Department of Traditional Chinese Medicine, Changchun University of Traditional Chinese Medicine, Changchun, Jilin, China.
Department of Respiratory Medicine, Affiliated Hospital of Changchun University of Traditional Chinese Medicine, Changchun, Jilin, China.
Medicine (Baltimore). 2024 Oct 11;103(41):e39921. doi: 10.1097/MD.0000000000039921.
Modern medical practice has confirmed the efficacy of Mahuang Fuzi Xixin Decoction (MHFZXXD) in treating elderly bronchial asthma, but its specific mechanisms of action remain to be clarified. Therefore, this study utilizes network pharmacology, molecular docking techniques, and molecular dynamics simulations to explore the key active components, core target genes, and potential mechanisms of MHFZXXD in the treatment of elderly bronchial asthma. Active components and related targets of MHFZXXD were identified through the retrieval and screening of the TCMSP, Swiss Targets Prediction, and Uniprot databases. Relevant targets for elderly bronchial asthma were searched using the GeneCards, OMIM, and Pharm GKB databases, followed by the selection of intersecting targets between the drug's active components and the disease. A PPI network diagram was created using String and Cytoscape software, and the intersecting targets of the disease and the active components of traditional Chinese medicine were imported into the DAVID database for GO and KEGG enrichment analysis to further explore their potential mechanisms of action. Subsequently, molecular docking and molecular dynamics simulations were performed using AutoDock Vina and Gromacs to verify the binding capacity and stability of the core genes with the key active components. The study results indicate that the active components of MHFZXXD, such as quercetin, luteolin, and kaempferol, target multiple genes including AKT1, EGF, MYC, TGFB1, PTEN, and CCND1. They exert effects through signaling pathways such as TNF, PI3K-Akt, and HIF-1. Molecular docking and dynamics simulations show that the core targets bind stably with the key active components. Overall, MHFZXXD may reduce inflammatory responses and improve hypoxic conditions and apoptosis during the progression of elderly bronchial asthma through multiple active components, targets, and signaling pathways, thereby delaying the malignant progression of the disease. This provides relevant evidence and experimental data for clinical treatment and further research.
现代医学实践已经证实了麻黄附子细辛汤(MHFZXXD)在治疗老年支气管哮喘方面的疗效,但具体作用机制仍需阐明。因此,本研究利用网络药理学、分子对接技术和分子动力学模拟方法,探讨 MHFZXXD 治疗老年支气管哮喘的关键活性成分、核心靶基因和潜在作用机制。通过 TCMSP、Swiss Targets Prediction 和 Uniprot 数据库检索和筛选,确定 MHFZXXD 的活性成分及相关靶点;利用 GeneCards、OMIM 和 Pharm GKB 数据库检索老年支气管哮喘相关靶点,筛选药物活性成分与疾病的 intersecting targets。使用 String 和 Cytoscape 软件构建 PPI 网络图,将 intersecting targets of the disease 和 the active components of traditional Chinese medicine 导入 DAVID 数据库进行 GO 和 KEGG 富集分析,进一步探讨其潜在作用机制。然后,利用 AutoDock Vina 和 Gromacs 进行分子对接和分子动力学模拟,验证核心基因与关键活性成分的结合能力和稳定性。研究结果表明,MHFZXXD 的活性成分如槲皮素、木犀草素和山奈酚等,靶向 AKT1、EGF、MYC、TGFB1、PTEN 和 CCND1 等多个基因,通过 TNF、PI3K-Akt 和 HIF-1 等信号通路发挥作用。分子对接和动力学模拟表明,核心靶点与关键活性成分结合稳定。综上所述,MHFZXXD 可能通过多种活性成分、靶标和信号通路,降低老年支气管哮喘进展过程中的炎症反应,改善缺氧和细胞凋亡状况,从而延缓疾病的恶性进展。这为临床治疗和进一步研究提供了相关证据和实验数据。