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Use of the caco-2 model in the screening of polluting substance toxicity.

作者信息

Velarde G, Ait-Aissa S, Gillet C, Rogerieux F, Lambre C, Vindimian E, Porcher J M

机构信息

Laboratoire de Biochimie et Toxicologie in vitro, Institut National de l'Environnement Industriel et des Risques (INERIS), F-60550 Verneuil-en-Halatte, France.

出版信息

Toxicol In Vitro. 1999 Aug-Oct;13(4-5):719-22. doi: 10.1016/s0887-2333(99)00055-7.

DOI:10.1016/s0887-2333(99)00055-7
PMID:20654540
Abstract

The aim of this work was to investigate the oral toxicity of representative chemicals chosen from each class of the list of 132 substances present in industrial effluents after the EEC Directive 76-464. Owing to its characterization as a model of the intestinal epithelium, the CaCo-2 cell line model was chosen. Cytotoxicity was assayed using the tetrazolium blue (MTT) test. For most of the substances, a linear correlation was observed between the octanol/water partition coefficient (log Kw) and the median inhibition concentration (IC(50)). This relationship between lipophilicity and toxicity is the hallmark of a narcotic mechanism of action. However, diethylamine appeared more toxic than the correlation would predict. Other amines were then tested (tert-butylamine, n-butylamine and benzylamine). All of these did not fit into the baseline correlation. The IC(50) were corrected by taking into account only the non-ionized, lipid insoluble, concentration at pH7.3. The amines still did not fit into the correlation, reinforcing the idea of a non-narcotic mechanism. The toxicity of a large number of substances can thus be predicted from their physico-chemical properties only when the substances exert a direct and non-specific effect. The amines appeared more toxic than substances with the same partition coefficient, showing that knowledge of the only lipophilicity is too restrictive to predict toxicity.

摘要

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