Protective Effect of Modified Suanmei-Tang on Metabolic-Associated Fatty Liver Disease: An Integrated Strategy of Network Pharmacology, Metabolomics, and Transcriptomics

被引:0
|
作者
Wang, Chao [1 ]
Zhao, Mei [2 ]
Yue, Yuanyuan [3 ]
Hu, Chao [2 ]
Zhou, Chunqiu [2 ]
Zhang, Zhongyi [2 ]
He, Yunliang [4 ]
Luo, Yaqi [4 ]
Shen, Tao [2 ]
Dang, Sijie [4 ]
Yang, Yang [4 ]
Zhang, Yong [2 ,4 ]
机构
[1] Qitai Hosp Sixth Div, Tradit Chinese Med Dept, Qitai 831899, Xinjiang, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Coll Basic Med, Chengdu 611137, Peoples R China
[3] Chengdu First Peoples Hosp, Dept Ultrasound, Chengdu 610095, Peoples R China
[4] Chinese Med Sci, Inst Tradit Chinese Med, Sichuan Acad, Chengdu 610014, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
modified Suanmei-Tang; MAFLD; transcriptomics; network pharmacology; metabolomics; NONALCOHOLIC STEATOHEPATITIS; MESSENGER-RNA; PATHOGENESIS; AUTOPHAGY;
D O I
10.2147/DDDT.S478072
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Modified Suanmei-Tang (MST) comprises four plants common to both traditional Chinese medicine and culinary applications, and it can potentially alleviate metabolic-associated fatty liver disease (MAFLD) triggered by a high-fat diet (HFD). Purpose: This research aims to investigate the impact and underlying mechanisms of MST in ameliorating MAFLD caused by an HFD. Methods: UHPLC-Q-Orbitrap-MS/MS was used to determine the constituents of MST and to evaluate its effects on MAFLD mouse models. Transcriptomics, network pharmacology, and bioinformatics analysis (including Kyoto Encyclopedia of Genes and Genomes and Gene Set Enrichment Analysis) were utilized to further clarify the mechanisms by which MST acts on MAFLD. The experimental methods included ELISA, real time quantitative PCR (RT-qPCR), Western blot, immunohistochemistry, molecular docking, and metabolomics. Transcriptomics was integrated with metabolomics to find correlations between differentially expressed genes and metabolites, and crucial genes were validated through RT-qPCR. Results: A total of 23 components of MST were identified. The formulation was found to alleviate metabolic disorders, obesity, insulin resistance, inflammation, and oxidative stress in mice with MAFLD. The findings indicate that MST promoted autophagy by suppressing phosphorylation in the PI3K/AKT/mTOR pathway and enhancing lipid management in the livers of MAFLD mice. Conclusion: MST could effectively improve lipid metabolism disorders and liver lipid deposition in MAFLD mice, and its mechanism might be related to regulating the PI3K/AKT/mTOR pathway to improve autophagy.
引用
收藏
页码:5161 / 5182
页数:22
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