IR@PKUHSC  > 北京大学第二临床医学院  > 北京大学肝病研究所
学科主题临床医学
Metabolic profiling analysis of a D-galactosamine/lipopolysaccharide-induced mouse model of fulminant hepatic failure
Feng, Bo1; Wu, Shengming1; Lv, Sa1; Liu, Feng1; Chen, Hongsong1; Yan, Xianzhong1; Li, Yu1; Dong, Fangting1; Wei, Lai1
关键词Metabonomics Gc/ms Fulminant Hepatic Failure
刊名JOURNAL OF PROTEOME RESEARCH
2007
DOI10.1021/pr0606326
6期:6页:2161-2167
收录类别SCI
文章类型Article
WOS标题词Science & Technology
类目[WOS]Biochemical Research Methods
研究领域[WOS]Biochemistry & Molecular Biology
关键词[WOS]ACUTE LIVER-FAILURE ; UNITED-STATES MULTICENTER ; D-GALACTOSAMINE ; AMINO-ACID ; RAT-LIVER ; H-1-NMR-BASED METABONOMICS ; FUNCTIONAL GENOMICS ; SERUM PHOSPHATE ; EARLY PREDICTOR ; BLOOD LACTATE
英文摘要

The purpose of this study was to characterize the changes in metabolic intermediates and to investigate the metabolic profile of a mouse model of fulminant hepatic failure (FHF), induced by D-galactosamine/ lipopolysaccharide (GaIN/LPS). Plasma metabolite levels were detected using gas chromatography/ time-of-flight mass spectrometry, and the acquired data were transferred into Simca-P and processed using principal components analysis ( PCA). In total, 45 metabolites were identified from the 267 distinct compounds found in the study. Whereas significant differences were noted in the plasma levels of the control and FHF groups, no differences in gluconeogenesis or glycolysis were noted following GaIN/LPS treatment. Our data also suggest that the production of ketone bodies, and the tricarboxylic acid and urea cycles, was inhibited. PCA data suggest that 5-hydroxyindoleacetic acid, glucose, beta-hydroxybutyrate, and phosphate parameters had the highest weights on each of the principal components, and that they were the most important metabolites contributing to the separation of groups. In conclusion, this metabonomic approach can be used as a powerful tool to characterize changes in metabolic intermediates and to search for metabolic markers under certain pathophysiological conditions, such as FHF. Our data also demonstrate that a combination of 5-hydroxyindoleacetic acid, glucose, beta-hydroxybutyrate, and phosphate concentrations in the plasma is a potential marker for FHF, as well as for the early prognosis of FHF.

语种英语
WOS记录号WOS:000246893500011
Citation statistics
Cited Times:46[WOS]   [WOS Record]     [Related Records in WOS]
文献类型期刊论文
条目标识符http://ir.bjmu.edu.cn/handle/400002259/50439
Collection北京大学第二临床医学院_北京大学肝病研究所
作者单位1.Peking Univ, Peoples Hosp, Inst Hepatol, Beijing 100044, Peoples R China
2.Natl Ctr Biomed Anal, Beijing 100039, Peoples R China
Recommended Citation
GB/T 7714
Feng, Bo,Wu, Shengming,Lv, Sa,et al. Metabolic profiling analysis of a D-galactosamine/lipopolysaccharide-induced mouse model of fulminant hepatic failure[J]. JOURNAL OF PROTEOME RESEARCH,2007,6(6):2161-2167.
APA Feng, Bo.,Wu, Shengming.,Lv, Sa.,Liu, Feng.,Chen, Hongsong.,...&Wei, Lai.(2007).Metabolic profiling analysis of a D-galactosamine/lipopolysaccharide-induced mouse model of fulminant hepatic failure.JOURNAL OF PROTEOME RESEARCH,6(6),2161-2167.
MLA Feng, Bo,et al."Metabolic profiling analysis of a D-galactosamine/lipopolysaccharide-induced mouse model of fulminant hepatic failure".JOURNAL OF PROTEOME RESEARCH 6.6(2007):2161-2167.
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