杏贝止咳颗粒治疗急性支气管炎的功效物质及作用机制研究

Study on the Effective Substances and Mechanism of Action of Xingbei Zhike Granules in the Treatment of Acute Bronchitis

  • 摘要:
    目的 阐明杏贝止咳颗粒治疗急性支气管炎的功效物质和作用机制。
    方法 通过网络药理学预测杏贝止咳颗粒潜在的功效物质和作用机制,随后通过大孔吸附树脂富集纯化得到功效物质并对其进行分离,通过体外炎症细胞模型筛选功效物质中抗炎活性成分,并建立关键成分(ECPs)组。最后利用脂多糖(LPS)气道滴鼻构建小鼠急性支气管炎模型,对杏贝止咳颗粒、功效物质、ECPs进行药效评价,采用RT-qPCR检测炎症介质的主要mRNA,Western blot检测NLRP3通路蛋白表达,并通过微生物群分析小鼠粪便中肠道菌群的多样性。
    结果 通过网络药理学预测杏贝止咳颗粒黄酮类成分具有抗炎功效,可能通过NLRP3信号通路治疗急性支气管炎。通过大孔吸附树脂得到60%乙醇洗脱部位为总黄酮部位(XBZK-60),XBZK-60分离得到5个黄酮类化合物,分别为甘草苷、木蝴蝶苷A、白杨素-7-O-β-D-葡萄糖醛酸苷、白杨素-7-O-龙胆二糖苷、木蝴蝶苷B,通过体外炎症细胞模型筛选木蝴蝶苷A、白杨素-7-O-β-D-葡萄糖醛酸苷、木蝴蝶苷B作为ECPs组。体内药效结果显示,与模型组相比,杏贝止咳颗粒组、XBZK-60组、ECPs组均能显著降低急性支气管炎小鼠肺泡灌洗液(BALF)中IL-6、IL-1β含量(P<0.05,P<0.01);RT-qPCR结果表明各给药组均能显著降低急性支气管小鼠肺组织中IL-6、IL-1α、IL-1β及TNF-α表达(P<0.01);Western blot结果表明各给药组均能显著下调急性支气管炎小鼠肺组织中Cleaved Caspase-1、ASC、NLRP3、TNF-α蛋白的表达(P<0.05,P<0.01);肠道微生物分析表明,各给药组肠道微生物丰度与丰富度均显著提升,肠道微生物中有益菌Lachnospiraceae_NK4A136_groupPrevotellaceae_UCG-001Colidextribacter数量均显著高于模型组。
    结论 总黄酮类成分是杏贝止咳颗粒治疗急性支气管炎的功效物质,可通过调控NLRP3信号通路来实现抗炎作用。其中,木蝴蝶苷A、木蝴蝶苷B以及白杨素-7-O-β-D-葡萄糖醛酸苷是总黄酮类中的关键成分。

     

    Abstract:
    OBJECTIVE To elucidate the effective substances and mechanism of action of Xingbei Zhike Granules in treating acute bronchitis.
    METHODS The potential effective substances and action mechanisms of Xingbei Zhike Granules were predicted through network pharmacology. Subsequently, the effective substances were enriched and purified by macroporous adsorption resin and separated. The anti-inflammatory effective components in the effective substances were screened through an in vitro inflammatory cell model, and a group of effective components (ECPs) was established. Finally, a mouse model of acute bronchitis was constructed by intranasal instillation of LPS to evaluate the pharmacological effects of Xingbei Zhike Granules, effective substances, and ECPs. RT-qPCR was used to detect the expression of main mRNAs and Western blot was used to detect the proteins of inflammatory mediators and the NLRP3 pathway, and the diversity of intestinal flora in mouse feces was analyzed through microbiota analysis.
    RESULTS Network pharmacology predicted that the flavonoid components of Xingbei Zhike Granules had anti-inflammatory effects and might treat acute bronchitis through the NLRP3 signaling pathway. The 60% ethanol elution fraction obtained by macroporous adsorption resin was the total flavonoid fraction (XBZK-60). Five flavonoid compounds were isolated from the total flavonoid fraction, namely liquiritin, oroxin A, chrysin-7-O-β-D-glucuronide, chrysin-7-O-gentiobioside, and oroxin B. Oroxin A, chrysin-7-O-β-D-glucuronide and oroxin B were screened as ECPs through an in vitro inflammatory cell model. The in vivo pharmacodynamic results showed that compared with the model group, the Xingbei Zhike Granules group, XBZK-60 group, and ECPs group could significantly reduce the content of IL-6 and IL-1β in the bronchoalveolar lavage fluid of mice with acute bronchitis (P<0.05, P<0.01). RT-qPCR results indicated that each administration group could significantly reduce the mRNA expression of IL-6, IL-1α, IL-1β and TNF-α in the lung tissues of mice with acute bronchitis (P<0.01). Western blot results showed that each administration group could significantly down-regulate the protein expression of Cleaved Caspase-1, ASC, NLRP3, and TNF-α in the lung tissues of mice with acute bronchitis (P<0.05, P<0.01). The gut microbiota analysis showed that compared with the model group, the abundance and richness of gut microbiota in each administration group were significantly increased, and the numbers of beneficial bacteria Lachnospiraceae_NK4A136_group, Prevotellaceae_UCG-001, and Colidextribacter in the gut microbiota were significantly higher than those in the model group.
    CONCLUSION Total flavonoid components are the effective substances of Xingbei Zhike Granules in the treatment of acute bronchitis, and they can achieve anti-inflammatory effects by regulating the NLRP3 signaling pathway. Among them, oroxin A, oroxin B and chrysin-7-O-β-D-glucuronide are the key components of the total flavonoids.

     

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