Literature DB >> 22806267

Activation patterns in superficial layers of neocortex change between experiences independent of behavior, environment, or the hippocampus.

Kaori Takehara-Nishiuchi1, Nathan Insel, Lan T Hoang, Zachary Wagner, Kathy Olson, Monica K Chawla, Sara N Burke, Carol A Barnes.   

Abstract

Previous work suggests that activation patterns of neurons in superficial layers of the neocortex are more sensitive to spatial context than activation patterns in deep cortical layers. A possible source of this laminar difference is the distribution of contextual information to the superficial cortical layers carried by hippocampal efferents that travel through the entorhinal cortex and subiculum. To evaluate the role that the hippocampus plays in determining context sensitivity in superficial cortical layers, behavior-induced expression of the immediate early gene Arc was examined in hippocampus-lesioned and control rats after exposing them to 2 distinct contexts. Contrary to expectations, hippocampal lesions had no observable effect on Arc expression in any neocortical layer relative to controls. Furthermore, another group of intact animals was exposed to the same environment twice, to determine the reliability of Arc-expression patterns across identical contextual and behavioral episodes. Although this condition included no difference in external input between 2 epochs, the significant layer differences in Arc expression still remained. Thus, laminar differences in activation or plasticity patterns are not likely to arise from hippocampal sources or differences in external inputs, but are more likely to be an intrinsic property of the neocortex.

Entities:  

Keywords:  context; episodic memory; hippocampus; immediate early gene; neocortex

Mesh:

Substances:

Year:  2012        PMID: 22806267      PMCID: PMC3733063          DOI: 10.1093/cercor/bhs209

Source DB:  PubMed          Journal:  Cereb Cortex        ISSN: 1047-3211            Impact factor:   5.357


  38 in total

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Authors:  B Bontempi; C Laurent-Demir; C Destrade; R Jaffard
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3.  Differential encoding of behavior and spatial context in deep and superficial layers of the neocortex.

Authors:  Sara N Burke; Monica K Chawla; Marsha R Penner; Brynne E Crowell; Paul F Worley; Carol A Barnes; Bruce L McNaughton
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4.  An investigation of the effects of hippocampal lesions in rats on pre- and postoperatively acquired spatial memory in a complex environment.

Authors:  Gordon Winocur; Morris Moscovitch; R Shayna Rosenbaum; Melanie Sekeres
Journal:  Hippocampus       Date:  2010-12       Impact factor: 3.899

5.  Spatial exploration induces ARC, a plasticity-related immediate-early gene, only in calcium/calmodulin-dependent protein kinase II-positive principal excitatory and inhibitory neurons of the rat forebrain.

Authors:  Almira Vazdarjanova; Victor Ramirez-Amaya; Nathan Insel; Thane K Plummer; Susanna Rosi; Shoaib Chowdhury; Dalia Mikhael; Paul F Worley; John F Guzowski; Carol A Barnes
Journal:  J Comp Neurol       Date:  2006-09-20       Impact factor: 3.215

6.  Arc, a growth factor and activity-regulated gene, encodes a novel cytoskeleton-associated protein that is enriched in neuronal dendrites.

Authors:  G L Lyford; K Yamagata; W E Kaufmann; C A Barnes; L K Sanders; N G Copeland; D J Gilbert; N A Jenkins; A A Lanahan; P F Worley
Journal:  Neuron       Date:  1995-02       Impact factor: 17.173

7.  Dynamics of the hippocampal ensemble code for space.

Authors:  M A Wilson; B L McNaughton
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8.  Differences in hippocampal neuronal population responses to modifications of an environmental context: evidence for distinct, yet complementary, functions of CA3 and CA1 ensembles.

Authors:  Almira Vazdarjanova; John F Guzowski
Journal:  J Neurosci       Date:  2004-07-21       Impact factor: 6.167

9.  CREB modulates excitability of nucleus accumbens neurons.

Authors:  Yan Dong; Thomas Green; Daniel Saal; Helene Marie; Rachael Neve; Eric J Nestler; Robert C Malenka
Journal:  Nat Neurosci       Date:  2006-03-05       Impact factor: 24.884

10.  CREB regulates excitability and the allocation of memory to subsets of neurons in the amygdala.

Authors:  Yu Zhou; Jaejoon Won; Mikael Guzman Karlsson; Miou Zhou; Thomas Rogerson; Jayaprakash Balaji; Rachael Neve; Panayiota Poirazi; Alcino J Silva
Journal:  Nat Neurosci       Date:  2009-09-27       Impact factor: 24.884

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  3 in total

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Authors:  Abbi R Hernandez; Jordan E Reasor; Leah M Truckenbrod; Keila T Campos; Quinten P Federico; Kaeli E Fertal; Katelyn N Lubke; Sarah A Johnson; Benjamin J Clark; Andrew P Maurer; Sara N Burke
Journal:  Neurobiol Aging       Date:  2018-06-30       Impact factor: 4.673

2.  Higher Arc Nucleus-to-Cytoplasm Ratio during Sleep in the Superficial Layers of the Mouse Cortex.

Authors:  Sakiko Honjoh; Luisa de Vivo; Hiroyuki Okuno; Haruhiko Bito; Giulio Tononi; Chiara Cirelli
Journal:  Front Neural Circuits       Date:  2017-08-23       Impact factor: 3.492

3.  Phasic and tonic neuron ensemble codes for stimulus-environment conjunctions in the lateral entorhinal cortex.

Authors:  Maryna Pilkiw; Nathan Insel; Younghua Cui; Caitlin Finney; Mark D Morrissey; Kaori Takehara-Nishiuchi
Journal:  Elife       Date:  2017-07-06       Impact factor: 8.140

  3 in total

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