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首页> 外文期刊>Environmental health perspectives. >Global Gene Expression Analysis in the Livers of Rat Offspring Perinatally Exposed to Low Doses of 2,2′,4,4′-Tetrabromodiphenyl Ether
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Global Gene Expression Analysis in the Livers of Rat Offspring Perinatally Exposed to Low Doses of 2,2′,4,4′-Tetrabromodiphenyl Ether

机译:低剂量的2,2',4,4'-四溴二苯醚暴露于大鼠子代的肝脏中的全局基因表达分析

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摘要

Background Polybrominated diphenyl ethers are a group of flame-retardant chemicals appearing increasingly in the environment. Their health effects and mechanisms of toxicity are poorly understood. Objectives We screened for the sensitive effects and mechanisms of toxicity of 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) by analyzing the gene expression profile in rats exposed to doses comparable to human exposure. Methods Wistar dams were exposed to vehicle or BDE-47 (0.002 and 0.2 mg/kg body weight) every fifth day from gestation day 15 to postnatal day 20 by injections to caudal vein. Total RNA was extracted from the livers of pups and hybridized to the whole-genome RNA expression microarrays. The list of genes 2-fold differentially expressed was exported to PANTHER and Ingenuity Systems for analysis of enriched ontology groups and molecular pathways. Results Oxidoreductase and transferase protein families were enriched in exposed rats as were these biological process categories: carbohydrate metabolism; electron transport; and lipid, fatty acid, and steroid metabolism. Four signaling pathways (cascades of activation of drug-metabolizing enzymes) and 10 metabolic pathways were significantly enriched. Drug-metabolizing enzymes appear to be regulated by BDE-47 through an aryl hydrocarbon receptor–independent mechanism. Direct interaction with retinoid X receptor or its upstream cascade may be involved. The main metabolic effects consisted of activation of metabolic pathways: α- and ω-oxidation of fatty acids, glycolysis, and starch hydrolysis. Conclusions Altered expression of genes involved in metabolic and signaling pathways and functions of the organism occurs after perinatal exposure of rat offspring to BDE-47 at doses relevant for the general population.
机译:背景技术多溴二苯醚是在环境中越来越多出现的一组阻燃化学品。人们对其健康影响和毒性机理了解甚少。目的我们通过分析暴露于与人类可比剂量的大鼠的基因表达谱,筛选了2,2',4,4'-四溴二苯醚(BDE-47)的敏感性效应和毒性机制。方法从妊娠第15天到出生后第20天,每隔五天,通过尾静脉注射将Wistar大坝暴露于媒介物或BDE-47(0.002和0.2 mg / kg体重)。从幼犬肝脏中提取总RNA,并与全基因组RNA表达微阵列杂交。将2倍差异表达的基因列表输出到PANTHER和Ingenuity Systems,以分析丰富的本体组和分子途径。结果暴露的大鼠中氧化还原酶和转移酶蛋白家族丰富,这些生物学过程类别为:碳水化合物代谢;电子传输以及脂质,脂肪酸和类固醇的代谢。四个信号通路(药物代谢酶的激活级联)和10个代谢通路被显着丰富。药物代谢酶似乎是通过BDE-47通过不依赖芳烃受体的机制来调节的。可能涉及与类维生素A X受体或其上游级联的直接相互作用。主要的代谢作用包括代谢途径的激活:脂肪酸的α-和ω-氧化,糖酵解和淀粉水解。结论围生期将大鼠后代暴露于与普通人群有关的剂量的BDE-47后,与该生物体的代谢,信号通路和功能有关的基因表达发生改变。

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