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Inonotus obliquus polysaccharide regulates gut microbiota of chronic pancreatitis in mice
Polysaccharide is efficient in attenuation of metabolic ailments and modulation of gut microbiota as prebiotics. The therapeutic effect of Inonotus obliquus polysaccharide (IOP) on chronic pancreatitis (CP) in mice has been validated in our previous study. However, it is not clear whether IOP is con...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309192/ https://www.ncbi.nlm.nih.gov/pubmed/28197985 http://dx.doi.org/10.1186/s13568-017-0341-1 |
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author | Hu, Yang Teng, Chunying Yu, Sumei Wang, Xin Liang, Jinsong Bai, Xin Dong, Liying Song, Tao Yu, Min Qu, Juanjuan |
author_facet | Hu, Yang Teng, Chunying Yu, Sumei Wang, Xin Liang, Jinsong Bai, Xin Dong, Liying Song, Tao Yu, Min Qu, Juanjuan |
author_sort | Hu, Yang |
collection | PubMed |
description | Polysaccharide is efficient in attenuation of metabolic ailments and modulation of gut microbiota as prebiotics. The therapeutic effect of Inonotus obliquus polysaccharide (IOP) on chronic pancreatitis (CP) in mice has been validated in our previous study. However, it is not clear whether IOP is conducive to maintaining the homeostasis between gut microbiota and host. The aim of this study is to testify the potential effects of IOP on gut microbiota composition and diversity in mice with CP. The changes in glutathione peroxidase (GSH-P(X)), total antioxidant capacity (TAOC), tumor necrosis factor alpha (TNF-α), transforming growth factor beta (TGF-β), lipase and trypsin levels were measured by commercial assay kits, meanwhile the gut microbiota composition and diversity were analyzed by high throughput sequencing. The IOP treatment increased GSH-P(X) and TAOC levels, and decreased TNF-α, TGF-β, lipase and trypsin levels in CP mice. It was also observed that gut microbiota in IOP treated groups were less diverse than others in terms of lower Shannon diversity index and Chao 1 estimator. IOP increased the proportion of Bacteroidetes and decreased that of Firmicutes at phylum level. Bacteroidetes was found positively correlated with GSH-P(X) and TAOC, and Firmicutes correlated with TNF-α, TGF-β, and lipase. In conclusion, administration of IOP could regulate gut microbiota composition and diversity to a healthy profile in mice with CP, and some bacterial phylum significantly correlated with characteristic parameters. |
format | Online Article Text |
id | pubmed-5309192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-53091922017-02-28 Inonotus obliquus polysaccharide regulates gut microbiota of chronic pancreatitis in mice Hu, Yang Teng, Chunying Yu, Sumei Wang, Xin Liang, Jinsong Bai, Xin Dong, Liying Song, Tao Yu, Min Qu, Juanjuan AMB Express Original Article Polysaccharide is efficient in attenuation of metabolic ailments and modulation of gut microbiota as prebiotics. The therapeutic effect of Inonotus obliquus polysaccharide (IOP) on chronic pancreatitis (CP) in mice has been validated in our previous study. However, it is not clear whether IOP is conducive to maintaining the homeostasis between gut microbiota and host. The aim of this study is to testify the potential effects of IOP on gut microbiota composition and diversity in mice with CP. The changes in glutathione peroxidase (GSH-P(X)), total antioxidant capacity (TAOC), tumor necrosis factor alpha (TNF-α), transforming growth factor beta (TGF-β), lipase and trypsin levels were measured by commercial assay kits, meanwhile the gut microbiota composition and diversity were analyzed by high throughput sequencing. The IOP treatment increased GSH-P(X) and TAOC levels, and decreased TNF-α, TGF-β, lipase and trypsin levels in CP mice. It was also observed that gut microbiota in IOP treated groups were less diverse than others in terms of lower Shannon diversity index and Chao 1 estimator. IOP increased the proportion of Bacteroidetes and decreased that of Firmicutes at phylum level. Bacteroidetes was found positively correlated with GSH-P(X) and TAOC, and Firmicutes correlated with TNF-α, TGF-β, and lipase. In conclusion, administration of IOP could regulate gut microbiota composition and diversity to a healthy profile in mice with CP, and some bacterial phylum significantly correlated with characteristic parameters. Springer Berlin Heidelberg 2017-02-14 /pmc/articles/PMC5309192/ /pubmed/28197985 http://dx.doi.org/10.1186/s13568-017-0341-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Hu, Yang Teng, Chunying Yu, Sumei Wang, Xin Liang, Jinsong Bai, Xin Dong, Liying Song, Tao Yu, Min Qu, Juanjuan Inonotus obliquus polysaccharide regulates gut microbiota of chronic pancreatitis in mice |
title | Inonotus obliquus polysaccharide regulates gut microbiota of chronic pancreatitis in mice |
title_full | Inonotus obliquus polysaccharide regulates gut microbiota of chronic pancreatitis in mice |
title_fullStr | Inonotus obliquus polysaccharide regulates gut microbiota of chronic pancreatitis in mice |
title_full_unstemmed | Inonotus obliquus polysaccharide regulates gut microbiota of chronic pancreatitis in mice |
title_short | Inonotus obliquus polysaccharide regulates gut microbiota of chronic pancreatitis in mice |
title_sort | inonotus obliquus polysaccharide regulates gut microbiota of chronic pancreatitis in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309192/ https://www.ncbi.nlm.nih.gov/pubmed/28197985 http://dx.doi.org/10.1186/s13568-017-0341-1 |
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