Ventral Tegmental Area Dopamine Neural Activity Switches Simultaneously with Rule Representations in the Medial Prefrontal Cortex and Hippocampus

Abstract

Multiple brain regions need to coordinate activity to support cognitive flexibility and behavioral adaptation. Neural activity in both the hippocampus (HPC) and medial prefrontal cortex (mPFC) is known to represent the spatial context and is sensitive to reward and rule alterations. Midbrain dopamine (DA) activity is key to reward-seeking behavior and learning. There is abundant evidence that midbrain DA modulates HPC and PFC activity. However, it remains underexplored how these networks engage dynamically and coordinate temporally when animals adjust their behavior according to changing reward contingencies. In particular, is there any relationship between DA reward prediction change during rule switching and rule representation changes in mPFC and CA1? We addressed these questions using simultaneous recordings of neuronal population activity from the hippocampal area CA1, mPFC, and ventral tegmental area (VTA) in male TH-Cre rats performing two spatial working memory tasks with frequent rule switches in blocks of trials. CA1 and mPFC ensembles showed rule-specific activity both during maze running and at reward locations, with mPFC rule coding more consistent across animals compared with CA1. Optogenetically tagged VTA DA neuron firing activity responded to and predicted reward outcome. We found that the correct prediction in DA emerged gradually over trials after rule switching in coordination with transitions in mPFC and CA1 ensemble representations of the current rule after a rule switch, followed by behavioral adaptation to the correct rule sequence. Therefore, our study demonstrates a crucial temporal coordination between the rule representation in mPFC/CA1, the dopamine reward signal, and behavioral strategy.