Abstract

The place cells and well-defined oscillatory population rhythms of the rodent hippocampus have served as a powerful model system in linking cells and circuits to memory function. While the initial three decades of place cell research primarily focused on the activity of neurons during exploration, the last twenty-five years have seen growing interest in the physiology of the hippocampus at rest. During slow-wave sleep and quiet wakefulness the hippocampus exhibits sharp-wave ripples (SWRs), short high-frequency, high-amplitude oscillations, that organize the reactivation or ‘replay’ of sequences of place cells, and interventions that disrupt SWRs impair learning. While the canonical model of SWRs generation have emphasized CA3 input to CA1 as the source of excitatory drive, recent work suggests there are multiple circuits, including the CA2 region, that can both influence, generate and organize SWRs, both from the oscillatory and information content perspectives in a task and state-dependent manner. This extended circuitry and its function must be considered for a true understanding of the role of the hippocampus in off-line processes such as planning and consolidation.

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