CARCINOGENIC CHROMIUM(VI) INDUCES OXIDATIVE STRESS IN CULTURED HUMAN LEUKEMIC T-LYMPHOCYTES. 1. GENERATIO OF HYDROGEN PEROXIDE DURIN INTRACELLULAR REDUCTION OF CHROMATE

S. Mattagajasingh, H. Misra
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引用次数: 3

Abstract

Treatment of human leukemic T-lymphocyte MOLT4 cells with potassium chromate, a chromium (VI) compound, increased the form ation of the oxidized compound dichlorofluorescein (DCF), a highly fluorescent compound, from the parent nonfluorescent compound, 2,7-dichlorofluorescin diacetate (DCF-DA). No such increase in DCF formation was observed when cells were treated with Cr(III) compounds. In cell-free system s, dichlorofluorescin diacetate was also oxidized to DCF by strong oxidants (such as hydrogen peroxide and hydroperoxides) in the presence of peroxidase, suggesting that Cr(VI) treatment increased the intracellular level of these peroxides in MOLT4 cells. The rate of generation of peroxides was found to be both dose and time dependent. These results suggest that accumulation of intracellular peroxides may, at least in part, be associated with chromium-induced genotoxicity and add to the emerging concept that these phenomena may, in part, be mediated via oxidative m echanisms.
致癌铬(vi)诱导培养的人白血病t淋巴细胞氧化应激。1. 细胞内铬酸盐还原过程中过氧化氢的产生
用铬酸钾(一种铬(VI)化合物)处理人白血病t淋巴细胞MOLT4细胞,增加了母体非荧光化合物2,7-二氯荧光素二醋酸酯(DCF- da)的氧化化合物二氯荧光素(DCF)的形成,这是一种高荧光化合物。当细胞用Cr(III)化合物处理时,没有观察到DCF形成的增加。在无细胞系统中,在过氧化物酶存在的情况下,双乙酸二氯荧光素也被强氧化剂(如过氧化氢和氢过氧化物)氧化为DCF,这表明Cr(VI)处理增加了MOLT4细胞中这些过氧化物的细胞内水平。发现过氧化物的生成速率与剂量和时间有关。这些结果表明,细胞内过氧化物的积累可能(至少部分)与铬诱导的遗传毒性有关,并增加了这些现象可能部分通过氧化机制介导的新兴概念。
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