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含二噁英的除草剂2,4,5-三氯苯氧基乙醇(TCPE)对突变及姐妹染色单体交换诱导的影响。

Effect of herbicide 2,4,5-trichlorophenoxyethanol (TCPE) containing dioxin on mutation and induction of sister chromatid exchanges.

作者信息

Tóth K, Oláh E, Somfai-Relle S, Sugár J

出版信息

Carcinogenesis. 1984 Dec;5(12):1725-8. doi: 10.1093/carcin/5.12.1725.

Abstract

Previous studies have indicated that both herbicide 2,4,5-trichlorophenoxyethanol (TCPE) and its contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) enhance liver tumor incidence in male Swiss mice in a dose-dependent manner. In this report the mutagenicity of TCPE (containing 0.1 p.p.m. TCDD) in the Salmonella/microsome assay was studied, and the effect of this herbicide on the colony-forming ability and on the frequency of sister chromatid exchange (SCE) in Chinese hamster cells were determined. TCPE (1-500 micrograms/plate) appeared non-mutagenic in strains TA 1535, TA 1537, TA 1538, TA 98 and TA 100 either in the absence or presence of S-9 mix from male Wistar rat, male Swiss mouse and male hamster liver pre-treated by Aroclor 1254, using the standard plate incorporation and the pre-incubation assay. Male mouse urine, after a single administration of TCPE to the animal, also proved to be non-mutagenic in strains TA 98 and TA 100. In mammalian cell systems, however, TCPE directly induced a dose related increase in SCE frequency. The dose required to double the control SCE frequency was in the slightly toxic range of the survival curve for TCPE. The cytotoxicity was diminished both in bacterial and mammalian systems in the presence of S-9 mix from male Swiss mouse liver. This S-9 mix strongly reduced SCE frequency induced by TCPE. The induction of SCE observed cannot be attributed to the contaminant TCDD alone, because the SCE production was not influenced by the appropriate low concentration of pure TCDD.

摘要

先前的研究表明,除草剂2,4,5-三氯苯氧基乙醇(TCPE)及其污染物2,3,7,8-四氯二苯并对二恶英(TCDD)均以剂量依赖方式提高雄性瑞士小鼠的肝癌发生率。在本报告中,研究了TCPE(含0.1 ppm TCDD)在沙门氏菌/微粒体试验中的致突变性,并测定了该除草剂对中国仓鼠细胞集落形成能力和姐妹染色单体交换(SCE)频率的影响。使用标准平板掺入法和预孵育试验,在不存在或存在经艾氏剂1254预处理的雄性Wistar大鼠、雄性瑞士小鼠和雄性仓鼠肝脏的S-9混合物的情况下,TCPE(1-500微克/平板)在TA 1535、TA 1537、TA 1538、TA 98和TA 100菌株中均未表现出致突变性。给动物单次注射TCPE后,雄性小鼠尿液在TA 98和TA 100菌株中也被证明无致突变性。然而,在哺乳动物细胞系统中,TCPE直接诱导SCE频率呈剂量相关增加。使对照SCE频率加倍所需的剂量处于TCPE存活曲线的轻微毒性范围内。在存在来自雄性瑞士小鼠肝脏的S-9混合物的情况下,细菌和哺乳动物系统中的细胞毒性均降低。这种S-9混合物强烈降低了TCPE诱导的SCE频率。观察到的SCE诱导不能仅归因于污染物TCDD,因为适当低浓度的纯TCDD不会影响SCE的产生。

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