4.3 Article

Flos Carthami Exerts Hepatoprotective Action in a Rat Model of Alcoholic Liver Injury via Modulating the Metabolomics Profile

Journal

Publisher

HINDAWI LTD
DOI: 10.1155/2022/8158699

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Funding

  1. National Natural Science Foundation of China [62162049]
  2. Mongolian Medicine Safety Evaluation and Innovation Team Project [MY20190003]
  3. Science and Technology Projects of Inner Mongolia Autonomous Region [2020GG0190]
  4. Natural Science Foundation of Inner Mongolia Autonomous Region of China [2021LHMS06007, 2019MS08036]
  5. Research Program of Science and Technology at Universities of Inner Mongolia Autonomous Region [NJZY20112]
  6. Program for Young Talents of Science and Technology in Universities of Inner Mongolia Autonomous Region [NJYT-19-B18]
  7. Grassland Talents-Mongolian Medicine Data Mining Key Technology Research Innovative Talent Team, Inner Mongolia University for Nationalities doctoral research start fund project [BS543]

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This study aimed to identify the changes in the metabolomics profile of liver tissue damaged by alcohol consumption and explore the potential protective effects of flos carthami. The findings demonstrated that flos carthami attenuated alcohol-induced injury and resulted in changes in the metabolic profiles.
This study was intended to identify the shifts in the metabolomics profile of the hepatic tissue damaged by alcohol consumption and verify the potential restorative action of flos carthami (the flowers of Carthamus tinctorius, FC) in the protection of alcohol-induced injury by attenuating the level of identified metabolites. Rats were treated with FC and subsequently subjected to alcohol administration. The serum samples were subjected to liquid chromatography-mass spectrometry (LC-MS)-based metabolomics followed by statistical and bioinformatics analyses. The clustering of the samples showed an obvious separation in the principal component analysis (PCA) plot, and the scores plot of the orthogonal partial least squares-discriminant analysis (OPLS-DA) model allowed the distinction among the three groups. Among the 3211 total metabolites, 1088 features were significantly different between the control and alcohol-treated groups, while 367 metabolites were identified as differential metabolites between the alcohol- and FC-treated rat groups. Time series clustering approach indicated that 910 metabolites in profile 6 were upregulated by alcohol but subsequently reversed by FC treatment; among them, the top 10 metabolites based on the variable importance in projection (VIP) scores were 1-methyladenine, phenylglyoxylic acid, N-acetylvaline, mexiletine, L-fucose, propylthiouracil, dopamine 4-sulfate, isoleucylproline, (R)-salsolinol, and monomethyl phthalate. The Pearson correlation analysis and network construction revealed 96 hub metabolites that were upregulated in the alcohol liver injury model group but were downregulated by FC. This study confirmed the hepatoprotective effects of FC against alcohol-induced liver injury and the related changes in the metabolic profiles, which will contribute to the understanding and the treatment of alcohol-induced acute liver injury.

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