Abstract
Adapting flexibly to changing circumstances is guided by memory of past choices, their outcomes in similar circumstances, and a method for choosing amongst potential actions. The hippocampus (HPC) is needed to remember episodes, and the prefrontal cortex (PFC) helps guide memory retrieval. Single unit activity in the HPC and PFC correlates with such cognitive functions. Previous work recorded CA1 and mPFC activity as male rats performed a spatial reversal task in a plus maze that requires both structures, found that PFC activity helps reactivate HPC representations of pending goal choices, but did not describe frontotemporal interactions after choices. We describe these interactions after choices here. CA1 activity tracked both current goal location and the past starting location of single trials; PFC activity tracked current goal location better than past start location. CA1 and PFC reciprocally modulated each other’s representations both before and after goal choices. After choices, CA1 activity predicted changes in PFC activity in subsequent trials and the magnitude of this prediction correlated with faster learning. In contrast, PFC start arm activity more strongly modulating CA1 activity after choices correlated with slower learning. Together, the results suggest post-choice HPC activity conveys retrospective signals to the PFC which combines different paths to common goals into “rules.” In subsequent trials, pre-choice mPFC activity modulates prospective CA1 signals informing goal selection.
SIGNIFICANCE STATEMENT:
Hippocampal (HPC) and prefrontal cortical (PFC) activity supports cognitive flexibility in changing circumstances. HPC signals represent behavioral episodes that link the start, choice, and goal of paths. PFC signals represent “rules” that guide goal-directed actions. While prior studies described HPC-PFC interactions preceding decisions in the plus maze, post-decision interactions were not investigated. Here, we show post-choice HPC and PFC activity distinguished the start and goal of paths, and CA1 signaled the past start of each trial more accurately than mPFC. Post-choice CA1 activity modulated subsequent PFC activity so rewarded actions were more likely to occur. Together, the results show that in changing circumstances, HPC retrospective codes modulate subsequent PFC coding, which in turn modulates HPC prospective codes that predict choices.
Footnotes
The authors declare no competing financial interests.
This work was supported by NIMH – National Institutes of Mental Health, USA (NIMH 2R01MH073689, NIMH MH118297, and NIMH MH119523 to M.L.S.) and the NVIDIA Corporation.
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