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Modulating toll-like receptor-mediated inflammatory responses following exposure of whole cell and lipopolysaccharide component from Porphyromonas gingivalis in wistar rat models

OBJECTIVE: To explore host innate inflammatory response and the signal pathway induced by Porphyromonas gingivalis by measuring level of toll-like receptor 2 (TLR2) and TLR4 activity. MATERIALS AND METHODS: Animal experimental study with pretest-posttest controlled group design were done between Jan...

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Autores principales: Nelwan, Sindy Cornelia, Nugraha, Ricardo Adrian, Endaryanto, Anang, Retno, Indrawati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727724/
https://www.ncbi.nlm.nih.gov/pubmed/29279665
http://dx.doi.org/10.4103/ejd.ejd_147_17
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author Nelwan, Sindy Cornelia
Nugraha, Ricardo Adrian
Endaryanto, Anang
Retno, Indrawati
author_facet Nelwan, Sindy Cornelia
Nugraha, Ricardo Adrian
Endaryanto, Anang
Retno, Indrawati
author_sort Nelwan, Sindy Cornelia
collection PubMed
description OBJECTIVE: To explore host innate inflammatory response and the signal pathway induced by Porphyromonas gingivalis by measuring level of toll-like receptor 2 (TLR2) and TLR4 activity. MATERIALS AND METHODS: Animal experimental study with pretest-posttest controlled group design were done between January 1 and December 10, 2016.. Total of 28 wistar rats had been used, randomized into 7 groups, each were given various dose of intra-sulcural injection of Porphyromonas gingivalis lipopolysaccharide. STATISTICAL ANALYSIS: Normality were measured by Shapiro–Wilk test, while statistical analysis made by ANOVA, t test, Pearson, and linear regression model.. RESULTS: At day 0, no significant difference TLR2 and TLR4 level were measured. At day 4, there is a slight difference between TLR2 and TLR4 level in each group. At day 11, there is a significant difference between TLR2 and TLR4 level in each group. Group with exposure of whole cell will develop greater TLR2 but lower TLR4 level. In the contrary, group with exposure of LPS will develop greater TLR4 but lower TLR2 level. CONCLUSION: Our data supported that P. gingivalis played a vital role in the pathogenesis of pathogen-induced inflammatory responses in which TLR2 and TLR4 have different molecular mechanisms following recognition of pathogens and inflammatory response.
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spelling pubmed-57277242017-12-26 Modulating toll-like receptor-mediated inflammatory responses following exposure of whole cell and lipopolysaccharide component from Porphyromonas gingivalis in wistar rat models Nelwan, Sindy Cornelia Nugraha, Ricardo Adrian Endaryanto, Anang Retno, Indrawati Eur J Dent Original Article OBJECTIVE: To explore host innate inflammatory response and the signal pathway induced by Porphyromonas gingivalis by measuring level of toll-like receptor 2 (TLR2) and TLR4 activity. MATERIALS AND METHODS: Animal experimental study with pretest-posttest controlled group design were done between January 1 and December 10, 2016.. Total of 28 wistar rats had been used, randomized into 7 groups, each were given various dose of intra-sulcural injection of Porphyromonas gingivalis lipopolysaccharide. STATISTICAL ANALYSIS: Normality were measured by Shapiro–Wilk test, while statistical analysis made by ANOVA, t test, Pearson, and linear regression model.. RESULTS: At day 0, no significant difference TLR2 and TLR4 level were measured. At day 4, there is a slight difference between TLR2 and TLR4 level in each group. At day 11, there is a significant difference between TLR2 and TLR4 level in each group. Group with exposure of whole cell will develop greater TLR2 but lower TLR4 level. In the contrary, group with exposure of LPS will develop greater TLR4 but lower TLR2 level. CONCLUSION: Our data supported that P. gingivalis played a vital role in the pathogenesis of pathogen-induced inflammatory responses in which TLR2 and TLR4 have different molecular mechanisms following recognition of pathogens and inflammatory response. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5727724/ /pubmed/29279665 http://dx.doi.org/10.4103/ejd.ejd_147_17 Text en Copyright: © 2017 European Journal of Dentistry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Nelwan, Sindy Cornelia
Nugraha, Ricardo Adrian
Endaryanto, Anang
Retno, Indrawati
Modulating toll-like receptor-mediated inflammatory responses following exposure of whole cell and lipopolysaccharide component from Porphyromonas gingivalis in wistar rat models
title Modulating toll-like receptor-mediated inflammatory responses following exposure of whole cell and lipopolysaccharide component from Porphyromonas gingivalis in wistar rat models
title_full Modulating toll-like receptor-mediated inflammatory responses following exposure of whole cell and lipopolysaccharide component from Porphyromonas gingivalis in wistar rat models
title_fullStr Modulating toll-like receptor-mediated inflammatory responses following exposure of whole cell and lipopolysaccharide component from Porphyromonas gingivalis in wistar rat models
title_full_unstemmed Modulating toll-like receptor-mediated inflammatory responses following exposure of whole cell and lipopolysaccharide component from Porphyromonas gingivalis in wistar rat models
title_short Modulating toll-like receptor-mediated inflammatory responses following exposure of whole cell and lipopolysaccharide component from Porphyromonas gingivalis in wistar rat models
title_sort modulating toll-like receptor-mediated inflammatory responses following exposure of whole cell and lipopolysaccharide component from porphyromonas gingivalis in wistar rat models
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727724/
https://www.ncbi.nlm.nih.gov/pubmed/29279665
http://dx.doi.org/10.4103/ejd.ejd_147_17
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