Prediction of phototoxic potential using human A431 cells and mouse 3T3 cells.

Molecular toxicology Pub Date : 1987-09-01
P A Duffy, A Bennett, M Roberts, O P Flint
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Abstract

An assay using established cell lines, human A431 epidermal cells and mouse 3T3 fibroblasts, has been developed to predict the phototoxic potential of compounds. The test determines the viability of the two cell lines in response to UV light in both the presence and absence of the test compound. The end point for cytotoxicity is determined from the mitochondrial dehydrogenase conversion of a tetrazolium salt (MTT) to a colored formazan product. The cytotoxicity of the test compound is established prior to UV exposure, and the highest no-effect concentration observed is then applied to cells that are subsequently exposed to different periods of UVA and UVA plus UVB light. A phototoxic effect is considered to have occurred when a biologically significant enhancement of toxicity is shown for the UV light with the compound present when compared to that of UV light alone. The test system has been validated with 30 compounds classified as strong, idiosyncratic, and negative based on the frequency of reported adverse reactions in humans. The in vitro phototoxicity assay was able to highlight the potential for phototoxicity in the strong category of phototoxic compounds and several of the idiosyncratic compounds. Only one of the negative compounds produced any activity in the assay in terms of enhancing UV toxicity. Some of the compounds were shown to protect the cells from the toxic effects of UV exposure.

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利用人A431细胞和小鼠3T3细胞预测光毒性电位。
使用已建立的细胞系,人类A431表皮细胞和小鼠3T3成纤维细胞,已经开发出一种测定方法来预测化合物的光毒性潜力。该测试确定了两种细胞系在存在和不存在测试化合物的情况下对紫外光的反应的活力。细胞毒性的终点是由线粒体脱氢酶将四氮唑盐(MTT)转化为彩色甲酸产物确定的。测试化合物的细胞毒性是在紫外线照射之前确定的,然后将观察到的最高无效应浓度应用于随后暴露于UVA和UVA加UVB光的不同时期的细胞。当与单独的紫外光相比,存在该化合物的紫外光显示出生物学上显著的毒性增强时,就认为发生了光毒性效应。该测试系统已经用30种化合物进行了验证,根据报告的人类不良反应的频率,这些化合物被分类为强效、特异性和阴性。体外光毒性试验能够在强光毒性化合物和一些特殊化合物中突出潜在的光毒性。在试验中,只有一种阴性化合物在增强紫外线毒性方面产生任何活性。一些化合物被证明可以保护细胞免受紫外线照射的毒性影响。
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