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Loss of hippocampal function impairs pattern separation on a mouse touch-screen operant paradigm
Megan Josey1, Jonathan L Brigman2
1Department of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
Neurobiology of Learning and Memory
|August 13, 2015
Summary
Mice with ventral hippocampus damage struggle with pattern separation tasks. A touch-screen method effectively measures this hippocampal function, crucial for memory and relevant to neuropsychiatric diseases.
Area of Science:
- Neuroscience
- Cognitive Psychology
- Behavioral Neuroscience
Background:
- The hippocampus is vital for learning and memory, with its dysfunction linked to neuropsychiatric disorders.
- Current preclinical models require refined behavioral measures for hippocampal function.
- Automated tasks are being developed to better assess spatial memory and pattern separation.
Purpose of the Study:
- To evaluate a touchscreen-based delayed nonmatching-to-location (TUNL) task for assessing hippocampal-dependent pattern separation in mice.
- To investigate the impact of ventral hippocampus lesions on pattern separation performance in this automated paradigm.
Main Methods:
- Mice with ventral hippocampus lesions and control mice were trained on a touchscreen TUNL task.
- The task involved discriminating between initially presented and subsequently presented stimuli with varying spatial separations and delays.
- Performance was assessed based on acquisition rates and sensitivity to changes in stimulus separation and delay duration.
Main Results:
- Ventral hippocampus-lesioned mice showed impaired performance as stimulus separation decreased.
- Unlike in rats, consistently increasing delays did not significantly impair lesion mice.
- Variable delays within a session significantly impaired performance in lesioned mice.
Conclusions:
- The touchscreen TUNL paradigm is a sensitive measure of hippocampal-dependent pattern separation in mice.
- This automated task is valuable for studying the effects of hippocampal dysfunction in preclinical models of disease.
- The findings highlight the utility of refined behavioral assays for understanding memory deficits.

