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Mutation-related differences in exploratory, spatial, and depressive-like behavior in pcd and Lurcher cerebellar
Jan Tuma1, Yaroslav Kolinko2, Frantisek Vozeh1
1Laboratory of Neurodegenerative Disorders, Faculty of Medicine in Pilsen, Biomedical Centre, Charles University in Prague Pilsen, Czech Republic ; Department of Pathophysiology, Faculty of Medicine in Pilsen, Charles University in Prague Pilsen, Czech Republic.
This study compared spatial navigation, learning, and memory in pcd and Lurcher cerebellar mutant mice. Lurcher mice exhibited better overall performance than pcd mice, despite deficits in both models.
Area of Science:
- Neuroscience
- Behavioral Neuroscience
- Genetics
Background:
- The cerebellum's role extends beyond motor control to cognitive and affective functions.
- Understanding cerebellar disorders requires studying genetic models like pcd and Lurcher mice.
- These models exhibit varying mutations and genetic backgrounds, impacting disease manifestation.
Purpose of the Study:
- To compare spatial navigation, learning, and memory in pcd and Lurcher cerebellar mutant mice.
- To assess behavioral differences in exploration, motivation, and cognitive tasks.
Main Methods:
- Mice were tested in an open field for exploratory behavior.
- The Morris water maze assessed spatial navigation with visible and hidden platforms.
- The forced swimming test evaluated motivation and depressive-like behavior.
Main Results:
- Lurcher mice displayed distinct open field exploration and reduced depressive-like behavior compared to pcd mice.
- Both mutants showed severe spatial navigation deficits, but Lurcher mice performed better overall.
- Lurcher mice utilized visual cues for navigation and showed a preference for the visible platform in probe trials.
Conclusions:
- Cerebellar mutant mice, pcd and Lurcher, exhibit differential cognitive and behavioral phenotypes.
- Lurcher mice demonstrate some visual guidance capabilities despite spatial learning impairments.
- These findings contribute to understanding cerebellar function and dysfunction in genetic models.

