Agrawal R C, Mehrotra N k
Laboratory of Environmental Carcinogenesis, Industrial Toxicology Research Center, Lucknow, India.
Food Chem Toxicol. 1997 Oct-Nov;35(10-11):1081-4. doi: 10.1016/s0278-6915(97)87275-4.
Propoxur is a widely used dithiocarbamate pesticide. In the present set of investigations, mutagenicity of propoxur (in formulation) was studied using the micronucleus assay in bone marrow of Swiss mice. Single intraperitoneal (i.p.) administration of 25 mg/kg body weight dose of propoxur, which is a maximum tolerated dose (MTD), significantly induced the micronucleus formation in bone marrow cells after a 24- and 48-hr exposure. A half and a quarter of the MTD (12.5 and 6.25 mg/kg) were found ineffective to induce the micronuclei formation after 24- and 48-hr time periods by the i.p. route. However, the PCE:NCE ratio was inhibited significantly with all the dose levels at both time periods. Oral administration of propoxur at different dose levels also induced micronuclei formation. A single application of 50 and 25 mg/kg dose levels of propoxur, which are MTD and 50% of MTD, also significantly induced micronuclei formation after 24- and 48-hr time periods in bone marrow cells of Swiss mice as compared with solvent control group, whereas a 12.5 mg/kg dose of propoxur was ineffective in inducing micronuclei formation. Single application of indole-3-carbinol (I3C), a glucobrassicin derivative present in cruciferous vegetables, significantly inhibited the propoxur-induced micronuclei formation when it was given at the dose level of 500 mg/kg body weight 48 hr before the single application of propoxur. Therefore, it seems that propoxur is mutagenic in the above test systems and I3C inhibited the mutagenicity of propoxur significantly.
残杀威是一种广泛使用的二硫代氨基甲酸盐类农药。在本系列研究中,使用瑞士小鼠骨髓微核试验研究了残杀威(制剂形式)的致突变性。腹腔注射(i.p.)25mg/kg体重剂量的残杀威(这是最大耐受剂量,MTD),在暴露24小时和48小时后,显著诱导了骨髓细胞中的微核形成。通过腹腔注射途径,MTD的一半和四分之一(12.5mg/kg和6.25mg/kg)在24小时和48小时时间段后未发现能有效诱导微核形成。然而,在两个时间段内,所有剂量水平都显著抑制了嗜多染红细胞(PCE)与正常红细胞(NCE)的比例。不同剂量水平的残杀威口服给药也诱导了微核形成。与溶剂对照组相比,单次应用50mg/kg和25mg/kg剂量水平的残杀威(分别为MTD和MTD的50%),在瑞士小鼠骨髓细胞中暴露24小时和48小时后也显著诱导了微核形成,而12.5mg/kg剂量的残杀威在诱导微核形成方面无效。吲哚-3-甲醇(I3C)是十字花科蔬菜中存在的一种葡糖硫苷衍生物,在单次应用残杀威前48小时以500mg/kg体重的剂量给药时,能显著抑制残杀威诱导的微核形成。因此,在上述测试系统中,残杀威似乎具有致突变性,而I3C能显著抑制残杀威的致突变性。