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Effect of telmisartan on levels of IL-1, TNF-α, down-regulated COX-2, MMP-2, MMP-9 and RANKL/RANK in an experimental periodontitis model

AIM: The aim of this study was to evaluate the effect of telmisartan (TELM) on inflammation, oxidation and the expression of matrix metalloproteinases (MMPs) and the expression RANKL/RANK/OPG in the periodontal tissue of a rat model for ligature-induced periodontitis. MATERIALS AND METHODS: Male Wis...

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Autores principales: Araújo, Aurigena A, Souza, Tatiana O, Moura, Lígia M, Brito, Gerly A C, Aragão, Karoline S, Araújo, Lorena S, Medeiros, Caroline A X, Alves, Maria S C F, Araújo, Raimundo F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274974/
https://www.ncbi.nlm.nih.gov/pubmed/24118063
http://dx.doi.org/10.1111/jcpe.12160
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author Araújo, Aurigena A
Souza, Tatiana O
Moura, Lígia M
Brito, Gerly A C
Aragão, Karoline S
Araújo, Lorena S
Medeiros, Caroline A X
Alves, Maria S C F
Araújo, Raimundo F
author_facet Araújo, Aurigena A
Souza, Tatiana O
Moura, Lígia M
Brito, Gerly A C
Aragão, Karoline S
Araújo, Lorena S
Medeiros, Caroline A X
Alves, Maria S C F
Araújo, Raimundo F
author_sort Araújo, Aurigena A
collection PubMed
description AIM: The aim of this study was to evaluate the effect of telmisartan (TELM) on inflammation, oxidation and the expression of matrix metalloproteinases (MMPs) and the expression RANKL/RANK/OPG in the periodontal tissue of a rat model for ligature-induced periodontitis. MATERIALS AND METHODS: Male Wistar albino rats were randomly divided into five groups of 10 rats each: (i) non-ligated, given water; (ii) ligated, given water; (iii) ligated, given 1 mg/kg TELM; (iv) ligated, given 5 mg/kg TELM; and (v) ligated, given 10 mg/kg TELM. All groups were treated with saline or TELM for 10 days. Periodontal tissue was analysed by histopathology; by the immunohistochemical examination of COX-2, MMP-2, MMP-9 and the RANKL/RANK/OPG pathway; and by ELISA analysis of the levels of IL-1β, IL-10, TNF-α, myeloperoxidase (MPO), malonaldehyde (MDA) and glutathione (GSH). RESULTS: Treatment with 10 mg/kg TELM resulted in reduced concentrations of MPO, MDA (p < 0.05) and the pro-inflammatory cytokine IL-1β (p < 0.05); reduced expression of MMP-2, MMP-9, RANK, RANKL and COX-2; and an increase in OPG. The levels of TNF-α were significantly reduced in all TELM-treated groups. CONCLUSIONS: These findings confirm the involvement of TELM in reducing the inflammatory response, oxidative stress and bone loss in ligature-induced periodontitis in rats.
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spelling pubmed-42749742014-12-29 Effect of telmisartan on levels of IL-1, TNF-α, down-regulated COX-2, MMP-2, MMP-9 and RANKL/RANK in an experimental periodontitis model Araújo, Aurigena A Souza, Tatiana O Moura, Lígia M Brito, Gerly A C Aragão, Karoline S Araújo, Lorena S Medeiros, Caroline A X Alves, Maria S C F Araújo, Raimundo F J Clin Periodontol Periodontal Diseases AIM: The aim of this study was to evaluate the effect of telmisartan (TELM) on inflammation, oxidation and the expression of matrix metalloproteinases (MMPs) and the expression RANKL/RANK/OPG in the periodontal tissue of a rat model for ligature-induced periodontitis. MATERIALS AND METHODS: Male Wistar albino rats were randomly divided into five groups of 10 rats each: (i) non-ligated, given water; (ii) ligated, given water; (iii) ligated, given 1 mg/kg TELM; (iv) ligated, given 5 mg/kg TELM; and (v) ligated, given 10 mg/kg TELM. All groups were treated with saline or TELM for 10 days. Periodontal tissue was analysed by histopathology; by the immunohistochemical examination of COX-2, MMP-2, MMP-9 and the RANKL/RANK/OPG pathway; and by ELISA analysis of the levels of IL-1β, IL-10, TNF-α, myeloperoxidase (MPO), malonaldehyde (MDA) and glutathione (GSH). RESULTS: Treatment with 10 mg/kg TELM resulted in reduced concentrations of MPO, MDA (p < 0.05) and the pro-inflammatory cytokine IL-1β (p < 0.05); reduced expression of MMP-2, MMP-9, RANK, RANKL and COX-2; and an increase in OPG. The levels of TNF-α were significantly reduced in all TELM-treated groups. CONCLUSIONS: These findings confirm the involvement of TELM in reducing the inflammatory response, oxidative stress and bone loss in ligature-induced periodontitis in rats. BlackWell Publishing Ltd 2013-12 2013-10-10 /pmc/articles/PMC4274974/ /pubmed/24118063 http://dx.doi.org/10.1111/jcpe.12160 Text en © 2013 The Authors. Journal of Clinical Periodontology published by John Wiley & Sons Ltd http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Periodontal Diseases
Araújo, Aurigena A
Souza, Tatiana O
Moura, Lígia M
Brito, Gerly A C
Aragão, Karoline S
Araújo, Lorena S
Medeiros, Caroline A X
Alves, Maria S C F
Araújo, Raimundo F
Effect of telmisartan on levels of IL-1, TNF-α, down-regulated COX-2, MMP-2, MMP-9 and RANKL/RANK in an experimental periodontitis model
title Effect of telmisartan on levels of IL-1, TNF-α, down-regulated COX-2, MMP-2, MMP-9 and RANKL/RANK in an experimental periodontitis model
title_full Effect of telmisartan on levels of IL-1, TNF-α, down-regulated COX-2, MMP-2, MMP-9 and RANKL/RANK in an experimental periodontitis model
title_fullStr Effect of telmisartan on levels of IL-1, TNF-α, down-regulated COX-2, MMP-2, MMP-9 and RANKL/RANK in an experimental periodontitis model
title_full_unstemmed Effect of telmisartan on levels of IL-1, TNF-α, down-regulated COX-2, MMP-2, MMP-9 and RANKL/RANK in an experimental periodontitis model
title_short Effect of telmisartan on levels of IL-1, TNF-α, down-regulated COX-2, MMP-2, MMP-9 and RANKL/RANK in an experimental periodontitis model
title_sort effect of telmisartan on levels of il-1, tnf-α, down-regulated cox-2, mmp-2, mmp-9 and rankl/rank in an experimental periodontitis model
topic Periodontal Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274974/
https://www.ncbi.nlm.nih.gov/pubmed/24118063
http://dx.doi.org/10.1111/jcpe.12160
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