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Evaluation of a collagen matrix in a mandible defect in rats submitted to the use of bisphosphonates

PURPOSE: To assess the effect of a collagen matrix (Mucograft(®)) on the inflammatory process in a semi-critical experimental defect model in rats treated with bisphosphonates. METHODS: Eighteen Wistar rats were randomly divided into three groups: saline (CG), alendronate (ALD) 5mg/kg (AG) or zoledr...

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Autores principales: Cunha, Vanessa Vasconcelos, Silva, Paulo Goberlânio de Barros, Lemos, José Vitor Mota, Martins, Joyce Ohana Lima, Freitas, Milena Oliveira, Avelar, Rafael Linard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709902/
https://www.ncbi.nlm.nih.gov/pubmed/33263607
http://dx.doi.org/10.1590/s0102-865020200100000005
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author Cunha, Vanessa Vasconcelos
Silva, Paulo Goberlânio de Barros
Lemos, José Vitor Mota
Martins, Joyce Ohana Lima
Freitas, Milena Oliveira
Avelar, Rafael Linard
author_facet Cunha, Vanessa Vasconcelos
Silva, Paulo Goberlânio de Barros
Lemos, José Vitor Mota
Martins, Joyce Ohana Lima
Freitas, Milena Oliveira
Avelar, Rafael Linard
author_sort Cunha, Vanessa Vasconcelos
collection PubMed
description PURPOSE: To assess the effect of a collagen matrix (Mucograft(®)) on the inflammatory process in a semi-critical experimental defect model in rats treated with bisphosphonates. METHODS: Eighteen Wistar rats were randomly divided into three groups: saline (CG), alendronate (ALD) 5mg/kg (AG) or zoledronic acid (ZA) 0.2mg/kg (ZG). ALD was administered orally for 10 weeks and ZA was administered intravascularly on days 0, 7 and 14 and 49. On day 42, a 2mm defect was created and filled with Mucograft(®) collagen matrix. The contralateral side was filled with a clot (control side). The animals were euthanized 70 days after the beginning of the experiment and the hemimandibles were radiographically and histologically (counting of empty osteocyte lacunae (%), apoptotic (%) and total osteoclasts, neutrophil and mononuclear inflammatory cells) analyzed. The variables were submitted to ANOVA/Bonferroni and t test (parametric data) (p <0.05, GraphPad Prism 5.0). RESULTS: Significant bone repair occurred in the groups treated with Mucograft(®). High number of total inflammatory cells and neutrophils cells were showed in AG (p=0.026 and p=0.035) and AZ groups (p=0.005, p=0.034) on the control sides associated with delayed bone repair and the presence of devitalized bone tissue in AG and ZG on the Mucograft(®) side. CONCLUSION: Mucograft(®) collagen matrix attenuated the inflammatory process in a mandible defect in rats submitted to the use of bisphosphonates (AG and ZG).
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spelling pubmed-77099022020-12-07 Evaluation of a collagen matrix in a mandible defect in rats submitted to the use of bisphosphonates Cunha, Vanessa Vasconcelos Silva, Paulo Goberlânio de Barros Lemos, José Vitor Mota Martins, Joyce Ohana Lima Freitas, Milena Oliveira Avelar, Rafael Linard Acta Cir Bras Original Article PURPOSE: To assess the effect of a collagen matrix (Mucograft(®)) on the inflammatory process in a semi-critical experimental defect model in rats treated with bisphosphonates. METHODS: Eighteen Wistar rats were randomly divided into three groups: saline (CG), alendronate (ALD) 5mg/kg (AG) or zoledronic acid (ZA) 0.2mg/kg (ZG). ALD was administered orally for 10 weeks and ZA was administered intravascularly on days 0, 7 and 14 and 49. On day 42, a 2mm defect was created and filled with Mucograft(®) collagen matrix. The contralateral side was filled with a clot (control side). The animals were euthanized 70 days after the beginning of the experiment and the hemimandibles were radiographically and histologically (counting of empty osteocyte lacunae (%), apoptotic (%) and total osteoclasts, neutrophil and mononuclear inflammatory cells) analyzed. The variables were submitted to ANOVA/Bonferroni and t test (parametric data) (p <0.05, GraphPad Prism 5.0). RESULTS: Significant bone repair occurred in the groups treated with Mucograft(®). High number of total inflammatory cells and neutrophils cells were showed in AG (p=0.026 and p=0.035) and AZ groups (p=0.005, p=0.034) on the control sides associated with delayed bone repair and the presence of devitalized bone tissue in AG and ZG on the Mucograft(®) side. CONCLUSION: Mucograft(®) collagen matrix attenuated the inflammatory process in a mandible defect in rats submitted to the use of bisphosphonates (AG and ZG). Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2020-11-30 /pmc/articles/PMC7709902/ /pubmed/33263607 http://dx.doi.org/10.1590/s0102-865020200100000005 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cunha, Vanessa Vasconcelos
Silva, Paulo Goberlânio de Barros
Lemos, José Vitor Mota
Martins, Joyce Ohana Lima
Freitas, Milena Oliveira
Avelar, Rafael Linard
Evaluation of a collagen matrix in a mandible defect in rats submitted to the use of bisphosphonates
title Evaluation of a collagen matrix in a mandible defect in rats submitted to the use of bisphosphonates
title_full Evaluation of a collagen matrix in a mandible defect in rats submitted to the use of bisphosphonates
title_fullStr Evaluation of a collagen matrix in a mandible defect in rats submitted to the use of bisphosphonates
title_full_unstemmed Evaluation of a collagen matrix in a mandible defect in rats submitted to the use of bisphosphonates
title_short Evaluation of a collagen matrix in a mandible defect in rats submitted to the use of bisphosphonates
title_sort evaluation of a collagen matrix in a mandible defect in rats submitted to the use of bisphosphonates
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709902/
https://www.ncbi.nlm.nih.gov/pubmed/33263607
http://dx.doi.org/10.1590/s0102-865020200100000005
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