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Unconventional animal models for traumatic brain injury and chronic traumatic encephalopathy

Traumatic brain injury (TBI) is one of the main causes of death worldwide. It is a complex injury that influences cellular physiology, causes neuronal cell death, and affects molecular pathways in the brain. This in turn can result in sensory, motor, and behavioral alterations that deeply impact the...

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Autores principales: Ackermans, Nicole L., Varghese, Merina, Wicinski, Bridget, Torres, Joshua, De Gasperi, Rita, Pryor, Dylan, Elder, Gregory A., Gama Sosa, Miguel A., Reidenberg, Joy S., Williams, Terrie M., Hof, Patrick R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596618/
https://www.ncbi.nlm.nih.gov/pubmed/34255876
http://dx.doi.org/10.1002/jnr.24920
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author Ackermans, Nicole L.
Varghese, Merina
Wicinski, Bridget
Torres, Joshua
De Gasperi, Rita
Pryor, Dylan
Elder, Gregory A.
Gama Sosa, Miguel A.
Reidenberg, Joy S.
Williams, Terrie M.
Hof, Patrick R.
author_facet Ackermans, Nicole L.
Varghese, Merina
Wicinski, Bridget
Torres, Joshua
De Gasperi, Rita
Pryor, Dylan
Elder, Gregory A.
Gama Sosa, Miguel A.
Reidenberg, Joy S.
Williams, Terrie M.
Hof, Patrick R.
author_sort Ackermans, Nicole L.
collection PubMed
description Traumatic brain injury (TBI) is one of the main causes of death worldwide. It is a complex injury that influences cellular physiology, causes neuronal cell death, and affects molecular pathways in the brain. This in turn can result in sensory, motor, and behavioral alterations that deeply impact the quality of life. Repetitive mild TBI can progress into chronic traumatic encephalopathy (CTE), a neurodegenerative condition linked to severe behavioral changes. While current animal models of TBI and CTE such as rodents, are useful to explore affected pathways, clinical findings therein have rarely translated into clinical applications, possibly because of the many morphofunctional differences between the model animals and humans. It is therefore important to complement these studies with alternative animal models that may better replicate the individuality of human TBI. Comparative studies in animals with naturally evolved brain protection such as bighorn sheep, woodpeckers, and whales, may provide preventive applications in humans. The advantages of an in‐depth study of these unconventional animals are threefold. First, to increase knowledge of the often‐understudied species in question; second, to improve common animal models based on the study of their extreme counterparts; and finally, to tap into a source of biological inspiration for comparative studies and translational applications in humans.
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spelling pubmed-85966182021-11-22 Unconventional animal models for traumatic brain injury and chronic traumatic encephalopathy Ackermans, Nicole L. Varghese, Merina Wicinski, Bridget Torres, Joshua De Gasperi, Rita Pryor, Dylan Elder, Gregory A. Gama Sosa, Miguel A. Reidenberg, Joy S. Williams, Terrie M. Hof, Patrick R. J Neurosci Res Reviews Traumatic brain injury (TBI) is one of the main causes of death worldwide. It is a complex injury that influences cellular physiology, causes neuronal cell death, and affects molecular pathways in the brain. This in turn can result in sensory, motor, and behavioral alterations that deeply impact the quality of life. Repetitive mild TBI can progress into chronic traumatic encephalopathy (CTE), a neurodegenerative condition linked to severe behavioral changes. While current animal models of TBI and CTE such as rodents, are useful to explore affected pathways, clinical findings therein have rarely translated into clinical applications, possibly because of the many morphofunctional differences between the model animals and humans. It is therefore important to complement these studies with alternative animal models that may better replicate the individuality of human TBI. Comparative studies in animals with naturally evolved brain protection such as bighorn sheep, woodpeckers, and whales, may provide preventive applications in humans. The advantages of an in‐depth study of these unconventional animals are threefold. First, to increase knowledge of the often‐understudied species in question; second, to improve common animal models based on the study of their extreme counterparts; and finally, to tap into a source of biological inspiration for comparative studies and translational applications in humans. John Wiley and Sons Inc. 2021-07-13 2021-10 /pmc/articles/PMC8596618/ /pubmed/34255876 http://dx.doi.org/10.1002/jnr.24920 Text en © 2021 The Authors. Journal of Neuroscience Research published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, 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 Reviews
Ackermans, Nicole L.
Varghese, Merina
Wicinski, Bridget
Torres, Joshua
De Gasperi, Rita
Pryor, Dylan
Elder, Gregory A.
Gama Sosa, Miguel A.
Reidenberg, Joy S.
Williams, Terrie M.
Hof, Patrick R.
Unconventional animal models for traumatic brain injury and chronic traumatic encephalopathy
title Unconventional animal models for traumatic brain injury and chronic traumatic encephalopathy
title_full Unconventional animal models for traumatic brain injury and chronic traumatic encephalopathy
title_fullStr Unconventional animal models for traumatic brain injury and chronic traumatic encephalopathy
title_full_unstemmed Unconventional animal models for traumatic brain injury and chronic traumatic encephalopathy
title_short Unconventional animal models for traumatic brain injury and chronic traumatic encephalopathy
title_sort unconventional animal models for traumatic brain injury and chronic traumatic encephalopathy
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596618/
https://www.ncbi.nlm.nih.gov/pubmed/34255876
http://dx.doi.org/10.1002/jnr.24920
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