Literature DB >> 25378167

Back to the future: preserved hippocampal network activity during reverse ambulation.

Andrew P Maurer1, Adam W Lester2, Sara N Burke1, Jonathan J Ferng2, Carol A Barnes3.   

Abstract

During movement, there is a transition of activity across the population, such that place-field centers ahead of the rat are sequentially activated in the order that they will be encountered. Although the mechanisms responsible for this sequence updating are unknown, two classes of models can be considered. The first class involves head-direction information for activating neurons in the order that their place fields will be traversed. An alternative model contends that motion and turn-related information from the posterior parietal cortex shift the subset of active hippocampal cells across the population. To explicitly test these two models, rodents were trained to run backward on a linear track, placing movement in opposition with head orientation. Although head-direction did not change between running conditions, place-field activity remapped and there was an increase in place-field size during backward running compared with forward. The population activity, however, could still be used to reconstruct the location of the rat accurately. Moreover, theta phase precession was maintained in both running conditions, indicating preservation of place-field sequences on short-time scales. The observation that sequence encoding persists even when the animal is orientated away from the direction of movement favors the concept that posterior parietal cortical mechanisms may be partially responsible for updating hippocampal activity patterns.
Copyright © 2014 the authors 0270-6474/14/3415022-10$15.00/0.

Entities:  

Keywords:  oscillations; phase precession; place cells; population vector; sequence learning; theta

Mesh:

Year:  2014        PMID: 25378167      PMCID: PMC4220031          DOI: 10.1523/JNEUROSCI.1129-14.2014

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  76 in total

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Authors:  Kamran Diba; György Buzsáki
Journal:  Nat Neurosci       Date:  2007-09-02       Impact factor: 24.884

2.  Head-direction cells recorded from the postsubiculum in freely moving rats. II. Effects of environmental manipulations.

Authors:  J S Taube; R U Muller; J B Ranck
Journal:  J Neurosci       Date:  1990-02       Impact factor: 6.167

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Authors:  L T Thompson; P J Best
Journal:  Brain Res       Date:  1990-02-19       Impact factor: 3.252

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Authors:  R U Muller; J L Kubie; J B Ranck
Journal:  J Neurosci       Date:  1987-07       Impact factor: 6.167

5.  Cortical representation of motion during unrestrained spatial navigation in the rat.

Authors:  B L McNaughton; S J Mizumori; C A Barnes; B J Leonard; M Marquis; E J Green
Journal:  Cereb Cortex       Date:  1994 Jan-Feb       Impact factor: 5.357

6.  Phase relationship between hippocampal place units and the EEG theta rhythm.

Authors:  J O'Keefe; M L Recce
Journal:  Hippocampus       Date:  1993-07       Impact factor: 3.899

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Authors:  M A Wilson; B L McNaughton
Journal:  Science       Date:  1993-08-20       Impact factor: 47.728

8.  Spatial information content and reliability of hippocampal CA1 neurons: effects of visual input.

Authors:  E J Markus; C A Barnes; B L McNaughton; V L Gladden; W E Skaggs
Journal:  Hippocampus       Date:  1994-08       Impact factor: 3.899

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Authors:  R U Muller; E Bostock; J S Taube; J L Kubie
Journal:  J Neurosci       Date:  1994-12       Impact factor: 6.167

Review 10.  Cellular bases of hippocampal EEG in the behaving rat.

Authors:  G Buzsáki; L W Leung; C H Vanderwolf
Journal:  Brain Res       Date:  1983-10       Impact factor: 3.252

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  10 in total

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Review 2.  Grid Cells and Place Cells: An Integrated View of their Navigational and Memory Function.

Authors:  Honi Sanders; César Rennó-Costa; Marco Idiart; John Lisman
Journal:  Trends Neurosci       Date:  2015-11-24       Impact factor: 13.837

3.  A neural-level model of spatial memory and imagery.

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4.  Entorhinal-CA3 Dual-Input Control of Spike Timing in the Hippocampus by Theta-Gamma Coupling.

Authors:  Antonio Fernández-Ruiz; Azahara Oliva; Gergő A Nagy; Andrew P Maurer; Antal Berényi; György Buzsáki
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5.  Independent theta phase coding accounts for CA1 population sequences and enables flexible remapping.

Authors:  Angus Chadwick; Mark C W van Rossum; Matthew F Nolan
Journal:  Elife       Date:  2015-02-02       Impact factor: 8.140

6.  Experience-Related Changes in Place Cell Responses to New Sensory Configuration That Does Not Occur in the Natural Environment in the Rat Hippocampus.

Authors:  Dan Zou; Hiroshi Nishimaru; Jumpei Matsumoto; Yusaku Takamura; Taketoshi Ono; Hisao Nishijo
Journal:  Front Pharmacol       Date:  2017-08-23       Impact factor: 5.810

7.  Flexible theta sequence compression mediated via phase precessing interneurons.

Authors:  Angus Chadwick; Mark Cw van Rossum; Matthew F Nolan
Journal:  Elife       Date:  2016-12-08       Impact factor: 8.140

8.  Altered neural odometry in the vertical dimension.

Authors:  Giulio Casali; Daniel Bush; Kate Jeffery
Journal:  Proc Natl Acad Sci U S A       Date:  2019-02-15       Impact factor: 11.205

9.  Ripple band phase precession of place cell firing during replay.

Authors:  Daniel Bush; H Freyja Ólafsdóttir; Caswell Barry; Neil Burgess
Journal:  Curr Biol       Date:  2021-11-02       Impact factor: 10.834

10.  Advantages and detection of phase coding in the absence of rhythmicity.

Authors:  Daniel Bush; Neil Burgess
Journal:  Hippocampus       Date:  2020-02-17       Impact factor: 3.753

  10 in total

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