Deciphering the mechanism of Sang Ju Yin in ameliorating acute lung injury: An integrated systems pharmacology approach encompassing chemical composition analysis, network pharmacology, metabolomics, molecular docking and molecular biology

系统药理学 系统生物学 药理学 分子药理学 计算生物学 机制(生物学) 生物 化学 药品 生物化学 受体 哲学 认识论
作者
Ruinan Ren,Fang Wang,Guiping Zhao,Qi Yu,Jinling Zhang,Wenbao Wang,Tianyang WANG,Song Lin,Lin Yan
出处
期刊: 卷期号:53 (5): 100527-100527
标识
DOI:10.1016/j.cjac.2025.100527
摘要

• The therapeutic effect of SJY anti-ALI is revealed by network pharmacology. • The impact of SJY on ALI rats is explored by LC/MS- 1 H NMR metabolomics. • Integration of network pharmacology-metabolomics is used to guide SJY's mechanism. • The impact of SJY on AA metabolism is proven by molecular docking, qRT-PCR and WB. Sang Ju Yin (SJY), a renowned traditional Chinese medicinal formula, has been widely utilized in acute lung injury (ALI) management. Yet, its underlying therapeutic mechanisms remain obscure. This study devised an innovative and integrated methodology, merging advanced chemical analysis with biological assays, to elucidate SJY's action mechanism in ALI treatment. Initially, UFLC-ESI-QTOF-MS was employed to precisely analyze SJY's chemical constituents. Subsequently, network pharmacology predicted potential targets and signaling pathways for SJY's beneficial effects. In parallel, pharmacodynamic evaluation was performed on ALI rats. Utilizing LC-MS and 1 H NMR metabolomics techniques with an innovative data fusion strategy, potential biomarkers and perturbed metabolic pathways were identified. Crucially, integrating network pharmacology and metabolomics insights yielded a holistic understanding of the mechanism. Finally, verification experiments involving molecular docking, Western Blot, and qRT-PCR were carried out. Notably, potential key bioactive components including apigenin were identified for SJY's anti-ALI activity. Marked perturbations in representative pathways such as arachidonic acid (AA) metabolism and PI3K-Akt pathway were obtained after SJY administration. Furthermore, integrated data spotlighted PTGS2, PLA2, and AA metabolism as pivotal, linking predicted targets and metabolic alterations for SJY in ALI treatment. In summary, this study uncovers SJY's mechanism in ALI treatment, presenting an advanced interdisciplinary framework. It deepens our comprehension of traditional Chinese medicine's role in ALI, setting a new standard for research at the chemistry-pharmacology interface.
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