利用细菌和啮齿动物骨髓细胞评价琥珀酸磺基碘-5、Rokamid MRZ 17、Rokacet RZG7P2和Roksol TL-7的遗传毒性。

E Janik-Spiechowicz, K Wyszyńska, B Przybojewska, B Barański, E Dziubałtowska, W Chwiałkowskaliro
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引用次数: 0

摘要

采用三个短期试验评价了四种表面活性剂的遗传毒性活性。分别是:Ames、沙门氏菌还原试验(TA97a、TA98、TA100和TA102)、Balb C小鼠骨髓微核试验、SFIS和Balb C小鼠体内姐妹染色单体交换(SCE)分析。在腹腔注射所有四种化合物后,雌雄小鼠微核pce的频率均未超过控制值。在小鼠骨髓细胞沙门氏菌基因突变试验和SCE诱导试验中,三种制剂——磺基琥珀酸盐IO-5、Rokacet MRZ 17和Rokacet RZG7P2均产生阴性反应。Roksol TL-7在含S9和不含S9的沙门氏菌检测菌株(用Aroclor 1254预处理的大鼠肝脏制备)中诱导移码和碱基对替换突变。在0.2微升Roksol TL-7 /板剂量下,鼠伤寒沙门氏菌TA97a(有和没有S9代谢激活)和鼠伤寒沙门氏菌TA100(有S9代谢激活)的检测结果明显阳性(每个板的应答数增加了两倍以上)。Roksol TL-7引起小鼠骨髓细胞SCE水平轻微升高。在剂量为50、75和100 mg/kg时,观察到SCE频率显著增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genotoxicity assessment of sulfosuccinate IO-5, Rokamid MRZ 17, Rokacet RZG7P2 and Roksol TL-7 using bacteria and bone marrow rodent cells.

Three short-term tests were used for evaluation of the genotoxic activity of four surface active agents. These were: Ames, Salmonella reversion assay using 4 tester strains (TA97a, TA98, TA100 and TA102), the micronucleus test int the bone marrow of Balb C mice and in vivo sister chromatid exchange (SCE) analysis in SFIS or Balb C mice. The frequency of micronucleated PCEs did not exceed the control values in mice of both sexes after intraperitoneal administration of all four compounds. Three preparations--Sulfosuccinate IO-5, Rokamid MRZ 17 and Rokacet RZG7P2 produced a negative response in Salmonella strains gene mutation assay and SCE induction test in mouse bone marrow cells. The Roksol TL-7 induced frameshift and base-pair substitution mutations in Salmonella tester strains both with and without S9 (prepared from the liver of rats which had been pretreated with Aroclor 1254). Evidently positive results (more than a twofold increase in the number of revertants per plate) were observed in tester strain S. typhimurium TA97a (with and without S9 metabolic activation) and S. typhimurium TA100 (with S9 metabolic activation) at a dose of 0.2 microliter Roksol TL-7 per plate. Roksol TL-7 caused slight increase in the SCE level in mouse bone marrow cells. A significant increase in SCE frequency was observed at doses of 50, 75 and 100 mg/kg.

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