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Development of an Ex Vivo Protocol to Model Bone Fracture in Laying Hens Resulting from Collisions

Fractures of the keel bone, a bone extending ventrally from the sternum, are a serious health and welfare problem in free range laying hens. Recent findings suggest that a major cause of keel damage within extensive systems is collisions with internal housing structures, though investigative efforts...

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Autores principales: Toscano, Michael J., Wilkins, Lindsay J., Millburn, Georgina, Thorpe, Katherine, Tarlton, John F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681979/
https://www.ncbi.nlm.nih.gov/pubmed/23785487
http://dx.doi.org/10.1371/journal.pone.0066215
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author Toscano, Michael J.
Wilkins, Lindsay J.
Millburn, Georgina
Thorpe, Katherine
Tarlton, John F.
author_facet Toscano, Michael J.
Wilkins, Lindsay J.
Millburn, Georgina
Thorpe, Katherine
Tarlton, John F.
author_sort Toscano, Michael J.
collection PubMed
description Fractures of the keel bone, a bone extending ventrally from the sternum, are a serious health and welfare problem in free range laying hens. Recent findings suggest that a major cause of keel damage within extensive systems is collisions with internal housing structures, though investigative efforts have been hindered by difficulties in examining mechanisms and likely influencing factors at the moment of fracture. The objectives of this study were to develop an ex vivo impact protocol to model bone fracture in hens caused by collision, to assess impact and bird-related factors influencing fracture occurrence and severity, and to identify correlations of mechanical and structural properties between different skeletal sites. We induced keel bone fractures in euthanized hens using a drop-weight impact tester able to generate a range of impact energies, producing fractures that replicate those commonly found in commercial settings. The results demonstrated that impact energies of a similar order to those expected in normal housing were able to produce fractures, and that greater collision energies resulted in an increased likelihood of fractures and of greater severity. Relationships were also seen with keel’s lateral surface bone mineral density, and the peak reactive force (strength) at the base of the manubrial spine. Correlations were also identified between the keel and long bones with respect to both strength and bone mineral density. This is the first study able to relate impact and bone characteristics with keel bone fracture at the moment of collision. Greater understanding of these relationships will provide means to reduce levels of breakage and severity in commercial systems.
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spelling pubmed-36819792013-06-19 Development of an Ex Vivo Protocol to Model Bone Fracture in Laying Hens Resulting from Collisions Toscano, Michael J. Wilkins, Lindsay J. Millburn, Georgina Thorpe, Katherine Tarlton, John F. PLoS One Research Article Fractures of the keel bone, a bone extending ventrally from the sternum, are a serious health and welfare problem in free range laying hens. Recent findings suggest that a major cause of keel damage within extensive systems is collisions with internal housing structures, though investigative efforts have been hindered by difficulties in examining mechanisms and likely influencing factors at the moment of fracture. The objectives of this study were to develop an ex vivo impact protocol to model bone fracture in hens caused by collision, to assess impact and bird-related factors influencing fracture occurrence and severity, and to identify correlations of mechanical and structural properties between different skeletal sites. We induced keel bone fractures in euthanized hens using a drop-weight impact tester able to generate a range of impact energies, producing fractures that replicate those commonly found in commercial settings. The results demonstrated that impact energies of a similar order to those expected in normal housing were able to produce fractures, and that greater collision energies resulted in an increased likelihood of fractures and of greater severity. Relationships were also seen with keel’s lateral surface bone mineral density, and the peak reactive force (strength) at the base of the manubrial spine. Correlations were also identified between the keel and long bones with respect to both strength and bone mineral density. This is the first study able to relate impact and bone characteristics with keel bone fracture at the moment of collision. Greater understanding of these relationships will provide means to reduce levels of breakage and severity in commercial systems. Public Library of Science 2013-06-13 /pmc/articles/PMC3681979/ /pubmed/23785487 http://dx.doi.org/10.1371/journal.pone.0066215 Text en © 2013 Toscano et al http://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 author and source are properly credited.
spellingShingle Research Article
Toscano, Michael J.
Wilkins, Lindsay J.
Millburn, Georgina
Thorpe, Katherine
Tarlton, John F.
Development of an Ex Vivo Protocol to Model Bone Fracture in Laying Hens Resulting from Collisions
title Development of an Ex Vivo Protocol to Model Bone Fracture in Laying Hens Resulting from Collisions
title_full Development of an Ex Vivo Protocol to Model Bone Fracture in Laying Hens Resulting from Collisions
title_fullStr Development of an Ex Vivo Protocol to Model Bone Fracture in Laying Hens Resulting from Collisions
title_full_unstemmed Development of an Ex Vivo Protocol to Model Bone Fracture in Laying Hens Resulting from Collisions
title_short Development of an Ex Vivo Protocol to Model Bone Fracture in Laying Hens Resulting from Collisions
title_sort development of an ex vivo protocol to model bone fracture in laying hens resulting from collisions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681979/
https://www.ncbi.nlm.nih.gov/pubmed/23785487
http://dx.doi.org/10.1371/journal.pone.0066215
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