Carr Russell L, Nail Carole A
Center for Environmental Health Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, Mississippi 39762, USA.
Toxicol Sci. 2008 Nov;106(1):186-92. doi: 10.1093/toxsci/kfn164. Epub 2008 Aug 14.
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.
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。