Ginseng-Containing Sijunzi Decoction Ameliorates Ulcerative Colitis by Orchestrating Gut Homeostasis in Microbial Modulation and Intestinal Barrier Integrity

Author:

Wu Yuqi1,Zheng Yanfei1,Wang Xiaolu1,Tang Ping1,Guo Wenqian1,Ma Han1,Zhang Anqi1,Li Delong1,Xie Yuxin1,Wang Chong-Zhi2,Yao Haiqiang1,Wan Jin-Yi1,Yuan Chun-Su2

Affiliation:

1. School of Traditional Chinese Medicine and National Institute of TCM Constitution & Preventive Medicine, Beijing University of Chinese, Medicine, Beijing 100029, P. R. China

2. Tang Center for Herbal Medicine Research and Department of Anesthesia & Critical Care, The University of Chicago, Chicago, IL 60637, USA

Abstract

Ulcerative colitis (UC) has become a global epidemic, and the lack of an effective cure highlights the necessity and urgency to explore novel therapies. Sijunzi Decoction (SJZD), a classical Chinese herbal formula, has been comprehensively applied and clinically proven effective in treating UC; however, the pharmacological mechanism behind its therapeutic benefits is largely obscure. Here, we find that SJZD can restore microbiota homeostasis and intestinal barrier integrity in DSS-induced colitis. SJZD significantly alleviated the colonic tissue damage and improved the goblet cell count, MUC2 secretion, and tight junction protein expressions, which indicated enhanced intestinal barrier integrity. SJZD remarkedly suppressed the abundance of phylum Proteobacteria and genus Escherichia-Shigella, which are typical features of microbial dysbiosis. Escherichia-Shigella was negatively correlated with body weight and colon length, and positively correlated with disease activity index and IL-1[Formula: see text]. Furthermore, through gut microbiota depletion, we confirmed that SJZD exerted anti-inflammatory activities in a gut microbiota-dependent manner, and fecal microbiota transplantation (FMT) validated the mediating role of gut microbiota in the SJZD treatment of UC. Through gut microbiota, SJZD modulates the biosynthesis of bile acids (BAs), especially tauroursodeoxycholic acid (TUDCA), which has been identified as the signature BA during SJZD treatment. Cumulatively, our findings disclose that SJZD attenuates UC via orchestrating gut homeostasis in microbial modulation and intestinal barrier integrity, thus offering a promising alternative approach to the clinical management of UC.

Funder

the Fundamental Research Funds for the Central Universities

Beijing University of Chinese Medicine High-level Talent Start-up Research Project

the National Natural Science Foundation of China

Publisher

World Scientific Pub Co Pte Ltd

Subject

Complementary and alternative medicine,General Medicine

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