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在无蛋白培养基和完全培养基中测定的MEIC参考化学品细胞毒性的比较。

Comparison of the cytotoxicity of the MEIC reference chemicals measured in protein free and in complete culture medium.

作者信息

Dierickx Paul J

机构信息

Instituut voor Volksgezondheid, Afdeling Toxikologie, Laboratorium Biochemische Toxikologie, Wytsmanstraat 14, B-1050 Brussels, Belgium.

出版信息

Toxicol In Vitro. 2005 Oct;19(7):859-64. doi: 10.1016/j.tiv.2005.06.009. Epub 2005 Jul 28.

Abstract

In order to investigate if a protein free cytotoxicity assay could improve the prediction of human acute toxicity, the cytotoxicity of 40 MEIC reference chemicals was measured by the neutral red uptake inhibition after 24h in protein free culture medium on rat hepatoma-derived Fa32 cells. The results were compared with the corresponding values obtained in complete culture medium, including 10% fetal calf serum. Potassium cyanide, arsenic trioxide, mercuric chloride, hexachlorophene and pentachlorophenol were much more cytotoxic in PF medium, as was the case to a lower extent for 16 other chemicals. The cytotoxicity of 8 chemicals was only changed to a limited extent when tested in PF medium, suggesting that serum proteins do not strongly interact with their cytotoxicity. Eleven other chemicals were less cytotoxic in PF medium, maybe because of too poor physiological conditions. Although a large number of differences in cytotoxicity were observed in function of the medium used for the assay, a good correlation was observed between both series of data (r(2)=0.946). The correlation between the cytotoxicity in PF medium and the human acute toxicity is lower (r(2)=0.647) than that in complete medium (r(2)=0.746). The results show that further research is necessary in order to improve the in vitro/in vivo correlations by introducing protein-dependent considerations.

摘要

为了研究无蛋白细胞毒性试验是否能改善对人类急性毒性的预测,在无蛋白培养基中,采用中性红摄取抑制法测定了40种MEIC参考化学品对大鼠肝癌衍生的Fa32细胞24小时后的细胞毒性。将结果与在含10%胎牛血清的完全培养基中获得的相应值进行比较。氰化钾、三氧化二砷、氯化汞、六氯酚和五氯酚在无蛋白培养基中的细胞毒性更强,其他16种化学品的情况则稍弱。8种化学品在无蛋白培养基中测试时细胞毒性仅发生有限变化,表明血清蛋白与其细胞毒性之间没有强烈相互作用。另外11种化学品在无蛋白培养基中的细胞毒性较小,可能是因为生理条件太差。尽管根据用于试验的培养基不同观察到大量细胞毒性差异,但两个数据集之间仍观察到良好的相关性(r(2)=0.946)。无蛋白培养基中的细胞毒性与人类急性毒性之间的相关性(r(2)=0.647)低于完全培养基中的相关性(r(2)=0.746)。结果表明,为了通过引入蛋白质相关因素来改善体外/体内相关性,有必要进行进一步研究。

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