反复暴露于低浓度毒死蜱对幼年大鼠血清酯酶的抑制作用。

Jenna A Mosier, Rachel L Hybart, Aubrey M Lewis, Navatha Alugubelly, Afzaal N Mohammed, Russell L Carr
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引用次数: 0

摘要

毒死蜱(CPF)是一种有机磷杀虫剂,由于与发育暴露相关的毒性报道而引起了极大的关注。虽然CPF的典型毒性机制涉及对脑乙酰胆碱酯酶(AChE)的抑制,但我们已经报道,暴露于不产生任何脑AChE抑制的CPF水平的幼年大鼠在晚年会导致神经行为改变。然而,目前尚不清楚暴露于这些低水平CPF对血液酯酶活性的影响,酯酶活性不仅经常被用作暴露的生物标志物,而且还被用作风险评估中的设定暴露水平。为了确定这一点,从出生后第10天到第16天,雄性和雌性大鼠幼崽口服玉米油(对照)或0.5、0.75或1.0 mg/kg CPF。最终暴露后12 h,测定血清胆碱酯酶(ChE)、丁基胆碱酯酶(BChE)和羧酸酯酶(CES),以及红细胞(RBC)和脑乙酰胆碱酯酶(AChE)活性。在所有酶的对照组和单独处理中,没有性别差异。只有最高剂量1.0 mg/kg CPF能显著抑制脑AChE(22-24%),但所有剂量均能显著抑制血中酯酶,其中抑制作用最大的是血清CES(65-85%),其次是血清BChE(57-76%)、RBC AChE(35-65%),最后是血清ChE(16-32%)。我们的数据证实,血液酯酶在CPF剂量下被抑制,CPF改变神经行为表现,但对脑乙酰胆碱酯酶活性没有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inhibition of Serum Esterases in Juvenile Rats Repeatedly Exposed to Low Levels of Chlorpyrifos.

Inhibition of Serum Esterases in Juvenile Rats Repeatedly Exposed to Low Levels of Chlorpyrifos.

Inhibition of Serum Esterases in Juvenile Rats Repeatedly Exposed to Low Levels of Chlorpyrifos.

Chlorpyrifos (CPF) is an organophosphorus insecticide that has gained significant attention cue to the reported toxicity associated with developmental exposure. While the canonical mechanism of toxicity of CPF involves the inhibition of brain acetylcholinesterase (AChE), we have reported that exposure of juvenile rats to levels of CPF that do not yield any inhibition of brain AChE results in neurobehavioral alterations at later ages. However, it is unclear what effect exposure to these low levels of CPF has on blood esterase activities which are frequently used not only as biomarkers of exposure but also to set exposure levels in risk assessment. To determine this, male and female rat pups were exposed orally from postnatal day 10 to 16 to either corn oil (vehicle) or 0.5, 0.75, or 1.0 mg/kg CPF. At 12 h after the final exposure, serum cholinesterase (ChE), butyrylcholinesterase (BChE), and carboxylesterase (CES), and red blood cell (RBC) and brain AChE activities were determined. There were no differences between sexes in either the controls or individual treatments for all enzymes. Only the highest dosage of 1.0 mg/kg CPF yielded significant brain AChE inhibition (22-24%) but all dosages significantly inhibited the blood esterases with inhibition being highest with serum CES (65-85%) followed by serum BChE (57-76%), RBC AChE (35-65%), and then serum ChE (16-32%). Our data verify that blood esterases are inhibited at dosages of CPF that alter neurobehavioral performance in the absence of effects on brain AChE activity.

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