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首页> 外文期刊>Toxicological Sciences >Developmental Neurotoxicity of Organophosphorous Pesticides: Fetal and Neonatal Exposure to Chlorpyrifos Alters Sex-Specific Behaviors at Adulthood in Mice
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Developmental Neurotoxicity of Organophosphorous Pesticides: Fetal and Neonatal Exposure to Chlorpyrifos Alters Sex-Specific Behaviors at Adulthood in Mice

机译:有机磷农药的发育神经毒性:毒死rif的胎儿和新生儿暴露改变了成年小鼠的性别特定行为

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Developmental exposure to the organophosphorous insecticide chlorpyrifos (CPF) induces long-term effects on brain and behavior in laboratory rodents. We evaluated in adult mice the behavioral effects of either fetal and/or neonatal CPF exposure at doses not inhibiting fetal and neonatal brain cholinesterase. CPF (3 or 6 mg/kg) was given by oral treatment to pregnant females on gestational days 15–18 and offspring were treated sc (1 or 3 mg/kg) on postnatal days (PNDs) 11–14. Serum and brain acetylcholinesterase (AChE) activity was evaluated at birth and 24 h from termination of postnatal treatments. On PND 70, male mice were assessed for spontaneous motor activity in an open-field test and in a socioagonistic encounter with an unfamiliar conspecific. Virgin females underwent a maternal induction test following presentation of foster pups. Both sexes were subjected to a plus-maze test to evaluate exploration and anxiety levels. Gestational and postnatal CPF exposure (higher doses) affected motor activity in the open field and enhanced synergically agonistic behavior. Postnatal CPF exposure increased maternal responsiveness toward pups in females. Mice of both sexes exposed to postnatal CPF showed reduced anxiety response in the plus-maze, an effect greater in females. Altogether, developmental exposure to CPF at doses that do not cause brain AChE inhibition induces long-term alterations in sex-specific behavior patterns of the mouse species. Late neonatal exposure on PNDs 11–14 was the most effective in causing behavioral changes. These findings support the hypothesis that developmental CPF may represent a risk factor for increased vulnerability to neurodevelopmental disorders in humans.
机译:发育暴露于有机磷杀虫剂毒死rif(CPF)会对实验室啮齿动物的大脑和行为产生长期影响。我们评估了成年小鼠在不抑制胎儿和新生儿脑胆碱酯酶剂量下胎儿和/或新生儿CPF暴露的行为影响。在妊娠第15-18天通过口服治疗向怀孕的女性给予CPF(3或6 mg / kg),在出生后第11-14天对后代进行皮下注射(1或3 mg / kg)。在出生时和终止产后治疗后24小时评估血清和脑乙酰胆碱酯酶(AChE)活性。在PND 70上,在野外测试中以及与陌生同种动物发生社会激动相遇时,对雄性小鼠的自发运动活动进行了评估。初生女性在寄养幼犬后接受母体诱导测试。男女都接受了迷宫测试,以评估探索和焦虑程度。妊娠期和产后CPF暴露(较高剂量)影响了旷野中的运动活动并增强了协同激动行为。产后CPF暴露增加了母体对雌性幼崽的反应能力。暴露于出生后CPF的两性小鼠在迷宫中表现出降低的焦虑反应,对女性的影响更大。总而言之,以不引起大脑AChE抑制的剂量暴露于CPF会引起小鼠物种的性别特异性行为模式的长期改变。 PND 11-14上新生儿的晚期暴露是引起行为改变的最有效方法。这些发现支持以下假设:发育性CPF可能代表增加人类对神经发育障碍的脆弱性的危险因素。

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