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Anti-inflammatory effects of olanexidine gluconate on oral epithelial cells
BACKGROUND: Periodontitis is a biofilm-induced chronic inflammatory condition of the periodontium. Chemokines produced by the innate and acquired immune responses play a significant role in disease progression. Reducing biofilm formation and inflammatory response caused by chemokines is vital for pr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839112/ https://www.ncbi.nlm.nih.gov/pubmed/31703580 http://dx.doi.org/10.1186/s12903-019-0932-0 |
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author | Nii, Takuya Yumoto, Hiromichi Hirota, Katsuhiko Miyake, Yoichiro |
author_facet | Nii, Takuya Yumoto, Hiromichi Hirota, Katsuhiko Miyake, Yoichiro |
author_sort | Nii, Takuya |
collection | PubMed |
description | BACKGROUND: Periodontitis is a biofilm-induced chronic inflammatory condition of the periodontium. Chemokines produced by the innate and acquired immune responses play a significant role in disease progression. Reducing biofilm formation and inflammatory response caused by chemokines is vital for preventing and treating periodontitis. Previously, we observed that treatment with 0.1% olanexidine gluconate (OLG) inhibited biofilm formation on saliva-coated hydroxyapatite. This study aimed to evaluate the anti-inflammatory effect of OLG on oral epithelial cells. METHODS: We examined if OLG could inhibit the inflammatory responses caused by Porphyromonas gingivalis (P. gingivalis) lipopolysaccharide (LPS) and heat-killed P. gingivalis in immortalized human oral keratinocytes (RT7). RESULTS: Treatment of RT7 with non-cytotoxic OLG concentrations significantly inhibited the production of inflammatory chemokines such as interleukin 8 (IL-8), C-C motif ligand 20 (CCL20), and growth-related oncogene protein-α (GRO-α), which are stimulated by P. gingivalis LPS in a concentration-dependent manner. Moreover, the inhibitory effects were observed regardless of the treatment time with P. gingivalis LPS (6, 12, or 24 h). OLG also significantly inhibited chemokine production stimulated by heat-killed P. gingivalis. CONCLUSIONS: The findings of this study suggest that treatment with OLG inhibits chronic inflammatory reactions in oral mucosal cells, such as periodontitis, caused by oral bacteria. |
format | Online Article Text |
id | pubmed-6839112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68391122019-11-12 Anti-inflammatory effects of olanexidine gluconate on oral epithelial cells Nii, Takuya Yumoto, Hiromichi Hirota, Katsuhiko Miyake, Yoichiro BMC Oral Health Research Article BACKGROUND: Periodontitis is a biofilm-induced chronic inflammatory condition of the periodontium. Chemokines produced by the innate and acquired immune responses play a significant role in disease progression. Reducing biofilm formation and inflammatory response caused by chemokines is vital for preventing and treating periodontitis. Previously, we observed that treatment with 0.1% olanexidine gluconate (OLG) inhibited biofilm formation on saliva-coated hydroxyapatite. This study aimed to evaluate the anti-inflammatory effect of OLG on oral epithelial cells. METHODS: We examined if OLG could inhibit the inflammatory responses caused by Porphyromonas gingivalis (P. gingivalis) lipopolysaccharide (LPS) and heat-killed P. gingivalis in immortalized human oral keratinocytes (RT7). RESULTS: Treatment of RT7 with non-cytotoxic OLG concentrations significantly inhibited the production of inflammatory chemokines such as interleukin 8 (IL-8), C-C motif ligand 20 (CCL20), and growth-related oncogene protein-α (GRO-α), which are stimulated by P. gingivalis LPS in a concentration-dependent manner. Moreover, the inhibitory effects were observed regardless of the treatment time with P. gingivalis LPS (6, 12, or 24 h). OLG also significantly inhibited chemokine production stimulated by heat-killed P. gingivalis. CONCLUSIONS: The findings of this study suggest that treatment with OLG inhibits chronic inflammatory reactions in oral mucosal cells, such as periodontitis, caused by oral bacteria. BioMed Central 2019-11-08 /pmc/articles/PMC6839112/ /pubmed/31703580 http://dx.doi.org/10.1186/s12903-019-0932-0 Text en © The Author(s). 2019 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Nii, Takuya Yumoto, Hiromichi Hirota, Katsuhiko Miyake, Yoichiro Anti-inflammatory effects of olanexidine gluconate on oral epithelial cells |
title | Anti-inflammatory effects of olanexidine gluconate on oral epithelial cells |
title_full | Anti-inflammatory effects of olanexidine gluconate on oral epithelial cells |
title_fullStr | Anti-inflammatory effects of olanexidine gluconate on oral epithelial cells |
title_full_unstemmed | Anti-inflammatory effects of olanexidine gluconate on oral epithelial cells |
title_short | Anti-inflammatory effects of olanexidine gluconate on oral epithelial cells |
title_sort | anti-inflammatory effects of olanexidine gluconate on oral epithelial cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839112/ https://www.ncbi.nlm.nih.gov/pubmed/31703580 http://dx.doi.org/10.1186/s12903-019-0932-0 |
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