Literature DB >> 18434518

Differential involvement of the basolateral amygdala and mediodorsal thalamus in instrumental action selection.

Sean B Ostlund1, Bernard W Balleine.   

Abstract

Although it has been shown that the basolateral amygdala (BLA) and the mediodorsal thalamus (MD) are critical for goal-directed instrumental performance, much remains unknown about the respective contributions of these structures to action selection. The current study assessed the effects of post-training BLA and MD lesions on several tests of instrumental action selection. We found that MD damage disrupted the influence of pavlovian cues over action selection but left intact rats' ability to select actions based on either the expected value or the discriminative stimulus properties of the outcome. In contrast, BLA lesions impaired performance on all three tests of action selection. Because both lesion types disrupted the influence of cues that signal reward over instrumental performance, we then investigated the involvement of these structures in pavlovian contingency learning using a task in which the predictive status of one of two cues is degraded by delivering its outcome noncontingently during the intertrial interval. As expected, the sham group selectively suppressed their conditioned approach performance to the cue that no longer signaled its outcome but continued to respond to the control stimulus. In contrast, both lesioned groups were impaired on this task. Interestingly, whereas the MD group displayed a nonspecific reduction in responding to both cues, the BLA group continued to show high levels of responding to both cues as if their performance was completely insensitive to this contingency manipulation. These findings demonstrate that the BLA and MD make important yet distinct contributions to instrumental action selection.

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Year:  2008        PMID: 18434518      PMCID: PMC2652225          DOI: 10.1523/JNEUROSCI.5472-07.2008

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  26 in total

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Authors:  P Blundell; G Hall; S Killcross
Journal:  J Neurosci       Date:  2001-11-15       Impact factor: 6.167

2.  Outcome-specific conditioned inhibition in Pavlovian backward conditioning.

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Journal:  Learn Behav       Date:  2003-11       Impact factor: 1.986

3.  The effect of lesions of the basolateral amygdala on instrumental conditioning.

Authors:  Bernard W Balleine; A Simon Killcross; Anthony Dickinson
Journal:  J Neurosci       Date:  2003-01-15       Impact factor: 6.167

4.  Relations between Pavlovian-instrumental transfer and reinforcer devaluation.

Authors:  Peter C Holland
Journal:  J Exp Psychol Anim Behav Process       Date:  2004-04

5.  General and outcome-specific forms of Pavlovian-instrumental transfer: the effect of shifts in motivational state and inactivation of the ventral tegmental area.

Authors:  Laura H Corbit; Patricia H Janak; Bernard W Balleine
Journal:  Eur J Neurosci       Date:  2007-11-14       Impact factor: 3.386

Review 6.  The organization of networks within the orbital and medial prefrontal cortex of rats, monkeys and humans.

Authors:  D Ongür; J L Price
Journal:  Cereb Cortex       Date:  2000-03       Impact factor: 5.357

7.  Different roles for orbitofrontal cortex and basolateral amygdala in a reinforcer devaluation task.

Authors:  Charles L Pickens; Michael P Saddoris; Barry Setlow; Michela Gallagher; Peter C Holland; Geoffrey Schoenbaum
Journal:  J Neurosci       Date:  2003-12-03       Impact factor: 6.167

8.  Coordination of actions and habits in the medial prefrontal cortex of rats.

Authors:  Simon Killcross; Etienne Coutureau
Journal:  Cereb Cortex       Date:  2003-04       Impact factor: 5.357

9.  Lesions of mediodorsal thalamus and anterior thalamic nuclei produce dissociable effects on instrumental conditioning in rats.

Authors:  Laura H Corbit; Janice L Muir; Bernard W Balleine
Journal:  Eur J Neurosci       Date:  2003-09       Impact factor: 3.386

10.  The role of prelimbic cortex in instrumental conditioning.

Authors:  Laura H Corbit; Bernard W Balleine
Journal:  Behav Brain Res       Date:  2003-11-30       Impact factor: 3.332

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  85 in total

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2.  On habits and addiction: An associative analysis of compulsive drug seeking.

Authors:  Sean B Ostlund; Bernard W Balleine
Journal:  Drug Discov Today Dis Models       Date:  2008

3.  μ- and δ-opioid-related processes in the accumbens core and shell differentially mediate the influence of reward-guided and stimulus-guided decisions on choice.

Authors:  Vincent Laurent; Beatrice Leung; Nigel Maidment; Bernard W Balleine
Journal:  J Neurosci       Date:  2012-02-01       Impact factor: 6.167

Review 4.  The Origins and Organization of Vertebrate Pavlovian Conditioning.

Authors:  Michael S Fanselow; Kate M Wassum
Journal:  Cold Spring Harb Perspect Biol       Date:  2015-11-09       Impact factor: 10.005

5.  Micro-opioid receptor activation in the basolateral amygdala mediates the learning of increases but not decreases in the incentive value of a food reward.

Authors:  Kate M Wassum; Ingrid C Cely; Bernard W Balleine; Nigel T Maidment
Journal:  J Neurosci       Date:  2011-02-02       Impact factor: 6.167

6.  A visual, position-independent instrumental reinforcer devaluation task for rats.

Authors:  Elizabeth A West; Patrick A Forcelli; Alice Murnen; Karen Gale; Ludise Malkova
Journal:  J Neurosci Methods       Date:  2010-11-17       Impact factor: 2.390

7.  Mediodorsal thalamus hypofunction impairs flexible goal-directed behavior.

Authors:  Sébastien Parnaudeau; Kathleen Taylor; Scott S Bolkan; Ryan D Ward; Peter D Balsam; Christoph Kellendonk
Journal:  Biol Psychiatry       Date:  2014-03-26       Impact factor: 13.382

Review 8.  Human and rodent homologies in action control: corticostriatal determinants of goal-directed and habitual action.

Authors:  Bernard W Balleine; John P O'Doherty
Journal:  Neuropsychopharmacology       Date:  2010-01       Impact factor: 7.853

9.  Differential effects of amygdala, orbital prefrontal cortex, and prelimbic cortex lesions on goal-directed behavior in rhesus macaques.

Authors:  Sarah E V Rhodes; Elisabeth A Murray
Journal:  J Neurosci       Date:  2013-02-20       Impact factor: 6.167

10.  Transient inactivation of basolateral amygdala during selective satiation disrupts reinforcer devaluation in rats.

Authors:  Elizabeth A West; Patrick A Forcelli; Alice T Murnen; David L McCue; Karen Gale; Ludise Malkova
Journal:  Behav Neurosci       Date:  2012-08       Impact factor: 1.912

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