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2
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Age-dependent pharmacokinetic and pharmacodynamic response in preweanling rats following oral exposure to the organophosphorus insecticide chlorpyrifos.断奶前大鼠经口暴露于有机磷杀虫剂毒死蜱后年龄依赖性的药代动力学和药效学反应。
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Impaired reproductive development in sons of women occupationally exposed to pesticides during pregnancy.孕期职业性接触杀虫剂的女性所生儿子的生殖发育受损。
Environ Health Perspect. 2008 Apr;116(4):566-72. doi: 10.1289/ehp.10790.
2
The effect of route, vehicle, and divided doses on the pharmacokinetics of chlorpyrifos and its metabolite trichloropyridinol in neonatal Sprague-Dawley rats.给药途径、载体及分次给药对新生Sprague-Dawley大鼠体内毒死蜱及其代谢物3,5,6-三氯-2-吡啶醇药代动力学的影响。
Toxicol Sci. 2007 Dec;100(2):360-73. doi: 10.1093/toxsci/kfm239. Epub 2007 Oct 10.
3
Alteration of neurotrophins in the hippocampus and cerebral cortex of young rats exposed to chlorpyrifos and methyl parathion.暴露于毒死蜱和甲基对硫磷的幼鼠海马体和大脑皮层中神经营养因子的改变。
Toxicol Sci. 2007 Dec;100(2):445-55. doi: 10.1093/toxsci/kfm248. Epub 2007 Sep 24.
4
Pesticide urinary metabolite levels of children in eastern North Carolina farmworker households.北卡罗来纳州东部农场工人家庭儿童的农药尿液代谢物水平。
Environ Health Perspect. 2007 Aug;115(8):1254-60. doi: 10.1289/ehp.9975.
5
Altered muscarinic acetylcholine receptor subtype binding in neonatal rat brain following exposure to chlorpyrifos or methyl parathion.新生大鼠脑内毒蕈碱型乙酰胆碱受体亚型结合在暴露于毒死蜱或甲基对硫磷后发生改变。
Toxicol Sci. 2007 Nov;100(1):118-27. doi: 10.1093/toxsci/kfm195. Epub 2007 Jul 31.
6
Developmental exposure to terbutaline and chlorpyrifos, separately or sequentially, elicits presynaptic serotonergic hyperactivity in juvenile and adolescent rats.在幼年和青春期大鼠中,单独或先后发育性暴露于特布他林和毒死蜱会引发突触前5-羟色胺能亢进。
Brain Res Bull. 2007 Jul 12;73(4-6):301-9. doi: 10.1016/j.brainresbull.2007.04.004. Epub 2007 May 11.
7
Assessing transferable residues from intermittent exposure to flea control collars containing the organophosphate insecticide chlorpyrifos.评估因间歇性接触含有有机磷酸酯杀虫剂毒死蜱的跳蚤控制项圈而产生的可转移残留。
J Expo Sci Environ Epidemiol. 2007 Nov;17(7):656-66. doi: 10.1038/sj.jes.7500570. Epub 2007 Mar 28.
8
Potential uses of biomonitoring data: a case study using the organophosphorus pesticides chlorpyrifos and malathion.生物监测数据的潜在用途:以有机磷农药毒死蜱和马拉硫磷为例的案例研究
Environ Health Perspect. 2006 Nov;114(11):1763-9. doi: 10.1289/ehp.9062.
9
Effect of developmental exposure to chlorpyrifos on the expression of neurotrophin growth factors and cell-specific markers in neonatal rat brain.发育阶段接触毒死蜱对新生大鼠大脑中神经营养生长因子和细胞特异性标志物表达的影响。
Toxicol Sci. 2006 Aug;92(2):500-6. doi: 10.1093/toxsci/kfl004. Epub 2006 May 4.
10
Age-dependent pharmacokinetic and pharmacodynamic response in preweanling rats following oral exposure to the organophosphorus insecticide chlorpyrifos.断奶前大鼠经口暴露于有机磷杀虫剂毒死蜱后年龄依赖性的药代动力学和药效学反应。
Toxicology. 2006 Mar 1;220(1):13-25. doi: 10.1016/j.tox.2005.11.011. Epub 2005 Dec 15.

不同给药模式对断奶前晚期大鼠反复接触毒死蜱后胆碱酯酶抑制作用的影响。

Effect of different administration paradigms on cholinesterase inhibition following repeated chlorpyrifos exposure in late preweanling rats.

作者信息

Carr Russell L, Nail Carole A

机构信息

Center for Environmental Health Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, Mississippi 39762, USA.

出版信息

Toxicol Sci. 2008 Nov;106(1):186-92. doi: 10.1093/toxsci/kfn164. Epub 2008 Aug 14.

DOI:10.1093/toxsci/kfn164
PMID:18703558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2563141/
Abstract

Chlorpyrifos (CPS) is widely used in agricultural settings and residue analysis has suggested that children in agricultural communities are at risk of exposure. This has resulted in a large amount of literature investigating the potential for CPS-induced developmental neurotoxic effects. Two developmental routes of administration of CPS are orally in corn oil at a rate of 0.5 ml/kg and subcutaneously in dimethyl sulfoxide (DMSO) at a rate of 1.0 ml/kg. For comparison between these methods, rat pups were exposed daily from days 10 to 16 to CPS (5 mg/kg) either orally dissolved in corn oil or subcutaneously dissolved in DMSO, both at rates of either 0.5 or 1.0 ml/kg. A representative vehicle/route group was present for each treatment. Both the low and high volume CPS in DMSO subcutaneous groups were lower than that of the low and high volume CPS in oil oral groups. At 4 h following the final administration, serum carboxylesterase was inhibited > 90% with all treatments. For cholinesterase activity in the cerebellum, medulla-pons, forebrain, and hindbrain, and serum, inhibition in the CPS-oil groups was similar and inhibition in the CPS-DMSO groups was similar. However, significantly greater inhibition was present in the high volume CPS-DMSO group as compared to the CPS-oil groups. Inhibition in the low volume CPS-DMSO group was generally between that in the CPS-oil groups and the high volume CPS-DMSO group. These data suggest that using DMSO as a vehicle for CPS may alter the level of brain ChE inhibition.

摘要

毒死蜱(CPS)在农业环境中广泛使用,残留分析表明农业社区的儿童有接触风险。这导致了大量文献研究CPS诱导发育性神经毒性作用的可能性。CPS的两种发育给药途径分别是以0.5毫升/千克的剂量口服溶于玉米油中,以及以1.0毫升/千克的剂量皮下注射溶于二甲基亚砜(DMSO)中。为了比较这些方法,从出生后第10天到第16天,将幼鼠每天暴露于CPS(5毫克/千克),要么口服溶于玉米油中,要么皮下注射溶于DMSO中,剂量均为0.5或1.0毫升/千克。每种处理都有一个代表性的溶媒/途径组。DMSO皮下注射组的低剂量和高剂量CPS均低于玉米油口服组的低剂量和高剂量CPS。在最后一次给药后4小时,所有处理的血清羧酸酯酶均被抑制>90%。对于小脑、延髓脑桥、前脑和后脑以及血清中的胆碱酯酶活性,CPS-油组的抑制作用相似,CPS-DMSO组的抑制作用也相似。然而,与CPS-油组相比,高剂量CPS-DMSO组的抑制作用明显更大。低剂量CPS-DMSO组的抑制作用一般介于CPS-油组和高剂量CPS-DMSO组之间。这些数据表明,使用DMSO作为CPS的溶媒可能会改变脑胆碱酯酶的抑制水平。