Gut microbiota-derived tryptophan metabolites regulated by Wuji Wan to attenuate colitis through AhR signaling activation.
10.1016/j.apsb.2024.11.009
- Author:
Wanghui JING
1
;
Sijing DONG
1
;
Yinyue XU
1
;
Jingjing LIU
2
;
Jiawei REN
1
;
Xue LIU
1
;
Min ZHU
1
;
Menggai ZHANG
1
;
Hehe SHI
1
;
Na LI
1
;
Peng XIA
3
;
Haitao LU
2
;
Sicen WANG
1
Author Information
1. School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an 710061, China.
2. School of Chinese Medicine, Hong Kong Traditional Chinese Medicine Phenome Center, State Key Laboratory of Environmental and Biological Analysis, Hong Kong Baptist University, Hong Kong 999077, China.
3. Department of Surgical Oncology, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China.
- Publication Type:Journal Article
- Keywords:
Aryl hydrocarbon receptor;
Colitis;
Gut microbiota;
Indole-3-acetic acid;
Intestinal barrier;
Lactobacillus;
Tryptophan metabolite;
Wuji Wan
- From:
Acta Pharmaceutica Sinica B
2025;15(1):205-223
- CountryChina
- Language:English
-
Abstract:
Disruption of the intestinal mucosal barrier caused by gut dysbiosis and metabolic imbalance is the underlying pathology of inflammatory bowel disease (IBD). Traditional Chinese medicine Wuji Wan (WJW) is commonly used to treat digestive system disorders and showed therapeutic potential for IBD. In this interdisciplinary study, we aim to investigate the pharmacological effects of WJW against experimental colitis by combining functional metabolomics and gut-microbiota sequencing techniques. Treatment with WJW altered the profile of the intestinal microbiota and notably increased the abundance of Lactobacillus, thereby facilitating the conversion of tryptophan into indole-3-acetic acid (IAA) and indoleacrylic acid (IA). These indole derivatives activated the aryl hydrocarbon receptor (AhR) pathway, which reduced colonic inflammation and restored the expression of intestinal barrier proteins. Interestingly, the beneficial effects of WJW on gut barrier function improvement and tryptophan metabolism were disappeared in the absence of gut microbiota. Finally, pre-treatment with the AhR antagonist CH-223191 confirmed the essential role of IAA-mediated AhR activation in the therapeutic effects of WJW. Overall, WJW enhanced intestinal barrier function and reduced colonic inflammation in a murine colitis model by modulating Lactobacillus-IAA-AhR signaling pathway. This study provides novel insights into colitis pathogenesis and presents an effective therapeutic and preventive approach against IBD.
