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Revisiting Traumatic Brain Injury: From Molecular Mechanisms to Therapeutic Interventions
Studying the complex molecular mechanisms involved in traumatic brain injury (TBI) is crucial for developing new therapies for TBI. Current treatments for TBI are primarily focused on patient stabilization and symptom mitigation. However, the field lacks defined therapies to prevent cell death, oxid...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601301/ https://www.ncbi.nlm.nih.gov/pubmed/33003373 http://dx.doi.org/10.3390/biomedicines8100389 |
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author | Jarrahi, Abbas Braun, Molly Ahluwalia, Meenakshi Gupta, Rohan V. Wilson, Michael Munie, Stephanie Ahluwalia, Pankaj Vender, John R. Vale, Fernando L. Dhandapani, Krishnan M. Vaibhav, Kumar |
author_facet | Jarrahi, Abbas Braun, Molly Ahluwalia, Meenakshi Gupta, Rohan V. Wilson, Michael Munie, Stephanie Ahluwalia, Pankaj Vender, John R. Vale, Fernando L. Dhandapani, Krishnan M. Vaibhav, Kumar |
author_sort | Jarrahi, Abbas |
collection | PubMed |
description | Studying the complex molecular mechanisms involved in traumatic brain injury (TBI) is crucial for developing new therapies for TBI. Current treatments for TBI are primarily focused on patient stabilization and symptom mitigation. However, the field lacks defined therapies to prevent cell death, oxidative stress, and inflammatory cascades which lead to chronic pathology. Little can be done to treat the mechanical damage that occurs during the primary insult of a TBI; however, secondary injury mechanisms, such as inflammation, blood-brain barrier (BBB) breakdown, edema formation, excitotoxicity, oxidative stress, and cell death, can be targeted by therapeutic interventions. Elucidating the many mechanisms underlying secondary injury and studying targets of neuroprotective therapeutic agents is critical for developing new treatments. Therefore, we present a review on the molecular events following TBI from inflammation to programmed cell death and discuss current research and the latest therapeutic strategies to help understand TBI-mediated secondary injury. |
format | Online Article Text |
id | pubmed-7601301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76013012020-11-01 Revisiting Traumatic Brain Injury: From Molecular Mechanisms to Therapeutic Interventions Jarrahi, Abbas Braun, Molly Ahluwalia, Meenakshi Gupta, Rohan V. Wilson, Michael Munie, Stephanie Ahluwalia, Pankaj Vender, John R. Vale, Fernando L. Dhandapani, Krishnan M. Vaibhav, Kumar Biomedicines Review Studying the complex molecular mechanisms involved in traumatic brain injury (TBI) is crucial for developing new therapies for TBI. Current treatments for TBI are primarily focused on patient stabilization and symptom mitigation. However, the field lacks defined therapies to prevent cell death, oxidative stress, and inflammatory cascades which lead to chronic pathology. Little can be done to treat the mechanical damage that occurs during the primary insult of a TBI; however, secondary injury mechanisms, such as inflammation, blood-brain barrier (BBB) breakdown, edema formation, excitotoxicity, oxidative stress, and cell death, can be targeted by therapeutic interventions. Elucidating the many mechanisms underlying secondary injury and studying targets of neuroprotective therapeutic agents is critical for developing new treatments. Therefore, we present a review on the molecular events following TBI from inflammation to programmed cell death and discuss current research and the latest therapeutic strategies to help understand TBI-mediated secondary injury. MDPI 2020-09-29 /pmc/articles/PMC7601301/ /pubmed/33003373 http://dx.doi.org/10.3390/biomedicines8100389 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Jarrahi, Abbas Braun, Molly Ahluwalia, Meenakshi Gupta, Rohan V. Wilson, Michael Munie, Stephanie Ahluwalia, Pankaj Vender, John R. Vale, Fernando L. Dhandapani, Krishnan M. Vaibhav, Kumar Revisiting Traumatic Brain Injury: From Molecular Mechanisms to Therapeutic Interventions |
title | Revisiting Traumatic Brain Injury: From Molecular Mechanisms to Therapeutic Interventions |
title_full | Revisiting Traumatic Brain Injury: From Molecular Mechanisms to Therapeutic Interventions |
title_fullStr | Revisiting Traumatic Brain Injury: From Molecular Mechanisms to Therapeutic Interventions |
title_full_unstemmed | Revisiting Traumatic Brain Injury: From Molecular Mechanisms to Therapeutic Interventions |
title_short | Revisiting Traumatic Brain Injury: From Molecular Mechanisms to Therapeutic Interventions |
title_sort | revisiting traumatic brain injury: from molecular mechanisms to therapeutic interventions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601301/ https://www.ncbi.nlm.nih.gov/pubmed/33003373 http://dx.doi.org/10.3390/biomedicines8100389 |
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