Drevon C, Kuroki T
Mutat Res. 1979 Jun;67(2):173-82. doi: 10.1016/0165-1218(79)90129-0.
The mutagenicity of vinyl chloride, vinylidene chloride (1,1-dichloroethylene) and chloroprene (2-chloro-1,3-butadiene) was tested in V79 Chinese hamster cells in the presence of a 15 000 x g liver supernatant from phenobarbitone-pre-treated rats and mice. Mutations in terms of 8-azaguanine and ouabain resistance were induced in a dose-related fasion by exposure to vapour of vinyl chloride in the presence of liver supernatant from phenobarbitone-pretreated rats. Vapours of vinylidene chloride and chloroprene induced a dose-related toxicity in the presence of liver supernatant from phenobarbitone-retreated rats, but these two compounds were not mutagenic in V79 Chinese hamster cells under the present assay conditions. The results are discussed with regard to the metabolic activation of the compounds and to the correlation with their carcinogenicity in man and experimental animals.
在存在来自苯巴比妥预处理大鼠和小鼠的15000×g肝脏上清液的情况下,在V79中国仓鼠细胞中测试了氯乙烯、偏二氯乙烯(1,1 - 二氯乙烯)和氯丁二烯(2 - 氯 - 1,3 - 丁二烯)的致突变性。在存在来自苯巴比妥预处理大鼠的肝脏上清液的情况下,通过暴露于氯乙烯蒸气以剂量相关的方式诱导了对8 - 氮杂鸟嘌呤和哇巴因抗性的突变。在存在来自苯巴比妥处理大鼠的肝脏上清液的情况下,偏二氯乙烯和氯丁二烯的蒸气诱导了剂量相关的毒性,但在本试验条件下,这两种化合物在V79中国仓鼠细胞中没有致突变性。就化合物的代谢活化以及与它们在人和实验动物中的致癌性的相关性对结果进行了讨论。