Mortensen S R, Hooper M J, Padilla S
Cellular and Molecular Toxicology Branch, Neurotoxicology Division (MD-74B), US Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
Toxicology. 1998 Jan 16;125(1):13-9. doi: 10.1016/s0300-483x(97)00157-1.
A growing body of evidence indicates that young animals exhibit an increased susceptibility to the lethal effects of cholinesterase (ChE)-inhibiting insecticides. Our laboratory is engaged in defining factors which may explain this age-related sensitivity. This report includes results from experiments designed to compare the developmental profiles, kinetic parameters and intrinsic (i.e. in vitro) sensitivity of developing male rat brain acetylcholinesterase (AChE) activity to carbamate and organophosphorus anticholinesterases. Total ChE activity in whole brain for each age was composed of about 90% AChE and 10% butyrylcholinesterase (BuChE) activity for the six ages examined. Brain AChE activity showed an age-related increase in Vmax until postnatal day 17 with no change in Km (average of all six ages approximately equal to 72 microM). Optimal substrate (acetylthiocholine) concentration for each age was 1 mM, and there was substrate inhibition (approximately 10%) at 2.5 mM. IC50s (the concentration of compound that inhibits 50% of the AChE activity in 30 min at 26 degrees C) defined concomitantly for postnatal day 4 and adult brain AChE using either aldicarb, carbaryl, chlorpyrifos-oxon or malaoxon were virtually identical at both ages with average IC50 values being: aldicarb = 2.4 microM, carbaryl = 1.7 microM, chlorpyrifos-oxon = 4.9 nM and malaoxon = 140 nM. In summary, AChE in young and adult brain differs mostly in specific activity while the Km(s), substrate profiles, and in vitro sensitivity to selected anticholinesterase insecticides are not different. Therefore, these data support the hypothesis that the greater sensitivity of the young animals to anticholinesterase pesticides is not due to the greater sensitivity of the target molecule AChE to these inhibitors.
越来越多的证据表明,幼龄动物对胆碱酯酶(ChE)抑制性杀虫剂的致死作用表现出更高的易感性。我们实验室致力于确定可能解释这种与年龄相关的敏感性的因素。本报告包括旨在比较发育中的雄性大鼠脑乙酰胆碱酯酶(AChE)活性对氨基甲酸酯类和有机磷抗胆碱酯酶的发育概况、动力学参数和内在(即体外)敏感性的实验结果。在所研究的六个年龄阶段,每个年龄全脑的总ChE活性约90%由AChE活性组成,10%由丁酰胆碱酯酶(BuChE)活性组成。脑AChE活性在出生后第17天之前表现出与年龄相关的Vmax增加,而Km没有变化(所有六个年龄的平均值约等于72 microM)。每个年龄的最佳底物(乙酰硫代胆碱)浓度为1 mM,在2.5 mM时存在底物抑制(约10%)。使用涕灭威、西维因、毒死蜱氧磷或马拉氧磷同时确定出生后第4天和成年脑AChE的IC50(在26℃下30分钟内抑制50%AChE活性的化合物浓度)在两个年龄阶段几乎相同,平均IC50值为:涕灭威 = 2.4 microM,西维因 = 1.7 microM,毒死蜱氧磷 = 4.9 nM,马拉氧磷 = 140 nM。总之,幼龄和成年脑AChE的主要区别在于比活性,而Km、底物谱以及对选定抗胆碱酯酶杀虫剂的体外敏感性并无差异。因此,这些数据支持以下假设,即幼龄动物对抗胆碱酯酶农药的更高敏感性并非由于靶分子AChE对这些抑制剂的更高敏感性。