Literature DB >> 23034954

Limbic system structures differentially contribute to exploratory trip organization of the rat.

Shawn S Winter1, Jenny R Köppen, Tialia B N Ebert, Douglas G Wallace.   

Abstract

The role of limbic system structures in spatial orientation continues to be debated. The hippocampus (HPC) has been implicated in encoding symbolic representations of environments (i.e., cognitive map), whereas entorhinal cortex (EC) function has been implicated in self-movement cue processing (i.e., dead reckoning). These distinctions largely depend on the electrophysiological characteristics of cells within these regions and behavioral tasks that typically fail to dissociate environmental and self-movement cue processing. Topographic and kinematic characteristics of exploratory trip organization have been shown to differentially depend on environmental and self-movement cue processing. The present study examines the effects of either HPC or EC lesions on exploratory trip organization under varying lighting conditions. HPC lesions selectively impaired all measures of performance under dark conditions, but spared all measures of performance under light conditions. EC lesions impaired kinematic measures related to distance estimation under all conditions and impaired all measures of performance under light conditions. These results provide evidence that the HPC is involved in processing self-movement cues but not environmental cues, and EC is involved in processing distance estimates generated from either self-movement or environmental cues. These observations provide further support for serial processing of self-movement cues through limbic system structures that converge on the HPC.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 23034954     DOI: 10.1002/hipo.22075

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


  9 in total

1.  Lesions of the hippocampus or dorsolateral striatum disrupt distinct aspects of spatial navigation strategies based on proximal and distal information in a cued variant of the Morris water task.

Authors:  James P Rice; Douglas G Wallace; Derek A Hamilton
Journal:  Behav Brain Res       Date:  2015-04-20       Impact factor: 3.332

2.  Effects of acquired vestibular pathology on the organization of mouse exploratory behavior.

Authors:  Mark T Banovetz; Rami I Lake; Ashley A Blackwell; Jenna R Osterlund Oltmanns; Ericka A Schaeffer; Ryan M Yoder; Douglas G Wallace
Journal:  Exp Brain Res       Date:  2021-02-08       Impact factor: 1.972

3.  Spatial navigation. Disruption of the head direction cell network impairs the parahippocampal grid cell signal.

Authors:  Shawn S Winter; Benjamin J Clark; Jeffrey S Taube
Journal:  Science       Date:  2015-02-05       Impact factor: 47.728

4.  Otolith dysfunction alters exploratory movement in mice.

Authors:  Philip A Blankenship; Lucia A Cherep; Tia N Donaldson; Sarah N Brockman; Alexandria D Trainer; Ryan M Yoder; Douglas G Wallace
Journal:  Behav Brain Res       Date:  2017-02-21       Impact factor: 3.332

5.  Sexually dimorphic organization of open field behavior following moderate prenatal alcohol exposure.

Authors:  Jenna R Osterlund Oltmanns; Ericka A Schaeffer; Monica Goncalves Garcia; Tia N Donaldson; Gabriela Acosta; Lilliana M Sanchez; Suzy Davies; Daniel D Savage; Douglas G Wallace; Benjamin J Clark
Journal:  Alcohol Clin Exp Res       Date:  2022-04-11       Impact factor: 3.928

6.  Passive Transport Disrupts Grid Signals in the Parahippocampal Cortex.

Authors:  Shawn S Winter; Max L Mehlman; Benjamin J Clark; Jeffrey S Taube
Journal:  Curr Biol       Date:  2015-09-17       Impact factor: 10.834

7.  Behavioral and Neural Subsystems of Rodent Exploration.

Authors:  Shannon M Thompson; Laura E Berkowitz; Benjamin J Clark
Journal:  Learn Motiv       Date:  2017-04-13

8.  Hypothalamic-pituitary-adrenal axis hypersensitivity in female rats on a post-weaning high-fat diet after chronic mild stress.

Authors:  Lian Liu; Junqiang Yang; Feng Qian; Chengbiao Lu
Journal:  Exp Ther Med       Date:  2017-05-23       Impact factor: 2.447

9.  Stellate Cells in the Medial Entorhinal Cortex Are Required for Spatial Learning.

Authors:  Sarah A Tennant; Lukas Fischer; Derek L F Garden; Klára Zsófia Gerlei; Cristina Martinez-Gonzalez; Christina McClure; Emma R Wood; Matthew F Nolan
Journal:  Cell Rep       Date:  2018-01-30       Impact factor: 9.423

  9 in total

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