA lesions in both cell lines. Cytotoxicity detected in V79 cells with help of PE test was in a good conformity with the level of DNA damage. MTT test has proved unsuitable, except for MMS-treated V79 cells. Compared with human cells HepG2, hamster cells V79 manifested approximately similar levels of SOD and CAT but ten times higher activity of GPx. Across all concentrations tested the most significant increase of activity-of the enzyme CAT was found in H2O2- and t-BHP-treated HepG2 cells, of the enzyme SOD in t-BHP- and MMS-treated V79 cells, and of the enzyme GPx in H2O2-treated V79 cells. We suggest that stimulation of enzyme activity by the relevant chemical compounds may result from transcriptional or post-transcriptional regulation of the expression of the genes CAT, SOD and GPx. Several authors suggest that moderate levels of toxic reactants can induce increase of AEs activities, while very high levels of reactants can induce their decrease, as a consequence of damage of the molecular machinery required to induce AEs. Based on a great amount of experiments, which were done and described within this paper, we can say that the above mentioned principle does not apply in general. Only the reactions of t-BHP affected HepG2 cells were consistent with this idea.
机译:我们调查了人类HepG2和仓鼠V79细胞中抗氧化剂酶(AEs),超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GPx)和过氧化氢酶(CAT)的活性,并用一定浓度的过氧化氢(H2O2),叔丁基过氧化氢处理(t-BHP)和甲磺酸甲酯(MMS)。同时评估了这些物质的细胞毒性和遗传毒性。我们发现,H2O2,t-BHP和MMS可预测地诱导两种细胞系中DNA损伤的浓度依赖性显着增加。借助PE检测在V79细胞中检测到的细胞毒性与DNA损伤水平高度吻合。事实证明,MTT测试不适合,除了经过MMS处理的V79细胞。与人类细胞HepG2相比,仓鼠细胞V79的SOD和CAT含量大致相似,但GPx的活性却高十倍。在所测试的所有浓度下,CAT酶的活性增加最为显着-在H2O2和t-BHP处理的HepG2细胞中,在T-BHP和MMS处理的V79细胞中发现SOD酶,以及GPx酶在H2O2处理的V79细胞中。我们建议相关化合物对酶活性的刺激可能是由于CAT,SOD和GPx基因表达的转录或转录后调控所致。几位作者建议,中等水平的有毒反应物可以诱导AEs活性增加,而非常高水平的反应物可以诱导AEs活性降低,这是诱导AEs所需的分子机制受到破坏的结果。根据本文中进行和描述的大量实验,我们可以说上述原理通常并不适用。仅受t-BHP影响的HepG2细胞的反应与该想法一致。

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