Delescluse C, Ledirac N, de Sousa G, Pralavorio M, Lesca P, Rahmani R
Laboratoire de Pharmaco-toxicologie Cellulaire et Moléculaire, Centre de Recherches INRA, Antibes, France.
Toxicol Lett. 1998 Aug;96-97:33-9. doi: 10.1016/s0378-4274(98)00047-2.
Insecticides deserve particular attention since the general population is potentially exposed to such chemicals through many routes. We therefore tested the comparative acute and chronic toxicity of chemicals belonging to the major insecticides families (DDT, malathion and tetrachlorvinphos, carbaryl, cypermethrin, diflubenzuron), in hepatocytes, HepG2 and HaCaT cell lines. Two kinds of end-points were used: cytotoxicity parameters and CYP1A1 induction. Except for cypermethrin and diflubenzuron, all these chemicals exerted a cytotoxic effect in hepatocytes and HaCaT, but not in HepG2 cells. However, the induction of the EROD activity appeared more sensitive since a response was detected at lower concentrations. Significant differences were observed between the cell types and the insecticides. Furthermore, these chemicals were unable to displace [3H]TCDD from its binding sites, suggesting that they would not be a ligand of the Ah receptor. The experimental approach used herein may be a good means for predicting the acute and chronic toxicity of pesticides.
由于普通人群可能通过多种途径接触到此类化学物质,杀虫剂值得特别关注。因此,我们在肝细胞、HepG2和HaCaT细胞系中测试了属于主要杀虫剂家族(滴滴涕、马拉硫磷和杀虫畏、西维因、氯氰菊酯、除虫脲)的化学物质的比较急性和慢性毒性。使用了两种终点指标:细胞毒性参数和CYP1A1诱导。除氯氰菊酯和除虫脲外,所有这些化学物质在肝细胞和HaCaT细胞中均表现出细胞毒性作用,但在HepG2细胞中未表现出细胞毒性作用。然而,EROD活性的诱导似乎更敏感,因为在较低浓度下就检测到了反应。在细胞类型和杀虫剂之间观察到了显著差异。此外,这些化学物质无法从其结合位点上取代[3H]TCDD,这表明它们不会是芳烃受体的配体。本文使用的实验方法可能是预测农药急性和慢性毒性的一种好方法。