Skip to main content

Main menu

  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
    • Special Collections
  • EDITORIAL BOARD
    • Editorial Board
    • ECR Advisory Board
    • Journal Staff
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
    • Accessibility
  • SUBSCRIBE

User menu

  • Log out
  • Log in
  • My Cart

Search

  • Advanced search
Journal of Neuroscience
  • Log out
  • Log in
  • My Cart
Journal of Neuroscience

Advanced Search

Submit a Manuscript
  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
    • Special Collections
  • EDITORIAL BOARD
    • Editorial Board
    • ECR Advisory Board
    • Journal Staff
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
    • Accessibility
  • SUBSCRIBE
PreviousNext
ARTICLE, Behavioral/Systems

The Effect of Lesions of the Insular Cortex on Instrumental Conditioning: Evidence for a Role in Incentive Memory

Bernard W. Balleine and Anthony Dickinson
Journal of Neuroscience 1 December 2000, 20 (23) 8954-8964; https://doi.org/10.1523/JNEUROSCI.20-23-08954.2000
Bernard W. Balleine
1Department of Psychology, University of California, Los Angeles, Los Angeles, California 90095, and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Anthony Dickinson
2Department of Experimental Psychology, University of Cambridge, Cambridge CB2 3EB, United Kingdom
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF
Loading

Article Figures & Data

Figures

  • Fig. 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 1.

    Experiment 1. Diagrams of coronal sections (0.48–1.7 mm anterior to bregma) on which the extent of cell loss observed after bilateral infusions of quinolinic acid aimed at the gustatory region of the insular cortex has been reconstructed from histology to reveal the largest (darker) and smallest (lighter) regions of damage induced in group GC. Thelines drawn on the right-hand hemisphere extending laterally from the corpus callosum (cc) and the claustrum (CL) reflect divisions between (from thetop) primary somatosensory (S), granular (GI), dorsal agranular (dAI), and ventral agranular (vAI) regions of insular cortex, respectively, as labeled on the lowermost section. rf, Rhinal fissure.

  • Fig. 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 2.

    Experiment 1. Photomicrograph showing a Nissl-stained coronal section through the insular cortex (∼1.0 mm anterior bregma). A shows this section in low magnification, whereas in B, the area enclosed by thedashed rectangle in A has been enlarged to give a clearer indication of the lesion boundaries (arrows). cc, Corpus callosum;rf, rhinal fissure.

  • Fig. 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 3.

    Experiment 1. The mean number of lever presses (left) and chain pulls (right) performed per outcome during instrumental acquisition on the FI 20 reinforcement schedule used in experiment 1. Data are averaged across blocks of five outcomes and are presented separately for group GC (filled circles) and group sham (open circles).

  • Fig. 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 4.

    Experiment 1. The number of lever presses and chain pulls (i.e., actions) per minute during instrumental training (left) and during the choice extinction test conducted after one of the training outcomes was devalued by a specific satiety treatment. Data from the extinction test are presented for group sham (middle) and group GC (right) averaged across 2 min periods with performance of the action that previously delivered the pre-fed, i.e., devalued (Deval), outcome (filled circles) presented separately from performance of the action that had delivered the non-pre-fed, i.e., valued (Val), outcome (open circles) for each group.

  • Fig. 5.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 5.

    Experiment 1. The number of lever presses and chain pulls (i.e., actions) per minute during the choice reward test conducted after one of the training outcomes was devalued by a specific satiety treatment. In contrast to the extinction test, performance of lever-press and chain-pull actions delivered the training outcomes on independent random ratio schedules. Data from the reward test are presented for group sham (left) and group GC (right) averaged across 2 min periods with performance of the action that previously delivered the pre-fed, i.e., devalued (Deval), outcome (filled circles) presented separately from performance of the action that had delivered the non-pre-fed, i.e., valued (Val), outcome (open circles) for each group.

  • Fig. 6.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 6.

    Experiment 2. Mean performance of lever-press and chain-pull actions per minute, averaged over 3 min periods, during each of the 4 d of contingency assessment (left four panels) and during the extinction test (right panel). Test performance is divided into two panels: A, showing the data from group sham; andB, showing the data from group GC. In this figure, performance of each action is presented separately in eachpanel according to whether the action-outcome contingency has been degraded, i.e., the outcome delivered by performing the action is the same as the one now delivered without performing the action (Same, filled circles) or has not been degraded, i.e., the outcome delivered by performing the action differs from that delivered without performing the action (Diff, open circles). In thepanel illustrating the extinction test, the previously degraded action-outcome contingency remains designated asSame and the nondegraded as Diff, although no outcomes of any kind were presented in this test.

  • Fig. 7.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 7.

    Experiment 3. Diagrams of coronal sections (0.48–1.7 mm anterior to bregma) on which the extent of cell loss observed after bilateral infusions of quinolinic acid aimed at the gustatory region of the insular cortex has been reconstructed from histology to reveal the largest (darker) and smallest (lighter) regions of damage induced in group GC. Abbreviations are as for Figure 1.

  • Fig. 8.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 8.

    Experiment 3. Performance of lever-press and chain-pull actions averaged across 4 min periods in the choice extinction test conducted after a post-training reduction in food deprivation. Before this test, all of the rats were allowed to learn about the effect of the shift in food deprivation on the incentive value of one of the two food outcomes used in training by giving them brief consummatory contact with that outcome in the new, i.e., low deprivation, state. The effect of this treatment on choice performance in extinction is presented for group sham (left) and group GC (right) with the performance of the action that, in training, delivered the outcome re-exposed in the low deprivation state (i.e., Deval, filled circles) plotted separately from performance of the other action (i.e., Val, open circles) in each group.

  • Fig. 9.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 9.

    Experiment 3. Rate of performance of the lever-press and chain-pull actions in the reacquisition tests conducted after the extinction test. Rats were shifted between high and low levels of deprivation with the effect of these shifts assessed on the relative performance of the devalued (Dev) and valued (Val) actions, as designated in the extinction test. The average rate of performance of each action was averaged across the two sessions conducted in each deprivation state and plotted separately for group sham (left) and group GC (right).

Back to top

In this issue

The Journal of Neuroscience: 20 (23)
Journal of Neuroscience
Vol. 20, Issue 23
1 Dec 2000
  • Table of Contents
  • Index by author
Email

Thank you for sharing this Journal of Neuroscience article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
The Effect of Lesions of the Insular Cortex on Instrumental Conditioning: Evidence for a Role in Incentive Memory
(Your Name) has forwarded a page to you from Journal of Neuroscience
(Your Name) thought you would be interested in this article in Journal of Neuroscience.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Print
View Full Page PDF
Citation Tools
The Effect of Lesions of the Insular Cortex on Instrumental Conditioning: Evidence for a Role in Incentive Memory
Bernard W. Balleine, Anthony Dickinson
Journal of Neuroscience 1 December 2000, 20 (23) 8954-8964; DOI: 10.1523/JNEUROSCI.20-23-08954.2000

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Respond to this article
Request Permissions
Share
The Effect of Lesions of the Insular Cortex on Instrumental Conditioning: Evidence for a Role in Incentive Memory
Bernard W. Balleine, Anthony Dickinson
Journal of Neuroscience 1 December 2000, 20 (23) 8954-8964; DOI: 10.1523/JNEUROSCI.20-23-08954.2000
Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • MATERIALS AND METHODS
    • RESULTS
    • DISCUSSION
    • Footnotes
    • REFERENCES
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF

Keywords

  • instrumental conditioning
  • gustatory cortex
  • insular cortex
  • devaluation
  • sensory-specific satiety
  • incentive learning
  • contingency
  • motivation
  • reward

Responses to this article

Respond to this article

Jump to comment:

No eLetters have been published for this article.

Related Articles

Cited By...

More in this TOC Section

ARTICLE

  • Intracranially Administered Anti-Αβ Antibodies Reduce β-Amyloid Deposition by Mechanisms Both Independent of and Associated with Microglial Activation
  • Neural Correlates of Competing Fear Behaviors Evoked by an Innately Aversive Stimulus
  • Distinct Developmental Modes and Lesion-Induced Reactions of Dendrites of Two Classes of Drosophila Sensory Neurons
Show more ARTICLE

Behavioral/Systems

  • Functional Heterogeneity in Human Olfactory Cortex: An Event-Related Functional Magnetic Resonance Imaging Study
  • Induction of Hippocampal Long-Term Potentiation during Waking Leads to Increased Extrahippocampal zif-268 Expression during Ensuing Rapid-Eye-Movement Sleep
  • Appetitive and Aversive Olfactory Learning in Humans Studied Using Event-Related Functional Magnetic Resonance Imaging
Show more Behavioral/Systems
  • Home
  • Alerts
  • Follow SFN on BlueSky
  • Visit Society for Neuroscience on Facebook
  • Follow Society for Neuroscience on Twitter
  • Follow Society for Neuroscience on LinkedIn
  • Visit Society for Neuroscience on Youtube
  • Follow our RSS feeds

Content

  • Early Release
  • Current Issue
  • Issue Archive
  • Collections

Information

  • For Authors
  • For Advertisers
  • For the Media
  • For Subscribers

About

  • About the Journal
  • Editorial Board
  • Privacy Notice
  • Contact
  • Accessibility
(JNeurosci logo)
(SfN logo)

Copyright © 2025 by the Society for Neuroscience.
JNeurosci Online ISSN: 1529-2401

The ideas and opinions expressed in JNeurosci do not necessarily reflect those of SfN or the JNeurosci Editorial Board. Publication of an advertisement or other product mention in JNeurosci should not be construed as an endorsement of the manufacturer’s claims. SfN does not assume any responsibility for any injury and/or damage to persons or property arising from or related to any use of any material contained in JNeurosci.