Literature DB >> 23175823

Hippocampal phase precession from dual input components.

Frances S Chance1.   

Abstract

Phase precession is a well known phenomenon in which a hippocampal place cell will fire action potentials at successively earlier phases (relative to the theta-band oscillations recorded in the local field potential) as an animal moves through the cell's receptive field (also known as a place field). We present a model in which CA1 pyramidal cell spiking is driven by dual input components arising from CA3 and EC3. The receptive fields of these two input components overlap but are offset in space from each other such that as the animal moves through the model place field, action potentials are driven first by the CA3 input component and then the EC3 input component. As CA3 synaptic input is known to arrive in CA1 at a later theta phase than EC3 input (Mizuseki et al., 2009; Montgomery et al., 2009), CA1 spiking advances in phase as the model transitions from CA3-driven spiking to EC3-driven spiking. Here spike phase is a function of animal location, placing our results in agreement with many experimental observations characterizing CA1 phase precession (O'Keefe and Recce, 1993; Huxter et al., 2003; Geisler et al., 2007). We predict that experimental manipulations that dramatically enhance or disrupt activity in either of these areas should have a significant effect on phase precession observed in CA1.

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Year:  2012        PMID: 23175823      PMCID: PMC6621772          DOI: 10.1523/JNEUROSCI.2786-12.2012

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


  16 in total

1.  Inhibitory suppression of heterogeneously tuned excitation enhances spatial coding in CA1 place cells.

Authors:  Christine Grienberger; Aaron D Milstein; Katie C Bittner; Sandro Romani; Jeffrey C Magee
Journal:  Nat Neurosci       Date:  2017-01-23       Impact factor: 24.884

2.  Modeling inheritance of phase precession in the hippocampal formation.

Authors:  Jorge Jaramillo; Robert Schmidt; Richard Kempter
Journal:  J Neurosci       Date:  2014-05-28       Impact factor: 6.167

3.  Silencing CA3 disrupts temporal coding in the CA1 ensemble.

Authors:  Steven J Middleton; Thomas J McHugh
Journal:  Nat Neurosci       Date:  2016-05-30       Impact factor: 24.884

Review 4.  Neural mechanisms of navigation involving interactions of cortical and subcortical structures.

Authors:  James R Hinman; Holger Dannenberg; Andrew S Alexander; Michael E Hasselmo
Journal:  J Neurophysiol       Date:  2018-02-14       Impact factor: 2.714

5.  Replay as wavefronts and theta sequences as bump oscillations in a grid cell attractor network.

Authors:  Louis Kang; Michael R DeWeese
Journal:  Elife       Date:  2019-11-18       Impact factor: 8.140

6.  Synaptic learning rules for sequence learning.

Authors:  Eric Torsten Reifenstein; Ikhwan Bin Khalid; Richard Kempter
Journal:  Elife       Date:  2021-04-16       Impact factor: 8.140

7.  Transformation of a Spatial Map across the Hippocampal-Lateral Septal Circuit.

Authors:  David Tingley; György Buzsáki
Journal:  Neuron       Date:  2018-05-17       Impact factor: 17.173

8.  Reversed theta sequences of hippocampal cell assemblies during backward travel.

Authors:  Anne Cei; Gabrielle Girardeau; Céline Drieu; Karim El Kanbi; Michaël Zugaro
Journal:  Nat Neurosci       Date:  2014-03-25       Impact factor: 24.884

9.  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
Journal:  Neuron       Date:  2017-03-08       Impact factor: 17.173

Review 10.  State-dependencies of learning across brain scales.

Authors:  Petra Ritter; Jan Born; Michael Brecht; Hubert R Dinse; Uwe Heinemann; Burkhard Pleger; Dietmar Schmitz; Susanne Schreiber; Arno Villringer; Richard Kempter
Journal:  Front Comput Neurosci       Date:  2015-02-26       Impact factor: 2.380

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