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      Metabolomic analysis of livers and serum from high-fat diet induced obese mice.

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          Abstract

          Liver and serum metabolites of obese and lean mice fed on high fat or normal diets were analyzed using ultraperformance liquid chromatography-quadrupole-time-of-flight mass spectrometry, gas chromatography-mass spectrometry, and partial least-squares-discriminant analysis (PLS-DA). Obese and lean groups were clearly discriminated from each other on PLS-DA score plot and major metabolites contributing to the discrimination were assigned as lipid metabolites (fatty acids, phosphatidylcholines (PCs), and lysophosphatidylcholines (lysoPCs)), lipid metabolism intermediates (betaine, carnitine, and acylcarnitines), amino acids, acidic compounds, monosaccharides, and serotonin. A high-fat diet increased lipid metabolites but decreased lipid metabolism intermediates and the NAD/NADH ratio, indicating that abnormal lipid and energy metabolism induced by a high-fat diet resulted in fat accumulation via decreased β-oxidation. In addition, this study revealed that the levels of many metabolites, including serotonin, betaine, pipecolic acid, and uric acid, were positively or negatively related to obesity-associated diseases. On the basis of these metabolites, we proposed a metabolic pathway related to high-fat diet-induced obesity. These metabolites can be used to better understand obesity and related diseases induced by a hyperlipidic diet. Furthermore, the level changes of these metabolites can be used to assess the risk of obesity and the therapeutic effect of obesity management.

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          Author and article information

          Journal
          J Proteome Res
          Journal of proteome research
          American Chemical Society (ACS)
          1535-3907
          1535-3893
          Feb 04 2011
          : 10
          : 2
          Affiliations
          [1 ] Research Division for Emerging Innovation Technology, Korea Food Research Institute, Sungnam, Kyongki, Republic of Korea.
          Article
          10.1021/pr100892r
          21047143
          0ff13c89-6b14-4419-aa8e-a54305ea87f9
          History

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