LC/MS-based non-targeted metabolomics for the investigation of general toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin in C57BL/6J and DBA/2J mice

被引:19
作者
Lin, Shuhai [1 ]
Yang, Zhu [2 ]
Shen, Yang [1 ,2 ]
Cai, Zongwei [1 ]
机构
[1] Hong Kong Baptist Univ, Dept Chem, Hong Kong, Hong Kong, Peoples R China
[2] Hong Kong Baptist Univ, Dept Phys, Hong Kong, Hong Kong, Peoples R China
关键词
LC/MS; Metabolomic; TCDD; Toxicity; Differentiating metabolite; MASS-SPECTROMETRY DATA; HEPATITIS-B; IDENTIFICATION; BIOMARKERS; METABONOMICS; PLASMA; METABOLITES; DISCOVERY; ALIGNMENT; RECEPTOR;
D O I
10.1016/j.ijms.2010.06.012
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Although numerous studies have been performed for the toxicological mechanisms of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), the metabolic changes of TCDD toxicity is less well understood. In this study, liquid chromatography/quadrupole time-of-flight mass spectrometry (LC/QTOFMS) was used for non-targeted metabolomics for understanding the different metabolic patterns associated with TCDD exposure in aryl hydrocarbon receptor (AhR) sensitive C57BL/6J (C6) and less sensitive DBA/2J (D2) mouse strains. The serum samples were analyzed and treated with metabolomic analysis in conjunction with multivariate data analysis. Metabolite identification was performed with interpreting high resolution MS data and MS/MS fragmentation, searching against databases and comparing with authentic compounds. Twelve differentiating metabolites (defined as a >= 1.5-fold change with a P <= 0.001) were highlighted in C6 mice versus control group, revealing lipid accumulation, fatty acid beta-oxidation, inflammation and alteration of amino acids as well as phase II drug-like metabolism. In contrast, only 2 differentiating metabolites were detected in D2 mouse model. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 36
页数:8
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