Abstract
Visual discrimination requires sensory processing followed by a perceptual decision. Despite a growing understanding of visual areas in this behavior, it is unclear what role top-down signals from prefrontal cortex play, in particular as a function of perceptual difficulty. To address this gap, we investigated how neurons in dorso-lateral frontal cortex (dl-FC) of freely-moving ferrets encode task variables in a two-alternative forced choice visual discrimination task with high- and low-contrast visual input. About two-thirds of all recorded neurons in dl-FC were modulated by at least one of the two task variables, task difficulty and target location. More neurons in dl-FC preferred the hard trials; no such preference bias was found for target location. In individual neurons, this preference for specific task types was limited to brief epochs. Finally, optogenetic stimulation confirmed the functional role of the activity in dl-FC before target touch; suppression of activity in pyramidal neurons with the ArchT silencing opsin resulted in a decrease in reaction time to touch the target but not to retrieve reward. In conclusion, dl-FC activity is differentially recruited for high perceptual difficulty in the freely-moving ferret and the resulting signal may provide top-down behavioral inhibition.
Highlights
We studied the role of ferret dorso-lateral frontal cortex (dl-FC) in sensory processing and action execution during a visual discrimination task that required freely-moving behavior
We found increased engagement of dl-FC for hard trials where the visual stimuli exhibited low contrast
The use of freely-moving animals combined with the layout of the behavioral chamber enabled us to study neuronal processes that were related to the movement of the animal, in particular the target location
Summary
Our aim was to understand higher-order cortical processing and how it relates to perceptual difficulty of visual discrimination
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