益肺通痹汤减轻博来霉素诱导的小鼠肺纤维化。
Yi-Fei-Tong-Bi Decoction Alleviates Bleomycin Induced Pulmonary Fibrosis in Mice.
作者信息
Du Kui, Wen Xingjian, Zhu Jie, Liang Rui, Wang Lu, Li Na, Zou Qinghua
机构信息
Department of Rheumatology and Immunology, First Affiliated Hospital of Army Medical University, Chongqing, People's Republic of China.
Chongqing Academy of Chinese Materia Medica, Chongqing, People's Republic of China.
出版信息
Drug Des Devel Ther. 2025 May 15;19:3983-3995. doi: 10.2147/DDDT.S515368. eCollection 2025.
BACKGROUND
Fei-Bi decoction, a Chinese ancient experience decoction collected in the book of Bianzhenglu (Syndrome Differentiation Record). Based on Fei-Bi Decoction, Yi-Fei-Tong-Bi decoction (YFTBD) is developed and has a significant effect in the treatment of pulmonary fibrosis. However, the underlying mechanisms of YFTBD affects pulmonary fibrosis remain to be elucidated.
PURPOSE
To investigate the protective effect and the underlying mechanism of YFTBD on bleomycin-induced pulmonary fibrosis in mice.
METHODS
The chemical components of water extract of YFTBD were analyzed by combining the high performance liquid chromatography (HPLC) coupled with mass spectrometry (MS). A mouse model was established by intratracheal injection of bleomycin, and the effects of YFTBD were evaluated through pathological staining, immunohistochemistry analyses, and Enzyme-Linked Immunosorbent Assay (ELISA). Subsequently, the effect of YFTBD on the gut microbiota of mice was analyzed by 16S rRNA high-throughput gene sequencing.
RESULTS
Compared with the model group, the survival rate and lung coefficient of mice with pulmonary fibrosis were increased after the intervention of YFTBD, the pathological morphology of lung tissue was improved, and the expression of the inflammatory factor levels were decreased. The expression of α-SMA, TGF-β1, p21, and p16 senescence-related proteins was significantly down-regulated. The expression of Smad7 and PGC-1α senescence-related proteins was significantly up-regulated. Meanwhile, gut microbiota analysis showed that YFTBD could induce changes in the abundance of , and NK4A136 group.
CONCLUSION
Our findings suggest that YFTBD could alleviate the bleomycin-induced pulmonary fibrosis in mice via regulating TGF-β1/Smad signaling pathway, inflammation and gut microbiota. It provides experimental evidence and a theoretical basis for the application of YFTBD in pulmonary fibrosis.
背景
肺痹汤是《辨证录》中收录的一首古代经验方。益肺通痹汤(YFTBD)是在肺痹汤的基础上研制而成,对肺纤维化的治疗有显著效果。然而,YFTBD影响肺纤维化的潜在机制仍有待阐明。
目的
探讨YFTBD对博莱霉素诱导的小鼠肺纤维化的保护作用及其潜在机制。
方法
采用高效液相色谱(HPLC)与质谱(MS)联用技术分析YFTBD水提取物的化学成分。通过气管内注射博莱霉素建立小鼠模型,并通过病理染色、免疫组织化学分析和酶联免疫吸附测定(ELISA)评估YFTBD的作用。随后,通过16S rRNA高通量基因测序分析YFTBD对小鼠肠道微生物群的影响。
结果
与模型组相比,YFTBD干预后肺纤维化小鼠的存活率和肺系数升高,肺组织病理形态改善,炎症因子水平表达降低。α-SMA、TGF-β1、p21和p16衰老相关蛋白的表达显著下调。Smad7和PGC-1α衰老相关蛋白的表达显著上调。同时,肠道微生物群分析表明,YFTBD可诱导NK4A136组丰度的变化。
结论
我们的研究结果表明,YFTBD可通过调节TGF-β1/Smad信号通路、炎症和肠道微生物群来减轻博莱霉素诱导的小鼠肺纤维化。为YFTBD在肺纤维化中的应用提供了实验证据和理论依据。