首页> 美国卫生研究院文献>Environmental Health Perspectives >Alterations in Central Nervous System Serotonergic and Dopaminergic Synaptic Activity in Adulthood after Prenatal or Neonatal Chlorpyrifos Exposure
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Alterations in Central Nervous System Serotonergic and Dopaminergic Synaptic Activity in Adulthood after Prenatal or Neonatal Chlorpyrifos Exposure

机译:产前或新生儿毒死rif暴露后成年后中枢神经系统血清素能和多巴胺能突触活性的变化

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摘要

Exposure to chlorpyrifos (CPF) alters neuronal development of serotonin (5HT) and dopamine systems, and we recently found long-term alterations in behaviors related to 5HT function. To characterize the synaptic mechanisms underlying these effects, we exposed developing rats to CPF regimens below the threshold for systemic toxicity, in three treatment windows: gestational days (GD) 17–20, postnatal days (PN) 1–4, or PN11–14. In early adulthood (PN60), we assessed basal neurotransmitter content and synaptic activity (turnover) in brain regions containing the major 5HT and dopamine projections. CPF exposure on GD17–20 or PN1–4 evoked long-term increases in 5HT turnover across multiple regions; the effects were not secondary to changes in neurotransmitter content, which was unaffected or even decreased. When the treatment window was shifted to PN11–14, there were no long-term effects. Dopamine turnover also showed significant increases after CPF exposure on GD17–20, but only when the dose was raised above the threshold for overt toxicity; however, hippocampal dopamine content was profoundly subnormal after exposures below or above the acute, toxic threshold, suggesting outright neurotoxicity. These results indicate that, in a critical developmental period, apparently nontoxic exposures to CPF produce lasting activation of 5HT systems in association with 5HT-associated behavioral anomalies.
机译:暴露于毒死rif(CPF)会改变5-羟色胺(5HT)和多巴胺系统的神经元发育,最近我们发现与5HT功能相关的行为发生了长期变化。为了表征这些作用的突触机制,我们在三个治疗窗口中将发育中的大鼠暴露于低于系统毒性阈值的CPF方案下:妊娠日(GD)17-20,产后日(PN)1-4或PN11-14 。在成年初期(PN60),我们评估了包含主要5HT和多巴胺投射的大脑区域的基础神经递质含量和突触活性(转变)。 GD17-20或PN1-4的CPF暴露引起多个地区5HT营业额的长期增加;这种作用并不随神经递质含量的变化而变化,而神经递质含量的变化并未受到影响甚至降低。当治疗窗口移至PN11-14时,没有长期影响。在GD17-20上CPF暴露后,多巴胺周转率也显示出显着增加,但仅当剂量增加到明显的毒性阈值以上时;然而,暴露于急性毒性阈值以下或之上后,海马多巴胺含量明显低于正常水平,表明完全神经毒性。这些结果表明,在关键的发育时期,显然无毒的CPF暴露会与5HT相关的行为异常相关联,从而持续激活5HT系统。

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