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Cerium Oxide Nanoparticles Improve Outcome after In Vitro and In Vivo Mild Traumatic Brain Injury

Mild traumatic brain injury results in aberrant free radical generation, which is associated with oxidative stress, secondary injury signaling cascades, mitochondrial dysfunction, and poor functional outcome. Pharmacological targeting of free radicals with antioxidants has been examined as an approa...

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Autores principales: Bailey, Zachary S., Nilson, Eric, Bates, John A., Oyalowo, Adewole, Hockey, Kevin S., Sajja, Venkata Siva Sai Sujith, Thorpe, Chevon, Rogers, Heidi, Dunn, Bryce, Frey, Aaron S., Billings, Marc J., Sholar, Christopher A., Hermundstad, Amy, Kumar, Challa, VandeVord, Pamela J., Rzigalinski, Beverly A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249477/
https://www.ncbi.nlm.nih.gov/pubmed/27733104
http://dx.doi.org/10.1089/neu.2016.4644
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author Bailey, Zachary S.
Nilson, Eric
Bates, John A.
Oyalowo, Adewole
Hockey, Kevin S.
Sajja, Venkata Siva Sai Sujith
Thorpe, Chevon
Rogers, Heidi
Dunn, Bryce
Frey, Aaron S.
Billings, Marc J.
Sholar, Christopher A.
Hermundstad, Amy
Kumar, Challa
VandeVord, Pamela J.
Rzigalinski, Beverly A.
author_facet Bailey, Zachary S.
Nilson, Eric
Bates, John A.
Oyalowo, Adewole
Hockey, Kevin S.
Sajja, Venkata Siva Sai Sujith
Thorpe, Chevon
Rogers, Heidi
Dunn, Bryce
Frey, Aaron S.
Billings, Marc J.
Sholar, Christopher A.
Hermundstad, Amy
Kumar, Challa
VandeVord, Pamela J.
Rzigalinski, Beverly A.
author_sort Bailey, Zachary S.
collection PubMed
description Mild traumatic brain injury results in aberrant free radical generation, which is associated with oxidative stress, secondary injury signaling cascades, mitochondrial dysfunction, and poor functional outcome. Pharmacological targeting of free radicals with antioxidants has been examined as an approach to treatment, but has met with limited success in clinical trials. Conventional antioxidants that are currently available scavenge a single free radical before they are destroyed in the process. Here, we report for the first time that a novel regenerative cerium oxide nanoparticle antioxidant reduces neuronal death and calcium dysregulation after in vitro trauma. Further, using an in vivo model of mild lateral fluid percussion brain injury in the rat, we report that cerium oxide nanoparticles also preserve endogenous antioxidant systems, decrease macromolecular free radical damage, and improve cognitive function. Taken together, our results demonstrate that cerium oxide nanoparticles are a novel nanopharmaceutical with potential for mitigating neuropathological effects of mild traumatic brain injury and modifying the course of recovery.
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spelling pubmed-72494772020-05-27 Cerium Oxide Nanoparticles Improve Outcome after In Vitro and In Vivo Mild Traumatic Brain Injury Bailey, Zachary S. Nilson, Eric Bates, John A. Oyalowo, Adewole Hockey, Kevin S. Sajja, Venkata Siva Sai Sujith Thorpe, Chevon Rogers, Heidi Dunn, Bryce Frey, Aaron S. Billings, Marc J. Sholar, Christopher A. Hermundstad, Amy Kumar, Challa VandeVord, Pamela J. Rzigalinski, Beverly A. J Neurotrauma Original Articles Mild traumatic brain injury results in aberrant free radical generation, which is associated with oxidative stress, secondary injury signaling cascades, mitochondrial dysfunction, and poor functional outcome. Pharmacological targeting of free radicals with antioxidants has been examined as an approach to treatment, but has met with limited success in clinical trials. Conventional antioxidants that are currently available scavenge a single free radical before they are destroyed in the process. Here, we report for the first time that a novel regenerative cerium oxide nanoparticle antioxidant reduces neuronal death and calcium dysregulation after in vitro trauma. Further, using an in vivo model of mild lateral fluid percussion brain injury in the rat, we report that cerium oxide nanoparticles also preserve endogenous antioxidant systems, decrease macromolecular free radical damage, and improve cognitive function. Taken together, our results demonstrate that cerium oxide nanoparticles are a novel nanopharmaceutical with potential for mitigating neuropathological effects of mild traumatic brain injury and modifying the course of recovery. Mary Ann Liebert, Inc., publishers 2020-06-15 2020-05-27 /pmc/articles/PMC7249477/ /pubmed/27733104 http://dx.doi.org/10.1089/neu.2016.4644 Text en © Zachary S. Bailey, et al., 2020; 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
Bailey, Zachary S.
Nilson, Eric
Bates, John A.
Oyalowo, Adewole
Hockey, Kevin S.
Sajja, Venkata Siva Sai Sujith
Thorpe, Chevon
Rogers, Heidi
Dunn, Bryce
Frey, Aaron S.
Billings, Marc J.
Sholar, Christopher A.
Hermundstad, Amy
Kumar, Challa
VandeVord, Pamela J.
Rzigalinski, Beverly A.
Cerium Oxide Nanoparticles Improve Outcome after In Vitro and In Vivo Mild Traumatic Brain Injury
title Cerium Oxide Nanoparticles Improve Outcome after In Vitro and In Vivo Mild Traumatic Brain Injury
title_full Cerium Oxide Nanoparticles Improve Outcome after In Vitro and In Vivo Mild Traumatic Brain Injury
title_fullStr Cerium Oxide Nanoparticles Improve Outcome after In Vitro and In Vivo Mild Traumatic Brain Injury
title_full_unstemmed Cerium Oxide Nanoparticles Improve Outcome after In Vitro and In Vivo Mild Traumatic Brain Injury
title_short Cerium Oxide Nanoparticles Improve Outcome after In Vitro and In Vivo Mild Traumatic Brain Injury
title_sort cerium oxide nanoparticles improve outcome after in vitro and in vivo mild traumatic brain injury
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249477/
https://www.ncbi.nlm.nih.gov/pubmed/27733104
http://dx.doi.org/10.1089/neu.2016.4644
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