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Effects of selective excitotoxic lesions of the nucleus accumbens core, anterior cingulate cortex, and central nucleus of the amygdala on autoshaping performance in rats.

Cardinal, Rudolf N., Parkinson, John A., Lachenal, Guillaume, Halkerston, Katherine M., Rudarakanchana, Nung, Hall, Jeremy, Morrison, Caroline H., Howes, Simon R., Robbins, Trevor W., Everitt, Barry J.·2002·Behavioral Neuroscience

DOI 10.1037/0735-7044.116.4.553

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Abstract

The nucleus accumbens core (AcbC), anterior cingulate cortex (ACC), and central nucleus of the amygdala (CeA) are required for normal acquisition of tasks based on stimulus-reward associations. However, it is not known whether they are involved purely in the learning process or are required for behavioral expression of a learned response. Rats were trained preoperatively on a Pavlovian autoshaping task in which pairing a visual conditioned stimulus (CS+) with food causes subjects to approach the CS+ while not approaching an unpaired stimulus (CS-). Subjects then received lesions of the AcbC, ACC, or CeA before being retested. AcbC lesions severely impaired performance; lesioned subjects approached the CS+ significantly less often than controls, failing to discriminate between the CS+ and CS-. ACC lesions also impaired performance but did not abolish discrimination entirely. CeA lesions had no effect on performance. Thus, the CeA is required for learning, but not expression, of a conditioned approach response, implying that it makes a specific contribution to the learning of stimulus-reward associations.

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The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
A neural substrate of prediction and reward
Schultz, W., Dayan, P., & Montague, P. R. (1997) · Science · doi:10.1126/science.275.5306.1593 · Cited by 9,388
Statistical Methods for Psychology.
Gudgeon, A. C., & Howell, D. C. (1994) · Journal of the Royal Statistical Society Series D (The Statistician) · doi:10.2307/2348956 · Cited by 8,277
Cognitive and emotional influences in anterior cingulate cortex
Bush, G., Luu, P., & Posner, M. I. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01483-2 · Cited by 6,259
Book Reviews: Keppel, Geoffrey. Design and Analysis: A Researcher’s Handbook . Englewood Cliffs, N. J.: Prentice Hall, 1973. 658 + xiii pp. $13.95
Beaton, A. E., & Keppel, G. (1975) · American Educational Research Journal · doi:10.2307/1162588 · Cited by 5,857
The Cognitive neurosciences
(2005) · Choice Reviews Online · doi:10.5860/choice.43-0626 · Cited by 4,726
The rat nervous system
Paxinos, G. (1985) · Cited by 3,715
A neural system for error detection and compensation
Gehring, W. J., Goss, B., Coles, M. G. H., Meyer, D. E., & Donchin, E. (1993) · Psychological Science · doi:10.1111/j.1467-9280.1993.tb00586.x · Cited by 2,862
The Psychology of Animal Learning
Hill, W. F., & Mackintosh, N. J. (1976) · The American Journal of Psychology · doi:10.2307/1421765 · Cited by 2,397
The Cognitive neurosciences
(1995) · Choice Reviews Online · doi:10.5860/choice.32-5931 · Cited by 2,337

Show all 84 references

Research works printed but not linked: 9

Amaral, 1992, Anatomical organization of the primate amygdaloid complex., 1
10.1037/0735-7044.111.5.908 · DOI
10.1037/0735-7044.111.5.920 · DOI
Cardinal, 2000, Effects of anterior cingulate cortex lesions on responding for conditioned reinforcement, discrete fear conditioning, autoshaping performance and Pavlovian-instrumental transfer., The European Journal of Neuroscience, 12, 88
Gabriel, 1980, Neuronal activity of cingulate cortex, anteroventral thalamus, and hippocampal formation in discriminative conditioning: Encoding and extraction of the significance of conditional stimuli., Vol. 9, 125
Keppel, 1982, Design and analysis: A researcher's handbook
Paxinos, 1998, The rat brain in stereotaxic coordinates
Tomie, 1989, Sign-tracking: The search for reward., 191
Zilles, 1995, Cortex: Areal and laminar structure., 649

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Self-citation
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Authors: Cardinal, R. N., Parkinson, J. A., Lachenal, G., Halkerston, K. M., Rudarakanchana, N., Hall, J., Morrison, C. H., Howes, S. R., Robbins, T. W., & Everitt, B. J.
Affiliations: University of Cambridge (GB)
ORCID: Cardinal, Rudolf N.
Parkinson, John A.
Rudarakanchana, Nung
Robbins, Trevor W.
Everitt, Barry J.
Venue: Behavioral Neuroscience
Publisher: American Psychological Association (APA)
Published: 2002
Volume: 116
Issue: 4
Pages: 553-567
ISSN: 0735-7044 (ISSN-L)
1939-0084
DOI: 10.1037/0735-7044.116.4.553
OpenAlex: W1980915028
Cited by: 201
References: 84
Citations by year: 2025: 3 · 2024: 2 · 2023: 5 · 2022: 3 · 2021: 3 · 2020: 2 · 2019: 15 · 2018: 3 · 2017: 9 · 2016: 8 · 2015: 12 · 2014: 6 · 2013: 16 · 2012: 11
FWCI: 4.21
Type: journal article
Language: en
Open access: closed
Locations: Behavioral Neuroscience (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Keywords: nucleus accumbens core, anterior cingulate cortex, central amygdala, excitotoxic lesions, autoshaping, classical conditioning, stimulus-reward associations, approach behavior, discrimination learning, conditioned stimulus, reward learning
MeSH terms: Amygdala, Animals, Cerebral Cortex, Conditioning, Classical, Discrimination Learning, Male, Nucleus Accumbens, Rats

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Effects of selective excitotoxic lesions of the nucleus accumbens core, anterior cingulate cortex, and central nucleus of the amygdala on autoshaping performance in rats.

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