Literature DB >> 11163635

Deficits in allothetic and idiothetic spatial behavior in rats with posterior cingulate cortex lesions.

I Q Whishaw1, H Maaswinkel, C L Gonzalez, B Kolb.   

Abstract

The cingulate cortex plays a central role in bridging neocortical and limbic structures involved in allothetic navigation, a form of navigation requiring the use of external cues. Animals can also navigate using idiothetic cues, which are cues generated by self-movement, but there have been no definitive tests of whether cingulate cortex also plays a role in idiothetic navigation. Rats with anterior cingulate (medial frontal) and posterior cingulate cortex (retrosplenial) suction ablations were trained to search for large food pellets on an open table, and the accuracy with which they returned home with the food was measured. In the idiothetic task they searched for food from a novel starting location under infrared light, and with surface olfactory cues displaced. The rats also received two tests of allothetic navigation. They were tested on a matching-to-place task in which they foraged for food from a number of successively presented new locations under normal room light, and they were trained to locate a hidden platform in a swimming pool (Morris place task). The group with posterior cingulate cortex lesions was severely impaired on all of the navigation tasks whereas the group with anterior cingulate cortex lesions displayed no deficit on the idiothetic task and only moderate deficits on the other tasks. The results demonstrate a role for posterior cingulate region in idiothetic navigation.

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Mesh:

Year:  2001        PMID: 11163635     DOI: 10.1016/s0166-4328(00)00312-0

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  35 in total

1.  Acetylcholine contributes to the integration of self-movement cues in head direction cells.

Authors:  Ryan M Yoder; Jeremy H M Chan; Jeffrey S Taube
Journal:  Behav Neurosci       Date:  2017-08       Impact factor: 1.912

2.  Navigating from hippocampus to parietal cortex.

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Journal:  Proc Natl Acad Sci U S A       Date:  2008-09-23       Impact factor: 11.205

3.  Impaired spatial performance in rats with retrosplenial lesions: importance of the spatial problem and the rat strain in identifying lesion effects in a swimming pool.

Authors:  K Troy Harker; Ian Q Whishaw
Journal:  J Neurosci       Date:  2002-02-01       Impact factor: 6.167

Review 4.  The retrosplenial-parietal network and reference frame coordination for spatial navigation.

Authors:  Benjamin J Clark; Christine M Simmons; Laura E Berkowitz; Aaron A Wilber
Journal:  Behav Neurosci       Date:  2018-08-09       Impact factor: 1.912

5.  Mapping resting-state brain networks in conscious animals.

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Journal:  J Neurosci Methods       Date:  2010-04-09       Impact factor: 2.390

6.  Coordinated activities of retrosplenial ensembles during resting-state encode spatial landmarks.

Authors:  HaoRan Chang; Ingrid M Esteves; Adam R Neumann; Jianjun Sun; Majid H Mohajerani; Bruce L McNaughton
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2020-04-06       Impact factor: 6.237

7.  Impaired head direction cell representation in the anterodorsal thalamus after lesions of the retrosplenial cortex.

Authors:  Benjamin J Clark; Joshua P Bassett; Sarah S Wang; Jeffrey S Taube
Journal:  J Neurosci       Date:  2010-04-14       Impact factor: 6.167

8.  Neural basis of stereotype-induced shifts in women's mental rotation performance.

Authors:  Maryjane Wraga; Molly Helt; Emily Jacobs; Kerry Sullivan
Journal:  Soc Cogn Affect Neurosci       Date:  2007-03       Impact factor: 3.436

9.  Organization of food protection behavior is differentially influenced by 192 IgG-saporin lesions of either the medial septum or the nucleus basalis magnocellularis.

Authors:  Megan M Martin; Shawn S Winter; Joseph L Cheatwood; Lynniece A Carter; Jeana L Jones; Scott L Weathered; Steven J Wagner; Douglas G Wallace
Journal:  Brain Res       Date:  2008-09-16       Impact factor: 3.252

10.  Acetylcholine efflux from retrosplenial areas and hippocampal sectors during maze exploration.

Authors:  Steven Anzalone; Jessica Roland; Brent Vogt; Lisa Savage
Journal:  Behav Brain Res       Date:  2009-03-03       Impact factor: 3.332

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