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Metabolomic analysis of urine from rats chronically dosed with acrylamide using NMR and LC/MS

机译:使用NMR和LC / MS对长期服用丙烯酰胺的大鼠尿液进行代谢组学分析

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摘要

Acrylamide (AA) is known to cause neurotox-icity, genotoxicity, reproductive, and carcinogenic effects in rodents and neurotoxicity in humans. A metabolomics study of urine samples from rats dosed with acrylamide for 14 days was undertaken to understand the mechanisms of and develop biomarkers for acrylamide-induced toxicity. NMR-based and LC/MS-based metabolomics methods were used to analyze metabolites in urine samples. Three mercapturic acid conjugates of acrylamide were detected using exact mass and principal component analysis (PCA) of urine samples. NMR analysis showed an increase in creatine and a decrease in taurine throughout the dosing period. Results showed that citric acid cycle metabolites were down-regulated later in the dosing period. Further, many amino acids were also up-regulated during the studyand may be related to the weight loss observed in this study. Taken together, the data suggest that both LC/MS-based and NMR-based metabolomics analysis can detect changes in endogenous metabolites related to glutathione, TCA cycle, and amino acid metabolism induced by AA administration over a 2 week dosing period.
机译:已知丙烯酰胺(AA)会在啮齿动物中引起神经毒性,遗传毒性,生殖和致癌作用,并对人类产生神经毒性。进行了一项代谢组学研究,研究了从大鼠中摄入丙烯酰胺14天的尿液样本,以了解丙烯酰胺诱导的毒性的机理并开发生物标志物。基于核磁共振和基于LC / MS的代谢组学方法用于分析尿液样品中的代谢物。使用尿液样品的精确质量和主成分分析(PCA)检测了三种丙烯酰胺的巯基酸共轭物。 NMR分析显示在整个给药期间肌酸增加,而牛磺酸减少。结果表明,柠檬酸循环代谢产物在给药后期被下调。此外,许多氨基酸在研究过程中也被上调,可能与这项研究中观察到的体重减轻有关。综上所述,数据表明基于LC / MS和基于NMR的代谢组学分析均可以检测到在2周的给药期间内与谷胱甘肽,TCA周期和AA诱导的氨基酸代谢有关的内源性代谢物的变化。

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