4.5 Article

Visual discrimination and inhibitory control deficits in mouse models of Down syndrome: A pilot study using rodent touchscreen technology

Journal

JOURNAL OF NEUROSCIENCE RESEARCH
Volume 101, Issue 4, Pages 492-507

Publisher

WILEY
DOI: 10.1002/jnr.25160

Keywords

cognition; Down syndrome; learning; memory; mouse models; touchscreen behavior; translation

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This study used rodent touchscreen paradigms to investigate learning deficits in mouse models of Down syndrome (DS). The Dp(16)1/Yey and Ts1Cje models showed learning deficits in visual discrimination (VD), with the Dp(16)1/Yey model exhibiting more pronounced deficits. Both models also displayed compulsive behavior and abnormal cortical inhibitory control during Extinction. The findings highlight the importance of mouse genetic background and absence of hyperactive behavior in successful learning in touchscreen testing.
Several non-verbal cognitive and behavioral tests have been developed to assess learning deficits in humans with Down syndrome (DS). Here we used rodent touchscreen paradigms in adult male mice to investigate visual discrimination (VD) learning and inhibitory control in the Dp(16)1/Yey (C57BL/6J genetic background), Ts65Dn (mixed B6 X C3H genetic background) and Ts1Cje (C57BL/6J genetic background) mouse models of DS. Dp(16)1/Yey and Ts1Cje models did not exhibit motivation or learning deficits during early pre-training, however, Ts1Cje mice showed a significant learning delay after the introduction of the incorrect stimulus (late pre-training), suggesting prefrontal cortex defects in this model. Dp(16)1/Yey and Ts1Cje mice display learning deficits in VD but these deficits were more pronounced in the Dp(16)1/Yey model. Both models also exhibited compulsive behavior and abnormal cortical inhibitory control during Extinction compared to WT littermates. Finally, Ts65Dn mice outperformed WT littermates in pre-training stages by initiating a significantly higher number of trials due to their hyperactive behavior. Both Ts65Dn and WT littermates showed poor performance during late pre-training and were not tested in VD. These studies demonstrate significant learning deficits and compulsive behavior in the Ts1Cje and Dp(16)1/Yey mouse models of DS. They also demonstrate that the mouse genetic background (C57BL/6J vs. mixed B6 X C3H) and the absence of hyperactive behavior are key determinants of successful learning in touchscreen behavioral testing. These data will be used to select the mouse model that best mimics cognitive deficits in humans with DS and evaluate the effects of future therapeutic interventions.

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