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孕期接触毒死蜱:胆碱酯酶和羧酸酯酶活性的剂量反应曲线

Gestational exposure to chlorpyrifos: dose response profiles for cholinesterase and carboxylesterase activity.

作者信息

Lassiter T L, Barone S, Moser V C, Padilla S

机构信息

Curriculum in Toxicology, University of North Carolina, Chapel Hill, USA.

出版信息

Toxicol Sci. 1999 Nov;52(1):92-100. doi: 10.1093/toxsci/52.1.92.

Abstract

This study investigates the in vivo dose response profiles of the target enzyme cholinesterase (ChE) and the detoxifying enzymes carboxylesterase (CaE) in the fetal and maternal compartments of pregnant rats dosed with chlorpyrifos [(O,O'-diethyl O-3,5,6-trichloro-2-pyridyl) phosphorothionate], a commonly used organophosphorus insecticide. Pregnant rats were dosed daily (po) with chlorpyrifos in corn oil (0, 3, 5, 7, or 10 mg/kg) on gestational days (GD) 14-18. Animals were sacrificed 5 h after the last chlorpyrifos dose (time of maximum brain cholinesterase inhibition) for analysis of ChE and CaE activity in maternal blood, liver, brain, placenta, and fetal liver and brain. The in vitro sensitivity (i.e., IC50, 30 min, 26 degrees C) of CaE also was determined by assaying the activity remaining after incubation with a range of chlorpyrifos-oxon concentrations. In vivo exposure to 10 mg/kg chlorpyrifos from GD14-18 caused overt maternal toxicity, with dose-related decreases in ChE activity more notable in maternal brain than fetal brain. Dose-related effects were also seen with chlorpyrifos-induced inhibition of fetal liver ChE and maternal brain CaE activities. Gestational exposure caused no inhibition of placental ChE or CaE, fetal brain CaE, or maternal blood CaE. ChE activities in the maternal blood and liver, as well as fetal and maternal liver CaE, however, were maximally inhibited by even the lowest dosage of chlorpyrifos. The in vitro sensitivity profiles of CaE to chlorpyrifos-oxon inhibition were valuable in predicting and verifying the in vivo CaE response profiles. Both the in vivo and in vitro findings indicated that fetal liver CaE inhibition was an extremely sensitive indicator of fetal chlorpyrifos exposure.

摘要

本研究调查了用毒死蜱[(O,O'-二乙基-O-3,5,6-三氯-2-吡啶基)硫代磷酸酯](一种常用的有机磷杀虫剂)对怀孕大鼠进行给药后,在胎儿和母体组织中靶酶胆碱酯酶(ChE)以及解毒酶羧酸酯酶(CaE)的体内剂量反应情况。怀孕大鼠在妊娠第14至18天每天经口给予玉米油中的毒死蜱(0、3、5、7或10mg/kg)。在最后一次给予毒死蜱剂量后5小时(脑胆碱酯酶抑制作用最强的时间)处死动物,以分析母体血液、肝脏、脑、胎盘以及胎儿肝脏和脑中ChE和CaE的活性。CaE的体外敏感性(即IC50,30分钟,26℃)也通过测定与一系列毒死蜱氧磷浓度孵育后剩余的活性来确定。在妊娠第14至18天体内暴露于10mg/kg毒死蜱会导致明显的母体毒性,ChE活性的剂量相关下降在母体脑中比胎儿脑中更显著。毒死蜱诱导的胎儿肝脏ChE和母体脑CaE活性抑制也呈现剂量相关效应。孕期暴露未抑制胎盘ChE或CaE、胎儿脑CaE或母体血液CaE。然而,即使是最低剂量的毒死蜱也能最大程度地抑制母体血液和肝脏中的ChE活性,以及胎儿和母体肝脏中的CaE活性。CaE对毒死蜱氧磷抑制的体外敏感性情况对于预测和验证体内CaE反应情况很有价值。体内和体外研究结果均表明,胎儿肝脏CaE抑制是胎儿暴露于毒死蜱的一个极其敏感的指标。

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