Deep behavioural phenotyping of the Q175 Huntington disease mouse model: effects of age, sex, and weight

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dc.contributor.authorKoch, Ellen T.
dc.contributor.authorCheng, Judy
dc.contributor.authorRamandi, Daniel
dc.contributor.authorSepers, Marja D.
dc.contributor.authorHsu, Alex
dc.contributor.authorFong, Tony
dc.contributor.authorMurphy, Timothy H.
dc.contributor.authorYttri, Eric
dc.contributor.authorRaymond, Lynn A.
dc.date.accessioned2024-05-26T00:03:59Z
dc.date.available2024-05-26T00:03:59Z
dc.date.issued2024-05-23
dc.date.updated2024-05-26T00:03:58Z
dc.description.abstractAbstract Background Huntington disease (HD) is a neurodegenerative disorder with complex motor and behavioural manifestations. The Q175 knock-in mouse model of HD has gained recent popularity as a genetically accurate model of the human disease. However, behavioural phenotypes are often subtle and progress slowly in this model. Here, we have implemented machine-learning algorithms to investigate behaviour in the Q175 model and compare differences between sexes and disease stages. We explore distinct behavioural patterns and motor functions in open field, rotarod, water T-maze, and home cage lever-pulling tasks. Results In the open field, we observed habituation deficits in two versions of the Q175 model (zQ175dn and Q175FDN, on two different background strains), and using B-SOiD, an advanced machine learning approach, we found altered performance of rearing in male manifest zQ175dn mice. Notably, we found that weight had a considerable effect on performance of accelerating rotarod and water T-maze tasks and controlled for this by normalizing for weight. Manifest zQ175dn mice displayed a deficit in accelerating rotarod (after weight normalization), as well as changes to paw kinematics specific to males. Our water T-maze experiments revealed response learning deficits in manifest zQ175dn mice and reversal learning deficits in premanifest male zQ175dn mice; further analysis using PyMouseTracks software allowed us to characterize new behavioural features in this task, including time at decision point and number of accelerations. In a home cage-based lever-pulling assessment, we found significant learning deficits in male manifest zQ175dn mice. A subset of mice also underwent electrophysiology slice experiments, revealing a reduced spontaneous excitatory event frequency in male manifest zQ175dn mice. Conclusions Our study uncovered several behavioural changes in Q175 mice that differed by sex, age, and strain. Our results highlight the impact of weight and experimental protocol on behavioural results, and the utility of machine learning tools to examine behaviour in more detailed ways than was previously possible. Specifically, this work provides the field with an updated overview of behavioural impairments in this model of HD, as well as novel techniques for dissecting behaviour in the open field, accelerating rotarod, and T-maze tasks.
dc.identifier.citationBMC Biology. 2024 May 23;22(1):121
dc.identifier.urihttps://doi.org/10.1186/s12915-024-01919-9
dc.identifier.urihttps://hdl.handle.net/1880/118851
dc.identifier.urihttps://doi.org/10.11575/PRISM/46448
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dc.titleDeep behavioural phenotyping of the Q175 Huntington disease mouse model: effects of age, sex, and weight
dc.typeJournal Article
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