Department of Pathophysiological Laboratory Sciences, Nagoya University Graduate School of Medicine, Nagoya 461-8673, Japan.
Toxicol Lett. 2011 May 30;203(1):28-32. doi: 10.1016/j.toxlet.2011.02.016. Epub 2011 Mar 3.
Pyrethroid insecticide (PYR) is used worldwide in agriculture and for indoor extermination of harmful insects. Urinary PYR metabolites (e.g. 3-phenoxybenzoic acid, 3PBA) have been used as the most sensitive biomarker for environmental PYR exposure since the late 1990s. In this study, we examined the effect of organophosphorus insecticide (OP) dichlorvos (DDVP) on excretion levels of urinary cis-permethrin-derived 3PBA in rats. Concentration of urinary 3PBA and cis-permethrin in plasma was monitored using gas chromatography-mass spectrometry and high-performance liquid chromatography after cis-permethrin injection (20 mg/kg) via the tail vein of rats pretreated intraperitoneally with DDVP (low dose, 0.3 mg/kg; high dose, 1.5 mg/kg). The amount of urinary 3PBA excretion over 48 h after cis-permethrin administration in control was 21.5±5.1 μg (mean±S.D.). In the low- and high-dose DDVP groups, the amounts of urinary 3PBA excretion were decreased to 81.1% (17.4±2.7 μg) and 70.3% (15.1±2.6 μg) of control, respectively. The plasma concentrations of cis-permethrin-derived 3-phenoxybenzyl alcohol (3PBAlc), which is a metabolite derived following hydrolysis of cis-permethrin, in high-dose DDVP group (0.18±0.01 μg) were significantly lower than in control (0.23±0.03 μg) 1h after cis-permethrin injection. Both in the control and high-dose DDVP group, no differences were observed in the excretion levels of urinary 3PBA after injection of 3PBAlc (25mg/kg, i.v.). These results suggested that the effect of DDVP on the amount of urinary 3PBA excretion was caused by the DDVP-induced modification of the cis-permethrin metabolic pathway. In conclusion, the possible decrease in urinary excretion level of 3PBA due to co-exposure to OPs should be considered in the biological monitoring of PYR exposure.
拟除虫菊酯杀虫剂(PYR)在全世界范围内用于农业和室内有害昆虫的消灭。自 20 世纪 90 年代末以来,尿液中 PYR 代谢物(例如 3-苯氧基苯甲酸,3PBA)一直被用作环境 PYR 暴露的最敏感生物标志物。在这项研究中,我们研究了有机磷杀虫剂敌敌畏(DDVP)对大鼠尿液中顺式氯菊酯衍生的 3PBA 排泄水平的影响。在大鼠尾静脉注射顺式氯菊酯(20mg/kg)之前,通过腹膜内预处理 DDVP(低剂量,0.3mg/kg;高剂量,1.5mg/kg),使用气相色谱-质谱法和高效液相色谱法监测尿液中 3PBA 和顺式氯菊酯的浓度。在对照组中,顺式氯菊酯给药后 48 小时内尿液中 3PBA 的排泄量为 21.5±5.1μg(平均值±标准差)。在低剂量和高剂量 DDVP 组中,尿液中 3PBA 的排泄量分别减少到对照组的 81.1%(17.4±2.7μg)和 70.3%(15.1±2.6μg)。高剂量 DDVP 组顺式氯菊酯衍生的 3-苯氧基苯甲醇(3PBAlc)的血浆浓度(顺式氯菊酯水解后的代谢物)在顺式氯菊酯给药后 1 小时(0.18±0.01μg)明显低于对照组(0.23±0.03μg)。在对照组和高剂量 DDVP 组中,静脉注射 3PBAlc(25mg/kg)后,尿液中 3PBA 的排泄水平没有差异。这些结果表明,DDVP 对尿液中 3PBA 排泄量的影响是由 DDVP 诱导的顺式氯菊酯代谢途径改变引起的。总之,在 PYR 暴露的生物监测中,应考虑到与 OPs 共同暴露导致 3PBA 尿液排泄水平降低的可能性。