Shen Yujin, Ma Xi, Du Zhenzhen, Li Yang, Mei Zhinan, Zhao Ling
School of Biology and Pharmaceutical Engineering, Wuhan Polytechnic University, Wuhan 430023, China.
Pharmaceuticals (Basel). 2025 Jul 18;18(7):1059. doi: 10.3390/ph18071059.
Allergic rhinitis (AR) is a prevalent allergic disorder characterized by a complex pathogenesis. Drawing on traditional Chinese medicine theory and contemporary pharmacological principles, this study developed an inhalation-based herbal formulation, ZHW, to explore a novel non-invasive therapeutic approach. To investigate the therapeutic effects of ZHW on AR and elucidate its underlying mechanisms and potential targets through an integrated analysis of network pharmacology and proteomics. The volatile components of ZHW were analyzed by gas chromatography-mass spectrometry (GC-MS). The mouse model of AR was induced by OVA sensitization. The therapeutic efficacy of ZHW was assessed based on nasal symptom scores, histopathological examination, and inflammatory cytokine levels. Furthermore, the underlying mechanisms and potential targets of ZHW were investigated through integrated network pharmacology and proteomics analyses. GC-MS analysis identified 39 bioactive compounds in ZHW. Inhalation treatment with ZHW demonstrated significant anti-allergic effects in OVA-sensitized mice, as evidenced by (1) reduced sneezing frequency and nasal rubbing behaviors; (2) decreased serum levels of IL-4, histamine, and OVA-specific IgE; (3) attenuated IL-4 concentrations in both nasal lavage fluid and lung tissue; (4) diminished nasal mucosal thickening; and (5) suppression of inflammatory cell infiltration. Integrated network pharmacology and proteomics analyses indicated that ZHW's therapeutic effects were mediated through the modulation of multiple pathways, including the PI3K-Akt signaling pathway, the B cell receptor signaling pathway, oxidative phosphorylation, and the FcεRI signaling pathway. Key molecular targets involved Rac1, MAPK1, and SYK. Molecular docking simulations revealed strong binding affinities between ZHW's primary bioactive constituents (linalool, levomenthol, linoleic acid, Linoelaidic acid, and n-Valeric acid cis-3-hexenyl ester) and these target proteins. The herbal formulation ZHW demonstrates significant efficacy in alleviating allergic rhinitis symptoms through multi-target modulation of key signaling pathways, including PI3K-Akt- and FcεRI-mediated inflammatory responses. These findings substantiate ZHW's therapeutic potential as a novel, non-invasive treatment for AR and provide a strong basis for the development of new AR therapies. Future clinical development will require systematic safety evaluation to ensure optimal therapeutic outcomes.
变应性鼻炎(AR)是一种常见的变应性疾病,其发病机制复杂。本研究借鉴中医理论和现代药理学原理,开发了一种基于吸入的中药制剂ZHW,以探索一种新型的非侵入性治疗方法。通过网络药理学和蛋白质组学的综合分析,研究ZHW对AR的治疗作用,阐明其潜在机制和潜在靶点。采用气相色谱-质谱联用(GC-MS)分析ZHW的挥发性成分。通过卵清蛋白(OVA)致敏建立AR小鼠模型。基于鼻症状评分、组织病理学检查和炎性细胞因子水平评估ZHW的治疗效果。此外,通过网络药理学和蛋白质组学的综合分析研究ZHW的潜在机制和潜在靶点。GC-MS分析鉴定出ZHW中的39种生物活性化合物。ZHW吸入治疗在OVA致敏小鼠中显示出显著的抗过敏作用,表现为:(1)打喷嚏频率和鼻摩擦行为减少;(2)血清白细胞介素-4(IL-4)、组胺和OVA特异性免疫球蛋白E(IgE)水平降低;(3)鼻灌洗液和肺组织中IL-4浓度降低;(4)鼻黏膜增厚减轻;(5)炎性细胞浸润受到抑制。网络药理学和蛋白质组学的综合分析表明,ZHW的治疗作用是通过调节多种途径介导的,包括磷脂酰肌醇-3激酶-蛋白激酶B(PI3K-Akt)信号通路、B细胞受体信号通路、氧化磷酸化和FcεRI信号通路。涉及的关键分子靶点有Rac1、丝裂原活化蛋白激酶1(MAPK1)和脾酪氨酸激酶(SYK)。分子对接模拟显示ZHW的主要生物活性成分(芳樟醇、左旋薄荷醇、亚油酸、反式亚油酸和顺-3-己烯基正戊酸酯)与这些靶蛋白之间具有很强的结合亲和力。中药制剂ZHW通过对关键信号通路(包括PI3K-Akt和FcεRI介导的炎症反应)的多靶点调节,在减轻变应性鼻炎症状方面显示出显著疗效。这些发现证实了ZHW作为一种新型非侵入性AR治疗方法的治疗潜力,并为开发新的AR治疗方法提供了有力依据。未来的临床开发需要进行系统的安全性评估,以确保最佳治疗效果。