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Automated quantitative gait analysis in animal models of movement disorders

BACKGROUND: Accurate and reproducible behavioral tests in animal models are of major importance in the development and evaluation of new therapies for central nervous system disease. In this study we investigated for the first time gait parameters of rat models for Parkinson's disease (PD), Hun...

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Autores principales: Vandeputte, Caroline, Taymans, Jean-Marc, Casteels, Cindy, Coun, Frea, Ni , Yicheng, Van Laere, Koen, Baekelandt, Veerle
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924851/
https://www.ncbi.nlm.nih.gov/pubmed/20691122
http://dx.doi.org/10.1186/1471-2202-11-92
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author Vandeputte, Caroline
Taymans, Jean-Marc
Casteels, Cindy
Coun, Frea
Ni , Yicheng
Van Laere, Koen
Baekelandt, Veerle
author_facet Vandeputte, Caroline
Taymans, Jean-Marc
Casteels, Cindy
Coun, Frea
Ni , Yicheng
Van Laere, Koen
Baekelandt, Veerle
author_sort Vandeputte, Caroline
collection PubMed
description BACKGROUND: Accurate and reproducible behavioral tests in animal models are of major importance in the development and evaluation of new therapies for central nervous system disease. In this study we investigated for the first time gait parameters of rat models for Parkinson's disease (PD), Huntington's disease (HD) and stroke using the Catwalk method, a novel automated gait analysis test. Static and dynamic gait parameters were measured in all animal models, and these data were compared to readouts of established behavioral tests, such as the cylinder test in the PD and stroke rats and the rotarod tests for the HD group. RESULTS: Hemiparkinsonian rats were generated by unilateral injection of the neurotoxin 6-hydroxydopamine in the striatum or in the medial forebrain bundle. For Huntington's disease, a transgenic rat model expressing a truncated huntingtin fragment with multiple CAG repeats was used. Thirdly, a stroke model was generated by a photothrombotic induced infarct in the right sensorimotor cortex. We found that multiple gait parameters were significantly altered in all three disease models compared to their respective controls. Behavioural deficits could be efficiently measured using the cylinder test in the PD and stroke animals, and in the case of the PD model, the deficits in gait essentially confirmed results obtained by the cylinder test. However, in the HD model and the stroke model the Catwalk analysis proved more sensitive than the rotarod test and also added new and more detailed information on specific gait parameters. CONCLUSION: The automated quantitative gait analysis test may be a useful tool to study both motor impairment and recovery associated with various neurological motor disorders.
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spelling pubmed-29248512010-08-21 Automated quantitative gait analysis in animal models of movement disorders Vandeputte, Caroline Taymans, Jean-Marc Casteels, Cindy Coun, Frea Ni , Yicheng Van Laere, Koen Baekelandt, Veerle BMC Neurosci Research Article BACKGROUND: Accurate and reproducible behavioral tests in animal models are of major importance in the development and evaluation of new therapies for central nervous system disease. In this study we investigated for the first time gait parameters of rat models for Parkinson's disease (PD), Huntington's disease (HD) and stroke using the Catwalk method, a novel automated gait analysis test. Static and dynamic gait parameters were measured in all animal models, and these data were compared to readouts of established behavioral tests, such as the cylinder test in the PD and stroke rats and the rotarod tests for the HD group. RESULTS: Hemiparkinsonian rats were generated by unilateral injection of the neurotoxin 6-hydroxydopamine in the striatum or in the medial forebrain bundle. For Huntington's disease, a transgenic rat model expressing a truncated huntingtin fragment with multiple CAG repeats was used. Thirdly, a stroke model was generated by a photothrombotic induced infarct in the right sensorimotor cortex. We found that multiple gait parameters were significantly altered in all three disease models compared to their respective controls. Behavioural deficits could be efficiently measured using the cylinder test in the PD and stroke animals, and in the case of the PD model, the deficits in gait essentially confirmed results obtained by the cylinder test. However, in the HD model and the stroke model the Catwalk analysis proved more sensitive than the rotarod test and also added new and more detailed information on specific gait parameters. CONCLUSION: The automated quantitative gait analysis test may be a useful tool to study both motor impairment and recovery associated with various neurological motor disorders. BioMed Central 2010-08-09 /pmc/articles/PMC2924851/ /pubmed/20691122 http://dx.doi.org/10.1186/1471-2202-11-92 Text en Copyright ©2010 Vandeputte et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Vandeputte, Caroline
Taymans, Jean-Marc
Casteels, Cindy
Coun, Frea
Ni , Yicheng
Van Laere, Koen
Baekelandt, Veerle
Automated quantitative gait analysis in animal models of movement disorders
title Automated quantitative gait analysis in animal models of movement disorders
title_full Automated quantitative gait analysis in animal models of movement disorders
title_fullStr Automated quantitative gait analysis in animal models of movement disorders
title_full_unstemmed Automated quantitative gait analysis in animal models of movement disorders
title_short Automated quantitative gait analysis in animal models of movement disorders
title_sort automated quantitative gait analysis in animal models of movement disorders
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924851/
https://www.ncbi.nlm.nih.gov/pubmed/20691122
http://dx.doi.org/10.1186/1471-2202-11-92
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