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Expression of Inflammatory Mediators in Periodontitis Over Established Diabetes: an Experimental Study in Rats

BACKGROUND: Diabetes mellitus is characterized by hyperglycemia ensuing from deficiencies in insulin action, secretion, or both. Hyperglycemia has wide-ranging molecular and cellular effects, leading to oxidative stress, up-regulation of pro-inflammatory responses, and vascular changes. OBJECTIVES:...

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Autores principales: Choubaya, Charbel, Chahine, Nathalie, Aoun, Georges, Anil, Sukumaran, Zalloua, Pierre, Salameh, Ziad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences of Bosnia and Herzegovina 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802681/
https://www.ncbi.nlm.nih.gov/pubmed/35169371
http://dx.doi.org/10.5455/medarh.2021.75.436-443
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author Choubaya, Charbel
Chahine, Nathalie
Aoun, Georges
Anil, Sukumaran
Zalloua, Pierre
Salameh, Ziad
author_facet Choubaya, Charbel
Chahine, Nathalie
Aoun, Georges
Anil, Sukumaran
Zalloua, Pierre
Salameh, Ziad
author_sort Choubaya, Charbel
collection PubMed
description BACKGROUND: Diabetes mellitus is characterized by hyperglycemia ensuing from deficiencies in insulin action, secretion, or both. Hyperglycemia has wide-ranging molecular and cellular effects, leading to oxidative stress, up-regulation of pro-inflammatory responses, and vascular changes. OBJECTIVES: The aim of this study was to evaluate the expressions of inflammatory markers involved in periodontal destructive process occurring in diabetes, periodontitis (PD), and both coexisting conditions. METHODS: A rat model was carried out using streptozotocin (STZ) to induce diabetes and Lipopolysaccharides (LPS) with teeth ligature to mimic periodontitis. The animals were distributed randomly into seven groups (n=12) and treated for 10 weeks with alternation between diabetes and PD. The relative quantification analysis of inflammatory markers expression: CRP, MMP-2-14, TIMP-2, IL-4, IFN-γ, was performed at the end of the experiments using western blot after protein isolation from periodontal tissue surrounding the ligation. RESULTS: The data showed that CRP, MMP-2, MMP-14, TIMP-2, and IFN-γ are involved in the process of periodontal inflammation associated with diabetes. A significant increase (p<0.05) in the expression of inflammatory markers was detected when PD is associated with preexisting diabetes in comparison with diabetes superimposed on preexisting PD. CONCLUSION: This study demonstrated that already established diabetes worsens periodontitis more than diabetes upcoming on existing periodontitis.
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spelling pubmed-88026812022-02-14 Expression of Inflammatory Mediators in Periodontitis Over Established Diabetes: an Experimental Study in Rats Choubaya, Charbel Chahine, Nathalie Aoun, Georges Anil, Sukumaran Zalloua, Pierre Salameh, Ziad Med Arch Original Paper BACKGROUND: Diabetes mellitus is characterized by hyperglycemia ensuing from deficiencies in insulin action, secretion, or both. Hyperglycemia has wide-ranging molecular and cellular effects, leading to oxidative stress, up-regulation of pro-inflammatory responses, and vascular changes. OBJECTIVES: The aim of this study was to evaluate the expressions of inflammatory markers involved in periodontal destructive process occurring in diabetes, periodontitis (PD), and both coexisting conditions. METHODS: A rat model was carried out using streptozotocin (STZ) to induce diabetes and Lipopolysaccharides (LPS) with teeth ligature to mimic periodontitis. The animals were distributed randomly into seven groups (n=12) and treated for 10 weeks with alternation between diabetes and PD. The relative quantification analysis of inflammatory markers expression: CRP, MMP-2-14, TIMP-2, IL-4, IFN-γ, was performed at the end of the experiments using western blot after protein isolation from periodontal tissue surrounding the ligation. RESULTS: The data showed that CRP, MMP-2, MMP-14, TIMP-2, and IFN-γ are involved in the process of periodontal inflammation associated with diabetes. A significant increase (p<0.05) in the expression of inflammatory markers was detected when PD is associated with preexisting diabetes in comparison with diabetes superimposed on preexisting PD. CONCLUSION: This study demonstrated that already established diabetes worsens periodontitis more than diabetes upcoming on existing periodontitis. Academy of Medical Sciences of Bosnia and Herzegovina 2021-12 /pmc/articles/PMC8802681/ /pubmed/35169371 http://dx.doi.org/10.5455/medarh.2021.75.436-443 Text en © 2021 Charbel Choubaya, Nathalie Chahine, Georges Aoun, Sukumaran Anil, Pierre Zalloua, Ziad Salameh https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Choubaya, Charbel
Chahine, Nathalie
Aoun, Georges
Anil, Sukumaran
Zalloua, Pierre
Salameh, Ziad
Expression of Inflammatory Mediators in Periodontitis Over Established Diabetes: an Experimental Study in Rats
title Expression of Inflammatory Mediators in Periodontitis Over Established Diabetes: an Experimental Study in Rats
title_full Expression of Inflammatory Mediators in Periodontitis Over Established Diabetes: an Experimental Study in Rats
title_fullStr Expression of Inflammatory Mediators in Periodontitis Over Established Diabetes: an Experimental Study in Rats
title_full_unstemmed Expression of Inflammatory Mediators in Periodontitis Over Established Diabetes: an Experimental Study in Rats
title_short Expression of Inflammatory Mediators in Periodontitis Over Established Diabetes: an Experimental Study in Rats
title_sort expression of inflammatory mediators in periodontitis over established diabetes: an experimental study in rats
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802681/
https://www.ncbi.nlm.nih.gov/pubmed/35169371
http://dx.doi.org/10.5455/medarh.2021.75.436-443
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