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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...

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Autores principales: Nii, Takuya, Yumoto, Hiromichi, Hirota, Katsuhiko, Miyake, Yoichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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.
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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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