Skip to content
Review Open access

Hippocampal-Cortical Circuits and Memory.

Aug 2026 · The Neuroscientist · pp. 10738584261469147 · 0 citations · 178 references
Medicine

TL;DR

Recurrent processing loops among the entorhinal cortex, hippocampus, and neocortex enable ongoing updating and integration of memory representations, challenging traditional sequential processing models and emphasizing the dynamic and interactive nature of these circuits.

Abstract

This review examines how distributed neural circuits involving the hippocampus, entorhinal cortex, and neocortex collectively support learning and memory functions. The hippocampus and entorhinal cortex are densely and bidirectionally connected, forming a core circuit that supports the formation of episodic memories as well as spatial learning and navigation. Their interactions with neocortical regions underlie decision making and the transformation of episodic experience into abstract concepts. These functions are supported by precisely timed interactions between neuronal ensembles across distributed circuits, coordinated by neural oscillations. During learning and navigation, theta oscillations synchronize the firing of neuronal ensembles and mediate the flow of information across structures. During periods of rest and sleep, hippocampal sharp-wave ripples coordinate the reactivation of experience-related activity patterns. Sharp-wave ripples mediate the transfer of memory traces from the hippocampus to the neocortex and their long-term consolidation. Rather than a unidirectional transfer from hippocampus to neocortex, emerging evidence reveals continuous bidirectional interactions throughout memory encoding, consolidation, and retrieval. Critically, recurrent processing loops among the entorhinal cortex, hippocampus, and neocortex enable ongoing updating and integration of memory representations, challenging traditional sequential processing models and emphasizing the dynamic and interactive nature of these circuits.

Read PDF

Similar papers

Open access Aug 2026

Circuit-specific reorganization of hippocampal-entorhinal-prefrontal subnetworks supports memory recall across the lifespan

The results refine prevailing systems consolidation theories by showing that memory consolidation is a circuit-specific and temporally ordered process, rather than a passive gradual phenomenon, and position the EC as a central and dynamic component of remote memory retrieval alongside the PFC.

Erika Atucha, Rukhshona Kayumova, Celia Fürst et al. · 0 citations
Open access Oct 2026

Selective Hippocampal Reactivation Driven by Neocortical Feedback Supports Memory Transfer in Predictive-Coding Networks

During sleep and quiet wakefulness, the brain spontaneously revisits neural activity patterns associated with previous experience, a phenomenon known as reactivation, or replay. Reactivation is thought to support systems consolidation, the process by which memory retrieval becomes progressively more dependent on neocor...

Saighi Paul · 0 citations
Open access Sep 2026

Transient excitability and synaptic consolidation support stable memory despite neural drift

A two-region recurrent network model of the hippocampus and anterior cingulate cortex is developed incorporating region-specific synaptic plasticity, excitability-dependent neuronal allocation, hippocampal-to-cortical coupling, and activity-dependent intrinsic plasticity to support a sequential mechanism in which hippo...

S. Wagle, C. Clopath · 0 citations
Open access Aug 2026

Distinct prefrontal-amygdala connectivity drives consolidated fear memories

These insights reveal that the consolidated engram requires the targeted engagement of a post-learning engram circuit, rather than a simple reactivation of neurons engaged during initial learning.

M. Kenna, James P. Kesby, Li Xu et al. · 0 citations
Open access Mar 2025

A cortical–hippocampal communication undergoes rebalancing after new learning

The brain’s ability to consolidate a wide range of memories while maintaining their distinctiveness across experiences remains poorly understood. Sharp-wave ripples, neural oscillations that occur predominantly within CA1 of the hippocampus during immobility and sleep, have been shown to play a critical role in the con...

Arron F. Hall, Dong V. Wang · 2 citations
Review Open access Sep 2026

Instructive signals drive learning through behavioral timescale synaptic plasticity in the hippocampus and beyond

Observations support a view of BTSP as a multi-factor plasticity rule that links synaptic, circuit, and systems-level processes, providing a biologically grounded framework for understanding how the brain rapidly incorporates new information.

L. Wilmerding, Fox Gourianova, Christine Grienberger · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.