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The Promise of Neuroprotective Agents in Parkinson’s Disease

Parkinson’s disease (PD) is characterized by loss of dopamine neurons in the substantia nigra of the brain. Since there are limited treatment options for PD, neuroprotective agents are currently being tested as a means to slow disease progression. Agents targeting oxidative stress, mitochondrial dys...

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Detalles Bibliográficos
Autores principales: Seidl, Stacey E., Potashkin, Judith A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221408/
https://www.ncbi.nlm.nih.gov/pubmed/22125548
http://dx.doi.org/10.3389/fneur.2011.00068
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author Seidl, Stacey E.
Potashkin, Judith A.
author_facet Seidl, Stacey E.
Potashkin, Judith A.
author_sort Seidl, Stacey E.
collection PubMed
description Parkinson’s disease (PD) is characterized by loss of dopamine neurons in the substantia nigra of the brain. Since there are limited treatment options for PD, neuroprotective agents are currently being tested as a means to slow disease progression. Agents targeting oxidative stress, mitochondrial dysfunction, and inflammation are prime candidates for neuroprotection. This review identifies Rasagiline, Minocycline, and creatine, as the most promising neuroprotective agents for PD, and they are all currently in phase III trials. Other agents possessing protective characteristics in delaying PD include stimulants, vitamins, supplements, and other drugs. Additionally, combination therapies also show benefits in slowing PD progression. The identification of neuroprotective agents for PD provides us with therapeutic opportunities for modifying the course of disease progression and, perhaps, reducing the risk of onset when preclinical biomarkers become available.
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spelling pubmed-32214082011-11-28 The Promise of Neuroprotective Agents in Parkinson’s Disease Seidl, Stacey E. Potashkin, Judith A. Front Neurol Neuroscience Parkinson’s disease (PD) is characterized by loss of dopamine neurons in the substantia nigra of the brain. Since there are limited treatment options for PD, neuroprotective agents are currently being tested as a means to slow disease progression. Agents targeting oxidative stress, mitochondrial dysfunction, and inflammation are prime candidates for neuroprotection. This review identifies Rasagiline, Minocycline, and creatine, as the most promising neuroprotective agents for PD, and they are all currently in phase III trials. Other agents possessing protective characteristics in delaying PD include stimulants, vitamins, supplements, and other drugs. Additionally, combination therapies also show benefits in slowing PD progression. The identification of neuroprotective agents for PD provides us with therapeutic opportunities for modifying the course of disease progression and, perhaps, reducing the risk of onset when preclinical biomarkers become available. Frontiers Research Foundation 2011-11-21 /pmc/articles/PMC3221408/ /pubmed/22125548 http://dx.doi.org/10.3389/fneur.2011.00068 Text en Copyright © 2011 Seidl and Potashkin. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Neuroscience
Seidl, Stacey E.
Potashkin, Judith A.
The Promise of Neuroprotective Agents in Parkinson’s Disease
title The Promise of Neuroprotective Agents in Parkinson’s Disease
title_full The Promise of Neuroprotective Agents in Parkinson’s Disease
title_fullStr The Promise of Neuroprotective Agents in Parkinson’s Disease
title_full_unstemmed The Promise of Neuroprotective Agents in Parkinson’s Disease
title_short The Promise of Neuroprotective Agents in Parkinson’s Disease
title_sort promise of neuroprotective agents in parkinson’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221408/
https://www.ncbi.nlm.nih.gov/pubmed/22125548
http://dx.doi.org/10.3389/fneur.2011.00068
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