Literature DB >> 10939340

Trajectory encoding in the hippocampus and entorhinal cortex.

L M Frank1, E N Brown, M Wilson.   

Abstract

We recorded from single neurons in the hippocampus and entorhinal cortex (EC) of rats to investigate the role of these structures in navigation and memory representation. Our results revealed two novel phenomena: first, many cells in CA1 and the EC fired at significantly different rates when the animal was in the same position depending on where the animal had come from or where it was going. Second, cells in deep layers of the EC, the targets of hippocampal outputs, appeared to represent the similarities between locations on spatially distinct trajectories through the environment. Our findings suggest that the hippocampus represents the animal's position in the context of a trajectory through space and that the EC represents regularities across different trajectories that could allow for generalization across experiences.

Entities:  

Keywords:  Non-programmatic

Mesh:

Year:  2000        PMID: 10939340     DOI: 10.1016/s0896-6273(00)00018-0

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  216 in total

1.  Experience-dependent changes in extracellular spike amplitude may reflect regulation of dendritic action potential back-propagation in rat hippocampal pyramidal cells.

Authors:  M C Quirk; K I Blum; M A Wilson
Journal:  J Neurosci       Date:  2001-01-01       Impact factor: 6.167

2.  Accumulation of hippocampal place fields at the goal location in an annular watermaze task.

Authors:  S A Hollup; S Molden; J G Donnett; M B Moser; E I Moser
Journal:  J Neurosci       Date:  2001-03-01       Impact factor: 6.167

3.  Contrasting patterns of receptive field plasticity in the hippocampus and the entorhinal cortex: an adaptive filtering approach.

Authors:  Loren M Frank; Uri T Eden; Victor Solo; Matthew A Wilson; Emery N Brown
Journal:  J Neurosci       Date:  2002-05-01       Impact factor: 6.167

4.  An analysis of neural receptive field plasticity by point process adaptive filtering.

Authors:  E N Brown; D P Nguyen; L M Frank; M A Wilson; V Solo
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-09       Impact factor: 11.205

5.  Spatial representation along the proximodistal axis of CA1.

Authors:  Espen J Henriksen; Laura L Colgin; Carol A Barnes; Menno P Witter; May-Britt Moser; Edvard I Moser
Journal:  Neuron       Date:  2010-10-06       Impact factor: 17.173

Review 6.  Elements of a neurobiological theory of the hippocampus: the role of activity-dependent synaptic plasticity in memory.

Authors:  R G M Morris; E I Moser; G Riedel; S J Martin; J Sandin; M Day; C O'Carroll
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2003-04-29       Impact factor: 6.237

7.  Learned association of allocentric and egocentric information in the hippocampus.

Authors:  Christian Hölscher; Wolfgang Jacob; Hanspeter A Mallot
Journal:  Exp Brain Res       Date:  2004-04-07       Impact factor: 1.972

8.  Dynamic coding of dorsal hippocampal neurons between tasks that differ in structure and memory demand.

Authors:  Henry L Hallock; Amy L Griffin
Journal:  Hippocampus       Date:  2012-10-04       Impact factor: 3.899

9.  Time Cells in the Hippocampus Are Neither Dependent on Medial Entorhinal Cortex Inputs nor Necessary for Spatial Working Memory.

Authors:  Marta Sabariego; Antonia Schönwald; Brittney L Boublil; David T Zimmerman; Siavash Ahmadi; Nailea Gonzalez; Christian Leibold; Robert E Clark; Jill K Leutgeb; Stefan Leutgeb
Journal:  Neuron       Date:  2019-05-02       Impact factor: 17.173

10.  Characterizing context-dependent differential firing activity in the hippocampus and entorhinal cortex.

Authors:  Michael J Prerau; Paul A Lipton; Howard B Eichenbaum; Uri T Eden
Journal:  Hippocampus       Date:  2014-02-03       Impact factor: 3.899

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