Traditional Chinese Medicine Department, Qitai Hospital of the Sixth Division, Xinjiang, 831899, People's Republic of China.
College of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, People's Republic of China.
Drug Des Devel Ther. 2024 Nov 13;18:5161-5182. doi: 10.2147/DDDT.S478072. eCollection 2024.
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).
This research aims to investigate the impact and underlying mechanisms of MST in ameliorating MAFLD caused by an HFD.
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.
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.
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.
改良酸梅汤(MST)由四种既属于中药又属于烹饪应用的植物组成,它可能缓解高脂肪饮食(HFD)引发的代谢相关脂肪性肝病(MAFLD)。
本研究旨在探讨 MST 改善 HFD 诱导的 MAFLD 的作用及其机制。
采用 UHPLC-Q-Orbitrap-MS/MS 法测定 MST 的成分,并评价其对 MAFLD 小鼠模型的作用。采用转录组学、网络药理学和生物信息学分析(包括京都基因与基因组百科全书和基因集富集分析)进一步阐明 MST 作用于 MAFLD 的机制。实验方法包括 ELISA、实时定量 PCR(RT-qPCR)、Western blot、免疫组织化学、分子对接和代谢组学。将转录组学与代谢组学相结合,寻找差异表达基因与代谢物之间的相关性,并通过 RT-qPCR 验证关键基因。
共鉴定出 MST 的 23 种成分。该配方可改善 MAFLD 小鼠的代谢紊乱、肥胖、胰岛素抵抗、炎症和氧化应激。研究结果表明,MST 通过抑制 PI3K/AKT/mTOR 通路的磷酸化和增强 MAFLD 小鼠肝脏的脂质代谢来促进自噬。
MST 可有效改善 MAFLD 小鼠的脂质代谢紊乱和肝脏脂质沉积,其机制可能与调节 PI3K/AKT/mTOR 通路以改善自噬有关。