Abstract |
Nonalcoholic fatty liver disease is considered to be the hepatic manifestation of metabolic syndrome and is usually related to high-fat, high- cholesterol diets. With the rationale that the identification and quantification of metabolites in different metabolic pathways may facilitate the discovery of clinically accessible biomarkers, we report the use of (1)H NMR metabolomics for quantitative profiling of liver extracts from LDLr(-/-) mice, a well-documented mouse model of fatty liver disease. A total of 55 metabolites were identified, and multivariate analyses in a diet- and time-comparative strategy were performed. Dietary cholesterol increased the hepatic concentrations of cholesterol, triglycerides, and oleic acid but also decreased the [PUFA/MUFA] ratio as well as the relative amount of long-chain polyunsaturated fatty acids in the liver. This was also accompanied by variations of the hepatic concentration of taurine, glutathione, methionine, and carnitine. Heat-map correlation analyses demonstrated that hepatic inflammation and development of steatosis correlated with cholesterol and triglyceride NMR derived signals, respectively. We conclude that dietary cholesterol is a causal factor in the development of both liver steatosis and hepatic inflammation.
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Authors | Maria Vinaixa, Miguel Angel Rodríguez, Anna Rull, Raúl Beltrán, Cinta Bladé, Jesús Brezmes, Nicolau Cañellas, Jorge Joven, Xavier Correig |
Journal | Journal of proteome research
(J Proteome Res)
Vol. 9
Issue 5
Pg. 2527-38
(May 07 2010)
ISSN: 1535-3907 [Electronic] United States |
PMID | 20402505
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cholesterol, Dietary
- Receptors, LDL
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Topics |
- Age Factors
- Animals
- Cholesterol, Dietary
(administration & dosage, metabolism)
- Cluster Analysis
- Disease Progression
- Fatty Liver
(metabolism)
- Histocytochemistry
- Inflammation
(metabolism)
- Male
- Metabolome
- Metabolomics
(methods)
- Mice
- Mice, Inbred C57BL
- Mice, Transgenic
- Multivariate Analysis
- Nuclear Magnetic Resonance, Biomolecular
- Receptors, LDL
(genetics, metabolism)
- Solubility
- Statistics, Nonparametric
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