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A Comprehensive Review of Experimental Rodent Models of Repeated Blast TBI

We reviewed the relevant literature delineating advances in the development of the experimental models of repeated blast TBI (rbTBI). It appears this subject is a relatively unexplored area considering the first work published in 2007 and the bulk of peer-reviewed papers was published post-2011. The...

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Autores principales: Skotak, Maciej, Townsend, Molly T., Ramarao, Kakulavarapu V., Chandra, Namas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776622/
https://www.ncbi.nlm.nih.gov/pubmed/31611839
http://dx.doi.org/10.3389/fneur.2019.01015
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author Skotak, Maciej
Townsend, Molly T.
Ramarao, Kakulavarapu V.
Chandra, Namas
author_facet Skotak, Maciej
Townsend, Molly T.
Ramarao, Kakulavarapu V.
Chandra, Namas
author_sort Skotak, Maciej
collection PubMed
description We reviewed the relevant literature delineating advances in the development of the experimental models of repeated blast TBI (rbTBI). It appears this subject is a relatively unexplored area considering the first work published in 2007 and the bulk of peer-reviewed papers was published post-2011. There are merely 34 papers published to date utilizing rodent rbTBI models. We performed an analysis and extracted basic parameters to capture the characteristics of the exposure conditions (the blast intensity, inter-exposure interval and the number of exposures), the age and weight of the animal models most commonly used in the studies, and their endpoints. Our analysis revealed three strains of rodents are predominantly used: Sprague Dawley and Long Evans rats and wild type (C57BL/6J) mice, and young adult animals 8 to 12-week-old are a preferred choice. Typical exposure conditions are the following: (1) peak overpressure in the 27–145 kPa (4–21 psi) range, (2) number of exposures: 2 (13.9%), 3 (63.9%), 5 (16.7%), or 12 (5.6%) with a single exposure used for a baseline comparison in 41.24% of the studies. Two inter-exposure interval durations were used: (1) short (1–30 min.) and (2) extended (24 h) between consecutive shock wave exposures. The experiments included characterization of repeated blast exposure effects on auditory, ocular and neurological function, with a focus on brain etiology in most of the published work. We present an overview of major histopathological findings, which are supplemented by studies implementing MRI (DTI) and behavioral changes after rbTBI in the acute (1–7 days post-injury), subacute (7–14 days), and chronic (>14 days) phases post-injury.
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spelling pubmed-67766222019-10-14 A Comprehensive Review of Experimental Rodent Models of Repeated Blast TBI Skotak, Maciej Townsend, Molly T. Ramarao, Kakulavarapu V. Chandra, Namas Front Neurol Neurology We reviewed the relevant literature delineating advances in the development of the experimental models of repeated blast TBI (rbTBI). It appears this subject is a relatively unexplored area considering the first work published in 2007 and the bulk of peer-reviewed papers was published post-2011. There are merely 34 papers published to date utilizing rodent rbTBI models. We performed an analysis and extracted basic parameters to capture the characteristics of the exposure conditions (the blast intensity, inter-exposure interval and the number of exposures), the age and weight of the animal models most commonly used in the studies, and their endpoints. Our analysis revealed three strains of rodents are predominantly used: Sprague Dawley and Long Evans rats and wild type (C57BL/6J) mice, and young adult animals 8 to 12-week-old are a preferred choice. Typical exposure conditions are the following: (1) peak overpressure in the 27–145 kPa (4–21 psi) range, (2) number of exposures: 2 (13.9%), 3 (63.9%), 5 (16.7%), or 12 (5.6%) with a single exposure used for a baseline comparison in 41.24% of the studies. Two inter-exposure interval durations were used: (1) short (1–30 min.) and (2) extended (24 h) between consecutive shock wave exposures. The experiments included characterization of repeated blast exposure effects on auditory, ocular and neurological function, with a focus on brain etiology in most of the published work. We present an overview of major histopathological findings, which are supplemented by studies implementing MRI (DTI) and behavioral changes after rbTBI in the acute (1–7 days post-injury), subacute (7–14 days), and chronic (>14 days) phases post-injury. Frontiers Media S.A. 2019-09-27 /pmc/articles/PMC6776622/ /pubmed/31611839 http://dx.doi.org/10.3389/fneur.2019.01015 Text en Copyright © 2019 Skotak, Townsend, Ramarao and Chandra. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Skotak, Maciej
Townsend, Molly T.
Ramarao, Kakulavarapu V.
Chandra, Namas
A Comprehensive Review of Experimental Rodent Models of Repeated Blast TBI
title A Comprehensive Review of Experimental Rodent Models of Repeated Blast TBI
title_full A Comprehensive Review of Experimental Rodent Models of Repeated Blast TBI
title_fullStr A Comprehensive Review of Experimental Rodent Models of Repeated Blast TBI
title_full_unstemmed A Comprehensive Review of Experimental Rodent Models of Repeated Blast TBI
title_short A Comprehensive Review of Experimental Rodent Models of Repeated Blast TBI
title_sort comprehensive review of experimental rodent models of repeated blast tbi
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776622/
https://www.ncbi.nlm.nih.gov/pubmed/31611839
http://dx.doi.org/10.3389/fneur.2019.01015
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