An Integrated Gut Microbiota and Network Pharmacology Study on Fuzi-Lizhong Pill for Treating Diarrhea-Predominant Irritable Bowel Syndrome

被引:38
|
作者
Zhang, Zhen [1 ,2 ]
Lim, Xia [1 ]
Huang, You [1 ]
Zhou, Jingwei [1 ]
Yang, Shasha [1 ]
Wei, Xinyi [1 ]
Lai, Wenjing [1 ]
Zhang, Xin [1 ]
Fu, Chaomei [1 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Pharm Coll, State Key Lab Southwestern Chinese Med Resources, Chengdu, Peoples R China
[2] Sichuan New Green Med Sci & Technol Dev Co Ltd, Key Lab Qual Control & Efficacy Evaluat Tradit Ch, Pengzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
irritable bowel syndrome; Fuzi-Lizhong pill; gut microbiota; network pharmacology; crucial targets; IGA RESPONSE; BACTERIA; HEALTH; BLOOD; CELLS;
D O I
10.3389/fphar.2021.746923
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diarrhea-predominant irritable bowel syndrome (IBS-D) is one of the most common chronic functional gastrointestinal diseases with limited treatments. Gut microbiota play an important role in chronic gastrointestinal diseases. In traditional Chinese medicine (TCM), Spleen-Yang deficiency (SYD) is one of the root causes of IBS-D. Fuzi-Lizhong pill (FLZP) is well known for its powerful capacity for treating SYD and has a good clinical effect on IBS-D. However, the mechanism of FLZP on the gut microbiota of IBS-D has not been fully clarified. Our present study aimed to reveal the mechanism of FLZP regulating gut microbiota of IBS-D. The body mass, CCK, MTL, and Bristol fecal character score were used to verify the establishment of the IBS-D model. IL-6, TNF, IL-1 beta, and IFN-gamma were crucial targets screened by network pharmacology and preliminarily verified by ELISA. Eighteen gut microbiota were important for the treatment of IBS-D with FLZP. Bacteroidetes, Blautia, Turicibacter, and Ruminococcus_torques_group were the crucial gut microbiota that FLZP inhibits persistent systemic inflammation in the IBS-D model. Lactobacillus is the crucial gut microbiota that FLZP renovates intestinal immune barrier in the IBS-D model. In summary, FLZP can affect bacterial diversity and community structures in the host and regulate inflammation and immune system to treat IBS-D.
引用
收藏
页数:14
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