Home cage-based insights into motor learning and strategy adaptation in a Huntington disease mouse model

Huntington disease (HD) is a genetic neurodegenerative disorder characterized by progressive motor dysfunction, cognitive decline, and neuropsychiatric symptoms. Assessing early motor skill deficits in HD mouse models is challenging with traditional behavioral tasks. This study uses a home cage-based lever-pulling task, PiPaw2.0, to evaluate motor learning in 6-7 months-old zQ175 knock-in HD mice in a more naturalistic environment. In this task, mice learn to pull a lever for a water reward, with the requirement to hold the lever within a specific goal range for a required hold time. As the mice improved, the required hold time increased, thereby gradually increasing the task demands. Both wild type (WT) and zQ175 mice initially showed similar task engagement, but zQ175 mice had significant deficits in adapting to increasing hold time. The WT mice refined their strategies over time, shifting from random to more precise lever pulls, while zQ175 mice failed to make this adjustment, maintaining erratic performance. Additionally, in group-housing WT mouse lever performance benefited from peer interactions, an effect absent in zQ175 mice. Post-task neural assessments revealed that WT mice developed experience-mediated synaptic plasticity in the left striatum (contralateral to lever-pulling paw), while zQ175 mice showed no significant changes, consistent with known corticostriatal plasticity impairments in HD mouse models. In conclusion, our findings demonstrate the effectiveness of group-housed, home cage-based assessments for evaluating motor learning and adaptation in HD mouse models. This study provides insights into the motor control and adaptive learning deficits in HD, emphasizing the value of automated home cage systems in advancing neurodegenerative disease research and highlighting the importance of peer influences on performance.

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Publication Details

Journal
PLoS ONE
Published
2025-02-13
DOI
https://doi.org/10.1371/journal.pone.0318663
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Home cage-based insights into motor learning and strategy adaptation in a Huntington disease mouse model

Daniel Ramandi, Brian Han, Lynn A. Raymond, Marja D. Sepers et al.
4 links
PLoS ONE
Genetic Neurodegenerative Diseases
article

Home cage-based insights into motor learning and strategy adaptation in a Huntington disease mouse model

Daniel Ramandi, Brian Han, Lynn A. Raymond, Marja D. Sepers, Timothy H. Murphy, Cameron L. Woodard, Z.-H. Wang
article en

Abstract

Huntington disease (HD) is a genetic neurodegenerative disorder characterized by progressive motor dysfunction, cognitive decline, and neuropsychiatric symptoms. Assessing early motor skill deficits in HD mouse models is challenging with traditional behavioral tasks. This study uses a home cage-based lever-pulling task, PiPaw2.0, to evaluate motor learning in 6-7 months-old zQ175 knock-in HD mice in a more naturalistic environment. In this task, mice learn to pull a lever for a water reward, with the requirement to hold the lever within a specific goal range for a required hold time. As the mice improved, the required hold time increased, thereby gradually increasing the task demands. Both wild type (WT) and zQ175 mice initially showed similar task engagement, but zQ175 mice had significant deficits in adapting to increasing hold time. The WT mice refined their strategies over time, shifting from random to more precise lever pulls, while zQ175 mice failed to make this adjustment, maintaining erratic performance. Additionally, in group-housing WT mouse lever performance benefited from peer interactions, an effect absent in zQ175 mice. Post-task neural assessments revealed that WT mice developed experience-mediated synaptic plasticity in the left striatum (contralateral to lever-pulling paw), while zQ175 mice showed no significant changes, consistent with known corticostriatal plasticity impairments in HD mouse models. In conclusion, our findings demonstrate the effectiveness of group-housed, home cage-based assessments for evaluating motor learning and adaptation in HD mouse models. This study provides insights into the motor control and adaptive learning deficits in HD, emphasizing the value of automated home cage systems in advancing neurodegenerative disease research and highlighting the importance of peer influences on performance.

PLoS ONEVol. 20(2)
Vancouver Coastal Health (CA), University of British Columbia (CA)
Faculty of Medicine, University of British Columbia, Canadian Institutes of Health Research, Department of Psychiatry, Faculty of Medicine, University of British Columbia, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 97%
Genetic Neurodegenerative Diseases
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