ABSTRACT
We have the capacity to follow arbitrary stimulus-response rules, meaning policies that determine how we will behave across circumstances. Yet, it is not clear how rules guide sensorimotor decision-making in the brain. Here, we recorded from neurons in three regions linked to decision-making, the orbitofrontal cortex, ventral striatum, and dorsal striatum, while macaques performed a rule-based decision-making task. We found that different rules warped the neural representations of chosen options by expanding rule-relevant coding dimensions relative to rule-irrelevant ones. Some cognitive theories suggest that warping could increase processing efficiency by facilitating rule-relevant computations at the expense of irrelevant ones. To test this idea, we modeled rules as the latent causes of decisions and identified a set of “rule-free” choices that could not be explained by simple rules. Contrasting these with rule-based choices revealed that following rules decreased the energetic cost of decision-making while warping the representational geometry of choice.
SIGNIFICANCE STATEMENT One important part of our ability to adapt flexibly to the world around us is our ability to implement arbitrary stimulus-response mappings, known as “rules”. Many studies have shown that when we follow a rule, its identity is encoded in neuronal firing rates. However, it remains unclear how rules regulate behavior. Here, we report that rules warp the way that sensorimotor information is represented in decision-making circuits: enhancing information that is relevant to the current rule at the expense of information that is irrelevant. These results imply that rules are implemented as a kind of attentional gate on what information is available for decision-making.