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Stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice
BACKGROUND/AIM: Ulcerative colitis (UC) has been implicated to imbalanced enteric flora and reduced microbial diversity. Stachyose is a kind of natural prebiotic which favorably modulate the composition of the gut microbiota. The present study aims to investigate the effects of stachyose on inflamma...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392292/ https://www.ncbi.nlm.nih.gov/pubmed/32270772 http://dx.doi.org/10.4103/sjg.SJG_580_19 |
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author | He, Liwen Zhang, Feiran Jian, Zhengyang Sun, Jiachen Chen, Jiamin Liapao, Vuekhang He, Qing |
author_facet | He, Liwen Zhang, Feiran Jian, Zhengyang Sun, Jiachen Chen, Jiamin Liapao, Vuekhang He, Qing |
author_sort | He, Liwen |
collection | PubMed |
description | BACKGROUND/AIM: Ulcerative colitis (UC) has been implicated to imbalanced enteric flora and reduced microbial diversity. Stachyose is a kind of natural prebiotic which favorably modulate the composition of the gut microbiota. The present study aims to investigate the effects of stachyose on inflammatory levels and gut microbiota of acute colitis mice. MATERIALS AND METHODS: In this study, the mice were randomly divided into four groups: (1) control group; (2) stachyose group; (3) dextran sulfate sodium (DSS) group; (4) stachyose + DSS group. Hemotoxylin and Eosin (H and E) staining was performed for the distal colon to examine the inflammation and tissue damage. The inflammatory cytokines including IL-6, IL-10, IL-17a, and TNF-α in serum were determined by ELISA assay. The differences in the gut microbiota were analyzed by 16S rDNA gene sequencing. RESULTS: Histological assay showed that the stachyose treatment significantly reduced the lesions of the colon in DSS-induced colitis. And the upregulated inflammatory cytokines induced by DSS were significantly inhibited by stachyose treatment. Additionally, the sequencing analysis showed that the stachyose changed the gut microbiota composition with a higher level of Akkermansia, as well as selectively increasing some probiotics, including Lactobacillus. CONCLUSIONS: Our results suggested that stachyose increased beneficial microbiota and bacterial diversity to alleviate acute colitis in mice, which might be a new promising option to UC patients. |
format | Online Article Text |
id | pubmed-7392292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-73922922020-08-12 Stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice He, Liwen Zhang, Feiran Jian, Zhengyang Sun, Jiachen Chen, Jiamin Liapao, Vuekhang He, Qing Saudi J Gastroenterol Original Article BACKGROUND/AIM: Ulcerative colitis (UC) has been implicated to imbalanced enteric flora and reduced microbial diversity. Stachyose is a kind of natural prebiotic which favorably modulate the composition of the gut microbiota. The present study aims to investigate the effects of stachyose on inflammatory levels and gut microbiota of acute colitis mice. MATERIALS AND METHODS: In this study, the mice were randomly divided into four groups: (1) control group; (2) stachyose group; (3) dextran sulfate sodium (DSS) group; (4) stachyose + DSS group. Hemotoxylin and Eosin (H and E) staining was performed for the distal colon to examine the inflammation and tissue damage. The inflammatory cytokines including IL-6, IL-10, IL-17a, and TNF-α in serum were determined by ELISA assay. The differences in the gut microbiota were analyzed by 16S rDNA gene sequencing. RESULTS: Histological assay showed that the stachyose treatment significantly reduced the lesions of the colon in DSS-induced colitis. And the upregulated inflammatory cytokines induced by DSS were significantly inhibited by stachyose treatment. Additionally, the sequencing analysis showed that the stachyose changed the gut microbiota composition with a higher level of Akkermansia, as well as selectively increasing some probiotics, including Lactobacillus. CONCLUSIONS: Our results suggested that stachyose increased beneficial microbiota and bacterial diversity to alleviate acute colitis in mice, which might be a new promising option to UC patients. Wolters Kluwer - Medknow 2020-04-06 /pmc/articles/PMC7392292/ /pubmed/32270772 http://dx.doi.org/10.4103/sjg.SJG_580_19 Text en Copyright: © 2020 Saudi Journal of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article He, Liwen Zhang, Feiran Jian, Zhengyang Sun, Jiachen Chen, Jiamin Liapao, Vuekhang He, Qing Stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice |
title | Stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice |
title_full | Stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice |
title_fullStr | Stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice |
title_full_unstemmed | Stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice |
title_short | Stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice |
title_sort | stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392292/ https://www.ncbi.nlm.nih.gov/pubmed/32270772 http://dx.doi.org/10.4103/sjg.SJG_580_19 |
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