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Hippocampus and trace conditioning of the rabbit's classically conditioned nictitating membrane response.

Solomon, Paul R, Vander Schaaf, Ellen R., Thompson, Richard F., Weisz, Donald J.·1986·Behavioral Neuroscience

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Abstract

Rabbits received classical conditioning of the nictitating membrane response (NMR) in a trace conditioning paradigm. In this paradigm, a 250-ms tone conditioned stimulus (CS) occurs, after which there is a 500-ms period of time in which no stimuli occur (the trace interval), followed by a 100-ms air puff unconditioned stimulus (UCS). In Experiment 1, lesions of the hippocampus or cingulate/retrosplenial cortex disrupted acquisition of the long-latency or adaptive conditioned response relative to unoperated controls and animals that received neocortical lesions that spared the cingulate/retrosplenial areas. When animals with hippocampal or cingulate/retrosplenial lesions were switched to a standard delay paradigm in which the CS and UCS were contiguous in time, they acquired in about the same number of trials as naive rabbits. In a second experiment multiple-unit activity in area CA1 of the hippocampus was examined during acquisition of the trace conditioned response (CR). Three groups of animals were tested: animals that had a 500-ms trace interval (Group T-500), animals that received explicitly unpaired presentations of the CS and UCS (Group UP), and animals that underwent conditioning with a 2,000-ms trace interval (Group T-2000). Animals in Group T-500 acquired the CR in about 500 trials. Early in training, and well before any CRs occurred, there was a substantial increase in neuronal activity in the hippocampus that began during the CS and persisted through the trace interval. There was also an increase in the UCS period that modeled the amplitude-time course of the behavioral unconditioned response. Later in conditioning as CRs emerged, there was no longer neuronal bursting throughout the CS + trace period. Rather, the activity shifted to later in the trace interval and formed a model of the amplitude-time course of the behavioral CR. Activity during the UCS period was similar to that seen earlier in conditioning. Animals in Group UP showed no behavioral conditioning and no increase in neuronal activity. Animals in Group T-2000 showed no long-latency behavioral conditioning and no increase in neuronal activity. The data are discussed in terms of the role of the hippocampus in conditioning during situations in which the CS and UCS are not contiguous in time.

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Physiology and Behavior
Falk, J. L. (1973) · Contemporary Psychology · doi:10.1037/0011818 · Cited by 2,288
Hippocampus, space, and memory
Olton, D. S., Becker, J. T., & Handelmann, G. E. (1979) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00062713 · Cited by 2,018
Cerebrocerebellar communication systems.
Allen, G. I., & Tsukahara, N. (1974) · Physiological Reviews · doi:10.1152/physrev.1974.54.4.957 · Cited by 1,084
A textbook of psychology.
Hebb, D. O. (1958) · W.B. Saunders eBooks · doi:10.1037/14200-000 · Cited by 1,011
The hippocampus and contextual retrieval of information from memory: A theory
Hirsh, R. (1974) · Behavioral Biology · doi:10.1016/s0091-6773(74)92231-7 · Cited by 957
Cerebellum: Essential Involvement in the Classically Conditioned Eyelid Response
McCormick, D. A., & Thompson, R. F. (1984) · Science · doi:10.1126/science.6701513 · Cited by 910
Self-citation
Experimental methods and instrumentation in psychology
Sidowski, J. B. (1966) · Medical Entomology and Zoology · Cited by 793
The Neuropsychology of Memory
Wertsch, J. V., Luria, A. R., & Haigh, B. (1977) · The American Journal of Psychology · doi:10.2307/1421747 · Cited by 604
The Neuropsychology of Human Memory
Squire, L. R. (1982) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.05.030182.001325 · Cited by 574
Neuronal Substrate of Classical Conditioning in the Hippocampus
Berger, T. W., Alger, B. E., & Thompson, R. F. (1976) · Science · doi:10.1126/science.1257783 · Cited by 523
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Gabriel, M., Kang, E., Poremba, A., Kubota, Y., Allen, M. T., Miller, D. P., & Steinmetz, J. E. (1996) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)81105-9 · Cited by 24
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Fortier, C. B., Disterhoft, J. F., & McGlinchey, R. E. (2000) · Neuropsychology · doi:10.1037//0894-4105.14.4.537 · Cited by 24
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Bussey, T. J., Barch, D. M., & Baxter, M. G. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.06.005 · Cited by 23
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Authors: Solomon, P. R., Vander Schaaf, E. R., Thompson, R. F., & Weisz, D. J.
Affiliations: Williams College (US)
Venue: Behavioral Neuroscience
Publisher: American Psychological Association (APA)
Published: 1986
Volume: 100
Issue: 5
Pages: 729-744
ISSN: 0735-7044 (ISSN-L)
1939-0084
DOI: 10.1037/0735-7044.100.5.729
OpenAlex: W1981891948
Cited by: 724
References: 54
Citations by year: 2026: 5 · 2025: 12 · 2024: 15 · 2023: 8 · 2022: 11 · 2021: 9 · 2020: 11 · 2019: 11 · 2018: 15 · 2017: 23 · 2016: 21 · 2015: 21 · 2014: 28 · 2013: 30 · 2012: 25
FWCI: 4.31
Type: journal article
Language: en
Open access: closed
Locations: Behavioral Neuroscience (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute of Mental Health (MH33381)
National Institute of Neurological Disorders and Stroke (5 F32NS 05694-03)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Keywords: hippocampus, trace conditioning, nictitating membrane response, classical conditioning, cingulate cortex, retrosplenial cortex, hippocampal lesions, trace interval, delay conditioning, air puff
MeSH terms: Animals, Brain Mapping, Cerebral Cortex, Conditioning, Classical, Conditioning, Eyelid, Gyrus Cinguli, Hippocampus, Limbic System, Nictitating Membrane, Rabbits, Sound, Touch

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Hippocampus and trace conditioning of the rabbit's classically conditioned nictitating membrane response.

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