Advances in non-dopaminergic pharmacological treatments of Parkinson's disease

Since the 1960’s treatments for Parkinson's disease (PD) have traditionally been directed to effectively restore or replace dopamine, with L-Dopa the gold standard. However, chronic L-Dopa use is associated with debilitating dyskinesias, limiting its effectiveness. This has created a need to de...

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Main Authors: Sandy eStayte, Bryce eVissel
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-05-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnins.2014.00113/full
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spelling doaj-f67b026b70124b85a6d4f27199d0e3812020-11-25T00:11:37ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2014-05-01810.3389/fnins.2014.0011386044Advances in non-dopaminergic pharmacological treatments of Parkinson's diseaseSandy eStayte0Sandy eStayte1Bryce eVissel2Bryce eVissel3Garvan Institute of Medical ResearchUNSW AustraliaGarvan Institute of Medical ResearchUNSW AustraliaSince the 1960’s treatments for Parkinson's disease (PD) have traditionally been directed to effectively restore or replace dopamine, with L-Dopa the gold standard. However, chronic L-Dopa use is associated with debilitating dyskinesias, limiting its effectiveness. This has created a need to develop new therapies that work in ways other than restoring or replacing dopamine. We provide a comprehensive overview of the emerging non-dopaminergic pharmacological treatments including drugs targeting adenosine, glutamate, adrenergic, and serotonin receptors, as well as GLP-1 agonists, calcium channel blockers, iron chelators, anti-inflammatories, neurotrophic factors and gene therapy, with a detailed overview of their success in animal models and their translation to human clinical trials. We suggest that further developments in the identification of novel therapeutics, particularly those offering disease-modifying effects, will consistently be met with challenges until improvements in clinical trial design and advances in understanding the basic science of PD are made. We consider how developments in genetics, the possibility that PD may consist of multiple disease states, and potential etiology in non-dopaminergic regions will influence drug development. We conclude that despite the challenges ahead patients have much cause for optimism that novel therapeutics that offer better disease management and/or which slow disease progression are inevitable.http://journal.frontiersin.org/Journal/10.3389/fnins.2014.00113/fullDopamineDyskinesiasGene TherapyTherapeuticsL-DopaParkinson's disease
collection DOAJ
language English
format Article
sources DOAJ
author Sandy eStayte
Sandy eStayte
Bryce eVissel
Bryce eVissel
spellingShingle Sandy eStayte
Sandy eStayte
Bryce eVissel
Bryce eVissel
Advances in non-dopaminergic pharmacological treatments of Parkinson's disease
Frontiers in Neuroscience
Dopamine
Dyskinesias
Gene Therapy
Therapeutics
L-Dopa
Parkinson's disease
author_facet Sandy eStayte
Sandy eStayte
Bryce eVissel
Bryce eVissel
author_sort Sandy eStayte
title Advances in non-dopaminergic pharmacological treatments of Parkinson's disease
title_short Advances in non-dopaminergic pharmacological treatments of Parkinson's disease
title_full Advances in non-dopaminergic pharmacological treatments of Parkinson's disease
title_fullStr Advances in non-dopaminergic pharmacological treatments of Parkinson's disease
title_full_unstemmed Advances in non-dopaminergic pharmacological treatments of Parkinson's disease
title_sort advances in non-dopaminergic pharmacological treatments of parkinson's disease
publisher Frontiers Media S.A.
series Frontiers in Neuroscience
issn 1662-453X
publishDate 2014-05-01
description Since the 1960’s treatments for Parkinson's disease (PD) have traditionally been directed to effectively restore or replace dopamine, with L-Dopa the gold standard. However, chronic L-Dopa use is associated with debilitating dyskinesias, limiting its effectiveness. This has created a need to develop new therapies that work in ways other than restoring or replacing dopamine. We provide a comprehensive overview of the emerging non-dopaminergic pharmacological treatments including drugs targeting adenosine, glutamate, adrenergic, and serotonin receptors, as well as GLP-1 agonists, calcium channel blockers, iron chelators, anti-inflammatories, neurotrophic factors and gene therapy, with a detailed overview of their success in animal models and their translation to human clinical trials. We suggest that further developments in the identification of novel therapeutics, particularly those offering disease-modifying effects, will consistently be met with challenges until improvements in clinical trial design and advances in understanding the basic science of PD are made. We consider how developments in genetics, the possibility that PD may consist of multiple disease states, and potential etiology in non-dopaminergic regions will influence drug development. We conclude that despite the challenges ahead patients have much cause for optimism that novel therapeutics that offer better disease management and/or which slow disease progression are inevitable.
topic Dopamine
Dyskinesias
Gene Therapy
Therapeutics
L-Dopa
Parkinson's disease
url http://journal.frontiersin.org/Journal/10.3389/fnins.2014.00113/full
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