Metabonomic characterization of early atherosclerosis in hamsters with induced cholesterol

被引:35
作者
Zha, Weibin [1 ]
A, Jiye [1 ]
Wang, Guangji [1 ]
Yan, Bei [1 ]
Gu, Shenghua [1 ]
Zhu, Xuanxuan [2 ]
Hao, Haiping [1 ]
Huang, Qing [1 ]
Sun, Jianguo [1 ]
Zhang, Ying [1 ]
Cao, Bei [1 ]
Ren, Hongcan [1 ]
机构
[1] China Pharmaceut Univ, Key Lab Drug Metab & Pharmacokinet, Nanjing 210038, Peoples R China
[2] Jiangsu Prov Hosp Tradit Chinese Med, Clin Res Inst, Dept Pharmacol, Nanjing, Peoples R China
关键词
Metabonomics; early atherosclerosis; hypercholesterolaemia; GC/MS; multivariate statistical analysis; LIPOPROTEIN RECEPTOR-ACTIVITY; INFLAMMATION; PLASMA; TRANSCRIPTOMICS; METABOLOMICS; EXPRESSION; BIOMARKERS;
D O I
10.1080/13547500903026401
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Atherosclerosis is a complicated and multifactorial disease, induced not only by genotype, but also, even more importantly, by environmental factors. Study on the metabolic perturbation of endogenous compounds may offer deeper insight into development of atherosclerosis. Gas chromatography/mass spectrometry (GC/MS)-based metabonomics was used to profile a metabolic fingerprint of serum obtained from hamsters with induced cholesterol. The deconvoluted GC/MS data were processed by multivariate statistical analysis tools, such as principal component analysis (PCA) and partial least squares projection to latent structure and discriminant analysis (PLS-DA). For the first time we showed a time-dependent development of the model animal from normal to hypercholesterolaemia, and further to early atherosclerosis. Twenty-one compounds were identified as markers involved in the development to atherosclerosis. Identification of the compounds suggests that amino acid metabolism and fatty acid oxidation are significantly perturbed following cholesterol overloading. The data provide novel information to approach the pathophysiological processes of the hypercholesterolaemia and atherosclerosis disease continuum.
引用
收藏
页码:372 / 380
页数:9
相关论文
共 31 条
[1]  
ALLAIN CC, 1974, CLIN CHEM, V20, P470
[2]   Correlations of elevated levels of hexacosanoate in erythrocyte membranes with risk factors for atherosclerosis [J].
Antoku, Y ;
Tsukamoto, K ;
Miyoshi, Y ;
Nagino, H ;
Anezaki, M ;
Suwa, K ;
Narabe, Y .
ATHEROSCLEROSIS, 2000, 153 (01) :169-173
[3]   Genome-wide expression studies of atherosclerosis - Critical issues in methodology, analysis, interpretation of transcriptomics data [J].
Bijnens, APJJ ;
Lutgens, E ;
Ayoubi, T ;
Kuiper, J ;
Horrevoets, AJ ;
Daemen, JAP .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (06) :1226-1235
[4]  
Brindle JT, 2002, NAT MED, V8, P1439, DOI 10.1038/nm802
[5]  
BUCOLO G, 1973, CLIN CHEM, V19, P476
[6]   FATTY-ACIDS REGULATE HEPATIC LOW-DENSITY-LIPOPROTEIN RECEPTOR ACTIVITY THROUGH REDISTRIBUTION OF INTRACELLULAR CHOLESTEROL POOLS [J].
DAUMERIE, CM ;
WOOLLETT, LA ;
DIETSCHY, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (22) :10797-10801
[7]   Metabolic profiling reveals a contribution of gut microbiota to fatty liver phenotype in insulin-resistant mice [J].
Dumas, Marc-Emmanuel ;
Barton, Richard H. ;
Toye, Ayo ;
Cloarec, Olivier ;
Blancher, Christine ;
Rothwell, Alice ;
Fearnside, Jane ;
Tatoud, Roger ;
Blanc, Veronique ;
Lindon, John C. ;
Mitchell, Steve C. ;
Holmes, Elaine ;
McCarthy, Mark I. ;
Scott, James ;
Gauguier, Dominique ;
Nicholson, Jeremy K. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (33) :12511-12516
[8]  
ERIKSSON L, 2001, MULTI MEGAVARIATE DA
[9]   HIV protease inhibitors and atherosclerosis [J].
Hui, DY .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (03) :317-318
[10]   Extraction and GC/MS analysis of the human blood plasma metabolome [J].
A, J ;
Trygg, J ;
Gullberg, J ;
Johansson, AI ;
Jonsson, P ;
Antti, H ;
Marklund, SL ;
Moritz, T .
ANALYTICAL CHEMISTRY, 2005, 77 (24) :8086-8094