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首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >In vitro genotoxicity of ethanol and acetaldehyde in human lymphocytes and the gastrointestinal tract mucosa cells.
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In vitro genotoxicity of ethanol and acetaldehyde in human lymphocytes and the gastrointestinal tract mucosa cells.

机译:乙醇和乙醛在人淋巴细胞和胃肠道粘膜细胞中的体外遗传毒性。

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摘要

The influence of ethanol and acetaldehyde on DNA in human lymphocytes, gastric mucosa (GM) and colonic mucosa (CM) was investigated by using the comet assay. All kinds of cells were exposed to ethanol and acetaldehyde in two regimens: the cells were incubated with either chemical and analysed or they were exposed first to ethanol, washed and then exposed to acetaldehyde and analysed. Lymphocytes were exposed to ethanol at final concentrations of 30 mM and acetaldehyde at 3 mM. GM cells were incubated with ethanol at 1 M and acetaldehyde at 100 mM. CM cells were exposed to ethanol at 10 mM and acetaldehyde at 100 mM. In combined exposure, the cells were subsequently exposed to ethanol and acetaldehyde at all combination of the concentrations of the agents. Ethanol caused DNA strand breaks, which were repaired during 4 hr, except when this agent was applied in GM cells at a concentration of 1 M. A dose-dependent decrease in the tail moment of all types of acetaldehyde-treated cells was observed. Similar results were obtained when a recognized DNA crosslinking agent, formaldehyde, was used. These results suggest that acetaldehyde may form crosslinks with DNA. These crosslinks were poorly repaired. CM cells showed the highest sensitivity of all cell types to ethanol than lymphocytes and GM cells. There were no differences in the sensitivity to acetaldehyde of all the cell types. Our results clearly indicate that ethanol and acetaldehyde can contribute to cancers of the digestive tract.
机译:通过彗星试验研究了乙醇和乙醛对人淋巴细胞,胃粘膜(GM)和结肠粘膜(CM)中DNA的影响。将所有类型的细胞以两种方案暴露于乙醇和乙醛中:将细胞与化学物质一起孵育并进行分析,或者先将它们暴露于乙醇中,洗涤后再暴露于乙醛中进行分析。将淋巴细胞暴露于终浓度为30 mM的乙醇中,并暴露于3 mM的乙醛中。 GM细胞与1 M的乙醇和100 mM的乙醛孵育。 CM细胞暴露于10 mM的乙醇和100 mM的乙醛。在联合暴露中,随后将细胞在试剂浓度的所有组合下暴露于乙醇和乙醛。乙醇引起的DNA链断裂,在4小时内得到修复,除非该试剂以1 M的浓度应用于GM细胞中。观察到,所有类型的乙醛处理过的细胞的尾矩均呈剂量依赖性降低。当使用公认的DNA交联剂甲醛时,可获得相似的结果。这些结果表明乙醛可能与DNA形成交联。这些交联修复不良。与淋巴细胞和GM细胞相比,CM细胞在所有细胞类型中对乙醇的敏感性最高。所有细胞类型对乙醛的敏感性没有差异。我们的结果清楚地表明,乙醇和乙醛可导致消化道癌症。

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