دورية أكاديمية

A novel network pharmacology strategy to decode mechanism of Wuling Powder in treating liver cirrhosis

التفاصيل البيبلوغرافية
العنوان: A novel network pharmacology strategy to decode mechanism of Wuling Powder in treating liver cirrhosis
المؤلفون: Qinwen Liu, Xiaowei Li, Yi Li, Qian Luo, Qiling Fan, Aiping Lu, Daogang Guan, Jiahui Li
المصدر: Chinese Medicine, Vol 19, Iss 1, Pp 1-17 (2024)
بيانات النشر: BMC, 2024.
سنة النشر: 2024
المجموعة: LCC:Other systems of medicine
مصطلحات موضوعية: Wuling Powder, Liver cirrhosis, Network pharmacology, Traditional Chinese Medicine, Other systems of medicine, RZ201-999
الوصف: Abstract Background Liver cirrhosis is a chronic liver disease with hepatocyte necrosis and lesion. As one of the TCM formulas Wuling Powder (WLP) is widely used in the treatment of liver cirrhosis. However, it’s key functional components and action mechanism still remain unclear. We attempted to explore the Key Group of Effective Components (KGEC) of WLP in the treatment of Liver cirrhosis through integrative pharmacology combined with experiments. Methods The components and potential target genes of WLP were extracted from published databases. A novel node importance calculation model considering both node control force and node bridging force is designed to construct the Function Response Space (FRS) and obtain key effector proteins. The genetic knapsack algorithm was employed to select KGEC. The effectiveness and reliability of KGEC were evaluated at the functional level by using gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. Finally, the effectiveness and potential mechanism of KGEC were confirmed by CCK-8, qPCR and Western blot. Results 940 effective proteins were obtained in FRS. KEGG pathways and GO terms enrichments analysis suggested that effective proteins well reflect liver cirrhosis characteristics at the functional level. 29 components of WLP were defined as KGEC, which covered 100% of the targets of the effective proteins. Additionally, the pathways enriched for the KGEC targets accounted for 83.33% of the shared genes between the targets and the pathogenic genes enrichment pathways. Three components scopoletin, caryophyllene oxide, and hydroxyzinamic acid from KGEC were selected for in vivo verification. The qPCR results demonstrated that all three components significantly reduced the mRNA levels of COL1A1 in TGF-β1-induced liver cirrhosis model. Furthermore, the Western blot assay indicated that these components acted synergistically to target the NF-κB, AMPK/p38, cAMP, and PI3K/AKT pathways, thus inhibiting the progression of liver cirrhosis. Conclusion In summary, we have developed a new model that reveals the key components and potential mechanisms of WLP for the treatment of liver cirrhosis. This model provides a reference for the secondary development of WLP and offers a methodological strategy for studying TCM formulas.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1749-8546
Relation: https://doaj.org/toc/1749-8546
DOI: 10.1186/s13020-024-00896-z
URL الوصول: https://doaj.org/article/a8d0ec3c9dcd4cfc8a7b57b639822627
رقم الأكسشن: edsdoj.8d0ec3c9dcd4cfc8a7b57b639822627
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17498546
DOI:10.1186/s13020-024-00896-z