4.7 Article

Metabolomic Characteristics of Liver and Cecum Contents in High-Fat-Diet-Induced Obese Mice Intervened with Lactobacillus plantarum FRT10

Journal

FOODS
Volume 11, Issue 16, Pages -

Publisher

MDPI
DOI: 10.3390/foods11162491

Keywords

obesity; Lactobacillus plantarum FRT10; UHPLC-QTOF/MS; metabolomics; biomarker; gut-liver axis

Funding

  1. National Key Research and Development Program of China [2017YFD0400303]
  2. National Natural Science Foundation of China [31802081]

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This study used liver and cecum contents metabonomics to analyze the metabolic profiles of obese mice and revealed the potential functions of Lactobacillus plantarum FRT10 in regulating liver and cecum contents metabolism. The results suggest that the anti-obesity effects of FRT10 may be related to alterations in glycerophospholipid metabolism, primary bile acid biosynthesis, amino metabolism, and purine and pyrimidine metabolism.
Obesity has become a major social problem related to health and quality of life. Our previous work demonstrated that Lactobacillus plantarum FRT10 alleviated obesity in high-fat diet (HFD)-fed mice by alleviating gut dysbiosis. However, the underlying functions of FRT10 in regulating liver and cecum contents metabolism remain unknown. Liver and cecum contents metabonomics combined with pathway analysis based on ultraperformance liquid chromatography-quadrupole-time-of-flight mass spectrometry (UHPLC-Q-TOF/MS) were performed to evaluate the alterations of metabolic profiles between obese control mice and obese mice in FRT10-treated groups. The orthogonal partial least squares discriminant analysis (OPLS-DA) score plots showed that there were significant differences in cecum contents and liver markers between experimental groups. In total, 26 potential biomarkers were identified in the liver and 15 in cecum contents that could explain the effect of FRT10 addition in HFD-fed mice. In addition, gut-liver axis analysis indicated that there was a strong correlation between cecum contents metabolites and hepatic metabolites. The mechanism of FRT10 against obesity might be related to the alterations in glycerophospholipid metabolism, primary bile acid biosynthesis, amino metabolism, and purine and pyrimidine metabolism. Studies on these metabolites could help us better understand the role of FRT10 in obesity induced by HFD.

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