Coexistence of Gait Disturbances and Chorea in Experimental Huntington’s Disease

Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease caused by an expanded CAG repeat. The clinical features are progressive motor dysfunction, cognitive deterioration, and psychiatric disturbances. Unpredictable choreic movements, among the most characteristic hallmarks, may...

Full description

Saved in:
Bibliographic Details
Main Authors: João Casaca-Carreira, Yasin Temel, Marloes van Zelst, Ali Jahanshahi
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Behavioural Neurology
Online Access:http://dx.doi.org/10.1155/2015/970204
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832568151423844352
author João Casaca-Carreira
Yasin Temel
Marloes van Zelst
Ali Jahanshahi
author_facet João Casaca-Carreira
Yasin Temel
Marloes van Zelst
Ali Jahanshahi
author_sort João Casaca-Carreira
collection DOAJ
description Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease caused by an expanded CAG repeat. The clinical features are progressive motor dysfunction, cognitive deterioration, and psychiatric disturbances. Unpredictable choreic movements, among the most characteristic hallmarks, may contribute to gait disturbances and loss of balance in HD individuals. In this study, we aimed to investigate and characterize the gait abnormalities and choreic movements in a transgenic rat model of HD (tgHD). TgHD presents typical neuropathological, neurophysiological, and behavioral aspects mimicking some of the key features of human HD and is the only described experimental model for HD that exhibits choreiform movements. We used the Catwalk, with emphasis on static and dynamic gait parameters, to test the hypothesis that at symptomatic age (9 months) the dynamic measures of gait in HD are altered and coexist with choreiform movements. Our results showed that the dynamic parameters seem to be more affected than static parameters at this age in tgHD rats. The number of steps and step cycles and swing speed of the paws were increased in tgHD rat in comparison to wild-type controls. Our study demonstrates that gait abnormalities coexist with chorea rather than being caused by it. These symptoms may originate from distinct networks in the basal ganglia and downstream connections.
format Article
id doaj-art-7ecb723b8d824019bee0876a13b7a700
institution Kabale University
issn 0953-4180
1875-8584
language English
publishDate 2015-01-01
publisher Wiley
record_format Article
series Behavioural Neurology
spelling doaj-art-7ecb723b8d824019bee0876a13b7a7002025-02-03T00:59:39ZengWileyBehavioural Neurology0953-41801875-85842015-01-01201510.1155/2015/970204970204Coexistence of Gait Disturbances and Chorea in Experimental Huntington’s DiseaseJoão Casaca-Carreira0Yasin Temel1Marloes van Zelst2Ali Jahanshahi3Department of Neuroscience, Maastricht University Medical Center, 6229 ER Maastricht, NetherlandsDepartment of Neuroscience, Maastricht University Medical Center, 6229 ER Maastricht, NetherlandsDepartment of Neuroscience, Maastricht University Medical Center, 6229 ER Maastricht, NetherlandsDepartment of Neuroscience, Maastricht University Medical Center, 6229 ER Maastricht, NetherlandsHuntington’s disease (HD) is an autosomal dominant neurodegenerative disease caused by an expanded CAG repeat. The clinical features are progressive motor dysfunction, cognitive deterioration, and psychiatric disturbances. Unpredictable choreic movements, among the most characteristic hallmarks, may contribute to gait disturbances and loss of balance in HD individuals. In this study, we aimed to investigate and characterize the gait abnormalities and choreic movements in a transgenic rat model of HD (tgHD). TgHD presents typical neuropathological, neurophysiological, and behavioral aspects mimicking some of the key features of human HD and is the only described experimental model for HD that exhibits choreiform movements. We used the Catwalk, with emphasis on static and dynamic gait parameters, to test the hypothesis that at symptomatic age (9 months) the dynamic measures of gait in HD are altered and coexist with choreiform movements. Our results showed that the dynamic parameters seem to be more affected than static parameters at this age in tgHD rats. The number of steps and step cycles and swing speed of the paws were increased in tgHD rat in comparison to wild-type controls. Our study demonstrates that gait abnormalities coexist with chorea rather than being caused by it. These symptoms may originate from distinct networks in the basal ganglia and downstream connections.http://dx.doi.org/10.1155/2015/970204
spellingShingle João Casaca-Carreira
Yasin Temel
Marloes van Zelst
Ali Jahanshahi
Coexistence of Gait Disturbances and Chorea in Experimental Huntington’s Disease
Behavioural Neurology
title Coexistence of Gait Disturbances and Chorea in Experimental Huntington’s Disease
title_full Coexistence of Gait Disturbances and Chorea in Experimental Huntington’s Disease
title_fullStr Coexistence of Gait Disturbances and Chorea in Experimental Huntington’s Disease
title_full_unstemmed Coexistence of Gait Disturbances and Chorea in Experimental Huntington’s Disease
title_short Coexistence of Gait Disturbances and Chorea in Experimental Huntington’s Disease
title_sort coexistence of gait disturbances and chorea in experimental huntington s disease
url http://dx.doi.org/10.1155/2015/970204
work_keys_str_mv AT joaocasacacarreira coexistenceofgaitdisturbancesandchoreainexperimentalhuntingtonsdisease
AT yasintemel coexistenceofgaitdisturbancesandchoreainexperimentalhuntingtonsdisease
AT marloesvanzelst coexistenceofgaitdisturbancesandchoreainexperimentalhuntingtonsdisease
AT alijahanshahi coexistenceofgaitdisturbancesandchoreainexperimentalhuntingtonsdisease