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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...

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Autores principales: Tanaka, Akihito, Kanmura, Shuji, Morinaga, Yuko, Kawabata, Katsuto, Arima, Shiho, Sasaki, Fumisato, Nasu, Yuichirou, Tanoue, Shiroh, Hashimoto, Shinichi, Takeshita, Masahiko, Takeda, Shiro, Ido, Akio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
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.
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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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