Inhibitory control of sharp-wave ripple duration during learning in hippocampal recurrent networks

The authors combine functional imaging, electrophysiology and molecular identification to examine the inhibitory control of hippocampal memory traces and uncover a role for specific populations of interneurons in regulating memory reactivation events during learning. Recurrent excitatory connections in hippocampal regions CA3 and CA2 are thought to play a key role in the generation of sharp-wave ripples (SWRs), electrophysiological oscillations tightly linked with learning and memory consolidation. However, it remains unknown how defined populations of inhibitory interneurons regulate these events during behavior. Here, we use large-scale, three-dimensional calcium imaging and retrospective molecular identification in the mouse hippocampus to characterize molecularly identified CA3 and CA2 interneuron activity during SWR-associated memory consolidation and spatial navigation. We describe subtype- and region-specific responses during behaviorally distinct brain states and find that SWRs are preceded by decreased cholecystokinin-expressing interneuron activity and followed by increased parvalbumin-expressing basket cell activity. The magnitude of these dynamics correlates with both SWR duration and behavior during hippocampal-dependent learning. Together these results assign subtype- and region-specific roles for inhibitory circuits in coordinating operations and learning-related plasticity in hippocampal recurrent circuits.

Automated summary

The authors used functional imaging, electrophysiology, and molecular identification to investigate how inhibitory interneurons regulate the inhibitory control of hippocampal memory traces during learning. They found that specific populations of interneurons play a role in memory reactivation events and the generation of sharp-wave ripples (SWRs). The activity of different types of interneurons correlates with SWR duration and behavior during hippocampal-dependent learning.