Deng Yongjun, Shen Limin, Zhu Huilan, Zhou Yanying, Hu Xin
Department of Otolaryngology, Shanghai Pudong New Area Guangming Hospital of Traditional Chinese Medicine, Shanghai, 201300, China.
Department of Otolaryngology, Renhe Hospital in Baoshan District, Shanghai, 200431, China.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Feb;398(2):1597-1612. doi: 10.1007/s00210-024-03353-8. Epub 2024 Aug 12.
Despite the complexity of allergic rhinitis (AR) pathogenesis, no FDA-approved drug has been developed to achieve optimal therapeutic effects. The present study explored the efficacy and mechanism of Huangqi (Hedysarum Multijugum Maxim)-Gancao (Glycyrrhizae Radix et Rhizoma or licorice) herb pair in treating AR by network pharmacology and experimental approaches. The bioactive ingredients of Huangqi and Gancao were identified and used to predict the targets of these herbs in AR and generate the pharmacological network. Ovalbumin (OVA)-induced AR mouse model was established to assess the anti-AR effect of the Huangqi decoction (HQD) prepared based on both herbs. We identified 90 active ingredients of the Huangqi-Gancao pair, targeting 69 AR-related genes. Quercetin (QUE) was identified as the hub ingredient of this pair, with 57 targets in AR. The protein-protein interaction (PPI) network analysis and molecular docking revealed IL1B, TNF, STAT1, IL6, PTGS2, RELA, IL2, NFKBIA, IFNG, IL10, IL1A, IRF1, EGFR, and CXCL10 as important targets of QUE in AR treatment. Experimentally, QUE or HQD significantly alleviated the AR-induced histopathological changes, AR symptoms, and IgE level and counteracted AR-induced expression changes of IFNG, IRF1, RELA, and NFKBIA. These effects were promoted by the NF-kB inhibitor helenalin, indicating that HQD and QUE counteracted AR in mice by regulating the IFNG/IRF1 signaling via the NF-κB pathway in AR mice. These findings shed light on the efficacy of the constituents of Huangqi-Gancao pair, their potential targets, and the molecular mechanisms of HQD in treating AR, which could advance the development of tailored therapeutic interventions for this disorder.
尽管变应性鼻炎(AR)发病机制复杂,但尚无经美国食品药品监督管理局(FDA)批准的药物能达到最佳治疗效果。本研究通过网络药理学和实验方法探讨了黄芪(多序岩黄芪)-甘草(甘草根及根茎)药对治疗AR的疗效及作用机制。鉴定了黄芪和甘草的生物活性成分,并用于预测这些草药在AR中的靶点并构建药理网络。建立卵清蛋白(OVA)诱导的AR小鼠模型,以评估基于这两种草药制备的黄芪汤(HQD)的抗AR作用。我们鉴定出黄芪-甘草药对的90种活性成分,靶向69个与AR相关的基因。槲皮素(QUE)被确定为该药对的核心成分,在AR中有57个靶点。蛋白质-蛋白质相互作用(PPI)网络分析和分子对接显示,白细胞介素1β(IL1B)、肿瘤坏死因子(TNF)、信号转导和转录激活因子1(STAT1)、白细胞介素6(IL6)、前列腺素内过氧化物合酶2(PTGS2)、RelA原癌基因(RELA)、白细胞介素2(IL2)、核因子κB抑制蛋白α(NFKBIA)、干扰素γ(IFNG)、白细胞介素10(IL10)、白细胞介素1α(IL1A)、干扰素调节因子1(IRF1)、表皮生长因子受体(EGFR)和CXC趋化因子配体10(CXCL10)是QUE在治疗AR中的重要靶点。实验表明,QUE或HQD可显著减轻AR诱导的组织病理学变化、AR症状和IgE水平,并抵消AR诱导的IFNG、IRF1、RELA和NFKBIA的表达变化。NF-κB抑制剂海伦内酯可增强这些作用,表明HQD和QUE通过调节AR小鼠中IFNG/IRF1信号通路的NF-κB途径来对抗小鼠的AR。这些发现揭示了黄芪-甘草药对成分的疗效、其潜在靶点以及HQD治疗AR的分子机制,这可能推动针对该疾病的定制治疗干预措施的开发。