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Neurophysiology of Drosophila Models of Parkinson's Disease

We provide an insight into the role Drosophila has played in elucidating neurophysiological perturbations associated with Parkinson's disease- (PD-) related genes. Synaptic signalling deficits are observed in motor, central, and sensory systems. Given the neurological impact of disease causing...

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Autores principales: West, Ryan J. H., Furmston, Rebecca, Williams, Charles A. C., Elliott, Christopher J. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414211/
https://www.ncbi.nlm.nih.gov/pubmed/25960916
http://dx.doi.org/10.1155/2015/381281
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author West, Ryan J. H.
Furmston, Rebecca
Williams, Charles A. C.
Elliott, Christopher J. H.
author_facet West, Ryan J. H.
Furmston, Rebecca
Williams, Charles A. C.
Elliott, Christopher J. H.
author_sort West, Ryan J. H.
collection PubMed
description We provide an insight into the role Drosophila has played in elucidating neurophysiological perturbations associated with Parkinson's disease- (PD-) related genes. Synaptic signalling deficits are observed in motor, central, and sensory systems. Given the neurological impact of disease causing mutations within these same genes in humans the phenotypes observed in fly are of significant interest. As such we observe four unique opportunities provided by fly nervous system models of Parkinson's disease. Firstly, Drosophila models are instrumental in exploring the mechanisms of neurodegeneration, with several PD-related mutations eliciting related phenotypes including sensitivity to energy supply and vesicular deformities. These are leading to the identification of plausible cellular mechanisms, which may be specific to (dopaminergic) neurons and synapses rather than general cellular phenotypes. Secondly, models show noncell autonomous signalling within the nervous system, offering the opportunity to develop our understanding of the way pathogenic signalling propagates, resembling Braak's scheme of spreading pathology in PD. Thirdly, the models link physiological deficits to changes in synaptic structure. While the structure-function relationship is complex, the genetic tractability of Drosophila offers the chance to separate fundamental changes from downstream consequences. Finally, the strong neuronal phenotypes permit relevant first in vivo drug testing.
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spelling pubmed-44142112015-05-10 Neurophysiology of Drosophila Models of Parkinson's Disease West, Ryan J. H. Furmston, Rebecca Williams, Charles A. C. Elliott, Christopher J. H. Parkinsons Dis Review Article We provide an insight into the role Drosophila has played in elucidating neurophysiological perturbations associated with Parkinson's disease- (PD-) related genes. Synaptic signalling deficits are observed in motor, central, and sensory systems. Given the neurological impact of disease causing mutations within these same genes in humans the phenotypes observed in fly are of significant interest. As such we observe four unique opportunities provided by fly nervous system models of Parkinson's disease. Firstly, Drosophila models are instrumental in exploring the mechanisms of neurodegeneration, with several PD-related mutations eliciting related phenotypes including sensitivity to energy supply and vesicular deformities. These are leading to the identification of plausible cellular mechanisms, which may be specific to (dopaminergic) neurons and synapses rather than general cellular phenotypes. Secondly, models show noncell autonomous signalling within the nervous system, offering the opportunity to develop our understanding of the way pathogenic signalling propagates, resembling Braak's scheme of spreading pathology in PD. Thirdly, the models link physiological deficits to changes in synaptic structure. While the structure-function relationship is complex, the genetic tractability of Drosophila offers the chance to separate fundamental changes from downstream consequences. Finally, the strong neuronal phenotypes permit relevant first in vivo drug testing. Hindawi Publishing Corporation 2015 2015-04-20 /pmc/articles/PMC4414211/ /pubmed/25960916 http://dx.doi.org/10.1155/2015/381281 Text en Copyright © 2015 Ryan J. H. West et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
West, Ryan J. H.
Furmston, Rebecca
Williams, Charles A. C.
Elliott, Christopher J. H.
Neurophysiology of Drosophila Models of Parkinson's Disease
title Neurophysiology of Drosophila Models of Parkinson's Disease
title_full Neurophysiology of Drosophila Models of Parkinson's Disease
title_fullStr Neurophysiology of Drosophila Models of Parkinson's Disease
title_full_unstemmed Neurophysiology of Drosophila Models of Parkinson's Disease
title_short Neurophysiology of Drosophila Models of Parkinson's Disease
title_sort neurophysiology of drosophila models of parkinson's disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414211/
https://www.ncbi.nlm.nih.gov/pubmed/25960916
http://dx.doi.org/10.1155/2015/381281
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