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Refining the mandibular osteoradionecrosis rat model by in vivo longitudinal µCT analysis

Osteoradionecrosis (ORN) is one of the most feared side effects of radiotherapy following cancers of the upper aero-digestive tract and leading to severe functional defects in patients. Today, our lack of knowledge about the physiopathology restricts the development of new treatments. In this study,...

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Autores principales: Dos Santos, Morgane, Demarquay, Christelle, Ermeneux, Louis, Aberkane, Fazia, Bléry, Pauline, Weiss, Pierre, Milliat, Fabien, Mathieu, Noëlle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8594779/
https://www.ncbi.nlm.nih.gov/pubmed/34782666
http://dx.doi.org/10.1038/s41598-021-01229-y
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author Dos Santos, Morgane
Demarquay, Christelle
Ermeneux, Louis
Aberkane, Fazia
Bléry, Pauline
Weiss, Pierre
Milliat, Fabien
Mathieu, Noëlle
author_facet Dos Santos, Morgane
Demarquay, Christelle
Ermeneux, Louis
Aberkane, Fazia
Bléry, Pauline
Weiss, Pierre
Milliat, Fabien
Mathieu, Noëlle
author_sort Dos Santos, Morgane
collection PubMed
description Osteoradionecrosis (ORN) is one of the most feared side effects of radiotherapy following cancers of the upper aero-digestive tract and leading to severe functional defects in patients. Today, our lack of knowledge about the physiopathology restricts the development of new treatments. In this study, we refined the ORN rat model and quantitatively studied the progression of the disease. We tested the impact of radiation doses from 20 to 40 Gy, delivered with incident 4MV X-ray beams on the left mandible of the inbred Lewis Rat. We used micro-computed tomography (µCT) to obtain in vivo images for longitudinal bone imaging and ex vivo images after animal perfusion with barium sulphate contrast agent for vessel imaging. We compared quantification methods by analyzing 3D images and 2D measurements to determine the most appropriate and precise method according to the degree of damage. We defined 25 Gy as the minimum irradiation dose combined with the median molar extraction necessary to develop non-regenerative bone necrosis. µCT image analyses were correlated with clinical and histological analyses. This refined model and accurate methods for bone and vessel quantification will improve our knowledge of the progression of ORN pathology and allow us to test the efficacy of new regenerative medicine procedures.
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spelling pubmed-85947792021-11-17 Refining the mandibular osteoradionecrosis rat model by in vivo longitudinal µCT analysis Dos Santos, Morgane Demarquay, Christelle Ermeneux, Louis Aberkane, Fazia Bléry, Pauline Weiss, Pierre Milliat, Fabien Mathieu, Noëlle Sci Rep Article Osteoradionecrosis (ORN) is one of the most feared side effects of radiotherapy following cancers of the upper aero-digestive tract and leading to severe functional defects in patients. Today, our lack of knowledge about the physiopathology restricts the development of new treatments. In this study, we refined the ORN rat model and quantitatively studied the progression of the disease. We tested the impact of radiation doses from 20 to 40 Gy, delivered with incident 4MV X-ray beams on the left mandible of the inbred Lewis Rat. We used micro-computed tomography (µCT) to obtain in vivo images for longitudinal bone imaging and ex vivo images after animal perfusion with barium sulphate contrast agent for vessel imaging. We compared quantification methods by analyzing 3D images and 2D measurements to determine the most appropriate and precise method according to the degree of damage. We defined 25 Gy as the minimum irradiation dose combined with the median molar extraction necessary to develop non-regenerative bone necrosis. µCT image analyses were correlated with clinical and histological analyses. This refined model and accurate methods for bone and vessel quantification will improve our knowledge of the progression of ORN pathology and allow us to test the efficacy of new regenerative medicine procedures. Nature Publishing Group UK 2021-11-15 /pmc/articles/PMC8594779/ /pubmed/34782666 http://dx.doi.org/10.1038/s41598-021-01229-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Dos Santos, Morgane
Demarquay, Christelle
Ermeneux, Louis
Aberkane, Fazia
Bléry, Pauline
Weiss, Pierre
Milliat, Fabien
Mathieu, Noëlle
Refining the mandibular osteoradionecrosis rat model by in vivo longitudinal µCT analysis
title Refining the mandibular osteoradionecrosis rat model by in vivo longitudinal µCT analysis
title_full Refining the mandibular osteoradionecrosis rat model by in vivo longitudinal µCT analysis
title_fullStr Refining the mandibular osteoradionecrosis rat model by in vivo longitudinal µCT analysis
title_full_unstemmed Refining the mandibular osteoradionecrosis rat model by in vivo longitudinal µCT analysis
title_short Refining the mandibular osteoradionecrosis rat model by in vivo longitudinal µCT analysis
title_sort refining the mandibular osteoradionecrosis rat model by in vivo longitudinal µct analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8594779/
https://www.ncbi.nlm.nih.gov/pubmed/34782666
http://dx.doi.org/10.1038/s41598-021-01229-y
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