National Exposure Research Laboratory, Office of Research and DevelopmentU.S. Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
Toxicol Sci. 2012 Dec;130(2):309-18. doi: 10.1093/toxsci/kfs245. Epub 2012 Aug 7.
Due to extensive use, human exposure to multiple pyrethroid insecticides occurs frequently. Studies of pyrethroid neurotoxicity suggest a common mode of toxicity and that pyrethroids should be considered cumulatively to model risk. The objective of this work was to use a pyrethroid mixture that reflects human exposure to common pyrethroids to develop comparative toxicokinetic profiles in rats, and then model the relationship between brain concentration and motor activity. Data from a national survey of child care centers were used to make a mixture reflecting proportions of the most prevalent pyrethroids: permethrin, cypermethrin, β-cyfluthrin, deltamethrin, and esfenvalerate. The mixture was administered orally at one of two concentrations (11.2 and 27.4 mg/kg) to adult male rats. At intervals from 1 to 24h, motor activity was assessed and the animals were sacrificed. Pyrethroid concentrations were measured in the blood, liver, fat, and brain. After controlling for dose, there were no differences in any tissue concentrations, except blood at the initial time point. Elimination half-lives for all pyrethroids in all tissues were < 7h. Brain concentrations of all pyrethroids (when cis- and trans-permethrin were pooled) at the initial time point were proportional to their relative doses. Decreases in motor activity indicated dose additivity, and the relationship between pyrethroid brain concentration and motor activity was described by a four-parameter sigmoidal E(max) model. This study links environmental data with toxicokinetic and neurobehavioral assays to support cumulative risk assessments of pyrethroid pesticides. The results support the additive model of pyrethroid effect on motor activity and suggest that variation in the neurotoxicity of individual pyrethroids is related to toxicodynamic rather than toxicokinetic differences.
由于广泛使用,人类经常接触多种拟除虫菊酯类杀虫剂。拟除虫菊酯类神经毒性的研究表明,它们具有共同的毒性模式,因此应将拟除虫菊酯类视为累积物来进行风险建模。本研究的目的是使用反映人类接触常见拟除虫菊酯混合物的混合物,在大鼠中建立比较毒代动力学特征,然后建立大脑浓度与运动活性之间的关系模型。本研究使用了一项全国性的儿童保育中心调查数据来制作反映最常见拟除虫菊酯(如氯菊酯、氯氰菊酯、β-氯氟氰菊酯、溴氰菊酯和甲氰菊酯)比例的混合物。将该混合物以两种浓度(11.2 和 27.4mg/kg)中的一种口服给予成年雄性大鼠。在 1 至 24 小时的时间间隔内,评估运动活性并对动物进行安乐死。在血液、肝脏、脂肪和大脑中测量拟除虫菊酯浓度。在控制剂量后,除了初始时间点的血液外,所有组织中的任何浓度均无差异。所有组织中所有拟除虫菊酯的消除半衰期均<7 小时。所有拟除虫菊酯(当顺式和反式氯菊酯混合时)在初始时间点的大脑浓度与其相对剂量成正比。运动活性的降低表明剂量相加,拟除虫菊酯大脑浓度与运动活性之间的关系可以用四参数 sigmoidal E(max)模型来描述。本研究将环境数据与毒代动力学和神经行为测定相结合,以支持对拟除虫菊酯类农药的累积风险评估。结果支持了拟除虫菊酯类对运动活性的加性效应模型,并表明个别拟除虫菊酯类神经毒性的差异与毒代动力学差异有关,而与毒动学差异无关。