基于网络药理学探讨十枣汤干预心力衰竭的作用机制OA
Discussion on the mechanism of the Shi Zao decoction in intervening heart failure based on network pharmacology
本研究探讨传统名方十枣汤在治疗心力衰竭中的作用机制,运用网络药理学方法进行系统剖析.研究整合多个数据平台及生物信息工具,构建复方组方与复杂疾病之间的多层交互网络.首先借助中药系统药理学数据库与分析平台,将口服生物利用度及类药性设为筛选条件,确定了 61 个有活性潜力的候选分子,得到相应的 237 个靶点基因.然后在 GeneCards 数据库、人类孟德尔遗传数据库(OMIM)和治疗靶标数据库(TTD)中检索心力衰竭相关靶点,结合相关性得分筛选去重后得出 614 个高度相关靶标;经过交集分析识别出 50 个交集靶点,之后导入 STRING 数据库构建蛋白质-蛋白质相互作用网络,结合 Cytoscape 拓扑结构参数筛选出网络核心节点,包括白细胞介素(interleukin,IL)-1B、IL-6、肿瘤坏死因子(tumor necrosis factor,TNF)等核心靶点,这些靶点在调控心力衰竭进程中具有关键地位.在"药材-活性化合物-作用靶点"网络构建过程中,槲皮素、山柰酚及 β-谷甾醇等成分显示出较高的网络连接度,据此猜测这些物质是本方的主要药效物质.对核心靶点开展基因本体论(GO)富集分析发现,相关基因广泛参与转录活动调控、细胞因子效应及机体免疫等过程;京都基因与基因组百科全书(KEGG)通路富集分析表明,十枣汤的潜在作用机制可能涉及晚期糖基化终末产物(advanced glycation end product,AGE)-晚期糖基化终末产物受体(advanced glycation end product receptor,RAGE)信号通路、动脉硬化及炎性调控等关键环节.从机制层面推测,槲皮素可能通过调节丝裂原活化蛋白激酶(mitogen-activated protein kinase,MAPK)通路调控凋亡相关蛋白表达,β-谷甾醇可通过减轻氧化应激及炎性反应实现心肌保护,山柰酚则有可能提高细胞内抗氧化能力,优化心肌微环境.总体而言,十枣汤呈现出"多靶点-多成分-多通路"综合干预优势,为其用于心力衰竭干预的机制探索及现代临床拓展提供了理论依据.
This study investigates the mechanism of action of the traditional Chinese medicine formula Shizao decoction(十 枣 汤)in heart failure.Employing network pharmacology methods for systematic analysis,the research integrates multiple data platforms and bioinformatics tools to construct a multi-layered interaction network between the compound formula and complex diseases.Firstly,by means of the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform(TCMSP),oral bioavailability and drug-likeness were set as screening criteria to identify 61 candidate molecules with potential activity,and the corresponding 237 target genes were obtained.Subsequently,Heart Failure(HF)-related targets were retrieved from GeneCards,the Online Mendelian Inheritance in Man(OMIM)database,and the Therapeutic Targets Database(TTD).After relevance score-based screening and deduplication,614 highly relevant targets were identified.Intersection analysis further pinpointed 50 overlapping targets which were imported into the STRING database to construct a protein-protein interaction network.Using Cytoscape topological parameters,core network nodes were identified,including key targets such as IL-1B,IL-6,and TNF,which play pivotal roles in regulating heart failure progression.During the construction of the"herbal medicine-active compound-target interaction"network,components such as quercetin,kaempferol,and β-sitosterol exhibited high network connectivity.This suggests these substances may be the primary bioactive constituents of the formula.GO analysis of core targets revealed widespread involvement in transcription regulation,cytokine effects,and immune processes.KEGG pathway enrichment analysis suggested potential mechanisms involving AGE-RAGE signaling,atherosclerosis,and inflammatory regulation.At the mechanistic level,quercetin may regulate apoptosis-related protein expression by modulating the MAPK signaling pathways,meanwile β-sitosterol may exert myocardial protection by alleviating oxidative stress and inflammatory responses,while kaempferol may enhance intracellular antioxidant capacity and optimize myocardial microenvironments.Overall,Shizao Tang demonstrates a comprehensive intervention advantage characterized by"multiple-target,multiple-component,multiple-pathway",which provides a theoretical basis for exploring its mechanisms in heart failure intervention and facilitating its translation into modern clinical application.
廖才刚;吴晗;陈云飞;魏东东;项杰鋆;张明玺
湖北中医药大学第一临床学院,湖北 武汉,430000湖北中医药大学第一临床学院,湖北 武汉,430000湖北中医药大学第一临床学院,湖北 武汉,430000湖北中医药大学第一临床学院,湖北 武汉,430000湖北中医药大学第一临床学院,湖北 武汉,430000湖北中医药大学附属武汉市中医医院,湖北 武汉,430000
医药卫生
心力衰竭十枣汤网络药理学
Heart failureThe Shizao decoctionNetwork pharmacology
《中医临床研究》 2026 (5)
112-118,7
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