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Protective effect and related mechanisms of curcumin in rat experimental periodontitis

BACKGROUND: Curcumin exhibits anti-inflammatory effects and has been suggested as a treatment for inflammatory diseases. The aim of this study was to investigate the effects of curcumin on the lipopolysaccharide induced inflammatory response in rat gingival fibroblasts in vitro and ligation-induced...

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Autores principales: Xiao, Chang-Jie, Yu, Xi-Jiao, Xie, Jian-Li, Liu, Shuang, Li, Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097422/
https://www.ncbi.nlm.nih.gov/pubmed/30115081
http://dx.doi.org/10.1186/s13005-018-0169-1
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author Xiao, Chang-Jie
Yu, Xi-Jiao
Xie, Jian-Li
Liu, Shuang
Li, Shu
author_facet Xiao, Chang-Jie
Yu, Xi-Jiao
Xie, Jian-Li
Liu, Shuang
Li, Shu
author_sort Xiao, Chang-Jie
collection PubMed
description BACKGROUND: Curcumin exhibits anti-inflammatory effects and has been suggested as a treatment for inflammatory diseases. The aim of this study was to investigate the effects of curcumin on the lipopolysaccharide induced inflammatory response in rat gingival fibroblasts in vitro and ligation-induced experimental periodontitis in vivo, and to speculate the possible anti-inflammatory mechanism of curcumin. METHODS: The gingival fibroblasts were incubated with different concentrations of curcumin in the absence or presence of lipopolysaccharide (LPS). Concentrations of interleukin-1β(IL-1β), tumor necrosis factor-α (TNF-α), osteoprotegerin (OPG) and soluble receptor activator of nuclear factor kappa-B ligand (RANKL) culture supernatants of rat gingival fibroblasts were determined by enzyme linked immunosorbent assay. The nuclear fraction of rat gingival fibroblasts was extracted and nuclear factor kappa-B (NF-κB) activation was assessed by western blotting to elucidate related mechanisms. Curcumin was given every two days by oral gavage. The gingival inflammation and alveolar bone loss between the first and second molars were observed by hematoxylin and eosin staining. Collagen fibers were observed by picro-sirius red staining. Alveolar bone loss was assessed by micro-CT analysis. RESULTS: Curcumin attenuated the production of IL-1β and TNF-α in rat gingival fibroblasts stimulated by LPS, and inhibited the LPS-induced decrease in OPG/sRANKL ratio and NF-κB activation. Curcumin significantly reduced gingival inflammation and modulated collagen fiber and alveolar bone loss in vivo. CONCLUSIONS: curcumin modulates inflammatory activity in rat periodontitis by inhibiting NF-κB activation and decreasing the OPG/sRANKL ratio induced by LPS.
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spelling pubmed-60974222018-08-20 Protective effect and related mechanisms of curcumin in rat experimental periodontitis Xiao, Chang-Jie Yu, Xi-Jiao Xie, Jian-Li Liu, Shuang Li, Shu Head Face Med Research BACKGROUND: Curcumin exhibits anti-inflammatory effects and has been suggested as a treatment for inflammatory diseases. The aim of this study was to investigate the effects of curcumin on the lipopolysaccharide induced inflammatory response in rat gingival fibroblasts in vitro and ligation-induced experimental periodontitis in vivo, and to speculate the possible anti-inflammatory mechanism of curcumin. METHODS: The gingival fibroblasts were incubated with different concentrations of curcumin in the absence or presence of lipopolysaccharide (LPS). Concentrations of interleukin-1β(IL-1β), tumor necrosis factor-α (TNF-α), osteoprotegerin (OPG) and soluble receptor activator of nuclear factor kappa-B ligand (RANKL) culture supernatants of rat gingival fibroblasts were determined by enzyme linked immunosorbent assay. The nuclear fraction of rat gingival fibroblasts was extracted and nuclear factor kappa-B (NF-κB) activation was assessed by western blotting to elucidate related mechanisms. Curcumin was given every two days by oral gavage. The gingival inflammation and alveolar bone loss between the first and second molars were observed by hematoxylin and eosin staining. Collagen fibers were observed by picro-sirius red staining. Alveolar bone loss was assessed by micro-CT analysis. RESULTS: Curcumin attenuated the production of IL-1β and TNF-α in rat gingival fibroblasts stimulated by LPS, and inhibited the LPS-induced decrease in OPG/sRANKL ratio and NF-κB activation. Curcumin significantly reduced gingival inflammation and modulated collagen fiber and alveolar bone loss in vivo. CONCLUSIONS: curcumin modulates inflammatory activity in rat periodontitis by inhibiting NF-κB activation and decreasing the OPG/sRANKL ratio induced by LPS. BioMed Central 2018-08-16 /pmc/articles/PMC6097422/ /pubmed/30115081 http://dx.doi.org/10.1186/s13005-018-0169-1 Text en © The Author(s). 2018 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
Xiao, Chang-Jie
Yu, Xi-Jiao
Xie, Jian-Li
Liu, Shuang
Li, Shu
Protective effect and related mechanisms of curcumin in rat experimental periodontitis
title Protective effect and related mechanisms of curcumin in rat experimental periodontitis
title_full Protective effect and related mechanisms of curcumin in rat experimental periodontitis
title_fullStr Protective effect and related mechanisms of curcumin in rat experimental periodontitis
title_full_unstemmed Protective effect and related mechanisms of curcumin in rat experimental periodontitis
title_short Protective effect and related mechanisms of curcumin in rat experimental periodontitis
title_sort protective effect and related mechanisms of curcumin in rat experimental periodontitis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097422/
https://www.ncbi.nlm.nih.gov/pubmed/30115081
http://dx.doi.org/10.1186/s13005-018-0169-1
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