Linking Cellular Mechanisms to Behavior: Entorhinal Persistent Spiking and Membrane Potential Oscillations May Underlie Path Integration, Grid Cell Firing, and Episodic Memory

The entorhinal cortex plays an important role in spatial memory and episodic memory functions. These functions may result from cellular mechanisms for integration of the afferent input to entorhinal cortex. This article reviews physiological data on persistent spiking and membrane potential oscilla...

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Main Authors: Michael E. Hasselmo, Mark P. Brandon
Format: Article
Language:English
Published: Hindawi Limited 2008-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2008/658323
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spelling doaj-069fa82287d7411da61ddd693f29743d2020-11-24T22:32:48ZengHindawi LimitedNeural Plasticity2090-59041687-54432008-01-01200810.1155/2008/658323658323Linking Cellular Mechanisms to Behavior: Entorhinal Persistent Spiking and Membrane Potential Oscillations May Underlie Path Integration, Grid Cell Firing, and Episodic MemoryMichael E. Hasselmo0Mark P. Brandon1Center for Memory and Brain, Department of Psychology and Program in Neuroscience, Boston University, 2 Cummington Sreet, Boston, MA 02215, USACenter for Memory and Brain, Department of Psychology and Program in Neuroscience, Boston University, 2 Cummington Sreet, Boston, MA 02215, USAThe entorhinal cortex plays an important role in spatial memory and episodic memory functions. These functions may result from cellular mechanisms for integration of the afferent input to entorhinal cortex. This article reviews physiological data on persistent spiking and membrane potential oscillations in entorhinal cortex then presents models showing how both these cellular mechanisms could contribute to properties observed during unit recording, including grid cell firing, and how they could underlie behavioural functions including path integration. The interaction of oscillations and persistent firing could contribute to encoding and retrieval of trajectories through space and time as a mechanism relevant to episodic memory.http://dx.doi.org/10.1155/2008/658323
collection DOAJ
language English
format Article
sources DOAJ
author Michael E. Hasselmo
Mark P. Brandon
spellingShingle Michael E. Hasselmo
Mark P. Brandon
Linking Cellular Mechanisms to Behavior: Entorhinal Persistent Spiking and Membrane Potential Oscillations May Underlie Path Integration, Grid Cell Firing, and Episodic Memory
Neural Plasticity
author_facet Michael E. Hasselmo
Mark P. Brandon
author_sort Michael E. Hasselmo
title Linking Cellular Mechanisms to Behavior: Entorhinal Persistent Spiking and Membrane Potential Oscillations May Underlie Path Integration, Grid Cell Firing, and Episodic Memory
title_short Linking Cellular Mechanisms to Behavior: Entorhinal Persistent Spiking and Membrane Potential Oscillations May Underlie Path Integration, Grid Cell Firing, and Episodic Memory
title_full Linking Cellular Mechanisms to Behavior: Entorhinal Persistent Spiking and Membrane Potential Oscillations May Underlie Path Integration, Grid Cell Firing, and Episodic Memory
title_fullStr Linking Cellular Mechanisms to Behavior: Entorhinal Persistent Spiking and Membrane Potential Oscillations May Underlie Path Integration, Grid Cell Firing, and Episodic Memory
title_full_unstemmed Linking Cellular Mechanisms to Behavior: Entorhinal Persistent Spiking and Membrane Potential Oscillations May Underlie Path Integration, Grid Cell Firing, and Episodic Memory
title_sort linking cellular mechanisms to behavior: entorhinal persistent spiking and membrane potential oscillations may underlie path integration, grid cell firing, and episodic memory
publisher Hindawi Limited
series Neural Plasticity
issn 2090-5904
1687-5443
publishDate 2008-01-01
description The entorhinal cortex plays an important role in spatial memory and episodic memory functions. These functions may result from cellular mechanisms for integration of the afferent input to entorhinal cortex. This article reviews physiological data on persistent spiking and membrane potential oscillations in entorhinal cortex then presents models showing how both these cellular mechanisms could contribute to properties observed during unit recording, including grid cell firing, and how they could underlie behavioural functions including path integration. The interaction of oscillations and persistent firing could contribute to encoding and retrieval of trajectories through space and time as a mechanism relevant to episodic memory.
url http://dx.doi.org/10.1155/2008/658323
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