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Oral administration of Lactobacillus plantarum 06CC2 prevents experimental colitis in mice via an anti-inflammatory response
Dysbiosis of the enteric microbiota causes gastrointestinal diseases, including colitis. The present study investigated the beneficial effect of Lactobacillus plantarum 06CC2 in experimental colitis in mice. An experimental colitis model in C57BL6 mice was induced using dextran sulfate sodium. Mice...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002978/ https://www.ncbi.nlm.nih.gov/pubmed/31922249 http://dx.doi.org/10.3892/mmr.2020.10925 |
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author | Tanaka, Akihito Kanmura, Shuji Morinaga, Yuko Kawabata, Katsuto Arima, Shiho Sasaki, Fumisato Nasu, Yuichirou Tanoue, Shiroh Hashimoto, Shinichi Takeshita, Masahiko Takeda, Shiro Ido, Akio |
author_facet | Tanaka, Akihito Kanmura, Shuji Morinaga, Yuko Kawabata, Katsuto Arima, Shiho Sasaki, Fumisato Nasu, Yuichirou Tanoue, Shiroh Hashimoto, Shinichi Takeshita, Masahiko Takeda, Shiro Ido, Akio |
author_sort | Tanaka, Akihito |
collection | PubMed |
description | Dysbiosis of the enteric microbiota causes gastrointestinal diseases, including colitis. The present study investigated the beneficial effect of Lactobacillus plantarum 06CC2 in experimental colitis in mice. An experimental colitis model in C57BL6 mice was induced using dextran sulfate sodium. Mice were orally administered 06CC2 (06CC2 group) or PBS only (control group) by gavage. The disease activity index (DAI), histological grading, and colon tissue and colonic lamina propria mononuclear cells (LPMCs) were examined macroscopically and histopathologically, and the expression levels of inflammation-associated cytokines (IL-6, IL-12, TNF-α and IL-10) in these samples were determined. Compared with the control group, the 06CC2 group exhibited a significantly lower DAI (1.5±0.8 vs. 0.2±0.3, respectively; P<0.05) and pathology score (6.3±1.5 vs. 3.8±1.3, respectively; P<0.05). IL-10 expression in colonic LPMCs was higher in the 06CC2 group than in the control group, although there was no significant difference in IFN-γ, IL-6 or IL-12 expression in colonic LPMCs between the two groups. In addition, 06CC2 stimulated the production of IL-10 from CD11b-positive cells and CD11c-positive cells in the colon. The 06CC2 strain induced IL-10 production in the colon and attenuated colon inflammation. |
format | Online Article Text |
id | pubmed-7002978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-70029782020-02-12 Oral administration of Lactobacillus plantarum 06CC2 prevents experimental colitis in mice via an anti-inflammatory response Tanaka, Akihito Kanmura, Shuji Morinaga, Yuko Kawabata, Katsuto Arima, Shiho Sasaki, Fumisato Nasu, Yuichirou Tanoue, Shiroh Hashimoto, Shinichi Takeshita, Masahiko Takeda, Shiro Ido, Akio Mol Med Rep Articles Dysbiosis of the enteric microbiota causes gastrointestinal diseases, including colitis. The present study investigated the beneficial effect of Lactobacillus plantarum 06CC2 in experimental colitis in mice. An experimental colitis model in C57BL6 mice was induced using dextran sulfate sodium. Mice were orally administered 06CC2 (06CC2 group) or PBS only (control group) by gavage. The disease activity index (DAI), histological grading, and colon tissue and colonic lamina propria mononuclear cells (LPMCs) were examined macroscopically and histopathologically, and the expression levels of inflammation-associated cytokines (IL-6, IL-12, TNF-α and IL-10) in these samples were determined. Compared with the control group, the 06CC2 group exhibited a significantly lower DAI (1.5±0.8 vs. 0.2±0.3, respectively; P<0.05) and pathology score (6.3±1.5 vs. 3.8±1.3, respectively; P<0.05). IL-10 expression in colonic LPMCs was higher in the 06CC2 group than in the control group, although there was no significant difference in IFN-γ, IL-6 or IL-12 expression in colonic LPMCs between the two groups. In addition, 06CC2 stimulated the production of IL-10 from CD11b-positive cells and CD11c-positive cells in the colon. The 06CC2 strain induced IL-10 production in the colon and attenuated colon inflammation. D.A. Spandidos 2020-03 2020-01-09 /pmc/articles/PMC7002978/ /pubmed/31922249 http://dx.doi.org/10.3892/mmr.2020.10925 Text en Copyright: © Tanaka et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Tanaka, Akihito Kanmura, Shuji Morinaga, Yuko Kawabata, Katsuto Arima, Shiho Sasaki, Fumisato Nasu, Yuichirou Tanoue, Shiroh Hashimoto, Shinichi Takeshita, Masahiko Takeda, Shiro Ido, Akio Oral administration of Lactobacillus plantarum 06CC2 prevents experimental colitis in mice via an anti-inflammatory response |
title | Oral administration of Lactobacillus plantarum 06CC2 prevents experimental colitis in mice via an anti-inflammatory response |
title_full | Oral administration of Lactobacillus plantarum 06CC2 prevents experimental colitis in mice via an anti-inflammatory response |
title_fullStr | Oral administration of Lactobacillus plantarum 06CC2 prevents experimental colitis in mice via an anti-inflammatory response |
title_full_unstemmed | Oral administration of Lactobacillus plantarum 06CC2 prevents experimental colitis in mice via an anti-inflammatory response |
title_short | Oral administration of Lactobacillus plantarum 06CC2 prevents experimental colitis in mice via an anti-inflammatory response |
title_sort | oral administration of lactobacillus plantarum 06cc2 prevents experimental colitis in mice via an anti-inflammatory response |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002978/ https://www.ncbi.nlm.nih.gov/pubmed/31922249 http://dx.doi.org/10.3892/mmr.2020.10925 |
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