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Development of animal model for Bisphosphonates-related osteonecrosis of the jaw (BRONJ)

BACKGROUND: The aim of this study is to develop a rat model of bisphosphonates-related osteonecrosis of the jaw (BRONJ) that would be verified with clinical, radiological and histological examination, and to confirm the influence of concurrent bisphosphonates and steroids use upon the occurrence and...

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Autores principales: Jang, Hyo-Won, Kim, Jin-Woo, Cha, In-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513231/
https://www.ncbi.nlm.nih.gov/pubmed/26217648
http://dx.doi.org/10.1186/s40902-015-0020-6
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author Jang, Hyo-Won
Kim, Jin-Woo
Cha, In-Ho
author_facet Jang, Hyo-Won
Kim, Jin-Woo
Cha, In-Ho
author_sort Jang, Hyo-Won
collection PubMed
description BACKGROUND: The aim of this study is to develop a rat model of bisphosphonates-related osteonecrosis of the jaw (BRONJ) that would be verified with clinical, radiological and histological examination, and to confirm the influence of concurrent bisphosphonates and steroids use upon the occurrence and aggravation of BRONJ. METHODS: Twenty seven rats were divided into 3 groups; Saline group (I), Zoledronate group (II), Zoledronate and Dexamethasone group (III). Rats got weekly intraperitoneal injection for 4 times and extraction of left maxillary and mandibular 1st, 2nd molars were followed. Consecutive injections were performed, and blood sampling for measurements of C-terminal crosslinked telopeptide of type I collagen and tartrate-resistant acid phosphate 5b rats were performed at the time of 2, 4 and 8 weeks. And then, rats were sacrificed and evaluated clinically, radiologically and histologically. RESULTS: 12/18 (66.6 %) of experimental group were diagnosed as BRONJ. There was no significant difference in incidence between zoledronate alone group (ll) and concurrent use of zoledronate and dexamethasone group (lll). CONCLUSIONS: Concurrent use of bisphosphonates and steroids increase incidence of BRONJ compared to saline group (l). Zoledronate alone group (ll) and concurrent use of zoledronate and dexamethasone group (lll) shows same incidence of BRONJ. Based on this study, the rat treated with bisphosphonates and steroids can be considered a novel, reliable and reproducible model to understand pathology of BRONJ.
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spelling pubmed-45132312015-07-25 Development of animal model for Bisphosphonates-related osteonecrosis of the jaw (BRONJ) Jang, Hyo-Won Kim, Jin-Woo Cha, In-Ho Maxillofac Plast Reconstr Surg Research BACKGROUND: The aim of this study is to develop a rat model of bisphosphonates-related osteonecrosis of the jaw (BRONJ) that would be verified with clinical, radiological and histological examination, and to confirm the influence of concurrent bisphosphonates and steroids use upon the occurrence and aggravation of BRONJ. METHODS: Twenty seven rats were divided into 3 groups; Saline group (I), Zoledronate group (II), Zoledronate and Dexamethasone group (III). Rats got weekly intraperitoneal injection for 4 times and extraction of left maxillary and mandibular 1st, 2nd molars were followed. Consecutive injections were performed, and blood sampling for measurements of C-terminal crosslinked telopeptide of type I collagen and tartrate-resistant acid phosphate 5b rats were performed at the time of 2, 4 and 8 weeks. And then, rats were sacrificed and evaluated clinically, radiologically and histologically. RESULTS: 12/18 (66.6 %) of experimental group were diagnosed as BRONJ. There was no significant difference in incidence between zoledronate alone group (ll) and concurrent use of zoledronate and dexamethasone group (lll). CONCLUSIONS: Concurrent use of bisphosphonates and steroids increase incidence of BRONJ compared to saline group (l). Zoledronate alone group (ll) and concurrent use of zoledronate and dexamethasone group (lll) shows same incidence of BRONJ. Based on this study, the rat treated with bisphosphonates and steroids can be considered a novel, reliable and reproducible model to understand pathology of BRONJ. Springer Berlin Heidelberg 2015-07-25 /pmc/articles/PMC4513231/ /pubmed/26217648 http://dx.doi.org/10.1186/s40902-015-0020-6 Text en © Jang et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research
Jang, Hyo-Won
Kim, Jin-Woo
Cha, In-Ho
Development of animal model for Bisphosphonates-related osteonecrosis of the jaw (BRONJ)
title Development of animal model for Bisphosphonates-related osteonecrosis of the jaw (BRONJ)
title_full Development of animal model for Bisphosphonates-related osteonecrosis of the jaw (BRONJ)
title_fullStr Development of animal model for Bisphosphonates-related osteonecrosis of the jaw (BRONJ)
title_full_unstemmed Development of animal model for Bisphosphonates-related osteonecrosis of the jaw (BRONJ)
title_short Development of animal model for Bisphosphonates-related osteonecrosis of the jaw (BRONJ)
title_sort development of animal model for bisphosphonates-related osteonecrosis of the jaw (bronj)
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513231/
https://www.ncbi.nlm.nih.gov/pubmed/26217648
http://dx.doi.org/10.1186/s40902-015-0020-6
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