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The role of gut microbiota associated metabolites in digestive disorders

Authors :
Na Li
Cheng Zhao
Pingnan Zhang
Songting Wu
Xiaotan Dou
Saifei Xu
Xiaoqi Zhang
Chunyan Peng
Ying Xie
Shuling Huang
Lin Zhou
Yonghua Shen
Lei Wang
Jinglin Wang
Chenggong Yu
Source :
Engineered Regeneration, Vol 5, Iss 2, Pp 228-246 (2024)
Publication Year :
2024
Publisher :
KeAi Communications Co., Ltd., 2024.

Abstract

The gut has been a focal point in the research of digestive system disorders. The internal microbiota generates metabolites that function as signaling molecules and substrates, interacting with the intestinal wall and influencing host physiology and pathology. Besides, the gut microbiota and metabolites owe highly diverse types and quantities, posing challenges for quantitative analysis, and monitoring frequent interactions between digestive tract metabolites and the intestinal wall remains a challenge. However, research targeting gut microbiota metabolites has elucidated their relevance to digestive diseases. By modulating metabolites such as short-chain fatty acids, bile acids, and lipopolysaccharides, it is possible to intervene in the progression of diseases such as inflammatory bowel disease and non-alcoholic fatty liver disease. Currently, research on gut microbiota is advancing, and more work is required to explore the interactions between host, microbes and underlying mechanisms. In this review, we have revisited the generation of gut microbiota-related metabolites, their impact on diseases, and modes of interaction, emphasizing the significant role of metabolites in digestive system disorders. It is believed that the linkage between gut microbiota and diseases in current research can be established through metabolites, providing a framework and foundation for research in the field of metabolomics and fundamental mechanisms.

Details

Language :
English
ISSN :
26661381
Volume :
5
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Engineered Regeneration
Publication Type :
Academic Journal
Accession number :
edsdoj.8a4748be5b5943be9e98c1f29589527f
Document Type :
article
Full Text :
https://doi.org/10.1016/j.engreg.2024.04.003