Mechanism and components of Hewei Jiangni Prescription in regulating MrgprX2/B2 to attenuate MC/DRG neuroimmune dysregulation and mitigate non-erosive reflux disease-associated esophageal hypersensitivity

医学 药方 机制(生物学) 回流 药理学 作用机理 迟发型超敏反应 免疫学 食道疾病 肠易激综合征 食管括约肌 发病机制 痛觉过敏
作者
Jiali Wang,Wenjing Pei,Lei Shi,Tangyou Mao,Xiaowei Chen,Jiali Liu,Yuan Cheng,Hui Jiang,Hao Huang,Juncong Hu,Zhang Shuangyuan,Xiaohong Li,Junxiang Li
出处
期刊:Journal of Ethnopharmacology [Elsevier BV]
卷期号:367: 121757-121757
标识
DOI:10.1016/j.jep.2026.121757
摘要

ETHNOPHARMACOLOGICAL RELEVANCE: The Hewei Jiangni Prescription (HP) is a traditional Chinese prescription, which has shown clinical benefits for many years in non-erosive reflux disease (NERD)-associated esophageal hypersensitivity. However, its mechanism of effects remains unclear. AIM OF THE STUDY: To investigate the mechanism of HP in treating NERD-associated esophageal hypersensitivity and identify its pharmacologically active components. MATERIALS AND METHODS: NERD-associated esophageal hypersensitivity model mice were treated with HP. Proteomics and protein interaction networks were employed to identify differentially regulated targets. Effects on key targets were validated in cell models and model mice using enzyme-linked immunosorbent assay, western blotting, reverse transcription‒quantitative polymerase chain reaction, and immunofluorescence. Bio-layer interference technology was used to identify HP components binding to targets, followed by liquid chromatography‒mass spectrometry identification and functional validation in cell models. RESULTS: levels, and decreasing the release of mast cell tryptase and calcitonin gene-related peptide. Vitexin was identified as one of the bioactive components of HP, reproducing its core pharmacological effects in vitro and exhibiting high affinity for the MRGX2 target. CONCLUSIONS: This study suggests that HP may attenuate neuroimmune dysregulation between mast cells and DRG neurons by regulating MrgprX2/B2, thereby mitigating NERD-associated esophageal hypersensitivity. Additionally, the study findings suggest that vitexin may be one of the bioactive components of HP.
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