Fan Xiaojing, Wang Xiye, Lian Jie, Pei Zhili, Jiang Mingyang, Bai Meirong
College of Engineering, Key Laboratory of Intelligent Manufacturing Technology, Inner Mongolia Minzu University, Tongliao 028000, China.
College of Chemistry and Chemical Engineering, Inner Mongolia Minzu University, Tongliao 028000, China.
Evid Based Complement Alternat Med. 2022 May 2;2022:8158699. doi: 10.1155/2022/8158699. eCollection 2022.
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 , 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.
本研究旨在确定酒精消费所致肝组织代谢组学特征的变化,并通过降低已鉴定代谢物的水平来验证红花(FC)在保护酒精诱导损伤方面的潜在恢复作用。大鼠经FC处理,随后给予酒精。血清样本进行基于液相色谱 - 质谱(LC - MS)的代谢组学分析,随后进行统计和生物信息学分析。样本聚类在主成分分析(PCA)图中显示出明显的分离,正交偏最小二乘判别分析(OPLS - DA)模型的得分图允许区分三组。在总共3211种代谢物中,对照组和酒精处理组之间有1088个特征有显著差异,而在酒精处理组和FC处理组大鼠之间有367种代谢物被鉴定为差异代谢物。时间序列聚类方法表明,谱6中的910种代谢物因酒精而上调,但随后经FC处理逆转;其中,基于投影变量重要性(VIP)得分的前10种代谢物是1 - 甲基腺嘌呤、苯甲酰甲酸、N - 乙酰缬氨酸、美西律、L - 岩藻糖、丙硫氧嘧啶、多巴胺4 - 硫酸盐、异亮氨酰脯氨酸、(R) - 萨索林醇和邻苯二甲酸单甲酯。Pearson相关分析和网络构建揭示了96种枢纽代谢物,它们在酒精性肝损伤模型组中上调,但经FC处理后下调。本研究证实了FC对酒精诱导的肝损伤具有保肝作用以及代谢谱的相关变化,这将有助于理解和治疗酒精诱导的急性肝损伤。