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Oral pathobiont induces systemic inflammation and metabolic changes associated with alteration of gut microbiota
Periodontitis has been implicated as a risk factor for metabolic disorders such as type 2 diabetes, atherosclerotic vascular diseases, and non-alcoholic fatty liver disease. Although bacteremias from dental plaque and/or elevated circulating inflammatory cytokines emanating from the inflamed gingiva...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010932/ https://www.ncbi.nlm.nih.gov/pubmed/24797416 http://dx.doi.org/10.1038/srep04828 |
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author | Arimatsu, Kei Yamada, Hitomi Miyazawa, Haruna Minagawa, Takayoshi Nakajima, Mayuka Ryder, Mark I. Gotoh, Kazuyoshi Motooka, Daisuke Nakamura, Shota Iida, Tetsuya Yamazaki, Kazuhisa |
author_facet | Arimatsu, Kei Yamada, Hitomi Miyazawa, Haruna Minagawa, Takayoshi Nakajima, Mayuka Ryder, Mark I. Gotoh, Kazuyoshi Motooka, Daisuke Nakamura, Shota Iida, Tetsuya Yamazaki, Kazuhisa |
author_sort | Arimatsu, Kei |
collection | PubMed |
description | Periodontitis has been implicated as a risk factor for metabolic disorders such as type 2 diabetes, atherosclerotic vascular diseases, and non-alcoholic fatty liver disease. Although bacteremias from dental plaque and/or elevated circulating inflammatory cytokines emanating from the inflamed gingiva are suspected mechanisms linking periodontitis and these diseases, direct evidence is lacking. We hypothesize that disturbances of the gut microbiota by swallowed bacteria induce a metabolic endotoxemia leading metabolic disorders. To investigate this hypothesis, changes in the gut microbiota, insulin and glucose intolerance, and levels of tissue inflammation were analysed in mice after oral administration of Porphyromonas gingivalis, a representative periodontopathogens. Pyrosequencing revealed that the population belonging to Bacteroidales was significantly elevated in P. gingivalis-administered mice which coincided with increases in insulin resistance and systemic inflammation. In P. gingivalis-administered mice blood endotoxin levels tended to be higher, whereas gene expression of tight junction proteins in the ileum was significantly decreased. These results provide a new paradigm for the interrelationship between periodontitis and systemic diseases. |
format | Online Article Text |
id | pubmed-4010932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40109322014-05-06 Oral pathobiont induces systemic inflammation and metabolic changes associated with alteration of gut microbiota Arimatsu, Kei Yamada, Hitomi Miyazawa, Haruna Minagawa, Takayoshi Nakajima, Mayuka Ryder, Mark I. Gotoh, Kazuyoshi Motooka, Daisuke Nakamura, Shota Iida, Tetsuya Yamazaki, Kazuhisa Sci Rep Article Periodontitis has been implicated as a risk factor for metabolic disorders such as type 2 diabetes, atherosclerotic vascular diseases, and non-alcoholic fatty liver disease. Although bacteremias from dental plaque and/or elevated circulating inflammatory cytokines emanating from the inflamed gingiva are suspected mechanisms linking periodontitis and these diseases, direct evidence is lacking. We hypothesize that disturbances of the gut microbiota by swallowed bacteria induce a metabolic endotoxemia leading metabolic disorders. To investigate this hypothesis, changes in the gut microbiota, insulin and glucose intolerance, and levels of tissue inflammation were analysed in mice after oral administration of Porphyromonas gingivalis, a representative periodontopathogens. Pyrosequencing revealed that the population belonging to Bacteroidales was significantly elevated in P. gingivalis-administered mice which coincided with increases in insulin resistance and systemic inflammation. In P. gingivalis-administered mice blood endotoxin levels tended to be higher, whereas gene expression of tight junction proteins in the ileum was significantly decreased. These results provide a new paradigm for the interrelationship between periodontitis and systemic diseases. Nature Publishing Group 2014-05-06 /pmc/articles/PMC4010932/ /pubmed/24797416 http://dx.doi.org/10.1038/srep04828 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images in this article are included in the article's Creative Commons license, unless indicated otherwise in the image credit; if the image is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the image. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Article Arimatsu, Kei Yamada, Hitomi Miyazawa, Haruna Minagawa, Takayoshi Nakajima, Mayuka Ryder, Mark I. Gotoh, Kazuyoshi Motooka, Daisuke Nakamura, Shota Iida, Tetsuya Yamazaki, Kazuhisa Oral pathobiont induces systemic inflammation and metabolic changes associated with alteration of gut microbiota |
title | Oral pathobiont induces systemic inflammation and metabolic changes associated with alteration of gut microbiota |
title_full | Oral pathobiont induces systemic inflammation and metabolic changes associated with alteration of gut microbiota |
title_fullStr | Oral pathobiont induces systemic inflammation and metabolic changes associated with alteration of gut microbiota |
title_full_unstemmed | Oral pathobiont induces systemic inflammation and metabolic changes associated with alteration of gut microbiota |
title_short | Oral pathobiont induces systemic inflammation and metabolic changes associated with alteration of gut microbiota |
title_sort | oral pathobiont induces systemic inflammation and metabolic changes associated with alteration of gut microbiota |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010932/ https://www.ncbi.nlm.nih.gov/pubmed/24797416 http://dx.doi.org/10.1038/srep04828 |
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