分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Bifidobacterium pseudolongum enriched by arctigenin orchestrates cough variant asthma via the acetate-aryl hydrocarbon receptor-interleukin-33 axis

Hong Jiang, Yongxiang Wang, Qimeng Tian, Yihang Sui, Jingge Sun, Ling Chen, Xiaoqiong Liu, Ninghua Tan

Journal:Journal of Pharmaceutical Analysis

IF:11.2

DOI:10.1016/j.jpha.2026.101610

PMID:

Published:2026-03-19

research field:分子生物学免疫学中医药学代谢组学微生物学呼吸病学

Abstract

Gut microbiota dysbiosis is significantly associated with the onset and progression of cough variant asthma (CVA). Targeting and improving gut microbiota dysbiosis may serve as a promising strategy for CVA. Suhuang antitussive capsule (SH) is the sole clinically approved traditional Chinese patent medicine specifically indicated for managing CVA. Herein, we initially identified arctigenin (AG) as one of the effective components detected and preliminarily screened from SH for its potential in treating CVA. AG significantly ameliorates ovalbumin (OVA)-induced CVA symptoms, alleviates gut dysbiosis, and improves intestinal barrier function. Specifically, AG alleviates CVA symptoms in a gut microbiota-dependent manner, as demonstrated by antibiotic treatment and fecal microbiota transplantation (FMT). 16S rRNA sequencing revealed that AG treatment could notably enrich the commensal bacterium Bifidobacterium pseudolongum ( B. pseudolongum ), which is typically reduced in CVA. The mono-colonization with B. pseudolongum also showed a reduction in CVA severity. GC-MS metabolomic analysis identified acetate as the key and main serum metabolite induced by B. pseudolongum . We demonstrated that acetate enters pulmonary circulation and activates the aryl hydrocarbon receptor (AHR). Validation using AHR antagonists, siRNA knockdown, Chromatin Immunoprecipitation (ChIP) assays, luciferase reporter experiments, and molecular docking confirmed that acetate-mediated AHR activation suppresses Interleukin-33 (IL-33) secretion from lung epithelial cells, thereby preventing CVA progression. These findings suggest AG, one of the effective components in SH, exhibits prebiotic-like effects to alleviate CVA and highlight the potential of targeting specific gut microbiota species for CVA treatment.

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