Center of Respiratory Disease, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Department of Respiratory, The Third Affiliated Hospital, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Drug Des Devel Ther. 2023 Jun 2;17:1613-1630. doi: 10.2147/DDDT.S406483. eCollection 2023.
Tuo-Min-Ding-Chuan Decoction (TMDCD) is an effective traditional Chinese medicine (TCM) formula granule for allergic asthma (AA). Previous studies proved its effects on controlling airway inflammations, while the specific mechanism was not clear.
We conducted a network pharmacology study to explore the molecular mechanism of TMDCD against AA with the public databases of TCMSP. Then, HUB genes were screened with the STRING database. DAVID database performed GO annotation and KEGG functional enrichment analysis of HUB genes, and it was verified with molecular docking by Autodock. Then, we built a classic ovalbumin-induced allergic asthma mice model to explore the mechanism of anti-inflammation effects of TMDCD.
In the network pharmacology study, we found out that the potential mechanism of TMDCD against AA might be related to NOD-like receptor (NLR) signaling pathway and Toll-like receptor (TLR) signaling pathway. In the experiment, TMDCD showed remarkable effects on alleviating airway inflammations, airway hyperresponsiveness (AHR), and airway remodeling in the asthmatic mice model. Further molecular biology and immunohistochemistry experiments suggested TMDCD could repress TLR4-NLRP3 pathway-mediated pyroptosis-related gene transcriptions to inhibit expressions of target proteins.
TMDCD could alleviate asthmatic mice model airway inflammations by regulating TLR4-NLRP3 pathway-mediated pyroptosis.
脱敏定喘汤(Tuo-Min-Ding-Chuan Decoction,TMDCD)是一种治疗过敏性哮喘(Allergic asthma,AA)的有效中药方剂颗粒。既往研究证实其具有控制气道炎症的作用,但具体机制尚不清楚。
我们通过 TCMSP 公共数据库进行网络药理学研究,以探讨 TMDCD 治疗 AA 的分子机制。然后,我们使用 STRING 数据库筛选 HUB 基因。DAVID 数据库对 HUB 基因进行 GO 注释和 KEGG 功能富集分析,并通过 Autodock 进行分子对接验证。然后,我们建立了经典的卵清蛋白诱导的过敏性哮喘小鼠模型,以探索 TMDCD 抗炎作用的机制。
在网络药理学研究中,我们发现 TMDCD 治疗 AA 的潜在机制可能与 NOD 样受体(NLR)信号通路和 Toll 样受体(TLR)信号通路有关。在实验中,TMDCD 对缓解哮喘小鼠模型的气道炎症、气道高反应性(Airway hyperresponsiveness,AHR)和气道重塑具有显著效果。进一步的分子生物学和免疫组织化学实验表明,TMDCD 可以抑制 TLR4-NLRP3 通路介导的焦亡相关基因转录,从而抑制靶蛋白的表达。
TMDCD 可以通过调节 TLR4-NLRP3 通路介导的焦亡来缓解哮喘小鼠模型的气道炎症。