Akyil Dilek, Konuk Muhsin, Eren Yasin, Liman Recep, Sağlam Esra
Molecular Biology and Genetic Department, Faculty of Sciences and Literatures, Afyon Kocatepe University, 03200, Afyonkarahisar, Turkey.
Molecular Biology and Genetics Department, Faculty of Engineering and Natural Sciences, Üsküdar University, Altunizade, 34662, Istanbul, Turkey.
Cytotechnology. 2017 Dec;69(6):865-874. doi: 10.1007/s10616-017-0099-y. Epub 2017 Jun 12.
We aimed to evaluate the mutagenic effect of Anilofos, organophosphate pesticide, by using Ames/Salmonella/microsome test. Its cytotoxic and genotoxic effects were also determined by chromosome aberration (CA), sister chromatid exchange (SCE) and micronucleus (MN) test in human peripheral blood lymphocytes. In the Ames test, five different concentrations of Anilofos were examined on TA97, TA98, TA100 and TA102 strains in the absence and presence of S9 fraction. According to the results all concentrations of this pesticide have not shown any mutagenic activity on TA97, TA100 and TA102 strains in the absence and presence of S9 fraction. But, 10, 100 and 1000 µg/plate concentrations of Anilofos were determined to be mutagenic on TA98 strain without S9 fraction. Lymphocytes were treated with various concentrations (25, 50, 100 and 200 µg/ml) of Anilofos for 24 and 48 h. The results of the assays showed that Anilofos did not induce SCE frequency, replication index and MN formation at all concentrations for both treatment periods. Anilofos significantly increased CA frequency at 100 and 200 µg/ml concentrations at 24 h treatment periods and at 50, 100 and 200 µg/ml concentrations in 48 h treatment periods. Additionally, it was determined that this pesticide decreased mitotic index and nuclear division index significantly. It was concluded that Anilofos has genotoxic and cytotoxic effects in human peripheral lymphocytes.
我们旨在通过艾姆斯/沙门氏菌/微粒体试验评估有机磷农药莎稗磷的致突变作用。还通过人外周血淋巴细胞的染色体畸变(CA)、姐妹染色单体交换(SCE)和微核(MN)试验来确定其细胞毒性和遗传毒性作用。在艾姆斯试验中,在不存在和存在S9组分的情况下,对TA97、TA98、TA100和TA102菌株检测了五种不同浓度的莎稗磷。根据结果,在不存在和存在S9组分的情况下,该农药的所有浓度对TA97、TA100和TA102菌株均未显示出任何致突变活性。但是,在无S9组分时,确定10、100和1000μg/平板浓度的莎稗磷对TA98菌株具有致突变性。用不同浓度(25、50、100和200μg/ml)的莎稗磷处理淋巴细胞24小时和48小时。检测结果表明,在两个处理时间段内,所有浓度的莎稗磷均未诱导SCE频率、复制指数和MN形成。在24小时处理时间段内,100和200μg/ml浓度以及在48小时处理时间段内50、100和200μg/ml浓度的莎稗磷显著增加了CA频率。此外,还确定该农药显著降低了有丝分裂指数和核分裂指数。得出的结论是,莎稗磷对人外周淋巴细胞具有遗传毒性和细胞毒性作用。