Literature DB >> 11508717

Perirhinal cortex and place-object conditional learning in the rat.

T J Bussey1, R Dias, E Amin, J L Muir, J P Aggleton.   

Abstract

The present study examined whether excitotoxic lesions of the perirhinal cortex can affect acquisition of a place-object conditional task in which object and spatial information must be integrated. Testing was carried out in a double Y-maze apparatus, in which rats learned a conditional rule of the type, "In Place X, choose Object A, not Object B (A+ vs. B-); in Place Y, choose Object B, not Object A (A- vs. B+)." Perirhinal cortex lesions significantly impaired acquisition of this task while sparing performance of an allocentric spatial memory task performed in a radial arm maze. Perirhinal cortex lesions also had no apparent effect on a 1-pair object discrimination task performed in the double Y maze or on retention and acquisition of 4-pair concurrent discrimination problems performed in a computer-automated touch screen testing apparatus. The results suggest that, although the perirhinal cortex and hippocampus can be functionally dissociated, their normal mode of operation includes the integration of object and spatial information.

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Mesh:

Year:  2001        PMID: 11508717     DOI: 10.1037//0735-7044.115.4.776

Source DB:  PubMed          Journal:  Behav Neurosci        ISSN: 0735-7044            Impact factor:   1.912


  15 in total

1.  On the dynamic nature of the engram: evidence for circuit-level reorganization of object memory traces following reactivation.

Authors:  Boyer D Winters; Mark C Tucci; Derek L Jacklin; James M Reid; James Newsome
Journal:  J Neurosci       Date:  2011-11-30       Impact factor: 6.167

Review 2.  Translational Assays for Assessment of Cognition in Rodent Models of Alzheimer's Disease and Dementia.

Authors:  A Shepherd; S Tyebji; A J Hannan; E L Burrows
Journal:  J Mol Neurosci       Date:  2016-09-16       Impact factor: 3.444

3.  A Critical Role for the Nucleus Reuniens in Long-Term, But Not Short-Term Associative Recognition Memory Formation.

Authors:  Gareth R I Barker; Elizabeth Clea Warburton
Journal:  J Neurosci       Date:  2018-02-15       Impact factor: 6.167

4.  Expression of HIV-Tat protein is associated with learning and memory deficits in the mouse.

Authors:  Amanda N Carey; Elizabeth I Sypek; Harminder D Singh; Marc J Kaufman; Jay P McLaughlin
Journal:  Behav Brain Res       Date:  2011-12-20       Impact factor: 3.332

5.  A computer-automated touchscreen paired-associates learning (PAL) task for mice: impairments following administration of scopolamine or dicyclomine and improvements following donepezil.

Authors:  Susan J Bartko; Ignasi Vendrell; Lisa M Saksida; Timothy J Bussey
Journal:  Psychopharmacology (Berl)       Date:  2010-11-18       Impact factor: 4.530

6.  Perirhinal cortex is necessary for acquiring, but not for retrieving object-place paired association.

Authors:  Yong Sang Jo; Inah Lee
Journal:  Learn Mem       Date:  2010-02-13       Impact factor: 2.460

7.  Disconnection of the hippocampal-perirhinal cortical circuits severely disrupts object-place paired associative memory.

Authors:  Yong Sang Jo; Inah Lee
Journal:  J Neurosci       Date:  2010-07-21       Impact factor: 6.167

8.  Recognition memory for complex visual discriminations is influenced by stimulus interference in rodents with perirhinal cortex damage.

Authors:  Paul E Gilbert; Raymond P Kesner
Journal:  Learn Mem       Date:  2003 Nov-Dec       Impact factor: 2.460

9.  The touchscreen cognitive testing method for rodents: how to get the best out of your rat.

Authors:  Timothy J Bussey; Tina L Padain; Elizabeth A Skillings; Boyer D Winters; A Jennifer Morton; Lisa M Saksida
Journal:  Learn Mem       Date:  2008-07-08       Impact factor: 2.460

10.  Interfering with Fos expression in rat perirhinal cortex impairs recognition memory.

Authors:  Ana Seoane; Christopher J Tinsley; Malcolm W Brown
Journal:  Hippocampus       Date:  2012-04-25       Impact factor: 3.899

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