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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2008-01-01
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Series: | Neural Plasticity |
Online Access: | http://dx.doi.org/10.1155/2008/658323 |
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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 |
work_keys_str_mv |
AT michaelehasselmo linkingcellularmechanismstobehaviorentorhinalpersistentspikingandmembranepotentialoscillationsmayunderliepathintegrationgridcellfiringandepisodicmemory AT markpbrandon linkingcellularmechanismstobehaviorentorhinalpersistentspikingandmembranepotentialoscillationsmayunderliepathintegrationgridcellfiringandepisodicmemory |
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