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Promising cannabinoid-based therapies for Parkinson’s disease: motor symptoms to neuroprotection

Parkinson’s disease (PD) is a slow insidious neurological disorder characterized by a loss of dopaminergic neurons in the midbrain. Although several recent preclinical advances have proposed to treat PD, there is hardly any clinically proved new therapeutic for its cure. Increasing evidence suggests...

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Autores principales: More, Sandeep Vasant, Choi, Dong-Kug
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404240/
https://www.ncbi.nlm.nih.gov/pubmed/25888232
http://dx.doi.org/10.1186/s13024-015-0012-0
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author More, Sandeep Vasant
Choi, Dong-Kug
author_facet More, Sandeep Vasant
Choi, Dong-Kug
author_sort More, Sandeep Vasant
collection PubMed
description Parkinson’s disease (PD) is a slow insidious neurological disorder characterized by a loss of dopaminergic neurons in the midbrain. Although several recent preclinical advances have proposed to treat PD, there is hardly any clinically proved new therapeutic for its cure. Increasing evidence suggests a prominent modulatory function of the cannabinoid signaling system in the basal ganglia. Hence, use of cannabinoids as a new therapeutic target has been recommended as a promising therapy for PD. The elements of the endocannabinoid system are highly expressed in the neural circuit of basal ganglia wherein they bidirectionally interact with dopaminergic, glutamatergic, and GABAergic signaling systems. As the cannabinoid signaling system undergoes a biphasic pattern of change during progression of PD, it explains the motor inhibition typically observed in patients with PD. Cannabinoid agonists such as WIN-55,212-2 have been demonstrated experimentally as neuroprotective agents in PD, with respect to their ability to suppress excitotoxicity, glial activation, and oxidative injury that causes degeneration of dopaminergic neurons. Additional benefits provided by cannabinoid related compounds including CE-178253, oleoylethanolamide, nabilone and HU-210 have been reported to possess efficacy against bradykinesia and levodopa-induced dyskinesia in PD. Despite promising preclinical studies for PD, use of cannabinoids has not been studied extensively at the clinical level. In this review, we reassess the existing evidence suggesting involvement of the endocannabinoid system in the cause, symptomatology, and treatment of PD. We will try to identify future threads of research that will help in the understanding of the potential therapeutic benefits of the cannabinoid system for treating PD.
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spelling pubmed-44042402015-04-21 Promising cannabinoid-based therapies for Parkinson’s disease: motor symptoms to neuroprotection More, Sandeep Vasant Choi, Dong-Kug Mol Neurodegener Review Parkinson’s disease (PD) is a slow insidious neurological disorder characterized by a loss of dopaminergic neurons in the midbrain. Although several recent preclinical advances have proposed to treat PD, there is hardly any clinically proved new therapeutic for its cure. Increasing evidence suggests a prominent modulatory function of the cannabinoid signaling system in the basal ganglia. Hence, use of cannabinoids as a new therapeutic target has been recommended as a promising therapy for PD. The elements of the endocannabinoid system are highly expressed in the neural circuit of basal ganglia wherein they bidirectionally interact with dopaminergic, glutamatergic, and GABAergic signaling systems. As the cannabinoid signaling system undergoes a biphasic pattern of change during progression of PD, it explains the motor inhibition typically observed in patients with PD. Cannabinoid agonists such as WIN-55,212-2 have been demonstrated experimentally as neuroprotective agents in PD, with respect to their ability to suppress excitotoxicity, glial activation, and oxidative injury that causes degeneration of dopaminergic neurons. Additional benefits provided by cannabinoid related compounds including CE-178253, oleoylethanolamide, nabilone and HU-210 have been reported to possess efficacy against bradykinesia and levodopa-induced dyskinesia in PD. Despite promising preclinical studies for PD, use of cannabinoids has not been studied extensively at the clinical level. In this review, we reassess the existing evidence suggesting involvement of the endocannabinoid system in the cause, symptomatology, and treatment of PD. We will try to identify future threads of research that will help in the understanding of the potential therapeutic benefits of the cannabinoid system for treating PD. BioMed Central 2015-04-08 /pmc/articles/PMC4404240/ /pubmed/25888232 http://dx.doi.org/10.1186/s13024-015-0012-0 Text en © More and Choi; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
More, Sandeep Vasant
Choi, Dong-Kug
Promising cannabinoid-based therapies for Parkinson’s disease: motor symptoms to neuroprotection
title Promising cannabinoid-based therapies for Parkinson’s disease: motor symptoms to neuroprotection
title_full Promising cannabinoid-based therapies for Parkinson’s disease: motor symptoms to neuroprotection
title_fullStr Promising cannabinoid-based therapies for Parkinson’s disease: motor symptoms to neuroprotection
title_full_unstemmed Promising cannabinoid-based therapies for Parkinson’s disease: motor symptoms to neuroprotection
title_short Promising cannabinoid-based therapies for Parkinson’s disease: motor symptoms to neuroprotection
title_sort promising cannabinoid-based therapies for parkinson’s disease: motor symptoms to neuroprotection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404240/
https://www.ncbi.nlm.nih.gov/pubmed/25888232
http://dx.doi.org/10.1186/s13024-015-0012-0
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