Investigation of the Hepatoprotective Effect of Prunus mume Sieb. et Zucc Extract in a Mouse Model of Alcoholic Liver Injury Through High-Resolution Metabolomics

被引:19
作者
Khan, Adnan [1 ]
Pan, Jeong Hoon [2 ,3 ]
Cho, Seongha [1 ]
Lee, Sojung [2 ]
Kim, Young Jun [2 ]
Park, Youngja H. [1 ]
机构
[1] Korea Univ, Coll Pharm, Metabol Lab, Sejong 339700, South Korea
[2] Korea Univ, Dept Food & Biotechnol, Sejong 30019, South Korea
[3] Univ Arkansas, Sch Human Environm Sci, Fayetteville, AR 72701 USA
关键词
alcoholism; herbal metabolomics; phytochemical analysis; ACTIVATED PROTEIN-KINASE; GANODERMA-LUCIDUM; OXIDATIVE STRESS; NITRIC-OXIDE; DISEASE; PHOSPHATIDYLCHOLINE; INFLAMMATION; CELLS; BRAIN; MICE;
D O I
10.1089/jmf.2016.3874
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study aimed to identify the changes in the metabolomics profile of liver damage caused by alcohol consumption and verify the beneficial effect of Prunus mume Sieb. et Zucc extract (PME) in protection of alcohol-induced injury by attenuating the level of identified metabolites. Mice were treated with PME and saline or untreated once daily for 5 days, followed by alcohol injection. The plasma samples were analyzed using liquid chromatography-mass spectrometrybased high-resolution metabolomics followed by a multivariate statistical analysis using MetaboAnalyst 3.0 to obtain significantly expressed metabolites, using a false discovery rate threshold of q = 0.05. Metabolites were annotated using Metlin database and mapped through Kyoto Encyclopedia of Genes and Genomes (KEGG). Among 4999 total features, 101 features were significant among alcohol-and PME-treated mice groups. All the samples cluster showed a clear separation in the heat map, and the scores plot of orthogonal partial least squares-discriminant analysis (OPLS-DA) model discriminated the three groups. Phosphatidylcholine, Saikosaponin BK1, Ganoderiol I, and N-2-[4-(3,3-dimethylallyloxy) phenyl] ethylcinnamide were among the significant compounds with a low intensity in alcohol group compared to PME group, suggesting that these compounds have a relation in the development of PME's protective effect. The study confirms the hepatoprotective, antioxidant, and anti-inflammatory effects of PME against alcohol-induced liver steatosis, inflammation, and apoptosis.
引用
收藏
页码:734 / 743
页数:10
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