Kacham R, Karanth S, Baireddy P, Liu J, Pope C
Department of Physiological Sciences, 264 McElroy Hall, Center for Veterinary Health Sciences, Oklahoma State University, Stillwater, OK 74078, USA.
Toxicol Appl Pharmacol. 2006 Jan 1;210(1-2):142-9. doi: 10.1016/j.taap.2005.09.014. Epub 2005 Nov 2.
We previously reported that sequence of exposure to chlorpyrifos and parathion in adult rats can markedly influence toxic outcome. In the present study, we evaluated the interactive toxicity of chlorpyrifos (8 mg/kg, po) and parathion (0.5 mg/kg, po) in neonatal (7 days old) rats. Rats were exposed to the insecticides either concurrently or sequentially (separated by 4 h) and sacrificed at 4, 8, and 24 h after the first exposure for biochemical measurements (cholinesterase activity in brain, plasma, and diaphragm and carboxylesterase activity in plasma and liver). The concurrently-exposed group showed more cumulative lethality (15/24) than either of the sequential dosing groups. With sequential dosing, rats treated initially with chlorpyrifos prior to parathion (C/P) exhibited higher lethality (7/23) compared to those treated with parathion before chlorpyrifos (P/C; 1/24). At 8 h after initial dosing, brain cholinesterase inhibition was significantly greater in the C/P group (59%) compared to the P/C group (28%). Diaphragm and plasma cholinesterase activity also followed a relatively similar pattern of inhibition. Carboxylesterase inhibition in plasma and liver was relatively similar among the treatment groups across time-points. Similar sequence-dependent differences in brain cholinesterase inhibition were also noted with lower binary exposures to chlorpyrifos (2 mg/kg) and parathion (0.35 mg/kg). In vitro and ex vivo studies compared relative oxon detoxification of carboxylesterases (calcium-insensitive) and A-esterases (calcium-sensitive) in liver homogenates from untreated and insecticide pretreated rats. Using tissues from untreated rats, carboxylesterases detoxified both chlorpyrifos oxon and paraoxon, while A-esterases only detoxified chlorpyrifos oxon. With parathion pretreatment, A-esterases still detoxified chlorpyrifos oxon while liver from chlorpyrifos pretreated rats had little apparent effect on paraoxon. We conclude that while neonatal rats are less capable than adults at detoxifying many organophosphorus insecticides including chlorpyrifos and parathion, toxicant-selective differences in detoxification play a role in sequence-dependent toxicity in both neonatal and adult rats with these two insecticides.
我们之前报道过,成年大鼠接触毒死蜱和对硫磷的顺序会显著影响毒性结果。在本研究中,我们评估了毒死蜱(8毫克/千克,经口)和对硫磷(0.5毫克/千克,经口)对新生(7日龄)大鼠的联合毒性。大鼠同时或先后(间隔4小时)接触杀虫剂,并在首次接触后4小时、8小时和24小时处死,进行生化测量(脑、血浆和膈肌中的胆碱酯酶活性以及血浆和肝脏中的羧酸酯酶活性)。同时接触组的累积致死率(15/24)高于任何一个先后给药组。先后给药时,先接触毒死蜱再接触对硫磷(C/P)的大鼠的致死率(7/23)高于先接触对硫磷再接触毒死蜱(P/C;1/24)的大鼠。在首次给药后8小时,C/P组的脑胆碱酯酶抑制率(59%)显著高于P/C组(28%)。膈肌和血浆胆碱酯酶活性也呈现出相对相似的抑制模式。各治疗组在不同时间点的血浆和肝脏羧酸酯酶抑制情况相对相似。在较低剂量的毒死蜱(2毫克/千克)和对硫磷(0.35毫克/千克)二元接触中,也观察到了脑胆碱酯酶抑制方面类似的顺序依赖性差异。体外和离体研究比较了未处理和经杀虫剂预处理大鼠肝脏匀浆中羧酸酯酶(钙不敏感)和A酯酶(钙敏感)对氧磷的相对解毒作用。使用未处理大鼠的组织,羧酸酯酶可使毒死蜱氧磷和对氧磷解毒,而A酯酶仅使毒死蜱氧磷解毒。经对硫磷预处理后,A酯酶仍可使毒死蜱氧磷解毒,而经毒死蜱预处理大鼠的肝脏对对氧磷几乎没有明显作用。我们得出结论,虽然新生大鼠在对包括毒死蜱和对硫磷在内的许多有机磷杀虫剂进行解毒方面比成年大鼠能力更弱,但解毒过程中对毒物的选择性差异在这两种杀虫剂对新生和成年大鼠的顺序依赖性毒性中发挥了作用。