Literature DB >> 1586352

Lesions of the rat postsubiculum impair performance on spatial tasks.

J S Taube1, J P Kesslak, C W Cotman.   

Abstract

Previous studies have identified a population of neurons in the postsubiculum that discharge as a function of the rat's head direction in the horizontal plane (Taube, Muller, & Ranck, 1990a). To assess the contribution of these cells in spatial learning, Long-Evans rats were tested in a variety of spatial and nonspatial tasks following bilateral electrolytic or neurotoxic lesions of the postsubiculum. Compared to unlesioned control animals, lesioned animals were impaired on two spatial tasks, a radial eight-arm maze task and a Morris water task, although the performance scores of both lesion groups improved over the course of behavioral testing. In contrast, lesioned animals were unimpaired on two nonspatial tasks, a cued version of the water maze task and a conditioned taste-aversion paradigm. In addition, lesioned animals showed transient hyperactivity in an open-field activity test. These results support the concept that neurons in the postsubiculum are part of a neural network involved in the processing of spatial information.

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Mesh:

Year:  1992        PMID: 1586352     DOI: 10.1016/0163-1047(92)90629-i

Source DB:  PubMed          Journal:  Behav Neural Biol        ISSN: 0163-1047


  36 in total

1.  Fear conditioning is disrupted by damage to the postsubiculum.

Authors:  Siobhan Robinson; David J Bucci
Journal:  Hippocampus       Date:  2011-11-11       Impact factor: 3.899

2.  Coupling between place cells and head direction cells during relative translations and rotations of distal landmarks.

Authors:  D Yoganarasimha; James J Knierim
Journal:  Exp Brain Res       Date:  2004-09-01       Impact factor: 1.972

3.  Theta frequency stimulation up-regulates the synaptic strength of the pathway from CA1 to subiculum region of hippocampus.

Authors:  Yan-You Huang; Eric R Kandel
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-27       Impact factor: 11.205

4.  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

5.  Intact landmark control and angular path integration by head direction cells in the anterodorsal thalamus after lesions of the medial entorhinal cortex.

Authors:  Benjamin J Clark; Jeffrey S Taube
Journal:  Hippocampus       Date:  2010-11-03       Impact factor: 3.899

6.  Failure of centrally placed objects to control the firing fields of hippocampal place cells.

Authors:  A Cressant; R U Muller; B Poucet
Journal:  J Neurosci       Date:  1997-04-01       Impact factor: 6.167

7.  Origins of landmark encoding in the brain.

Authors:  Ryan M Yoder; Benjamin J Clark; Jeffrey S Taube
Journal:  Trends Neurosci       Date:  2011-10-06       Impact factor: 13.837

Review 8.  Retrosplenial cortex and its role in cue-specific learning and memory.

Authors:  Travis P Todd; Danielle I Fournier; David J Bucci
Journal:  Neurosci Biobehav Rev       Date:  2019-05-02       Impact factor: 8.989

Review 9.  Cellular dynamical mechanisms for encoding the time and place of events along spatiotemporal trajectories in episodic memory.

Authors:  Michael E Hasselmo; Lisa M Giocomo; Mark P Brandon; Motoharu Yoshida
Journal:  Behav Brain Res       Date:  2009-12-16       Impact factor: 3.332

10.  Otoconia-deficient mice show selective spatial deficits.

Authors:  Ryan M Yoder; Seth L Kirby
Journal:  Hippocampus       Date:  2014-05-15       Impact factor: 3.899

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