Literature DB >> 10401637

Head direction cells in the primate pre-subiculum.

R G Robertson1, E T Rolls, P Georges-François, S Panzeri.   

Abstract

The function of the primate hippocampus and related structures was analysed by making recordings from the hippocampus, subiculum, presubiculum, and parahippocampal gyrus in monkeys actively walking in the laboratory. Head direction cells were found in the presubiculum. The firing rate of these cells was a function of the head direction of the monkey, with a response that was typically 10-100 times larger to the best as compared to the opposite direction. The mean half-amplitude width of the tuning of the cells was 76 degrees. The response of head direction cells in the presubiculum was not influenced by the place where the monkey was, there being the same tuning to head direction at different places in a room, and even outside the room. The response of these cells was also independent of the "spatial view" observed by the monkey, and also the position of the eyes in the head. The average information about head direction was 0.64 bits, about place was 0.10 bits, about spatial view was 0.27 bits, and about eye position was 0.04 bits. The cells maintained their tuning for periods of at least several minutes when the view details were obscured or the room was darkened. This representation of head direction could be useful together with the hippocampal spatial view cells and whole body motion cells found in primates in such spatial and memory functions as path integration.

Mesh:

Year:  1999        PMID: 10401637     DOI: 10.1002/(SICI)1098-1063(1999)9:3<206::AID-HIPO2>3.0.CO;2-H

Source DB:  PubMed          Journal:  Hippocampus        ISSN: 1050-9631            Impact factor:   3.899


  45 in total

1.  Rapid spatial reorientation and head direction cells.

Authors:  Michaël B Zugaro; Angelo Arleo; Alain Berthoz; Sidney I Wiener
Journal:  J Neurosci       Date:  2003-04-15       Impact factor: 6.167

2.  Vestibular, optokinetic, and cognitive contribution to the guidance of passive self-rotation toward instructed targets.

Authors:  Reinhart Jürgens; Grigorios Nasios; Wolfgang Becker
Journal:  Exp Brain Res       Date:  2003-05-10       Impact factor: 1.972

3.  The use of decoding to analyze the contribution to the information of the correlations between the firing of simultaneously recorded neurons.

Authors:  Leonardo Franco; Edmund T Rolls; Nikolaos C Aggelopoulos; Alessandro Treves
Journal:  Exp Brain Res       Date:  2004-01-13       Impact factor: 1.972

4.  Saccade direction encoding in the primate entorhinal cortex during visual exploration.

Authors:  Nathaniel J Killian; Steve M Potter; Elizabeth A Buffalo
Journal:  Proc Natl Acad Sci U S A       Date:  2015-12-07       Impact factor: 11.205

5.  Common Neural Representations for Visually Guided Reorientation and Spatial Imagery.

Authors:  Lindsay K Vass; Russell A Epstein
Journal:  Cereb Cortex       Date:  2017-02-01       Impact factor: 5.357

6.  Allocentric spatial referencing of neuronal activity in macaque posterior cingulate cortex.

Authors:  Heather L Dean; Michael L Platt
Journal:  J Neurosci       Date:  2006-01-25       Impact factor: 6.167

7.  Angular displacement perception modulated by force background.

Authors:  James R Lackner; Paul DiZio
Journal:  Exp Brain Res       Date:  2009-04-19       Impact factor: 1.972

8.  The role of attention on the integration of visual and inertial cues.

Authors:  Daniel R Berger; Heinrich H Bülthoff
Journal:  Exp Brain Res       Date:  2009-04-07       Impact factor: 1.972

9.  Deriving angular displacement from optic flow: a fMRI study.

Authors:  Volker Diekmann; Reinhart Jürgens; Wolfgang Becker
Journal:  Exp Brain Res       Date:  2009-03-20       Impact factor: 1.972

Review 10.  A new neural framework for visuospatial processing.

Authors:  Dwight J Kravitz; Kadharbatcha S Saleem; Chris I Baker; Mortimer Mishkin
Journal:  Nat Rev Neurosci       Date:  2011-04       Impact factor: 34.870

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