The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
Excitotoxic Lesions of the Amygdala Fail to Produce Impairment in Visual Learning for Auditory Secondary Reinforcement But Interfere with Reinforcer Devaluation Effects in Rhesus Monkeys
Open accessAbstract
Aspiration lesions of the amygdala were found previously to produce a severe impairment in visual discrimination learning for auditory secondary reinforcement in rhesus monkeys (Gaffan and Harrison, 1987). To determine whether excitotoxic amygdala lesions would also produce this effect, we trained four naive rhesus monkeys on the same task. The monkeys were required to learn 40 new visual discrimination problems per session in a situation in which visual choices were guided by an auditory secondary reinforcer that had been previously associated with food reward. Bilateral excitotoxic lesions of the amygdala had no effect on the rate of learning visual discrimination problems for auditory secondary reinforcement. We also tested the amygdalectomized monkeys on a reinforcer devaluation task and compared their performance with a group of three normal monkeys. The monkeys first learned to discriminate 60 pairs of objects, baited with two different food rewards. Each of the food rewards was then devalued by selective satiation in two separate experimental sessions. Normal controls tended to avoid displacing objects that covered the devalued food to a significantly greater degree than did the amygdalectomized monkeys, indicating that the excitotoxic amygdala damage interfered with reinforcer devaluation effects. Our results are consistent with the idea that the amygdala is necessary for learning the association between stimuli and the value of particular food rewards; however, the amygdala is not necessary for maintaining the value of secondary reinforcers, once they have been learned.
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In the citing paper
“Intact, control monkeys tend to avoid choosing objects associated with the devalued food, a finding called the ‘devaluation effect’.”
From Localization of Dysfunction in Major Depressive Disorder: Prefrontal Cortex and Amygdala (2011) · cites this paper as [74]
In the citing paper
“As illustrated in Figure 3A (pink), monkeys with bilateral amygdala lesions typically fail to show the devaluation effect or show it only in a strongly attenuated form.”
From Localization of Dysfunction in Major Depressive Disorder: Prefrontal Cortex and Amygdala (2011) · cites this paper as [74]
In the citing paper
“The monkeys chose objects according to their original preferences, with less influence of their selectively satiated state than in intact monkeys.”
From Localization of Dysfunction in Major Depressive Disorder: Prefrontal Cortex and Amygdala (2011) · cites this paper as [74]
In the citing paper
“Some monkeys received bilateral PFo ablations (blue) and others received a crossed surgical disconnection (green) of the amygdala and PFo (a unilateral amygdala lesion in one hemisphere along with unilateral PFo lesion in the other hemisphere, combined with section of the forebrain commissures). In all lesion groups, the devaluation effect was markedly attenuated.”
From Localization of Dysfunction in Major Depressive Disorder: Prefrontal Cortex and Amygdala (2011) · cites this paper as [74]
In the citing paper
“The same groups of operated monkeys showed little or no change in food preferences and worked for food like control monkeys.”
From Localization of Dysfunction in Major Depressive Disorder: Prefrontal Cortex and Amygdala (2011) · cites this paper as [74]
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Citations
Cites
Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229
Perirhinal and parahippocampal cortices of the macaque monkey: Cortical afferents
Suzuki, W., & Amaral, D. G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903500402 · Cited by 1,149
Involvement of the amygdala in stimulus-reward associations: interaction with the ventral striatum
Cador, M., Robbins, T. W., & Everitt, B. J. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90354-0 · Cited by 652
Hatfield, T., Han, J.-S., Conley, M., Gallagher, M., & Holland, P. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05256.1996 · Cited by 555
Everitt, B. J., Morris, K. A., O'Brien, A., & Robbins, T. W. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90145-e · Cited by 507
Neural substrates of visual stimulus-stimulus association in rhesus monkeys
Murray, E. A., Gaffan, D., & Mishkin, M. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-10-04549.1993 · Cited by 300
Self-citationThe amygdala complex: multiple roles in associative learning and attention.
Gallagher, M., & Holland, P. C. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.25.11771 · Cited by 300
Hypothalamic neuronal responses associated with the sight of food
Rolls, E. T., Burton, M. J., & Mora, F. (1976) · Brain Research · doi:10.1016/0006-8993(76)91048-9 · Cited by 290
Burns, L. H., Robbins, T. W., & Everitt, B. J. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90113-5 · Cited by 289
Dunn, L., & Everitt, B. J. (1988) · Behavioral Neuroscience · doi:10.1037//0735-7044.102.1.3 · Cited by 270
Research works printed but not linked: 5
- Everitt BJ Robbins TW (1992) Amygdala-ventral striatal interactions and reward-related processes. in The amygdala: neurobiological aspects of emotion, memory, and mental dysfunction, ed Aggleton JP (Wiley, New York), pp 401–429.
- 10.1523/JNEUROSCI.07-08-02285.1987 · DOI
- Goulet, 1996, Aspiration lesions of the amygdala disrupt rhinal cortical efferents to the mediodorsal nucleus of the thalamus in rhesus monkeys., Soc Neurosci Abstr, 22, 1867
- Holland, 1979, Differential effects of two ways of devaluing the unconditioned stimulus., J Exp Psychol, 5, 65
- O’ Boyle, 1993, Effects of excitotoxic amygdalo-hippocampal lesions on visual recognition in rhesus monkeys., Soc Neurosci Abstr, 19, 438
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Metadata
- Authors
- Málková, L., Gaffan, D., & Murray, E. A.
- Affiliations
- University of Oxford (GB)
- National Institutes of Health (US)
- ORCID
- Murray, Elisabeth A.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1997-08-01
- Volume
- 17
- Issue
- 15
- Pages
- 6011-6020
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6573210
- OpenAlex
- W1611064050
- Cited by
- 295
- References
- 35
- Citations by year
- 2025: 3 · 2024: 8 · 2023: 10 · 2022: 5 · 2021: 8 · 2020: 6 · 2019: 12 · 2018: 6 · 2017: 6 · 2016: 3 · 2015: 14 · 2014: 4 · 2013: 10 · 2012: 9
- FWCI
- 5.68
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Oxford
- Medical Research Council
- National Institute of Mental Health
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- amygdala, excitotoxic lesions, reinforcer devaluation, visual discrimination learning, rhesus monkeys, satiation, food reward, stimulus value, avoidance learning
- MeSH terms
- Acoustic Stimulation, Amygdala, Animals, Discrimination, Psychological, Female, Learning, Macaca mulatta, Male, Photic Stimulation, Reinforcement, Psychology
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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