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Recent Preclinical Insights Into the Treatment of Chronic Traumatic Encephalopathy

Chronic traumatic encephalopathy (CTE) is a neurodegenerative condition associated with significant mortality and morbidity. The central pathophysiological mechanisms by which repetitive cranial injury results in the neurodegeneration of CTE are poorly understood. Current well-established working mo...

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Autores principales: Breen, Patrick W., Krishnan, Vaishnav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381336/
https://www.ncbi.nlm.nih.gov/pubmed/32774238
http://dx.doi.org/10.3389/fnins.2020.00616
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author Breen, Patrick W.
Krishnan, Vaishnav
author_facet Breen, Patrick W.
Krishnan, Vaishnav
author_sort Breen, Patrick W.
collection PubMed
description Chronic traumatic encephalopathy (CTE) is a neurodegenerative condition associated with significant mortality and morbidity. The central pathophysiological mechanisms by which repetitive cranial injury results in the neurodegeneration of CTE are poorly understood. Current well-established working models emphasize a central role for trauma-induced excessive phosphorylation and accumulation of insoluble tangles of Tau protein. In this review, we summarize recent data from preclinical animal models of CTE where a series of candidate treatments have been carefully evaluated, including kinase inhibitors, antibody therapy, and anti-inflammatory therapies. We discuss the overall translational potential of these approaches and provide recommendations for future bench-to-bedside treatment strategies.
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spelling pubmed-73813362020-08-06 Recent Preclinical Insights Into the Treatment of Chronic Traumatic Encephalopathy Breen, Patrick W. Krishnan, Vaishnav Front Neurosci Neuroscience Chronic traumatic encephalopathy (CTE) is a neurodegenerative condition associated with significant mortality and morbidity. The central pathophysiological mechanisms by which repetitive cranial injury results in the neurodegeneration of CTE are poorly understood. Current well-established working models emphasize a central role for trauma-induced excessive phosphorylation and accumulation of insoluble tangles of Tau protein. In this review, we summarize recent data from preclinical animal models of CTE where a series of candidate treatments have been carefully evaluated, including kinase inhibitors, antibody therapy, and anti-inflammatory therapies. We discuss the overall translational potential of these approaches and provide recommendations for future bench-to-bedside treatment strategies. Frontiers Media S.A. 2020-07-07 /pmc/articles/PMC7381336/ /pubmed/32774238 http://dx.doi.org/10.3389/fnins.2020.00616 Text en Copyright © 2020 Breen and Krishnan. 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 Neuroscience
Breen, Patrick W.
Krishnan, Vaishnav
Recent Preclinical Insights Into the Treatment of Chronic Traumatic Encephalopathy
title Recent Preclinical Insights Into the Treatment of Chronic Traumatic Encephalopathy
title_full Recent Preclinical Insights Into the Treatment of Chronic Traumatic Encephalopathy
title_fullStr Recent Preclinical Insights Into the Treatment of Chronic Traumatic Encephalopathy
title_full_unstemmed Recent Preclinical Insights Into the Treatment of Chronic Traumatic Encephalopathy
title_short Recent Preclinical Insights Into the Treatment of Chronic Traumatic Encephalopathy
title_sort recent preclinical insights into the treatment of chronic traumatic encephalopathy
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381336/
https://www.ncbi.nlm.nih.gov/pubmed/32774238
http://dx.doi.org/10.3389/fnins.2020.00616
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