dc.contributor.author
Sun, Rongwan
dc.contributor.author
Gaerz, Marie-Christin
dc.contributor.author
Oeing, Christian
dc.contributor.author
Mai, Knut
dc.contributor.author
Brachs, Sebastian
dc.date.accessioned
2025-07-25T10:03:57Z
dc.date.available
2025-07-25T10:03:57Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/48357
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-48079
dc.description.abstract
Introduction: Holistic phenotyping of rodent models is increasing, with a growing awareness of the 3Rs and the fact that specialized experimental setups can also impose artificial restrictions. Activity is an important parameter for almost all basic and applied research areas involving laboratory animals. Locomotor activity, the main form of energy expenditure, influences metabolic rate, muscle mass, and body weight and is frequently investigated in metabolic disease research. Additionally, it serves as an indicator of animal welfare in therapeutic, pharmacological, and toxicological studies. Thus, accurate and effective measurement of activity is crucial. However, conventional monitoring systems often alter the housing environment and require handling, which can introduce artificial interference and lead to measurement inaccuracies.
Methods: Our study focused on evaluating circadian activity profiles derived from the DVC and comparing them with conventional activity measurements to validate them statistically and assess their reproducibility. We utilized data from metabolic studies, an Alzheimer’s disease model known for increased activity, and included DVC monitoring in a project investigating treatment effects on activity in a type-1-like diabetes model.
Results: The DVC data yielded robust, scientifically accurate, and consistent circadian profiles from group-housed mice, which is particularly advantageous for longitudinal experiments. The activity profiles from both systems were fully comparable, providing matching profiles. Using DVC monitoring, we confirmed the hyperactivity phenotype in an AD model and reproduced a decline in activity in type-1-like diabetes model.
Discussion: In our work, we derived robust circadian activity profiles from the DVC data of group-housed mice, which were scientifically accurate, reproducible and comparable to another activity measurement. This approach can not only improve animal welfare according to the 3R principles but can also be implement in high-throughput longitudinal studies. Furthermore, we discuss the advantages and limitations of DVC activity measurements to highlight its potential and avoid confounders.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
activity measurements
en
dc.subject
circadian profiles
en
dc.subject
continuous home cage monitoring
en
dc.subject
Alzheimer's disease
en
dc.subject
non-invasive
en
dc.subject
digital ventilated cage
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Accurate locomotor activity profiles of group-housed mice derived from home cage monitoring data
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
1456307
dcterms.bibliographicCitation.doi
10.3389/fnins.2024.1456307
dcterms.bibliographicCitation.journaltitle
Frontiers in Neuroscience
dcterms.bibliographicCitation.originalpublishername
Frontiers Media SA
dcterms.bibliographicCitation.volume
18
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
39371613
dcterms.isPartOf.eissn
1662-453X