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首页> 外文期刊>Environmental health perspectives. >Exposure to organophosphates reduces the expression of neurotrophic factors in neonatal rat brain regions: similarities and differences in the effects of chlorpyrifos and diazinon on the fibroblast growth factor superfamily.
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Exposure to organophosphates reduces the expression of neurotrophic factors in neonatal rat brain regions: similarities and differences in the effects of chlorpyrifos and diazinon on the fibroblast growth factor superfamily.

机译:暴露于有机磷酸盐会降低新生大鼠大脑区域中神经营养因子的表达:毒死rif和地嗪酮对成纤维细胞生长因子超家族作用的异同。

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摘要

BACKGROUND: The fibroblast growth factor (FGF) superfamily of neurotrophic factors plays critical roles in neural cell development, brain assembly, and recovery from neuronal injury. OBJECTIVES: We administered two organophosphate pesticides, chlorpyrifos and diazinon, to neonatal rats on postnatal days 1-4, using doses below the threshold for systemic toxicity or growth impairment, and spanning the threshold for barely detectable cholinesterase inhibition: 1 mg/kg/day chlorpyrifos and 1 or 2 mg/kg/day diazinon. METHODS: Using microarrays, we then examined the regional expression of mRNAs encoding the FGFs and their receptors (FGFRs) in the forebrain and brain stem. RESULTS: Chlorpyrifos and diazinon both markedly suppressed fgf20 expression in the forebrain and fgf2 in the brain stem, while elevating brain stem fgfr4 and evoking a small deficit in brain stem fgf22. However, they differed in that the effects on fgf2 and fgfr4 were significantly larger for diazinon, and the two agents also showed dissimilar, smaller effects on fgf11, fgf14, and fgfr1. CONCLUSIONS: The fact that there are similarities but also notable disparities in the responses to chlorpyrifos and diazinon, and that robust effects were seen even at doses that do not inhibit cholinesterase, supports the idea that organophosphates differ in their propensity to elicit developmental neurotoxicity, unrelated to their anticholinesterase activity. Effects on neurotrophic factors provide a mechanistic link between organophosphate injury to developing neurons and the eventual, adverse neurodevelopmental outcomes.
机译:背景:神经营养因子的成纤维细胞生长因子(FGF)超家族在神经细胞发育,脑部组装和神经元损伤的恢复中起着至关重要的作用。目的:我们在出生后的第1-4天给新生大鼠施用了两种有机磷酸盐杀虫剂毒死rif和地嗪酮,其剂量低于全身毒性或生长障碍的阈值,并且几乎不能检测到胆碱酯酶抑制的阈值:1 mg / kg /天毒死rif和1或2 mg / kg /天的二嗪农。方法:使用微阵列,然后我们检查了在前脑和脑干中编码FGF及其受体(FGFR)的mRNA的区域表达。结果:毒死rif和地嗪酮均显着抑制前脑中的fgf20表达和脑干中的fgf2,同时升高脑干fgfr4并引起脑干fgf22的少量缺陷。但是,他们的不同之处在于,二嗪农对fgf2和fgfr4的作用明显更大,并且两种药物对fgf11,fgf14和fgfr1的作用也不同,较小。结论:对毒死rif和二嗪农的反应存在相似性但也存在显着差异,并且即使在不抑制胆碱酯酶的剂量下也能见到强效作用,这一事实支持以下观点:有机磷酸酯在引起发育性神经毒性的倾向上存在差异,互不相关他们的抗胆碱酯酶活性。对神经营养因子的影响提供了有机磷对发育中的神经元的伤害与最终不良的神经发育结果之间的机制联系。

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