Abstract
Previous research in humans, macaques, and rodents has demonstrated a role of the medial frontal cortex in detecting errors, registering success, and exerting pro-active control on saccade production. The cortical circuitry accomplishing these computations is unknown. Here, we analyze neural spiking data from two monkeys collected using a linear electrode array to describe the functional properties of neurons across cortical layers in the dorsal and ventral banks of the caudal segments of anterior cingulate cortex (actually midcingulate cortex, MCC) during a visually-guided saccade countermanding task. Monkeys were rewarded for shifting gaze to a visual target unless, in infrequent random trials a stop signal appeared, which instructed the subject to cancel saccade initiation. Despite sampling over 900 neurons in MCC, less than 5% demonstrated significant modulation in response to a visual target. Typically, these responses were sustained, discharging until after saccade production. Around 70% of visually responsive neurons were most sensitive to a visual target appearing in one hemifield. Interestingly, as observed previously in SEF, MCC visual neurons showed an unexpected preference for ipsilateral visual stimuli. MCC visual neurons were modulated significantly later than those in occipital and temporal visual areas, as well as other frontal regions such as frontal and supplementary eye fields. Although we found no difference in visual onset latencies between the dorsal and ventral banks, task-related visual response latency varied across cortical layers. These findings provide the first report of the functional architecture of visual signals in two discrete regions of cingulate cortex and provide important constraints for microcircuit models of these areas.