WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience behavioral testing systems
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

The Journal of Neuroscience, January 31, 2007, 27(5):1054-1062; doi:10.1523/JNEUROSCI.3616-06.2007

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (14)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Izquierdo, A.
Right arrow Articles by Murray, E. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Izquierdo, A.
Right arrow Articles by Murray, E. A.

 Previous Article  |  Next Article 

Behavioral/Systems/Cognitive
Selective Bilateral Amygdala Lesions in Rhesus Monkeys Fail to Disrupt Object Reversal Learning

Alicia Izquierdo and Elisabeth A. Murray

Section on the Neurobiology of Learning and Memory, Laboratory of Neuropsychology, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892

Correspondence should be addressed to Dr. Alicia Izquierdo, California State University, Los Angeles, College of Natural and Social Sciences, Department of Psychology, 5151 State University Drive, Los Angeles, CA 90032. Email: AIzquie{at}calstatela.edu

Neuropsychological studies in nonhuman primates have led to the view that the amygdala plays an essential role in stimulus–reward association. The main evidence in support of this idea is that bilateral aspirative or radiofrequency lesions of the amygdala yield severe impairments on object reversal learning, a task that assesses the ability to shift choices of objects based on the presence or absence of food reward (i.e., reward contingency). The behavioral effects of different lesion techniques, however, can vary. The present study therefore evaluated the effects of selective, excitotoxic lesions of the amygdala in rhesus monkeys on object reversal learning. For comparison, we tested the same monkeys on a task known to be sensitive to amygdala damage, the reinforcer devaluation task. Contrary to previous results based on less selective lesion techniques, monkeys with complete excitotoxic amygdala lesions performed object reversal learning as quickly as controls. As predicted, however, the same operated monkeys were impaired in making object choices after devaluation of the associated food reinforcer. The results suggest two conclusions. First, the results demonstrate that the amygdala makes a selective contribution to stimulus–reward association; the amygdala is critical for guiding object choices after changes in reward value but not after changes in reward contingency. Second, the results implicate a critical contribution to object reversal learning of structures nearby the amygdala, perhaps the subjacent rhinal cortex.

Key words: emotion; stimulus–reward association; decision making; reward value; reward contingency; macaque monkey; rhinal cortex; reinforcement


Received Aug. 21, 2006; revised Nov. 2, 2006; accepted Nov. 21, 2006.

Correspondence should be addressed to Dr. Alicia Izquierdo, California State University, Los Angeles, College of Natural and Social Sciences, Department of Psychology, 5151 State University Drive, Los Angeles, CA 90032. Email: AIzquie{at}calstatela.edu




This article has been cited by other articles:


Home page
J. Neurosci.Home page
P. H. Rudebeck and E. A. Murray
Amygdala and Orbitofrontal Cortex Lesions Differentially Influence Choices during Object Reversal Learning
J. Neurosci., August 13, 2008; 28(33): 8338 - 8343.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
M.S. Man, H.F. Clarke, and A.C. Roberts
The Role of the Orbitofrontal Cortex and Medial Striatum in the Regulation of Prepotent Responses to Food Rewards
Cereb Cortex, August 9, 2008; (2008) bhn137v1.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
Y. L. Reekie, K. Braesicke, M. S. Man, and A. C. Roberts
Uncoupling of behavioral and autonomic responses after lesions of the primate orbitofrontal cortex
PNAS, July 15, 2008; 105(28): 9787 - 9792.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. R. E. Wilson and D. Gaffan
Prefrontal-Inferotemporal Interaction Is Not Always Necessary for Reversal Learning
J. Neurosci., May 21, 2008; 28(21): 5529 - 5538.
[Abstract] [Full Text] [PDF]


Home page
Arch Gen PsychiatryHome page
E. C. Finger, A. A. Marsh, D. G. Mitchell, M. E. Reid, C. Sims, S. Budhani, D. S. Kosson, G. Chen, K. E. Towbin, E. Leibenluft, et al.
Abnormal Ventromedial Prefrontal Cortex Function in Children With Psychopathic Traits During Reversal Learning
Arch Gen Psychiatry, May 1, 2008; 65(5): 586 - 594.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. S. Mitchell, P. G. F. Browning, and M. G. Baxter
Neurotoxic Lesions of the Medial Mediodorsal Nucleus of the Thalamus Disrupt Reinforcer Devaluation Effects in Rhesus Monkeys
J. Neurosci., October 17, 2007; 27(42): 11289 - 11295.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
A. Izquierdo, T. K. Newman, J. D. Higley, and E. A. Murray
Genetic modulation of cognitive flexibility and socioemotional behavior in rhesus monkeys
PNAS, August 28, 2007; 104(35): 14128 - 14133.
[Abstract] [Full Text] [PDF]



-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2008 by Society for Neuroscience ONLINE ISSN: 1529-2401
-