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首页> 外文期刊>Metallomics. integrated biometal science >Serum metabolomics reveals that arsenic exposure disrupted lipid and amino acid metabolism in rats: a step forward in understanding chronic arsenic toxicity
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Serum metabolomics reveals that arsenic exposure disrupted lipid and amino acid metabolism in rats: a step forward in understanding chronic arsenic toxicity

机译:血清代谢组学揭示了砷暴露破坏了大鼠的脂质和氨基酸代谢:了解慢性砷毒性迈出了一大步

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Chronic arsenic exposure through drinking water threatens public health worldwide. Although its multiorgan toxicity has been reported, the impact of chronic arsenic exposure on the metabolic network remains obscure. In this study, male Sprague Dawley rats were exposed to 0.5, 2 or 10 ppm sodium arsenite for three months. An ultra-high performance liquid chromatography/mass spectrometry based metabolomics approach was utilized to unveil the global metabolic response to chronic arsenic exposure in rats. Distinct serum metabolome profiles were found to be associated with the doses. Eighteen differential metabolites were identified, and most of them showed dose-dependent responses to arsenic exposure. Metabolic abnormalities mainly involved lipid metabolism and amino acid metabolism. The metabolic alterations were further confirmed by hepatic gene expression. Expressions of cpt2, lcat, cact, crot and mtr were significantly elevated in high dose groups. This study provides novel evidence to support the association between arsenic exposure and metabolic disruption, and it contributes to understanding the mechanism of chronic arsenic toxicity.
机译:饮水对砷的长期暴露威胁着世界范围的公共健康。尽管已经报道了其多器官毒性,但是长期暴露于砷对代谢网络的影响仍然不清楚。在这项研究中,雄性Sprague Dawley大鼠被暴露于0.5、2或10 ppm的亚砷酸钠三个月。一种基于超高效液相色谱/质谱的代谢组学方法被用于揭示大鼠对慢性砷暴露的整体代谢反应。发现不同的血清代谢组谱与剂量有关。鉴定出18种差异代谢物,其中大多数表现出对砷暴露的剂量依赖性反应。代谢异常主要涉及脂质代谢和氨基酸代谢。肝基因表达进一步证实了代谢改变。高剂量组中cpt2,lcat,cact,crot和mtr的表达显着升高。这项研究提供了新的证据来支持砷暴露与代谢破坏之间的关联,并且有助于理解慢性砷毒性的机制。

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