Refined movement analysis in the staircase test reveals differential motor deficits in mouse models of stroke

Author:

Skrobot Matej1ORCID,Sa Rafael De1,Walter Josefine123,Vogt Arend1ORCID,Paulat Raik1,Lips Janet13,Mosch Larissa13,Mueller Susanne134ORCID,Dominiak Sina56,Sachdev Robert6,Boehm-Sturm Philipp134,Dirnagl Ulrich12378,Endres Matthias13789,Harms Christoph137ORCID,Wenger Nikolaus1

Affiliation:

1. Department of Neurology with Experimental Neurology, Charité – Universitätsmedizin Berlin, Berlin, Germany

2. QUEST Center for Transforming Biomedical Research, Berlin Institute of Health (BIH), Berlin, Germany

3. Center for Stroke Research Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany

4. NeuroCure Cluster of Excellence and Charité Core Facility 7T Experimental MRIs, Charité-Universitätsmedizin Berlin, Berlin, Germany

5. Institute of Biology, Humboldt University of Berlin, Berlin, Germany

6. Sussex Neuroscience, School of Life Sciences, University of Sussex, Brighton, UK

7. DZHK (German Center for Cardiovascular Research), Berlin, Germany

8. DZNE (German Center for Neurodegenerative Diseases), Berlin, Germany

9. DZPG (German Center of Mental Health), Berlin, Germany

Abstract

Accurate assessment of post-stroke deficits is crucial in translational research. Recent advances in machine learning offer precise quantification of rodent motor behavior post-stroke, yet detecting lesion-specific upper extremity deficits remains unclear. Employing proximal middle cerebral artery occlusion (MCAO) and cortical photothrombosis (PT) in mice, we assessed post-stroke impairments via the Staircase test. Lesion locations were identified using 7 T-MRI. Machine learning was applied to reconstruct forepaw kinematic trajectories and feature analysis was achieved with MouseReach, a new data-processing toolbox. Lesion reconstructions pinpointed ischemic centers in the striatum (MCAO) and sensorimotor cortex (PT). Pellet retrieval alterations were observed, but were unrelated to overall stroke volume. Instead, forepaw slips and relative reaching success correlated with increasing cortical lesion size in both models. Striatal lesion size after MCAO was associated with prolonged reach durations that occurred with delayed symptom onset. Further analysis on the impact of selective serotonin reuptake inhibitors in the PT model revealed no clear treatment effects but replicated strong effect sizes of slips for post-stroke deficit detection. In summary, refined movement analysis unveiled specific deficits in two widely-used mouse stroke models, emphasizing the value of deep behavioral profiling in preclinical stroke research to enhance model validity for clinical translation.

Publisher

SAGE Publications

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