National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency Research Triangle Park, NC, United States.
Toxicology. 2011 Nov 28;290(1):1-6. doi: 10.1016/j.tox.2011.08.002. Epub 2011 Aug 10.
The potential for human exposure to pyrethroid pesticides has prompted pharmacodynamic and pharmacokinetic research to better characterize risk. This work tested the hypothesis that blood and brain concentrations of the pyrethroid bifenthrin are predictive of neurotoxic effects. Adult male Long Evans rats received a single oral dose of bifenthrin dissolved in corn oil. Using figure-eight mazes, motor activity was measured for 1h at 4- and 7-h following exposure to bifenthrin (0-16mg/kg or 0-9mg/kg, respectively; n=4-8/group). Whole blood and brains were collected immediately following motor activity assays. Bifenthrin concentrations in blood and brain were quantified using HPLC/MS/MS. Bifenthrin exposure decreased motor activity from 20% to 70% in a dose-dependent manner at both time points. The relationship between motor activity data and administered dose, and blood and brain bifenthrin concentrations were described using a sigmoidal E(max) model. The relationships between motor activity and administered dose or blood concentrations were different between the 4- and 7-h time points. The relationship between motor activity and brain concentration was not significantly different between the two time points. These data suggest that momentary brain concentration of bifenthrin may be a more precise dose metric for predicting behavioral effects because the relationship between brain concentration and locomotor activity is independent of the time of exposure.
人类接触拟除虫菊酯类农药的可能性促使人们进行药效动力学和药代动力学研究,以更好地评估风险。这项工作检验了一个假设,即拟除虫菊酯类农药中的氯氟氰菊酯在血液和大脑中的浓度可以预测其神经毒性作用。成年雄性长耳大仓鼠(Long Evans rats)经口单次给予溶于玉米油的氯氟氰菊酯。在暴露于氯氟氰菊酯(0-16mg/kg 或 0-9mg/kg,分别为 4-7 小时;n=4-8/组)4-7 小时后,使用八字迷宫测试,在暴露后 1 小时测量运动活性。在运动活性测定后立即采集全血和大脑。使用 HPLC/MS/MS 定量测定血液和大脑中的氯氟氰菊酯浓度。氯氟氰菊酯暴露以剂量依赖性方式使运动活性从 20%降低到 70%,在两个时间点均如此。运动活性数据与给药剂量、血液和大脑中的氯氟氰菊酯浓度之间的关系用 S 型 E(max)模型描述。运动活性与给药剂量或血液浓度之间的关系在 4-7 小时时间点之间不同。运动活性与大脑浓度之间的关系在两个时间点之间没有显著差异。这些数据表明,氯氟氰菊酯在大脑中的瞬时浓度可能是预测行为效应的更精确剂量指标,因为大脑浓度与运动活性之间的关系独立于暴露时间。