Blanquart C, Romet S, Baeza A, Guennou C, Marano F
Laboratoire de Cytophysiologie et Toxicologie Cellulaire, Université Paris 7, 2 Place Jussieu, 75005 Paris, France.
Toxicol In Vitro. 1991;5(5-6):499-502. doi: 10.1016/0887-2333(91)90080-w.
Cytotoxic assays have been carried out to evaluate toxic effects of acrolein, mechlorethamin, parathion and paraoxon, using primary cultures of rabbit tracheal epithelium obtained by the explant outgrowth technique. The effect of drug exposure was first evaluated by the tetrazolium salt assay, neutral red uptake and release of cellular lactate dehydrogenase. These assays, previously developed for cell line cultures, were adapted to our model. In addition, we present in this paper an easy and rapid method to evaluate the effect of chemicals on cell proliferation. This was performed using an image analysis method, and was found to be the most sensitive marker to determine the acute toxicity of chemicals.
已进行细胞毒性试验,以评估丙烯醛、氮芥、对硫磷和对氧磷的毒性作用,试验采用通过外植体生长技术获得的兔气管上皮原代培养物。首先通过四唑盐试验、中性红摄取和细胞乳酸脱氢酶释放来评估药物暴露的影响。这些先前为细胞系培养开发的试验方法已适用于我们的模型。此外,我们在本文中提出了一种简单快速的方法来评估化学物质对细胞增殖的影响。这是通过图像分析方法进行的,并且被发现是确定化学物质急性毒性的最敏感指标。