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Dental extraction following zoledronate, induces osteonecrosis in rat´s jaw

BACKGROUND: Bisphosphonate-Related Osteonecrosis of the Jaw (BRONJ) is clinically characterized by the presence of exposed bone in the oral cavity that persists for more than eight weeks. Previous attempts to establish an animal model have not sufficiently considered disease features. Our aim was to...

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Autores principales: Vidal-Gutiérrez, Ximena, Gómez-Clavel, José-Francisco, Gaitán-Cepeda, Luis-Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359702/
https://www.ncbi.nlm.nih.gov/pubmed/28160593
http://dx.doi.org/10.4317/medoral.21609
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author Vidal-Gutiérrez, Ximena
Gómez-Clavel, José-Francisco
Gaitán-Cepeda, Luis-Alberto
author_facet Vidal-Gutiérrez, Ximena
Gómez-Clavel, José-Francisco
Gaitán-Cepeda, Luis-Alberto
author_sort Vidal-Gutiérrez, Ximena
collection PubMed
description BACKGROUND: Bisphosphonate-Related Osteonecrosis of the Jaw (BRONJ) is clinically characterized by the presence of exposed bone in the oral cavity that persists for more than eight weeks. Previous attempts to establish an animal model have not sufficiently considered disease features. Our aim was to establish an inexpensive and replicable animal model that develops BRONJ in a short time. MATERIAL AND METHODS: Thirty-two male Wistar rats were randomly divided into two groups: control and experimental. In the experimental group, we administered 0.06mg/kg intraperitoneal dose of zoledronic acid (ZA) 7 and 14 days prior to maxillary second molar extraction. At two, four and six weeks after tooth extraction, the animals were euthanized, and we dissected the maxilla following histological procedures. We stained serial slides with hematoxylin and eosin and Masson’s trichrome. The samples were harvested for macroscopic, radiologic and histological evaluation of bone changes. RESULTS: At two weeks postextraction, we observed exposed necrotic bone in dental socket areas in experimental groups. Radiological analysis revealed osteolytic lesions accompanied by extensive destruction and sequestrum formation in the same group. Histological examination confirmed the absence of necrotic bone in control groups in contrast with the experimental groups. The percentage of empty lacunae and the number of osteoclasts and the necrotic bone area were significantly increased (p<0.05) in the experimental groups. CONCLUSIONS: The animal model using ZA administration to prior dental extraction successfully mimicked human BRONJ lesions. Also, the model was easily replicated, inexpensive and showed different features than other previous BRONJ models. Key words:Bisphosphonates, osteonecrosis, dental extractions, animal model, BRONJ.
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spelling pubmed-53597022017-03-24 Dental extraction following zoledronate, induces osteonecrosis in rat´s jaw Vidal-Gutiérrez, Ximena Gómez-Clavel, José-Francisco Gaitán-Cepeda, Luis-Alberto Med Oral Patol Oral Cir Bucal Research BACKGROUND: Bisphosphonate-Related Osteonecrosis of the Jaw (BRONJ) is clinically characterized by the presence of exposed bone in the oral cavity that persists for more than eight weeks. Previous attempts to establish an animal model have not sufficiently considered disease features. Our aim was to establish an inexpensive and replicable animal model that develops BRONJ in a short time. MATERIAL AND METHODS: Thirty-two male Wistar rats were randomly divided into two groups: control and experimental. In the experimental group, we administered 0.06mg/kg intraperitoneal dose of zoledronic acid (ZA) 7 and 14 days prior to maxillary second molar extraction. At two, four and six weeks after tooth extraction, the animals were euthanized, and we dissected the maxilla following histological procedures. We stained serial slides with hematoxylin and eosin and Masson’s trichrome. The samples were harvested for macroscopic, radiologic and histological evaluation of bone changes. RESULTS: At two weeks postextraction, we observed exposed necrotic bone in dental socket areas in experimental groups. Radiological analysis revealed osteolytic lesions accompanied by extensive destruction and sequestrum formation in the same group. Histological examination confirmed the absence of necrotic bone in control groups in contrast with the experimental groups. The percentage of empty lacunae and the number of osteoclasts and the necrotic bone area were significantly increased (p<0.05) in the experimental groups. CONCLUSIONS: The animal model using ZA administration to prior dental extraction successfully mimicked human BRONJ lesions. Also, the model was easily replicated, inexpensive and showed different features than other previous BRONJ models. Key words:Bisphosphonates, osteonecrosis, dental extractions, animal model, BRONJ. Medicina Oral S.L. 2017-03 2017-02-04 /pmc/articles/PMC5359702/ /pubmed/28160593 http://dx.doi.org/10.4317/medoral.21609 Text en Copyright: © 2017 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ 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 Research
Vidal-Gutiérrez, Ximena
Gómez-Clavel, José-Francisco
Gaitán-Cepeda, Luis-Alberto
Dental extraction following zoledronate, induces osteonecrosis in rat´s jaw
title Dental extraction following zoledronate, induces osteonecrosis in rat´s jaw
title_full Dental extraction following zoledronate, induces osteonecrosis in rat´s jaw
title_fullStr Dental extraction following zoledronate, induces osteonecrosis in rat´s jaw
title_full_unstemmed Dental extraction following zoledronate, induces osteonecrosis in rat´s jaw
title_short Dental extraction following zoledronate, induces osteonecrosis in rat´s jaw
title_sort dental extraction following zoledronate, induces osteonecrosis in rat´s jaw
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359702/
https://www.ncbi.nlm.nih.gov/pubmed/28160593
http://dx.doi.org/10.4317/medoral.21609
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