Frontal circuit specialisations for decision making

There is widespread consensus that distributed circuits across prefrontal and anterior cingulate cortex (PFC/ACC) are critical for reward-based decision making. The circuit specialisations of these areas in primates were likely shaped by their foraging niche, in which decision making is typically sequential, attention-guided and temporally extended. Here, I argue that in humans and other primates, PFC/ACC circuits are functionally specialised in two ways. First, microcircuits found across PFC/ACC are highly recurrent in nature and have synaptic properties that support persistent activity across temporally extended cognitive tasks. These properties provide the basis of a computational account of time-varying neural activity within PFC/ACC as a decision is being made. Second, the macrocircuit connections (to other brain areas) differ between distinct PFC/ACC cytoarchitectonic subregions. This variation in macrocircuit connections explains why PFC/ACC subregions make unique contributions to reward-based decision tasks and how these contributions are shaped by attention. They predict dissociable neural representations to emerge in orbitofrontal, anterior cingulate and dorsolateral prefrontal cortex during sequential attention-guided choice, as recently confirmed in neurophysiological recordings.

Automated summary

There is a consensus that circuits in the prefrontal and anterior cingulate cortex play a critical role in reward-based decision making. The functional specialization of PFC/ACC circuits in humans and primates involve microcircuits that support persistent activity during cognitive tasks and macrocircuit connections that vary between different cytoarchitectonic subregions, contributing uniquely to reward-based decision tasks. This variation in circuit connections predicts distinctive neural representations in different regions of the brain during sequential attention-guided choice.