代谢组
代谢组学
化学
微生物群
新陈代谢
肠道菌群
生物化学
梭杆菌门
微生态学
代谢途径
脂质代谢
脂肪酸代谢
药理学
生物
色谱法
微生物学
生物信息学
16S核糖体RNA
拟杆菌
基因
作者
Min Cheng,Yuanfang Sun,Leqi Wang,Lirong Tan,Hui‐Zi Jin,Shi‐Kai Yan,Shasha Li,Xue Xiao
标识
DOI:10.1093/fqsafe/fyab010
摘要
Abstract Objective This study aimed to elucidate the possible mechanism of Gest-Aid Plus Oral Liquid (GAP) on healthcare function. Method Ultrahigh-performance liquid chromatography–quadrupole time-of-flight mass spectrometry-based metabolomics and 16S rDNA sequencing of gut microbiota were performed on serum and fecal samples of GAP and control rats. Additionally, short-chain fatty acids (SCFAs) and inflammatory cytokines in fecal samples were determined through gas chromatography–mass spectrometry and enzyme-linked immunosorbent assay kits. Result Metabolomics discovered 41 metabolites, which mainly involved amino acid metabolism, lipid metabolism, coenzyme factors, and vitamin metabolism. Administration of GAP increased abundance of Prevotella_9, Alloprevotella, Blautia, Phascolarctobacterium, Parabacteroides, and Fusicatenibacter, and six SCFAs were increased in the GAP group. Measurement of inflammatory cytokines showed that GAP had an anti-inflammatory effect in rats. Conclusion Administration of GAP greatly affects the aspartate metabolism and microecology of rats, enhances intestinal motility and gut barrier integrity and anti-inflammation. These findings not only have possible implications for further application of GAP, but also provide a link between the gut microbiome, SCFAs, inflammation and serum metabolites in rats.
科研通智能强力驱动
Strongly Powered by AbleSci AI