Cargando…

Ursolic acid improves the bacterial community mapping of the intestinal tract in liver fibrosis mice

Liver fibrosis often appears in chronic liver disease, with extracellular matrix (ECM) deposition as the main feature. Due to the presence of the liver-gut axis, the destruction of intestinal homeostasis is often accompanied by the development of liver fibrosis. The inconsistent ecological environme...

Descripción completa

Detalles Bibliográficos
Autores principales: Wan, Sizhe, Huang, Chenkai, Wang, Anjiang, Zhu, Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185030/
https://www.ncbi.nlm.nih.gov/pubmed/32355580
http://dx.doi.org/10.7717/peerj.9050
_version_ 1783526689056227328
author Wan, Sizhe
Huang, Chenkai
Wang, Anjiang
Zhu, Xuan
author_facet Wan, Sizhe
Huang, Chenkai
Wang, Anjiang
Zhu, Xuan
author_sort Wan, Sizhe
collection PubMed
description Liver fibrosis often appears in chronic liver disease, with extracellular matrix (ECM) deposition as the main feature. Due to the presence of the liver-gut axis, the destruction of intestinal homeostasis is often accompanied by the development of liver fibrosis. The inconsistent ecological environment of different intestinal sites may lead to differences in the microbiota. The traditional Chinese medicine ursolic acid (UA) has been proven to protect the liver from fibrosis. We investigated the changes in the microbiota of different parts of the intestine during liver fibrosis and the effect of UA on these changes based on high-throughput sequencing technology. Sequencing results suggest that the diversity and abundance of intestinal microbiota decline and the composition of the microbiota is disordered, the potentially beneficial Firmicutes bacteria are reduced, and the pathways for functional prediction are changed in the ilea and anal faeces of liver fibrosis mice compared with normal mice. However, in UA-treated liver fibrosis mice, these disorders improved. It is worth noting that the bacterial changes in the ilea and anal faeces are not consistent. In conclusion, in liver fibrosis, the microbiota of different parts of the intestines have different degrees of disorder, and UA can improve this disorder. This may be a potential mechanism for UA to achieve anti-fibrosis. This study provides theoretical guidance for the UA targeting of intestinal microbiota for the treatment of liver fibrosis.
format Online
Article
Text
id pubmed-7185030
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher PeerJ Inc.
record_format MEDLINE/PubMed
spelling pubmed-71850302020-04-30 Ursolic acid improves the bacterial community mapping of the intestinal tract in liver fibrosis mice Wan, Sizhe Huang, Chenkai Wang, Anjiang Zhu, Xuan PeerJ Microbiology Liver fibrosis often appears in chronic liver disease, with extracellular matrix (ECM) deposition as the main feature. Due to the presence of the liver-gut axis, the destruction of intestinal homeostasis is often accompanied by the development of liver fibrosis. The inconsistent ecological environment of different intestinal sites may lead to differences in the microbiota. The traditional Chinese medicine ursolic acid (UA) has been proven to protect the liver from fibrosis. We investigated the changes in the microbiota of different parts of the intestine during liver fibrosis and the effect of UA on these changes based on high-throughput sequencing technology. Sequencing results suggest that the diversity and abundance of intestinal microbiota decline and the composition of the microbiota is disordered, the potentially beneficial Firmicutes bacteria are reduced, and the pathways for functional prediction are changed in the ilea and anal faeces of liver fibrosis mice compared with normal mice. However, in UA-treated liver fibrosis mice, these disorders improved. It is worth noting that the bacterial changes in the ilea and anal faeces are not consistent. In conclusion, in liver fibrosis, the microbiota of different parts of the intestines have different degrees of disorder, and UA can improve this disorder. This may be a potential mechanism for UA to achieve anti-fibrosis. This study provides theoretical guidance for the UA targeting of intestinal microbiota for the treatment of liver fibrosis. PeerJ Inc. 2020-04-24 /pmc/articles/PMC7185030/ /pubmed/32355580 http://dx.doi.org/10.7717/peerj.9050 Text en ©2020 Wan et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Microbiology
Wan, Sizhe
Huang, Chenkai
Wang, Anjiang
Zhu, Xuan
Ursolic acid improves the bacterial community mapping of the intestinal tract in liver fibrosis mice
title Ursolic acid improves the bacterial community mapping of the intestinal tract in liver fibrosis mice
title_full Ursolic acid improves the bacterial community mapping of the intestinal tract in liver fibrosis mice
title_fullStr Ursolic acid improves the bacterial community mapping of the intestinal tract in liver fibrosis mice
title_full_unstemmed Ursolic acid improves the bacterial community mapping of the intestinal tract in liver fibrosis mice
title_short Ursolic acid improves the bacterial community mapping of the intestinal tract in liver fibrosis mice
title_sort ursolic acid improves the bacterial community mapping of the intestinal tract in liver fibrosis mice
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185030/
https://www.ncbi.nlm.nih.gov/pubmed/32355580
http://dx.doi.org/10.7717/peerj.9050
work_keys_str_mv AT wansizhe ursolicacidimprovesthebacterialcommunitymappingoftheintestinaltractinliverfibrosismice
AT huangchenkai ursolicacidimprovesthebacterialcommunitymappingoftheintestinaltractinliverfibrosismice
AT wanganjiang ursolicacidimprovesthebacterialcommunitymappingoftheintestinaltractinliverfibrosismice
AT zhuxuan ursolicacidimprovesthebacterialcommunitymappingoftheintestinaltractinliverfibrosismice