基于系统药理学方法探讨散风通窍滴丸治疗过敏性鼻炎的作用靶点及机制

Exploring the Target and Mechanism of Sanfeng Tongqiao Dropping Pills in the Treatment of Allergic Rhinitis Based on Systematic Pharmacological Methods

  • 摘要:
      目的  运用网络药理学研究方法筛选散风通窍滴丸(SFTQ)活性成分, 探讨其治疗过敏性鼻炎(Allergic rhinitis, AR)的靶点和作用机制。
      方法  利用中药系统药理学分析平台(TCMSP)筛选SFTQ的活性成分和作用靶点。运用TCMSP和TTD数据库筛选AR相关治疗靶点。通过Cytoscape构建SFTQ活性成分-AR疾病靶点网络, 预测潜在靶点。采用Davidv 6.8数据库对核心靶点进行KEGG通路富集分析。建立AR小鼠模型, 用不同剂量的SFTQ进行激发期干预, 通过行为学、病理切片HE染色、外周血EOS、IgE水平及颈部淋巴结中ILC2数量等指标进行评价。
      结果  筛选出42个活性成分, 16个潜在靶点。KEGG富集分析得到18条潜在信号通路, 主要涉及T细胞受体信号通路、HIF-1信号通路等。体内实验表明, SFTQ能显著减少AR小鼠喷嚏和挠鼻次数, 减轻黏膜增厚程度, 减少外周血中EOS, 降低血清中IgE水平, 同时能显著减少颈部淋巴结中ILC2的数量。
      结论  运用系统药理学方法, 揭示了SFTQ治疗AR的多成分、多靶点、多通路的特点, 为SFTQ的机制研究提供了可能的靶点和有效成分, 为更全面地认识及应用该方奠定了基础。

     

    Abstract:
      OBJECTIVE  To screen the active components of Sanfeng Tongqiao (SFTQ) by using network pharmacological method and to investigate the target and mechanism of SFTQ in the treatment of allergic rhinitis (AR).
      METHODS  The active components and targets of SFTQ were screened by TCMSP. TCMSP and TTD database were used to screen AR-related therapeutic targets. SFTQ active components-AR target network was constructed by Cytoscape to predict potential targets. KEGG pathway enrichment analysis was performed on Davidv 6.8 database. An AR mouse model was established, and different doses of SFTQ were used for intervention during the stimulation period. The results were evaluated through behavioral indicators, pathological sections, HE staining, peripheral blood EOS and IgE levels, and the number of ILC2 in cervical lymph nodes.
      RESULTS  42 active components and 16 potential targets were identified. KEGG enrichment analysis revealed 18 potential signaling pathways involving T cell receptor signaling pathway, HIF-1 signaling pathway, etc. In vivo, SFTQ significantly reduced the frequency of sneezing and rubbing, the degree of mucosal thickening, peripheral blood EOS, IgE level and the amount of ILC2 in cervical lymph nodes.
      CONCLUSION  Using systems pharmacology methods, the study revealed the multi-component, multi-target, and multi-pathway characteristics of SFTQ in treating AR, providing possible targets and active components for the mechanism study of SFTQ, and laying the foundation for a more comprehensive understanding and application of this prescription.

     

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