| Literature DB >> 34916934 |
Zhang Zhen1,2, Lin Xia1, Huang You1, Zhou Jingwei1, Yang Shasha1, Wei Xinyi1, Lai Wenjing1, Zhang Xin1, Fu Chaomei1.
Abstract
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-1β, and IFN-γ 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.Entities:
Keywords: Fuzi-Lizhong pill; crucial targets; gut microbiota; irritable bowel syndrome; network pharmacology
Year: 2021 PMID: 34916934 PMCID: PMC8670173 DOI: 10.3389/fphar.2021.746923
Source DB: PubMed Journal: Front Pharmacol ISSN: 1663-9812 Impact factor: 5.810