A 1H NMR-Based Metabonomic Investigation of Time-Related Metabolic Trajectories of the Plasma, Urine and Liver Extracts of Hyperlipidemic Hamsters

被引:91
作者
Jiang, Chun-ying [1 ,2 ,3 ]
Yang, Kang-min [1 ,2 ,3 ]
Yang, Liu [1 ,2 ,3 ]
Miao, Zhao-xia [1 ,2 ,3 ]
Wang, Ying-hong [1 ,2 ,3 ]
Zhu, Hai-bo [1 ,2 ,3 ]
机构
[1] Chinese Acad Med Sci, State Key Lab Bioact Subst & Funct Nat Med, Beijing 100730, Peoples R China
[2] Chinese Acad Med Sci, Minist Hlth, Key Lab Biosynth Nat Prod, Beijing 100730, Peoples R China
[3] Peking Union Med Coll, Beijing 100021, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 06期
关键词
MASS-SPECTROMETRY; H-1-NMR SPECTROSCOPY; ATHEROSCLEROSIS; SERUM; REVEALS; DISEASE; CHOLESTEROL; PROGRESSION; ASSIGNMENT; OXIDATION;
D O I
10.1371/journal.pone.0066786
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The hamster has been previously found to be a suitable model to study the changes associated with diet-induced hyperlipidemia in humans. Traditionally, studies of hyperlipidemia utilize serum-or plasma-based biochemical assays and histopathological evaluation. However, unbiased metabonomic technologies have the potential to identify novel biomarkers of disease. Thus, to obtain a better understanding of the progression of hyperlipidemia and discover potential biomarkers, we have used a proton nuclear magnetic resonance spectroscopy (H-1-NMR)-based metabonomics approach to study the metabolic changes occurring in the plasma, urine and liver extracts of hamsters fed a high-fat/high-cholesterol diet. Samples were collected at different time points during the progression of hyperlipidemia, and individual proton NMR spectra were visually and statistically assessed using two multivariate analyses (MVA): principal component analysis (PCA) and orthogonal partial least squares-discriminant analysis (OPLS-DA). Using the commercial software package Chenomx NMR suite, 40 endogenous metabolites in the plasma, 80 in the urine and 60 in the water-soluble fraction of liver extracts were quantified. NMR analysis of all samples showed a time-dependent transition from a physiological to a pathophysiological state during the progression of hyperlipidemia. Analysis of the identified biomarkers of hyperlipidemia suggests that significant perturbations of lipid and amino acid metabolism, as well as inflammation, oxidative stress and changes in gut microbiota metabolites, occurred following cholesterol overloading. The results of this study substantially broaden the metabonomic coverage of hyperlipidemia, enhance our understanding of the mechanism of hyperlipidemia and demonstrate the effectiveness of the NMR-based metabonomics approach to study a complex disease.
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