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Establishment of a novel rat model of blast-related diffuse axonal injury
Although studies concerning blast-related traumatic brain injury (bTBI) have demonstrated the significance of diffuse axonal injury (DAI), no standard models for this type of injury have been widely accepted. The present study investigated a mechanism of inducing DAI through real blast injury, which...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030930/ https://www.ncbi.nlm.nih.gov/pubmed/29977358 http://dx.doi.org/10.3892/etm.2018.6146 |
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author | Zhang, Jun-Hai Gu, Jian-Wen Li, Bing-Cang Gao, Fa-Bao Liao, Xiao-Ming Cui, Shao-Jie |
author_facet | Zhang, Jun-Hai Gu, Jian-Wen Li, Bing-Cang Gao, Fa-Bao Liao, Xiao-Ming Cui, Shao-Jie |
author_sort | Zhang, Jun-Hai |
collection | PubMed |
description | Although studies concerning blast-related traumatic brain injury (bTBI) have demonstrated the significance of diffuse axonal injury (DAI), no standard models for this type of injury have been widely accepted. The present study investigated a mechanism of inducing DAI through real blast injury, which was achieved by performing instantaneous high-speed swinging of the rat head, thus establishing a stable animal model of blast DAI. Adult Sprague-Dawley rats weighing 150±10 g were randomly divided into experimental (n=16), control (n=10) and sham control (n=6) groups. The frontal, parietal and occipital cortex of the rats in the experimental group were exposed, whereas those of the control group were unexposed; the sham control group rats were anesthetized and attached to the craniocerebral blast device without experiencing a blast. The rats were subjected to craniocerebral blast injury through a blast equivalent to 400 mg of trinitrotoluene using an electric detonator. Biomechanical parameters, and physical and behavioural changes of the sagittal head swing were measured using a high-speed camera. Magnetic resonance imaging (MRI) scans were conducted at 2, 12, 24 and 48 h after craniocerebral injury, only the experimental group indicated brain stem injury. The rats were sacrificed immediately following the MRI at 48 h for pathological examination of the brain stem using haematoxylin and eosin staining. The results indicated that 14 rats (87.5%) in the experimental group exhibited blast DAI, while no DAI was observed in the control and sham control groups, and the difference between the groups was significant (P<0.05). The present results indicated that this experimental design may serve to provide a stable model of blast DAI in rats. |
format | Online Article Text |
id | pubmed-6030930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-60309302018-07-05 Establishment of a novel rat model of blast-related diffuse axonal injury Zhang, Jun-Hai Gu, Jian-Wen Li, Bing-Cang Gao, Fa-Bao Liao, Xiao-Ming Cui, Shao-Jie Exp Ther Med Articles Although studies concerning blast-related traumatic brain injury (bTBI) have demonstrated the significance of diffuse axonal injury (DAI), no standard models for this type of injury have been widely accepted. The present study investigated a mechanism of inducing DAI through real blast injury, which was achieved by performing instantaneous high-speed swinging of the rat head, thus establishing a stable animal model of blast DAI. Adult Sprague-Dawley rats weighing 150±10 g were randomly divided into experimental (n=16), control (n=10) and sham control (n=6) groups. The frontal, parietal and occipital cortex of the rats in the experimental group were exposed, whereas those of the control group were unexposed; the sham control group rats were anesthetized and attached to the craniocerebral blast device without experiencing a blast. The rats were subjected to craniocerebral blast injury through a blast equivalent to 400 mg of trinitrotoluene using an electric detonator. Biomechanical parameters, and physical and behavioural changes of the sagittal head swing were measured using a high-speed camera. Magnetic resonance imaging (MRI) scans were conducted at 2, 12, 24 and 48 h after craniocerebral injury, only the experimental group indicated brain stem injury. The rats were sacrificed immediately following the MRI at 48 h for pathological examination of the brain stem using haematoxylin and eosin staining. The results indicated that 14 rats (87.5%) in the experimental group exhibited blast DAI, while no DAI was observed in the control and sham control groups, and the difference between the groups was significant (P<0.05). The present results indicated that this experimental design may serve to provide a stable model of blast DAI in rats. D.A. Spandidos 2018-07 2018-05-10 /pmc/articles/PMC6030930/ /pubmed/29977358 http://dx.doi.org/10.3892/etm.2018.6146 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Zhang, Jun-Hai Gu, Jian-Wen Li, Bing-Cang Gao, Fa-Bao Liao, Xiao-Ming Cui, Shao-Jie Establishment of a novel rat model of blast-related diffuse axonal injury |
title | Establishment of a novel rat model of blast-related diffuse axonal injury |
title_full | Establishment of a novel rat model of blast-related diffuse axonal injury |
title_fullStr | Establishment of a novel rat model of blast-related diffuse axonal injury |
title_full_unstemmed | Establishment of a novel rat model of blast-related diffuse axonal injury |
title_short | Establishment of a novel rat model of blast-related diffuse axonal injury |
title_sort | establishment of a novel rat model of blast-related diffuse axonal injury |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030930/ https://www.ncbi.nlm.nih.gov/pubmed/29977358 http://dx.doi.org/10.3892/etm.2018.6146 |
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