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In Vitro Studies on Atrazine Effects on Human Intestinal Cells

机译:阿特拉津对人体肠道细胞影响的体外研究

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Considering the importance of the oral route for human exposure to atrazine, we have investigated the possible effect of this herbicide on the human intestinal cells and the integrity of the epithelial barrier, using Caco-2 cells as the intestinal model in vitro. We evaluated possibile cytotoxic and genotoxic effects of atrazine in concentrations ranging from 1 to 250 μM on the Caco-2 cells at different stages of growth after short- and long-term exposure. Results from the tetrazolium blue (MTT) test and the Trypan blue exclusion assay showed that atrazine cytotoxicity was dose- and time-dependent. Obtained data indicated that atrazine at high concentrations (50 and 250 μM) was able to induce effects on Caco-2 proliferation and viability. Moreover, it was found that the long-term exposure to atrazine at the non-cytotoxic dose caused inhibition of the intestinal cell maturation and decreased the transepithelial electrical resistance, the indicator of the epithelial barrier integrity. Studies on the atrazine genotoxicity determined using the single cell microelectrophoresis assay indicated that atrazine did not induce DNA damages in the Caco-2 cells at concentrations of up to 50 μM, whereas enhancement in the DNA damage was observed at 250 μM. Altogether, our results indicate that atrazine at expected human oral exposure concentrations is not able to induce effects on the Caco-2 cell proliferation and viability, but may suppress the intestinal cell differentiation and reduce the cell monolayer integrity. We suggest that chronic exposure on low levels of atrazine may lead to alteration in the expression of the morphological and functional features of the Caco-2 cells related to the transport and barrier function of small intestinal enterocytes. In consequence, this may lead to alterations in the intestinal absorption process.
机译:考虑到口服途径对人暴露于阿特拉津的重要性,我们使用Caco-2细胞作为体外肠道模型,研究了该除草剂对人肠道细胞和上皮屏障完整性的可能影响。我们评估了短期和长期暴露后不同浓度的阿特拉津对Caco-2细胞在1至250μM浓度范围内可能产生的细胞毒性和遗传毒性作用。四唑蓝(MTT)测试和锥虫蓝排除试验的结果表明,阿特拉津的细胞毒性是剂量和时间依赖性的。获得的数据表明,高浓度(50和250μM)的阿特拉津能够诱导对Caco-2增殖和活力的影响。此外,发现长期暴露于无细胞毒性剂量的at去津可抑制肠细胞成熟并降低跨上皮电阻,这是上皮屏障完整性的指标。使用单细胞微电泳分析确定的阿特拉津遗传毒性研究表明,阿特拉津在高达50μM的浓度下不会在Caco-2细胞中诱导DNA损伤,而在250μM时观察到DNA损伤的增强。总而言之,我们的结果表明,在人类预期的口腔暴露浓度下的at去津不能诱导对Caco-2细胞增殖和活力的影响,但可能抑制肠细胞分化并降低细胞单层完整性。我们建议长期暴露于低水平的r去津可能会导致Caco-2细胞的形态和功能特征表达的改变,该表达与小肠肠上皮细胞的转运和屏障功能有关。结果,这可能导致肠道吸收过程的改变。

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