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NMR-based metabonomic analysis of the hepatotoxicity induced by combined exposure to PCBs and TCDD in rats

机译:基于NMR的代谢组学分析大鼠联合暴露于PCBs和TCDD引起的肝毒性

摘要

A metabonomic approach using (1)H NMR spectroscopy was adopted to investigate the metabonomic pattern of rat urine after oral administration of environmental endocrine disruptors (EDs) polychlorinated biphenyls (PCBs) and 2,3,7,8-tetrachlorodibenzo- p-dioxin (TCDD) alone or in combination and to explore the possible hepatotoxic mechanisms of combined exposure to PCBs and TCDD. (1)H NMR spectra of urines collected 24 h before and after exposure were analyzed via pattern recognition by using principal component analysis (PCA). Serum biochemistry and liver histopathology indicated significant hepatotoxicity in the rats of the combined group. The PCA scores plots of urinary (1)H NMR data showed that all the treatment groups could be easily distinguished from the control group, so could the PCBs or TCDD group and the combined group. The loadings plots of the PCA revealed remarkable increases in the levels of lactate, glucose, taurine, creatine. and 2-hydroxy-isovaleric acid and reductions in the levels of 2-oxoglutarate, citrate, succinate, hippurate, and trimethylamine-N-oxide in rat urine after exposure. These changes were more striking in the combined group. The changed metabolites may be considered possible biomarker for the hepatotoxicity. The present study demonstrates that combined exposure to PCBs and TCDD induced significant hepatotoxicity in rats, and mitochondrial dysfunction and fatty acid metabolism perturbations might contribute to the hepatotoxicity. There was good conformity between changes in the urine metabonomic pattern and those in serum biochemistry and liver histopathology. These results showed that the NMR-based metabonomic approach may provide a promising technique for the evaluation of the combined toxicity of EDs. (C) 2010 Elsevier Inc. All rights reserved.
机译:采用代谢组学方法使用(1)H NMR光谱研究口服环境内分泌干扰物(ED),多氯联苯(PCB)和2,3,7,8-四氯二苯并-对二恶英( TCDD)单独或组合使用,以探索将PCBs和TCDD联合暴露的可能的肝毒性机制。 (1)使用主成分分析(PCA)通过模式识别分析暴露前后24小时尿液的1 H NMR谱。血清生化和肝组织病理学表明联合组大鼠具有明显的肝毒性。尿(1)H NMR数据的PCA评分图显示,所有治疗组均可轻松与对照组区分开,PCBs或TCDD组以及合并组也可轻松区分开。 PCA的负荷图显示乳酸,葡萄糖,牛磺酸,肌酸水平显着增加。和2-羟基-异戊酸暴露后大鼠尿液中2-氧代戊二酸,柠檬酸,琥珀酸,马尿酸和三甲胺-N-氧化物的含量降低。这些变化在合并后的小组中更为显着。改变的代谢产物可能被认为是肝毒性的可能生物标志物。本研究表明,多氯联苯和TCDD共同暴露可引起大鼠明显的肝毒性,线粒体功能障碍和脂肪酸代谢紊乱可能会导致肝毒性。尿代谢组学模式的变化与血清生化和肝组织病理学的变化之间具有良好的一致性。这些结果表明,基于NMR的代谢组学方法可能为评估ED的联合毒性提供有希望的技术。 (C)2010 Elsevier Inc.保留所有权利。

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