Lingganwuweijiangxin Decoction suppresses allergic airway inflammation in Guinea pigs with cough variant asthma by regulating the treg/Th17 balance and the JAK1/STAT6 signaling pathway

医学 哮喘 免疫学 汤剂 STAT6 炎症 过敏 Treg细胞 气道 豚鼠 白细胞介素4 内科学 细胞因子 免疫系统 麻醉 白细胞介素2受体 T细胞
作者
Yu Lai,Fengyi He,Jingyi Tang,Xuannan Chen,Shiqing Yuan,Qi Zhang
出处
期刊:Journal of Asthma [Taylor & Francis]
卷期号:62 (8): 1280-1295 被引量:1
标识
DOI:10.1080/02770903.2025.2472357
摘要

Background Lingganwuweijiangxin Decoction (LD) is an effective prescription widely used to treat cough variant asthma (CVA) in traditional Chinese medicine, although its mechanisms remain unclear. This study investigates the therapeutic effects and underlying mechanisms of LD on CVA.Methods A guinea pig CVA model was treated with either LD or budesonide (BUD). Capsaicin aerosol-induced coughs were recorded. Pathological changes were then examined using hematoxylin and eosin staining, transmission electron microscopy, and Wright–Giemsa staining of bronchoalveolar lavage fluid (BALF). Inflammatory cytokines were measured by enzyme-linked immunosorbent assay. mRNA expression levels of transcription factors forkhead box P3 (Foxp3), retinoic acid-related orphan receptor γt (RORγt), Janus kinase 1 (JAK1), signal transducer and activator of transcription 6 (STAT6), the transient receptor potential ankyrin 1 (TRPA1), and transient receptor potential vanilloid 1 (TRPV1) in lung tissue were detected by real-time reverse transcription polymerase chain reaction, and protein levels of these markers were assessed by Western blotting.Results Compared to the control group, the model group showed significantly more coughs, which were markedly reduced by LD treatment (p = 0.0083 and p = 0.0117). LD treatment also decreased inflammatory cell infiltration, alveolar epithelial hyperplasia, and mitochondrial swelling in ciliated cells, consistent with the lung tissue injury score (p < 0.0001). LD significantly reduced the ovalbumin-induced elevation of TRPA1 (p < 0.01 and p < 0.0001), TRPV1 (p < 0.01 and p < 0.0001), and substance P (SP) levels (p < 0.05). Moreover, LD treatment increased Foxp3 mRNA (p = 0.0013) and protein expression (p < 0.0001) and reduced RORγt mRNA (p < 0.0001). LD also decreased JAK1 and STAT6 transcription (p = 0.0021, p < 0.0001, respectively), with consistent effects observed at the protein level (p < 0.0001).Conclusions LD significantly reduced coughs and airway inflammation in the CVA guinea pig model by regulating TRPA1, TRPV1, SP, regulatory T cell/T helper 17 cell balance, and the JAK1/STAT6 signaling pathway. These effects were comparable to BUD, suggesting that LD may be a viable alternative treatment for CVA.
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