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Therapeutic potential of systemic brain rejuvenation strategies for neurodegenerative disease

Neurodegenerative diseases are a devastating group of conditions that cause progressive loss of neuronal integrity, affecting cognitive and motor functioning in an ever-increasing number of older individuals. Attempts to slow neurodegenerative disease advancement have met with little success in the...

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Autores principales: Horowitz, Alana M., Villeda, Saul A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539850/
https://www.ncbi.nlm.nih.gov/pubmed/28815019
http://dx.doi.org/10.12688/f1000research.11437.1
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author Horowitz, Alana M.
Villeda, Saul A.
author_facet Horowitz, Alana M.
Villeda, Saul A.
author_sort Horowitz, Alana M.
collection PubMed
description Neurodegenerative diseases are a devastating group of conditions that cause progressive loss of neuronal integrity, affecting cognitive and motor functioning in an ever-increasing number of older individuals. Attempts to slow neurodegenerative disease advancement have met with little success in the clinic; however, a new therapeutic approach may stem from classic interventions, such as caloric restriction, exercise, and parabiosis. For decades, researchers have reported that these systemic-level manipulations can promote major functional changes that extend organismal lifespan and healthspan. Only recently, however, have the functional effects of these interventions on the brain begun to be appreciated at a molecular and cellular level. The potential to counteract the effects of aging in the brain, in effect rejuvenating the aged brain, could offer broad therapeutic potential to combat dementia-related neurodegenerative disease in the elderly. In particular, results from heterochronic parabiosis and young plasma administration studies indicate that pro-aging and rejuvenating factors exist in the circulation that can independently promote or reverse age-related phenotypes. The recent demonstration that human umbilical cord blood similarly functions to rejuvenate the aged brain further advances this work to clinical translation. In this review, we focus on these blood-based rejuvenation strategies and their capacity to delay age-related molecular and functional decline in the aging brain. We discuss new findings that extend the beneficial effects of young blood to neurodegenerative disease models. Lastly, we explore the translational potential of blood-based interventions, highlighting current clinical trials aimed at addressing therapeutic applications for the treatment of dementia-related neurodegenerative disease in humans.
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spelling pubmed-55398502017-08-15 Therapeutic potential of systemic brain rejuvenation strategies for neurodegenerative disease Horowitz, Alana M. Villeda, Saul A. F1000Res Review Neurodegenerative diseases are a devastating group of conditions that cause progressive loss of neuronal integrity, affecting cognitive and motor functioning in an ever-increasing number of older individuals. Attempts to slow neurodegenerative disease advancement have met with little success in the clinic; however, a new therapeutic approach may stem from classic interventions, such as caloric restriction, exercise, and parabiosis. For decades, researchers have reported that these systemic-level manipulations can promote major functional changes that extend organismal lifespan and healthspan. Only recently, however, have the functional effects of these interventions on the brain begun to be appreciated at a molecular and cellular level. The potential to counteract the effects of aging in the brain, in effect rejuvenating the aged brain, could offer broad therapeutic potential to combat dementia-related neurodegenerative disease in the elderly. In particular, results from heterochronic parabiosis and young plasma administration studies indicate that pro-aging and rejuvenating factors exist in the circulation that can independently promote or reverse age-related phenotypes. The recent demonstration that human umbilical cord blood similarly functions to rejuvenate the aged brain further advances this work to clinical translation. In this review, we focus on these blood-based rejuvenation strategies and their capacity to delay age-related molecular and functional decline in the aging brain. We discuss new findings that extend the beneficial effects of young blood to neurodegenerative disease models. Lastly, we explore the translational potential of blood-based interventions, highlighting current clinical trials aimed at addressing therapeutic applications for the treatment of dementia-related neurodegenerative disease in humans. F1000Research 2017-08-01 /pmc/articles/PMC5539850/ /pubmed/28815019 http://dx.doi.org/10.12688/f1000research.11437.1 Text en Copyright: © 2017 Horowitz AM and Villeda SA http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Horowitz, Alana M.
Villeda, Saul A.
Therapeutic potential of systemic brain rejuvenation strategies for neurodegenerative disease
title Therapeutic potential of systemic brain rejuvenation strategies for neurodegenerative disease
title_full Therapeutic potential of systemic brain rejuvenation strategies for neurodegenerative disease
title_fullStr Therapeutic potential of systemic brain rejuvenation strategies for neurodegenerative disease
title_full_unstemmed Therapeutic potential of systemic brain rejuvenation strategies for neurodegenerative disease
title_short Therapeutic potential of systemic brain rejuvenation strategies for neurodegenerative disease
title_sort therapeutic potential of systemic brain rejuvenation strategies for neurodegenerative disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539850/
https://www.ncbi.nlm.nih.gov/pubmed/28815019
http://dx.doi.org/10.12688/f1000research.11437.1
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