Evidence map›Paper›PMID 38783261›Full record

ArticleBMC biology2024

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

Ellen T Koch, Judy Cheng, Daniel Ramandi, Marja D Sepers, Alex Hsu, Tony Fong, Timothy H Murphy, Eric Yttri, Lynn A Raymond

Abstract read
In one paragraph

Article in BMC biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ellen T KochDepartment of Psychiatry, Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, Canada. ellen.koch@ucalgary.ca.
Judy ChengDepartment of Psychiatry, Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, Canada.
Daniel RamandiDepartment of Psychiatry, Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, Canada.
Marja D SepersDepartment of Psychiatry, Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, Canada.
Alex HsuDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA, USA.
Tony FongDepartment of Psychiatry, Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, Canada.
Timothy H MurphyDepartment of Psychiatry, Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, Canada.
Eric YttriDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA, USA.
Lynn A RaymondDepartment of Psychiatry, Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, Canada.

Funding

CRCNS Circuit-Level Mechanisms of Adaptive decision-makingR01DA053014 · NIDA · CARNEGIE-MELLON UNIVERSITY · PI VERSTYNEN, TIMOTHY D · 2020 to 2022
$1.0M
CIHR 143210CIHR 178043CIHR 180631National Science Foundation 1548562NIDA NIH HHS R01 DA053014NIH HHS DA053014
6 · The paper itself

Abstract

backgroundHuntington 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.

resultsIn 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.

conclusionsOur 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.

Indexed as

Behavior, AnimalBody WeightDisease Models, AnimalHuntington DiseasePhenotypeAge FactorsAnimalsFemaleMachine LearningMaleMaze LearningMiceSex FactorsBehaviourHuntington diseaseMachine learningMotor learningMotor skillNaturalistic behaviour; response learningNeuroscienceOpen fieldRotarodStriatumT-maze

Identifiers

PMID38783261
PMCPMC11119712

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.