氨基甲酸酯类杀虫剂pirimor50®对蚕豆根尖分生组织和人淋巴细胞培养的遗传毒性影响及其代谢提取物处理

R. Valencia-Quintana, S. Gómez-Arroyo, J. Sánchez-Alarcón, M. Milić, J. L. Olivares, S. Waliszewski, J. Cortés-Eslava, R. Villalobos-pietrini, M. Calderón-Segura
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引用次数: 9

摘要

摘要:本研究的目的是评估pirimor50®,一种以匹利麦布为基础的配方(50%活性成分),在人淋巴细胞培养物和蚕豆根分生组织中的遗传毒性作用。此外,目的是研究用哺乳动物微粒体S9和植物S10代谢组分或S10混合代谢转化提取物(在蚕豆原根用pirimore -50®处理后)进行杀虫剂处理的综合影响。采用姐妹染色单体交换法(sce)测定细胞周期进展和增殖(M1-M3中期比例和复制指数比值- ri)。植物促生长原激活采用两种方法:体内激活- pirimor50®作用于植物4小时,然后将S10混合物加入淋巴细胞;并且,用primoro -50®和S10或S9处理体外活化淋巴细胞2小时。0.01 mg mL-1直接处理可显著提高分生组织中SCE的频率。在淋巴细胞中,1 mg mL-1时SCE显著升高,0.5 mg mL-1时RI和M1-M3中期比例降低,2.5 mg mL-1时细胞分裂停止。S10混合淋巴细胞处理2-2.5 mg mL-1时SCE值显著升高,3 mg mL-1时细胞死亡。用pirimor50®联合S9或S10治疗淋巴细胞,SCE发生率略有升高,但对RI降低有显著影响,S9治疗时最低。由于没有关于pirimor50基因毒性的数据,本研究是第一个评估和比较其在动物和植物两种生物测定中的直接作用,以及植物和动物代谢对其基因毒性潜力的影响的研究之一。
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Genotoxic effects of the carbamate insecticide Pirimor-50® in Vicia faba root tip meristems and human lymphocyte culture after direct application and treatment with its metabolic extracts
Abstract The aim of the study was to evaluate genotoxic effects of Pirimor-50®, a pirimicarb-based formulation (50 % active ingredient), in human lymphocyte cultures and Vicia faba root meristems. Furthermore, the objective was to examine a combined influence of insecticide treatment with mammalian microsomal S9 and vegetal S10 metabolic fractions or S10 mix metabolic transformation extracts (after Vicia faba primary roots treatment with Pirimor-50®). We used sister chromatid exchange assay-SCE and measured cell cycle progression and proliferation (proportion of M1-M3 metaphases and replication index ratio-RI). Two processes were used for plant promutagen activation: in vivo activation-Pirimor-50® was applied for 4 h to the plant and then S10 mix was added to lymphocytes; and, in vitro activation-lymphocytes were treated with Pirimor-50® and S10 or S9 for 2 h. Direct treatment induced significantly higher SCE frequencies in meristems at 0.01 mg mL-1. In lymphocytes, significantly higher SCE was at 1 mg mL-1 with decrease in RI and M1-M3 metaphase proportions at 0.5 mg mL-1 and cell division stop at 2.5 mg mL1. S10 mix lymphocyte treatment showed significantly elevated SCE values at 2-2.5 mg mL-1, with cell death at 3 mg mL-1. Lymphocyte treatment with Pirimor-50® together with S9 or S10 showed slightly elevated SCE frequency but had a significant influence on RI decrease, with lowest values in S9 treatment. Since no data are available on the genotoxicity of Pirimor-50®, this study is one of the first to evaluate and compare its direct effect in two bioassays, animal and vegetal, and also the effect of plant and animal metabolism on its genotoxic potential.
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