Literature DB >> 23575841

Functional disconnection of the orbitofrontal cortex and basolateral amygdala impairs acquisition of a rat gambling task and disrupts animals' ability to alter decision-making behavior after reinforcer devaluation.

Fiona D Zeeb1, Catharine A Winstanley.   

Abstract

An inability to adjust choice preferences in response to changes in reward value may underlie key symptoms of many psychiatric disorders, including chemical and behavioral addictions. We developed the rat gambling task (rGT) to investigate the neurobiology underlying complex decision-making processes. As in the Iowa Gambling task, the optimal strategy is to avoid choosing larger, riskier rewards and to instead favor options associated with smaller rewards but less loss and, ultimately, greater long-term gain. Given the demonstrated importance of the orbitofrontal cortex (OFC) and basolateral amygdala (BLA) in acquisition of the rGT and Iowa Gambling task, we used a contralateral disconnection lesion procedure to assess whether functional connectivity between these regions is necessary for optimal decision-making. Disrupting the OFC-BLA pathway retarded acquisition of the rGT. Devaluing the reinforcer by inducing sensory-specific satiety altered decision-making in control groups. In contrast, disconnected rats did not update their choice preference following reward devaluation, either when the devalued reward was still delivered or when animals needed to rely on stored representations of reward value (i.e., during extinction). However, all rats exhibited decreased premature responding and slower response latencies after satiety manipulations. Hence, disconnecting the OFC and BLA did not affect general behavioral changes caused by reduced motivation, but instead prevented alterations in the value of a specific reward from contributing appropriately to cost-benefit decision-making. These results highlight the role of the OFC-BLA pathway in the decision-making process and suggest that communication between these areas is vital for the appropriate assessment of reward value to influence choice.

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Year:  2013        PMID: 23575841      PMCID: PMC6619089          DOI: 10.1523/JNEUROSCI.3971-12.2013

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


  36 in total

1.  Thalamic-cortical-striatal circuitry subserves working memory during delayed responding on a radial arm maze.

Authors:  S B Floresco; D N Braaksma; A G Phillips
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

2.  Changes in functional connectivity in orbitofrontal cortex and basolateral amygdala during learning and reversal training.

Authors:  G Schoenbaum; A A Chiba; M Gallagher
Journal:  J Neurosci       Date:  2000-07-01       Impact factor: 6.167

3.  Control of response selection by reinforcer value requires interaction of amygdala and orbital prefrontal cortex.

Authors:  M G Baxter; A Parker; C C Lindner; A D Izquierdo; E A Murray
Journal:  J Neurosci       Date:  2000-06-01       Impact factor: 6.167

4.  Effects of selective thalamic and prelimbic cortex lesions on two types of visual discrimination and reversal learning.

Authors:  Y Chudasama; T J Bussey; J L Muir
Journal:  Eur J Neurosci       Date:  2001-09       Impact factor: 3.386

5.  Decision-making deficits, linked to a dysfunctional ventromedial prefrontal cortex, revealed in alcohol and stimulant abusers.

Authors:  A Bechara; S Dolan; N Denburg; A Hindes; S W Anderson; P E Nathan
Journal:  Neuropsychologia       Date:  2001       Impact factor: 3.139

6.  Functional disconnection of the medial prefrontal cortex and subthalamic nucleus in attentional performance: evidence for corticosubthalamic interaction.

Authors:  Yogita Chudasama; Christelle Baunez; Trevor W Robbins
Journal:  J Neurosci       Date:  2003-07-02       Impact factor: 6.167

7.  Encoding predicted outcome and acquired value in orbitofrontal cortex during cue sampling depends upon input from basolateral amygdala.

Authors:  Geoffrey Schoenbaum; Barry Setlow; Michael P Saddoris; Michela Gallagher
Journal:  Neuron       Date:  2003-08-28       Impact factor: 17.173

Review 8.  The 5-choice serial reaction time task: behavioural pharmacology and functional neurochemistry.

Authors:  T W Robbins
Journal:  Psychopharmacology (Berl)       Date:  2002-08-09       Impact factor: 4.530

9.  Different contributions of the human amygdala and ventromedial prefrontal cortex to decision-making.

Authors:  A Bechara; H Damasio; A R Damasio; G P Lee
Journal:  J Neurosci       Date:  1999-07-01       Impact factor: 6.167

10.  The effects of d-amphetamine, chlordiazepoxide, alpha-flupenthixol and behavioural manipulations on choice of signalled and unsignalled delayed reinforcement in rats.

Authors:  R N Cardinal; T W Robbins; B J Everitt
Journal:  Psychopharmacology (Berl)       Date:  2000-11       Impact factor: 4.530

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  54 in total

1.  Identity-Specific Reward Representations in Orbitofrontal Cortex Are Modulated by Selective Devaluation.

Authors:  James D Howard; Thorsten Kahnt
Journal:  J Neurosci       Date:  2017-02-03       Impact factor: 6.167

2.  Hippocampal interplay with the nucleus accumbens is critical for decisions about time.

Authors:  Andrew R Abela; Yiran Duan; Yogita Chudasama
Journal:  Eur J Neurosci       Date:  2015-07-30       Impact factor: 3.386

3.  Disadvantageous decision-making on a rodent gambling task is associated with increased motor impulsivity in a population of male rats.

Authors:  Michael M Barrus; Jay G Hosking; Fiona D Zeeb; Melanie Tremblay; Catharine A Winstanley
Journal:  J Psychiatry Neurosci       Date:  2015-03       Impact factor: 6.186

4.  Pharmacological evidence that 5-HT2C receptor blockade selectively improves decision making when rewards are paired with audiovisual cues in a rat gambling task.

Authors:  Wendy K Adams; Chris Barkus; Jacqueline-Marie N Ferland; Trevor Sharp; Catharine A Winstanley
Journal:  Psychopharmacology (Berl)       Date:  2017-07-21       Impact factor: 4.530

5.  Basolateral Amygdala to Orbitofrontal Cortex Projections Enable Cue-Triggered Reward Expectations.

Authors:  Nina T Lichtenberg; Zachary T Pennington; Sandra M Holley; Venuz Y Greenfield; Carlos Cepeda; Michael S Levine; Kate M Wassum
Journal:  J Neurosci       Date:  2017-07-25       Impact factor: 6.167

Review 6.  Behavioral flexibility in rats and mice: contributions of distinct frontocortical regions.

Authors:  D A Hamilton; J L Brigman
Journal:  Genes Brain Behav       Date:  2015-01       Impact factor: 3.449

7.  Inactivation of the prelimbic or infralimbic cortex impairs decision-making in the rat gambling task.

Authors:  Fiona D Zeeb; P J J Baarendse; L J M J Vanderschuren; Catharine A Winstanley
Journal:  Psychopharmacology (Berl)       Date:  2015-09-21       Impact factor: 4.530

Review 8.  What the orbitofrontal cortex does not do.

Authors:  Thomas A Stalnaker; Nisha K Cooch; Geoffrey Schoenbaum
Journal:  Nat Neurosci       Date:  2015-05       Impact factor: 24.884

9.  Increased motor impulsivity in a rat gambling task during chronic ropinirole treatment: potentiation by win-paired audiovisual cues.

Authors:  Melanie Tremblay; Michael M Barrus; Paul J Cocker; Christelle Baunez; Catharine A Winstanley
Journal:  Psychopharmacology (Berl)       Date:  2019-01-31       Impact factor: 4.530

10.  Sex differences in a rat model of risky decision making.

Authors:  Caitlin A Orsini; Markie L Willis; Ryan J Gilbert; Jennifer L Bizon; Barry Setlow
Journal:  Behav Neurosci       Date:  2015-12-14       Impact factor: 1.912

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