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多组学研究揭示苯扎氯铵消毒剂改变小鼠新生大脑中的甾醇和脂质稳态。

Multiomics Investigation Reveals Benzalkonium Chloride Disinfectants Alter Sterol and Lipid Homeostasis in the Mouse Neonatal Brain.

作者信息

Herron Josi M, Hines Kelly M, Tomita Hideaki, Seguin Ryan P, Cui Julia Yue, Xu Libin

机构信息

Department of Medicinal Chemistry.

Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington 98195.

出版信息

Toxicol Sci. 2019 Sep 1;171(1):32-45. doi: 10.1093/toxsci/kfz139.

Abstract

Lipids are critical for neurodevelopment; therefore, disruption of lipid homeostasis by environmental chemicals is expected to have detrimental effects on this process. Previously, we demonstrated that the benzalkonium chlorides (BACs), a class of commonly used disinfectants, alter cholesterol biosynthesis and lipid homeostasis in neuronal cell cultures in a manner dependent on their alkyl chain length. However, the ability of BACs to reach the neonatal brain and alter sterol and lipid homeostasis during neurodevelopment in vivo has not been characterized. Therefore, the goal of this study was to use targeted and untargeted mass spectrometry and transcriptomics to investigate the effect of BACs on sterol and lipid homeostasis and to predict the mechanism of toxicity of BACs on neurodevelopmental processes. After maternal dietary exposure to 120 mg BAC/kg body weight/day, we quantified BAC levels in the mouse neonatal brain, demonstrating for the first time that BACs can cross the blood-placental barrier and enter the developing brain. Transcriptomic analysis of neonatal brains using RNA sequencing revealed alterations in canonical pathways related to cholesterol biosynthesis, liver X receptor-retinoid X receptor (LXR/RXR) signaling, and glutamate receptor signaling. Mass spectrometry analysis revealed decreases in total sterol levels and downregulation of triglycerides and diglycerides, which were consistent with the upregulation of genes involved in sterol biosynthesis and uptake as well as inhibition of LXR signaling. In conclusion, these findings demonstrate that BACs target sterol and lipid homeostasis and provide new insights for the possible mechanisms of action of BACs as developmental neurotoxicants.

摘要

脂质对神经发育至关重要;因此,环境化学物质破坏脂质稳态预计会对这一过程产生有害影响。此前,我们证明了苯扎氯铵(BACs),一类常用消毒剂,以一种依赖于其烷基链长度的方式改变神经元细胞培养物中的胆固醇生物合成和脂质稳态。然而,BACs在体内神经发育过程中到达新生大脑并改变甾醇和脂质稳态的能力尚未得到表征。因此,本研究的目的是使用靶向和非靶向质谱以及转录组学来研究BACs对甾醇和脂质稳态的影响,并预测BACs对神经发育过程的毒性作用机制。在母体饮食暴露于120毫克BAC/千克体重/天后,我们对小鼠新生大脑中的BAC水平进行了定量,首次证明BACs可以穿过血胎盘屏障并进入发育中的大脑。使用RNA测序对新生大脑进行转录组分析,揭示了与胆固醇生物合成、肝X受体-视黄醇X受体(LXR/RXR)信号传导以及谷氨酸受体信号传导相关的经典途径的改变。质谱分析显示总甾醇水平降低以及甘油三酯和甘油二酯下调,这与参与甾醇生物合成和摄取的基因上调以及LXR信号传导的抑制一致。总之,这些发现表明BACs靶向甾醇和脂质稳态,并为BACs作为发育性神经毒物的可能作用机制提供了新的见解。

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