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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2020
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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. |
format | Online Article Text |
id | pubmed-7249477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
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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