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Rodent models of Parkinson's disease: beyond the motor symptomatology
Parkinson's disease (PD) is classically characterized by motor symptoms; however, non-motor symptoms (NMS) are increasingly recognized as relevant in disease-state, given the associated alterations in mood (depression and anxiety) and cognition. Here, particularly in regards to NMS, we aimed to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840800/ https://www.ncbi.nlm.nih.gov/pubmed/24324416 http://dx.doi.org/10.3389/fnbeh.2013.00175 |
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author | Campos, Filipa L. Carvalho, Miguel M. Cristovão, Ana C. Je, Goun Baltazar, Graça Salgado, António J. Kim, Yoon-Seong Sousa, Nuno |
author_facet | Campos, Filipa L. Carvalho, Miguel M. Cristovão, Ana C. Je, Goun Baltazar, Graça Salgado, António J. Kim, Yoon-Seong Sousa, Nuno |
author_sort | Campos, Filipa L. |
collection | PubMed |
description | Parkinson's disease (PD) is classically characterized by motor symptoms; however, non-motor symptoms (NMS) are increasingly recognized as relevant in disease-state, given the associated alterations in mood (depression and anxiety) and cognition. Here, particularly in regards to NMS, we aimed to compare the motor, emotional and cognitive behavior of three animal models of PD that trigger dopaminergic (DAergic) degeneration on both brain hemispheres: (i) the 6-hydroxydopamine (6-OHDA, 8 or 6 μg) lesion model; (ii) the paraquat (PQ) induced model, and (iii) a genetic model based on α-synuclein overexpression (α-syn). 6-OHDA and α-syn vector were injected bilaterally in the substantia nigra pars compacta (SNpc) of adult male Wistar rats; as for PQ delivery, micro-osmotic pumps were implanted in the interscapular region. Motor deficits were observed in all models, with histological analysis of tyrosine hydroxylase positive cells in the SNpc revealing a significant loss of DAergic neurons in all animal models. In addition, the α-syn animal model also presented a reduction in exploratory activity, and the 6-OHDA and PQ animals displayed a significant increase in both depressive- and anxiety-like behavior. Interestingly, cognitive impairment (working memory) was only observed in the 6-OHDA model. Overall, these PD models are suitable for mimicking the motor symptoms associated to PD, with each encompassing other relevant NMS components of the disorder that may prove beneficial for further studies in PD. |
format | Online Article Text |
id | pubmed-3840800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-38408002013-12-09 Rodent models of Parkinson's disease: beyond the motor symptomatology Campos, Filipa L. Carvalho, Miguel M. Cristovão, Ana C. Je, Goun Baltazar, Graça Salgado, António J. Kim, Yoon-Seong Sousa, Nuno Front Behav Neurosci Neuroscience Parkinson's disease (PD) is classically characterized by motor symptoms; however, non-motor symptoms (NMS) are increasingly recognized as relevant in disease-state, given the associated alterations in mood (depression and anxiety) and cognition. Here, particularly in regards to NMS, we aimed to compare the motor, emotional and cognitive behavior of three animal models of PD that trigger dopaminergic (DAergic) degeneration on both brain hemispheres: (i) the 6-hydroxydopamine (6-OHDA, 8 or 6 μg) lesion model; (ii) the paraquat (PQ) induced model, and (iii) a genetic model based on α-synuclein overexpression (α-syn). 6-OHDA and α-syn vector were injected bilaterally in the substantia nigra pars compacta (SNpc) of adult male Wistar rats; as for PQ delivery, micro-osmotic pumps were implanted in the interscapular region. Motor deficits were observed in all models, with histological analysis of tyrosine hydroxylase positive cells in the SNpc revealing a significant loss of DAergic neurons in all animal models. In addition, the α-syn animal model also presented a reduction in exploratory activity, and the 6-OHDA and PQ animals displayed a significant increase in both depressive- and anxiety-like behavior. Interestingly, cognitive impairment (working memory) was only observed in the 6-OHDA model. Overall, these PD models are suitable for mimicking the motor symptoms associated to PD, with each encompassing other relevant NMS components of the disorder that may prove beneficial for further studies in PD. Frontiers Media S.A. 2013-11-26 /pmc/articles/PMC3840800/ /pubmed/24324416 http://dx.doi.org/10.3389/fnbeh.2013.00175 Text en Copyright © 2013 Campos, Carvalho, Cristovão, Je, Baltazar, Salgado, Kim and Sousa. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Campos, Filipa L. Carvalho, Miguel M. Cristovão, Ana C. Je, Goun Baltazar, Graça Salgado, António J. Kim, Yoon-Seong Sousa, Nuno Rodent models of Parkinson's disease: beyond the motor symptomatology |
title | Rodent models of Parkinson's disease: beyond the motor symptomatology |
title_full | Rodent models of Parkinson's disease: beyond the motor symptomatology |
title_fullStr | Rodent models of Parkinson's disease: beyond the motor symptomatology |
title_full_unstemmed | Rodent models of Parkinson's disease: beyond the motor symptomatology |
title_short | Rodent models of Parkinson's disease: beyond the motor symptomatology |
title_sort | rodent models of parkinson's disease: beyond the motor symptomatology |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840800/ https://www.ncbi.nlm.nih.gov/pubmed/24324416 http://dx.doi.org/10.3389/fnbeh.2013.00175 |
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