Exploring miRNA-related Molecular Targets of Erchen Decoction against Lipid Metabolism Disorder using a Network Pharmacologic Approach

被引:7
|
作者
Ding, Shanshan [1 ]
Chen, Qiliang [1 ,2 ]
Huang, Yiqing [1 ]
Li, Xiaomei [1 ]
Chai, Yujuan [3 ]
Li, Candong [1 ]
Asakawa, Tetsuya [1 ,4 ]
机构
[1] Fujian Univ Tradit Chinese Med, Res Base Tradit Chinese Med Syndrome, Fuzhou 350122, Peoples R China
[2] Guangzhou Univ Chinese Med, Sch Basic Med, Guangzhou 510006, Guangdong, Peoples R China
[3] Shenzhen Univ, Hlth Sci Ctr, Sch Med Engn, Shenzhen 518060, Peoples R China
[4] Hamamatsu Univ Sch Med, Dept Neurosurg, Hamamatsu, Shizuoka, Japan
基金
日本学术振兴会;
关键词
Lipid metabolism disorder; microRNA; network pharmacology approach; erchen decoction; molecular targets; high-fat diet; CIRCULATING MICRORNA SIGNATURE; EXPRESSION; OBESITY; CONTRIBUTES;
D O I
10.2174/1386207324666210302093300
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Erchen Decoction (ECD) is a complex herbal formulation widely used for treating lipid metabolism disorder (LMD) in China. This study aims to explore the microRNA (miRNA)-related molecular targets of ECD against LMD using a network pharmacology approach (NPA) Methods: We randomly divided 20 male Sprague Dawley rats into two groups; 10 rats were normal controls, and the other 10 rats were fed a high-fat diet (HED) for 12 weeks to establish an LMD model. Differentially expressed miRNAs (DE-miRs, HFD vs. Control) in the rats' liver tissues were identified by miRNA sequencing and validated with qRT-PCR. Finally, the miRNA-related molecular targets for ECD activity against LMD were identified using a standard NPA by finding the intersection between identified DE-miRs-related targets and ECD-related targets. Result: We identified 8 DE-miRs and 968 targets and compared them to 262 ECD-related targets. A final list of 22 candidate targets was identified. Using a confidence score of >0.4, the network of (protein-protein interaction) PPI relationships exhibited 22 nodes and 67 edges. The GO and KEGG enrichment analyses revealed 171 molecular targets and 59 pathways, which were associated with ECD against LMD. Conclusion: The identified molecular targets and pathways suggest that complex mechanisms are involved in ECD's mechanism of action, and immune-inflammation-related mechanisms are closely associated with the effects of ECD. The targets obtained in this study will guide future studies on the pharmacologic effects of ECD.
引用
收藏
页码:986 / 997
页数:12
相关论文
共 3 条
  • [1] Exploring the potential mechanism and molecular targets of Taohong Siwu Decoction against deep vein thrombosis based on network pharmacology and analysis docking
    Fan, Wei
    Liu, Jinhui
    Liu, Qingyan
    MEDICINE, 2024, 103 (02) : E36220
  • [2] Exploring the material basis and molecular targets of Changma Xifeng tablet in treating Tourette syndrome: an integrative approach of network pharmacology and miRNA analysis
    Peng, Jing
    Li, Qiaoling
    Liu, Linhui
    Gao, Ping
    Xing, Lipeng
    Chen, Li
    Liu, Hui
    Liu, Zhisheng
    METABOLIC BRAIN DISEASE, 2024, 39 (08) : 1573 - 1590
  • [3] An integrated approach using molecular docking, network pharmacology, and UPLC-Q-TOF-MS analysis to investigate the chemical makeup and mechanism of Xiaoqinglong decoction against asthma
    Wei, Shuang
    Li, Xueting
    Li, Xinyu
    Wang, Rui
    Wang, Yuming
    Li, Yubo
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2025, 1254