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毒死蜱的发育神经毒性:靶向神经胶质细胞。

Developmental neurotoxicity of chlorpyrifos: targeting glial cells.

机构信息

Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina, NC 27710, USA.

出版信息

Environ Toxicol Pharmacol. 2005 May;19(3):455-61. doi: 10.1016/j.etap.2004.12.007.

Abstract

The pesticide chlorpyrifos (CPF) causes neurobehavioral damage, even at doses that do not elicit acute cholinergic toxicity. CPF disrupts the developing brain during glial proliferation and differentiation. Since glial cells play critical roles in brain development and function, we hypothesized that CPF neurotoxicity involves alteration of glial cell development. CPF effects in C6 glioma cells mirrored effects in the intact brain: inhibited DNA synthesis; interfered with adenylyl cyclase (AC) signaling; obstructed DNA binding to transcription factors involved in cell differentiation; and enhanced reactive oxygen species (ROS) formation. CPF was administered to prenatal and neonatal rats and examined for markers of astrocytes, oligodendrocytes, and neurons. Widespread effects were elicited by exposure during the peak period of gliogenesis. Males were preferentially targeted during postnatal exposures while females experienced delayed effects following gestational exposure, commensurate with behavioral outcomes. Alterations in glial cell development contribute to CPF neurotoxicity, extending vulnerability to myelination, synaptic plasticity, and architectural modeling, which continue into adolescence.

摘要

杀虫剂毒死蜱(CPF)会导致神经行为损伤,即使在没有引起急性胆碱能毒性的剂量下也是如此。CPF 在神经胶质细胞增殖和分化过程中会破坏发育中的大脑。由于神经胶质细胞在大脑发育和功能中起着至关重要的作用,我们假设 CPF 的神经毒性涉及到神经胶质细胞发育的改变。CPF 在 C6 神经胶质瘤细胞中的作用与在完整大脑中的作用相似:抑制 DNA 合成;干扰腺苷酸环化酶(AC)信号转导;阻碍与细胞分化相关的转录因子与 DNA 的结合;并增强活性氧(ROS)的形成。CPF 被给予产前和新生大鼠,并检查星形胶质细胞、少突胶质细胞和神经元的标志物。在神经胶质发生的高峰期暴露会引起广泛的影响。雄性在出生后暴露时受到优先影响,而雌性在妊娠期暴露后则会出现延迟影响,与行为结果相一致。神经胶质细胞发育的改变导致 CPF 的神经毒性,增加了对髓鞘形成、突触可塑性和结构建模的易感性,这些过程会持续到青春期。

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