Suppr超能文献

固本防哮方通过调节微生物群-乙酸-Tregs轴改善小鼠哮喘缓解期症状

Gu-Ben-Fang-Xiao Decoction Ameliorated Murine Asthma in Remission Stage by Modulating Microbiota-Acetate-Tregs Axis.

作者信息

Dong Yingmei, Yan Hua, Zhao Xia, Lin Rui, Lin Lili, Ding Yuanyuan, Liu Liwei, Ren Lishun, Xing Qiongqiong, Ji Jianjian

机构信息

Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.

Jiangsu Key Laboratory of Pediatric Respiratory Disease, Institute of Pediatrics, Medical Metabolomics Center, Nanjing University of Chinese Medicine, Nanjing, China.

出版信息

Front Pharmacol. 2020 May 4;11:549. doi: 10.3389/fphar.2020.00549. eCollection 2020.

Abstract

Dysbiosis of gut microbiota is a critical factor in the pathogenesis of asthma. Manipulating gut microbiota is a promising therapeutic intervention in asthma, and is being extensively studied. Gu-Ben-Fang-Xiao Decoction (GBFXD), derived from traditional Chinese medicine, is an effective and safe therapeutic formula for asthma in remission stage (ARS). Herein, we showed that GBFXD treatment remarkably alleviated ARS by improving respiratory function and lung histopathology. Asthmatic mice displayed a dysbiosis of gut microbiota, represented by significantly increased abundance of and decreased abundance of in gut, while GBFXD treatment reversed the gut dysbiosis in asthmatic mice at phylum, family, and genus levels. Moreover, our data showed that GBFXD treatment increased the abundance of short-chain fatty acid (SCFA)-producing bacteria in asthmatic mice, such as , , and , which consequently led to elevated levels of SCFAs. Furthermore, GBFXD treatment significantly enhanced the regulatory T cell differentiation SCFAs, particularly acetate, in asthmatic mice. More critically, the protective effect of GBFXD was shown to be transmissible among asthmatic mice through co-housing microbiota transplantation. Antibiotic cocktail and acetate replenishment experiments also further substantiated the importance of SCFA-producing gut microbiota in GBFXD action. We, thus, demonstrated for the first time that gut microbiota dysbiosis existed in ARS. GBFXD could ameliorate ARS through the microbiota-acetate-Tregs axis.

摘要

肠道微生物群失调是哮喘发病机制中的一个关键因素。调控肠道微生物群是一种有前景的哮喘治疗干预手段,目前正在进行广泛研究。固本防哮汤(GBFXD)源自中药,是缓解期哮喘(ARS)的一种有效且安全的治疗方剂。在此,我们表明GBFXD治疗可通过改善呼吸功能和肺组织病理学显著缓解ARS。哮喘小鼠表现出肠道微生物群失调,其特征为肠道中[具体菌1]丰度显著增加而[具体菌2]丰度降低,而GBFXD治疗在门、科和属水平上逆转了哮喘小鼠的肠道失调。此外,我们的数据表明GBFXD治疗增加了哮喘小鼠中产生短链脂肪酸(SCFA)的细菌的丰度,如[具体菌3]、[具体菌4]和[具体菌5],从而导致SCFAs水平升高。此外,GBFXD治疗显著增强了哮喘小鼠中SCFAs,特别是乙酸盐介导的调节性T细胞分化。更关键的是,GBFXD的保护作用通过同笼微生物群移植在哮喘小鼠之间具有可传递性。抗生素鸡尾酒和乙酸盐补充实验也进一步证实了产生SCFA的肠道微生物群在GBFXD作用中的重要性。因此,我们首次证明ARS中存在肠道微生物群失调。GBFXD可通过微生物群 - 乙酸盐 - 调节性T细胞轴改善ARS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33ac/7212778/85b3534962a0/fphar-11-00549-g008.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验