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首页> 外文期刊>Chemico-biological interactions >An in vitro model for evaluation of vaporous toxicity of trichloroethylene and tetrachloroethylene to CHO-K1 cells.
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An in vitro model for evaluation of vaporous toxicity of trichloroethylene and tetrachloroethylene to CHO-K1 cells.

机译:用于评估三氯乙烯和四氯乙烯对CHO-K1细胞的蒸气毒性的体外模型。

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摘要

Toxicokinetics of trichloroethylene (TCE) and tetrachloroethylene (PER) in culture medium and their toxicity to CHO-K1 cells were investigated by employing an in vitro vapor exposure system. Cells were cultured in a 60 mm petri dish with a 25 mm glass dish glued in the central area. TCE or PER was added to the central glass dish so that it would evaporate and dissolve in the surrounding medium in which cells were growing. The results showed that the concentration of TCE or PER in medium increased significantly within 20 min and then decreased very rapidly with time. After a 24 h incubation, the residual of TCE or PER in the medium was very low, but was displayed in a dose-dependent manner. Treatment of cells with either TCE or PER resulted in a dose- and time-dependent inhibition of cell growth. A significantly increase in the frequency of micronuclei (MN) was also observed with either TCE or PER treatment. Low doses of TCE (5-20 microl) or PER (1-5 microl) significantly enhanced the intracellular glutathione (GSH) level. However, the level of GSH rapidly decreased with higher doses of TCE (40-80 microl) or PER (10-20 microl). Depletion of cellular GSH showed no effect on the sensitivity of cells to TCE or PER treatment. GSH-conjugation has been proposed as an activation mechanism to account for the nephrotoxicity of TCE and PER, however the toxicity of TCE and PER to CHO-K1 cells is probably mediated through a distinct mechanism.
机译:通过使用体外蒸气暴露系统研究了三氯乙烯(TCE)和四氯乙烯(PER)在培养基中的毒代动力学及其对CHO-K1细胞的毒性。在60mm培养皿中培养细胞,其中25mm玻璃皿粘在中心区域。将TCE或PER添加到中央玻璃皿中,以使其蒸发并溶解在细胞正在生长的周围培养基中。结果表明,培养基中TCE或PER的浓度在20分钟内显着增加,然后随时间迅速降低。孵育24小时后,培养基中TCE或PER的残留量非常低,但呈剂量依赖性。用TCE或PER处理细胞会导致剂量和时间依赖性的细胞生长抑制。通过TCE或PER处理,还观察到微核(MN)频率显着增加。低剂量的TCE(5-20​​微升)或PER(1-5微升)可显着提高细胞内谷胱甘肽(GSH)水平。然而,随着更高剂量的TCE(40-80微升)或PER(10-20微升),GSH的含量迅速下降。细胞GSH的耗竭对细胞对TCE或PER处理的敏感性没有影响。已经提出将GSH缀合作为考虑到TCE和PER的肾毒性的激活机制,但是TCE和PER对CHO-K1细胞的毒性可能是通过不同的机制介导的。

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