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Relating Histopathology and Mechanical Strain in Experimental Contusion Spinal Cord Injury in a Rat Model

During traumatic spinal cord injury (SCI), the spinal cord is subject to external displacements that result in damage of neural tissues. These displacements produce complex internal deformations, or strains, of the spinal cord parenchyma. The aim of this study is to determine a relationship between...

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Autores principales: Bhatnagar, Tim, Liu, Jie, Yung, Andrew, Cripton, Peter, Kozlowski, Piotr, Tetzlaff, Wolfram, Oxland, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035832/
https://www.ncbi.nlm.nih.gov/pubmed/26729511
http://dx.doi.org/10.1089/neu.2015.4200
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author Bhatnagar, Tim
Liu, Jie
Yung, Andrew
Cripton, Peter
Kozlowski, Piotr
Tetzlaff, Wolfram
Oxland, Thomas
author_facet Bhatnagar, Tim
Liu, Jie
Yung, Andrew
Cripton, Peter
Kozlowski, Piotr
Tetzlaff, Wolfram
Oxland, Thomas
author_sort Bhatnagar, Tim
collection PubMed
description During traumatic spinal cord injury (SCI), the spinal cord is subject to external displacements that result in damage of neural tissues. These displacements produce complex internal deformations, or strains, of the spinal cord parenchyma. The aim of this study is to determine a relationship between these internal strains during SCI and primary damage to spinal cord gray matter (GM) in an in vivo rat contusion model. Using magnetic resonance imaging and novel image registration methods, we measured three-dimensional (3D) mechanical strain in in vivo rat cervical spinal cord (n = 12) during an imposed contusion injury. We then assessed expression of the neuronal transcription factor, neuronal nuclei (NeuN), in ventral horns of GM (at the epicenter of injury as well as at intervals cranially and caudally), immediately post-injury. We found that minimum principal strain was most strongly correlated with loss of NeuN stain across all animals (R(2) = 0.19), but varied in strength between individual animals (R(2) = 0.06–0.52). Craniocaudal distribution of anatomical damage was similar to measured strain distribution. A Monte Carlo simulation was used to assess strain field error, and minimum principal strain (which ranged from 8% to 36% in GM ventral horns) exhibited a standard deviation of 2.6% attributed to the simulated error. This study is the first to measure 3D deformation of the spinal cord and relate it to patterns of ensuing tissue damage in an in vivo model. It provides a platform on which to build future studies addressing the tolerance of spinal cord tissue to mechanical deformation.
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spelling pubmed-50358322016-10-04 Relating Histopathology and Mechanical Strain in Experimental Contusion Spinal Cord Injury in a Rat Model Bhatnagar, Tim Liu, Jie Yung, Andrew Cripton, Peter Kozlowski, Piotr Tetzlaff, Wolfram Oxland, Thomas J Neurotrauma Original Articles During traumatic spinal cord injury (SCI), the spinal cord is subject to external displacements that result in damage of neural tissues. These displacements produce complex internal deformations, or strains, of the spinal cord parenchyma. The aim of this study is to determine a relationship between these internal strains during SCI and primary damage to spinal cord gray matter (GM) in an in vivo rat contusion model. Using magnetic resonance imaging and novel image registration methods, we measured three-dimensional (3D) mechanical strain in in vivo rat cervical spinal cord (n = 12) during an imposed contusion injury. We then assessed expression of the neuronal transcription factor, neuronal nuclei (NeuN), in ventral horns of GM (at the epicenter of injury as well as at intervals cranially and caudally), immediately post-injury. We found that minimum principal strain was most strongly correlated with loss of NeuN stain across all animals (R(2) = 0.19), but varied in strength between individual animals (R(2) = 0.06–0.52). Craniocaudal distribution of anatomical damage was similar to measured strain distribution. A Monte Carlo simulation was used to assess strain field error, and minimum principal strain (which ranged from 8% to 36% in GM ventral horns) exhibited a standard deviation of 2.6% attributed to the simulated error. This study is the first to measure 3D deformation of the spinal cord and relate it to patterns of ensuing tissue damage in an in vivo model. It provides a platform on which to build future studies addressing the tolerance of spinal cord tissue to mechanical deformation. Mary Ann Liebert, Inc. 2016-09-15 2016-09-15 /pmc/articles/PMC5035832/ /pubmed/26729511 http://dx.doi.org/10.1089/neu.2015.4200 Text en © Tim Bhatnagar et al., 2016; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Articles
Bhatnagar, Tim
Liu, Jie
Yung, Andrew
Cripton, Peter
Kozlowski, Piotr
Tetzlaff, Wolfram
Oxland, Thomas
Relating Histopathology and Mechanical Strain in Experimental Contusion Spinal Cord Injury in a Rat Model
title Relating Histopathology and Mechanical Strain in Experimental Contusion Spinal Cord Injury in a Rat Model
title_full Relating Histopathology and Mechanical Strain in Experimental Contusion Spinal Cord Injury in a Rat Model
title_fullStr Relating Histopathology and Mechanical Strain in Experimental Contusion Spinal Cord Injury in a Rat Model
title_full_unstemmed Relating Histopathology and Mechanical Strain in Experimental Contusion Spinal Cord Injury in a Rat Model
title_short Relating Histopathology and Mechanical Strain in Experimental Contusion Spinal Cord Injury in a Rat Model
title_sort relating histopathology and mechanical strain in experimental contusion spinal cord injury in a rat model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035832/
https://www.ncbi.nlm.nih.gov/pubmed/26729511
http://dx.doi.org/10.1089/neu.2015.4200
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