Literature DB >> 35396329

Aberrant Phase Precession of Lateral Septal Cells in a Maternal Immune Activation Model of Schizophrenia Risk May Disrupt the Integration of Location with Reward.

Lucinda J Speers1, Robert Schmidt2, David K Bilkey3.   

Abstract

Spatial memory and reward processing are known to be disrupted in schizophrenia. Since the lateral septum (LS) may play an important role in the integration of location and reward, we examined the effect of maternal immune activation (MIA), a known schizophrenia risk factor, on spatial representation in the rat LS. In support of a previous study, we found that spatial location is represented as a phase code in the rostral LS of adult male rats, so that LS cell spiking shifts systematically against the phase of the hippocampal, theta-frequency, local field potential as an animal moves along a track toward a reward (phase precession). Whereas shallow precession slopes were observed in control group cells, they were steeper in the MIA animals, such that firing frequently precessed across several theta cycles as the animal moved along the length of the apparatus, with subsequent ambiguity in the phase representation of location. Furthermore, an analysis of the phase trajectories of the control group cells revealed that the population tended to converge toward a common firing phase as the animal approached the reward location. This suggested that phase coding in these cells might signal both reward location and the distance to reward. By comparison, the degree of phase convergence in the MIA-group cells was weak, and the region of peak convergence was distal to the reward location. These findings suggest that a schizophrenia risk factor disrupts the phase-based encoding of location-reward relationships in the LS, potentially smearing reward representations across space.SIGNIFICANCE STATEMENT It is unclear how spatial or contextual information generated by hippocampal cells is converted to a code that can be used to signal reward location in regions, such as the VTA. Here we provide evidence that the firing phase of cells in the lateral septum, a region that links the two areas, may code reward location in the firing phase of cells. This phase coding is disrupted in a maternal immune activation model of schizophrenia risk such that representations of reward may be smeared across space in maternal immune activation animals. This could potentially underlie erroneous reward processing and misattribution of salience in schizophrenia.
Copyright © 2022 the authors.

Entities:  

Keywords:  lateral septum; maternal immune activation; phase precession; schizophrenia

Mesh:

Year:  2022        PMID: 35396329      PMCID: PMC9121831          DOI: 10.1523/JNEUROSCI.0039-22.2022

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.709


  79 in total

1.  Hippocampal theta sequences.

Authors:  David J Foster; Matthew A Wilson
Journal:  Hippocampus       Date:  2007       Impact factor: 3.899

2.  Dissociation between the experience-dependent development of hippocampal theta sequences and single-trial phase precession.

Authors:  Ting Feng; Delia Silva; David J Foster
Journal:  J Neurosci       Date:  2015-03-25       Impact factor: 6.167

3.  Theta sequences are essential for internally generated hippocampal firing fields.

Authors:  Yingxue Wang; Sandro Romani; Brian Lustig; Anthony Leonardo; Eva Pastalkova
Journal:  Nat Neurosci       Date:  2014-12-22       Impact factor: 24.884

4.  The role of CA3-LS-VTA loop in the formation of conditioned place preference induced by context-associated reward memory for morphine.

Authors:  Jin-Xiang Jiang; Huan Liu; Zhen-Zhen Huang; Yue Cui; Xue-Qin Zhang; Xiao-Long Zhang; Yu Cui; Wen-Jun Xin
Journal:  Addict Biol       Date:  2016-11-11       Impact factor: 4.280

5.  Recognition of visual stimuli and memory for spatial context in schizophrenic patients and healthy volunteers.

Authors:  Gildas Brébion; Anthony S David; Lyn S Pilowsky; Hugh Jones
Journal:  J Clin Exp Neuropsychol       Date:  2004-11       Impact factor: 2.475

6.  Self-motion and the hippocampal spatial metric.

Authors:  Alejandro Terrazas; Michael Krause; Peter Lipa; Katalin M Gothard; Carol A Barnes; Bruce L McNaughton
Journal:  J Neurosci       Date:  2005-08-31       Impact factor: 6.167

7.  Late prenatal immune activation in mice leads to behavioral and neurochemical abnormalities relevant to the negative symptoms of schizophrenia.

Authors:  Byron K Y Bitanihirwe; Daria Peleg-Raibstein; Forouhar Mouttet; Joram Feldon; Urs Meyer
Journal:  Neuropsychopharmacology       Date:  2010-08-25       Impact factor: 7.853

8.  Impairment on the hippocampal-dependent virtual Morris water task in schizophrenia.

Authors:  Faith M Hanlon; Michael P Weisend; Derek A Hamilton; Aaron P Jones; Robert J Thoma; Mingxiong Huang; Kimberly Martin; Ronald A Yeo; Gregory A Miller; Jose M Cañive
Journal:  Schizophr Res       Date:  2006-07-14       Impact factor: 4.939

9.  Adaptation to chronic PCP results in hyperfunctional NMDA and hypofunctional GABA(A) synaptic receptors.

Authors:  B Yu; C Wang; J Liu; K M Johnson; J P Gallagher
Journal:  Neuroscience       Date:  2002       Impact factor: 3.590

10.  Phase precession in the human hippocampus and entorhinal cortex.

Authors:  Salman E Qasim; Itzhak Fried; Joshua Jacobs
Journal:  Cell       Date:  2021-05-11       Impact factor: 66.850

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.