Khan Adnan, Pan Jeong Hoon, Cho Seongha, Lee Sojung, Kim Young Jun, Park Youngja H
1 Metabolomics Laboratory, College of Pharmacy, Korea University , Sejong, Korea.
2 Department of Food and Biotechnology, Korea University , Sejong, Korea.
J Med Food. 2017 Aug;20(8):734-743. doi: 10.1089/jmf.2016.3874. Epub 2017 Jun 26.
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 spectrometry-based 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.
本研究旨在确定酒精消费所致肝损伤的代谢组学特征变化,并通过降低已鉴定代谢物的水平来验证乌梅提取物(PME)对酒精诱导损伤的保护作用。小鼠每天接受一次PME和生理盐水处理或不处理,持续5天,随后注射酒精。使用基于液相色谱 - 质谱的高分辨率代谢组学分析血浆样本,然后使用MetaboAnalyst 3.0进行多变量统计分析,以获得显著表达的代谢物,使用错误发现率阈值q = 0.05。代谢物使用Metlin数据库进行注释,并通过京都基因与基因组百科全书(KEGG)进行映射。在总共4999个特征中,101个特征在酒精处理组和PME处理组的小鼠中具有显著性。所有样本聚类在热图中显示出明显的分离,正交偏最小二乘判别分析(OPLS - DA)模型的得分图区分了三组。与PME组相比,磷脂酰胆碱、柴胡皂苷BK1、灵芝二醇I和N - 2 - [4 - (3,3 - 二甲基烯丙氧基)苯基]乙基肉桂酰胺是酒精组中强度较低的显著化合物,表明这些化合物与PME保护作用的发展有关。该研究证实了PME对酒精诱导的肝脂肪变性、炎症和细胞凋亡具有保肝、抗氧化和抗炎作用。