Literature DB >> 16921500

Behavioral correlates of the distributed coding of spatial context.

Michael I Anderson1, Sarah Killing, Caitlin Morris, Alan O'Donoghue, Dikennam Onyiagha, Rosemary Stevenson, Madeleine Verriotis, Kathryn J Jeffery.   

Abstract

Hippocampal place cells respond heterogeneously to elemental changes of a compound spatial context, suggesting that they form a distributed code of context, whereby context information is shared across a population of neurons. The question arises as to what this distributed code might be useful for. The present study explored two possibilities: one, that it allows contexts with common elements to be disambiguated, and the other, that it allows a given context to be associated with more than one outcome. We used two naturalistic measures of context processing in rats, rearing and thigmotaxis (boundary-hugging), to explore how rats responded to contextual novelty and to relate this to the behavior of place cells. In experiment 1, rats showed dishabituation of rearing to a novel reconfiguration of familiar context elements, suggesting that they perceived the reconfiguration as novel, a behavior that parallels that of place cells in a similar situation. In experiment 2, rats were trained in a place preference task on an open-field arena. A change in the arena context triggered renewed thigmotaxis, and yet navigation continued unimpaired, indicating simultaneous representation of both the altered contextual and constant spatial cues. Place cells similarly exhibited a dual population of responses, consistent with the hypothesis that their activity underlies spatial behavior. Together, these experiments suggest that heterogeneous context encoding (or "partial remapping") by place cells may function to allow the flexible assignment of associations to contexts, a faculty that could be useful in episodic memory encoding. Copyright (c) 2006 Wiley-Liss, Inc.

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Year:  2006        PMID: 16921500     DOI: 10.1002/hipo.20206

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


  13 in total

1.  Framing of grid cells within and beyond navigation boundaries.

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2.  Dominance of the proximal coordinate frame in determining the locations of hippocampal place cell activity during navigation.

Authors:  Jennifer J Siegel; Joshua P Neunuebel; James J Knierim
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3.  Pattern separation in the dentate gyrus: a role for the CA3 backprojection.

Authors:  Catherine E Myers; Helen E Scharfman
Journal:  Hippocampus       Date:  2010-08-03       Impact factor: 3.899

4.  Objects and landmarks: hippocampal place cells respond differently to manipulations of visual cues depending on size, perspective, and experience.

Authors:  Kristin M Scaplen; Arune A Gulati; Victoria L Heimer-McGinn; Rebecca D Burwell
Journal:  Hippocampus       Date:  2014-08-13       Impact factor: 3.899

Review 5.  Theoretical accounts of spatial learning: a neurobiological view (commentary on Pearce, 2009).

Authors:  Kathryn J Jeffery
Journal:  Q J Exp Psychol (Hove)       Date:  2010-03-04       Impact factor: 2.143

6.  Distinct pathways for rule-based retrieval and spatial mapping of memory representations in hippocampal neurons.

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Journal:  J Neurosci       Date:  2013-01-16       Impact factor: 6.167

Review 7.  Place cells, grid cells, attractors, and remapping.

Authors:  Kathryn J Jeffery
Journal:  Neural Plast       Date:  2011-11-03       Impact factor: 3.599

8.  Hippocampal lesions impair rapid learning of a continuous spatial alternation task.

Authors:  Steve M Kim; Loren M Frank
Journal:  PLoS One       Date:  2009-05-08       Impact factor: 3.240

9.  Novelty and anxiolytic drugs dissociate two components of hippocampal theta in behaving rats.

Authors:  Christine E Wells; Doran P Amos; Ali Jeewajee; Vincent Douchamps; John Rodgers; John O'Keefe; Neil Burgess; Colin Lever
Journal:  J Neurosci       Date:  2013-05-15       Impact factor: 6.167

Review 10.  A specific role for septohippocampal acetylcholine in memory?

Authors:  Alexander Easton; Vincent Douchamps; Madeline Eacott; Colin Lever
Journal:  Neuropsychologia       Date:  2012-08-03       Impact factor: 3.139

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