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Baihe Dihuang-Danshen Decoction in Myocardial Ischemia-reperfusion Injury: Network Pharmacology and Experimental Validation

小桶 药理学 对接(动物) 计算生物学 下调和上调 系统药理学 体内 安全药理学 医学 作用机理 基因 汤剂 细胞损伤 毒性 急性毒性 交互网络 化学 基因表达 免疫系统 多巴胺转运体 基因表达谱 数量结构-活动关系 生物信息学 运输机
作者
Ling Huang,Liang Zhang,Qiang Xu,Wei-Jia Huang,Shizhong Zhang,Cuihua Liu,Kuncheng Qiu
出处
期刊:Current Computer - Aided Drug Design [Bentham Science Publishers]
卷期号:22
标识
DOI:10.2174/0115734099391795251203142647
摘要

INTRODUCTION: Myocardial ischemia-reperfusion injury (MIRI) significantly impairs the prognosis of cardiac surgery. Baihe Dihuang-Danshen Decoction (BDDSD), a Chinese herbal formula, has shown efficacy against MIRI. This study combined network pharmacology and experimental validation to identify the core compounds and mechanisms of BDDSD. METHODS: The compounds of BDDSD were identified through the TCMSP and BATMAN databases. Potential targets were determined by intersecting MIRI-related differential genes with BDDSD compound targets. A protein-protein interaction (PPI) network was constructed using the STING platform. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were performed using the Metascape database. A TF-gene network and a gene-miRNA network were generated using the NetworkAnalyst platform. Immune infiltration analysis was conducted using CIBERSORT. In vivo verification was then performed, followed by molecular docking analysis. RESULTS: The analysis revealed that BDDSD's cardioprotective effects against MIRI are mediated by six core compounds (e.g., Tanshinone IIA, Cryptotanshinone), which synergistically modulate key targets (e.g., IL6, HMOX1). In rats, BDDSD treatment reduced myocardial structural damage. Notably, MIRI-induced upregulation of mRNA expression of all six core targets was significantly suppressed by BDDSD. Molecular docking confirmed strong compound-target binding, further validating BDDSD's efficacy in MIRI. DISCUSSION: Our study elucidated the mechanisms underlying BDDSD's action in MIRI treatment. However, given that BDDSD operates through multiple components and targets, the complex interactions between these compounds require further investigation. Additionally, comprehensive toxicity assessments in preclinical models are needed to establish its safety profile. CONCLUSION: This study provides a comprehensive overview of the core compounds, potential targets, and mechanisms of BDDSD in MIRI treatment, offering a foundation for further research into the pathological mechanisms of MIRI and the therapeutic potential of traditional Chinese herbal decoctions.
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