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Hippocampus and trace conditioning of the rabbit's classically conditioned nictitating membrane response.
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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“These deficits are strikingly similar to those reported in hippocampal-lesioned mammals [216,226,227,228,229,230,231], and reveal that the hippocampal pallium of teleost fish is critical for the temporal dimension of the associative memories required for trace classical conditioning.”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [230]
Citations
Cites
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
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-citationExperimental methods and instrumentation in psychology
Sidowski, J. B. (1966) · Medical Entomology and Zoology · Cited by 793
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
Self-citation
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Sorted by citations
Learning enhances adult neurogenesis in the hippocampal formation
Gould, E., Beylin, A., Tanapat, P., Reeves, A., & Shors, T. J. (1999) · Nature Neuroscience · doi:10.1038/6365 · Cited by 2,157
Neurogenesis in the adult is involved in the formation of trace memories
Shors, T. J., Miesegaes, G. R., Beylin, A. V., Zhao, M., Rydel, T. A., & Gould, E. (2001) · Nature · doi:10.1038/35066584 · Cited by 2,014
The stressed hippocampus, synaptic plasticity and lost memories
Kim, J. J., & Diamond, D. M. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn849 · Cited by 1,543
CENTRAL CHOLINERGIC SYSTEMS AND COGNITION
Everitt, B. J., & Robbins, T. W. (1997) · Annual Review of Psychology · doi:10.1146/annurev.psych.48.1.649 · Cited by 1,348
Neuronal Reward and Decision Signals: From Theories to Data
Schultz, W. (2015) · Physiological Reviews · doi:10.1152/physrev.00023.2014 · Cited by 1,126
Two functional components of the hippocampal memory system
Eichenbaum, H., Otto, T., & Cohen, N. J. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035391 · Cited by 1,114
Adult neurogenesis: from precursors to network and physiology
Abrous, D. N., Koehl, M., & Le Moal, M. (2005) · Physiological Reviews · doi:10.1152/physrev.00055.2003 · Cited by 971
Biology and the Future of Psychoanalysis: A New Intellectual Framework for Psychiatry Revisited
Kandel, E. R. (1999) · American Journal of Psychiatry · doi:10.1176/ajp.156.4.505 · Cited by 905
Neurogenesis may relate to some but not all types of hippocampal‐dependent learning
Shors, T. J., Townsend, D. A., Zhao, M., Kozorovitskiy, Y., & Gould, E. (2002) · Hippocampus · doi:10.1002/hipo.10103 · Cited by 853
COGNITIVE NEUROSCIENCE OF HUMAN MEMORY
Gabrieli, J. D. E. (1998) · Annual Review of Psychology · doi:10.1146/annurev.psych.49.1.87 · Cited by 808
The propositional nature of human associative learning
Mitchell, C. J., Houwer, J. D., & Lovibond, P. F. (2009) · Behavioral and Brain Sciences · doi:10.1017/s0140525x09000855 · Cited by 789
Molecular mechanisms of memory acquisition, consolidation and retrieval
Abel, T. G., & Lattal, K. M. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00194-x · Cited by 709
The Neuroscience of Mammalian Associative Learning
Fanselow, M. S., & Poulos, A. M. (2005) · Annual Review of Psychology · doi:10.1146/annurev.psych.56.091103.070213 · Cited by 683
Hippocampectomy disrupts trace eye-blink conditioning in rabbits.
Moyer, J. R., Deyo, R. A., & Disterhoft, J. F. (2015) · Behavioral Neuroscience · doi:10.1037/bne0000079 · Cited by 664
Neural circuits and mechanisms involved in Pavlovian fear conditioning: A critical review
Kim, J. J., & Jung, M. W. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.06.005 · Cited by 636
Impaired fear conditioning following unilateral temporal lobectomy in humans
LaBar, K., LeDoux, J., Spencer, D., & Phelps, E. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06846.1995 · Cited by 631
Neural Substrates of Eyeblink Conditioning: Acquisition and RetentionPreprint
Christian, K. M., & Thompson, R. F. (2003) · Learning & Memory · doi:10.1101/lm.59603 · Cited by 609
Self-citationAnticipated moments: temporal structure in attention
Nobre, A. C., & van Ede, F. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.141 · Cited by 615
Nobre, A. C., Correa, Á., & Coull, J. T. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.07.006 · Cited by 572
Kim, J. J., Clark, R. E., & Thompson, R. F. (1995) · Behavioral Neuroscience · doi:10.1037//0735-7044.109.2.195 · Cited by 499
Self-citationShors, T. J., Chua, C., & Falduto, J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-16-06292.2001 · Cited by 496
Organization of Memory Traces in the Mammalian Brain
Thompson, R. F., & Krupa, D. J. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.002511 · Cited by 458
Self-citationThe Serial Reaction Time Task: Implicit Motor Skill Learning?: Figure 1.
Robertson, E. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2747-07.2007 · Cited by 484
Trace Eyeblink Conditioning Increases CA1 Excitability in a Transient and Learning-Specific Manner
Moyer, J. R., Thompson, L. T., & Disterhoft, J. F. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-17-05536.1996 · Cited by 403
Büchel, C., Dolan, R. J., Armony, J. L., & Friston, K. J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-24-10869.1999 · Cited by 409
Associative Memory Formation Increases the Observation of Dendritic Spines in the Hippocampus
Leuner, B., Falduto, J., & Shors, T. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00659.2003 · Cited by 403
How Can Hearing Loss Cause Dementia?
Griffiths, T. D., Lad, M., Kumar, S., Holmes, E., McMurray, B., Maguire, E. A., Billig, A. J., & Sedley, W. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.003 · Cited by 389
Neural dynamics of adaptive timing and temporal discrimination during associative learning
Grossberg, S., & Schmajuk, N. A. (1989) · Neural Networks · doi:10.1016/0893-6080(89)90026-9 · Cited by 367
Implicit Perceptual Anticipation Triggered by Statistical Learning
Turk‐Browne, N. B., Scholl, B. J., Johnson, M. K., & Chun, M. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0858-10.2010 · Cited by 384
Classical fear conditioning in functional neuroimaging
Büchel, C. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00078-7 · Cited by 360
Sex differences in learning processes of classical and operant conditioning
Dalla, C., & Shors, T. J. (2009) · Physiology & Behavior · doi:10.1016/j.physbeh.2009.02.035 · Cited by 347
Evolution of declarative memory
Manns, J. R., & Eichenbaum, H. (2006) · Hippocampus · doi:10.1002/hipo.20205 · Cited by 345
Takehara‐Nishiuchi, K., Kawahara, S., & Kirino, Y. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-30-09897.2003 · Cited by 343
Ezzyat, Y., & Davachi, L. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.042 · Cited by 321
Long-term potentiation: What's learning got to do with it?
Shors, T. J., & Matzel, L. D. (1997) · Behavioral and Brain Sciences · doi:10.1017/s0140525x97001593 · Cited by 320
Geinisman, Y., deToledo‐Morrell, L., Morrell, F., & Heller, R. E. (1995) · Progress in Neurobiology · doi:10.1016/0301-0082(94)00047-l · Cited by 327
Thompson, R. F. (2004) · Annual Review of Psychology · doi:10.1146/annurev.psych.56.091103.070239 · Cited by 314
Self-citationStress-Induced Facilitation of Classical Conditioning
Shors, T. J., Weiss, C., & Thompson, R. F. (1992) · Science · doi:10.1126/science.1636089 · Cited by 310
Self-citationHippocampal place cells, context, and episodic memory
Smith, D. M., & Mizumori, S. J. Y. (2006) · Hippocampus · doi:10.1002/hipo.20208 · Cited by 317
Trace but not delay fear conditioning requires attention and the anterior cingulate cortex
Han, C. J., O'Tuathaigh, C. M., van Trigt, L., Quinn, J. J., Fanselow, M. S., Mongeau, R., Koch, C., & Anderson, D. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2132313100 · Cited by 302
Effects of Stress and Hippocampal NMDA Receptor Antagonism on Recognition Memory in RatsPreprint
Baker, K. B., & Kim, J. J. (2002) · Learning & Memory · doi:10.1101/lm.46102 · Cited by 300
Memory systems in the brain and localization of a memory
Thompson, R. F., & Kim, J. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13438 · Cited by 300
Self-citationLeuner, B., Mendolia‐Loffredo, S., Kozorovitskiy, Y., Samburg, D., Gould, E., & Shors, T. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0204-04.2004 · Cited by 300
Chronic Pain and Chronic Stress: Two Sides of the Same Coin?
Abdallah, C. G., & Geha, P. (2017) · Chronic Stress · doi:10.1177/2470547017704763 · Cited by 311
Neural mechanisms of classical conditioning in mammals
Thompson, R. F. (1990) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1990.0161 · Cited by 274
Self-citationHolmes, A., Wrenn, C. C., Harris, A. P., Thayer, K. E., & Crawley, J. N. (2002) · Genes Brain & Behavior · doi:10.1046/j.1601-1848.2001.00005.x · Cited by 284
Mind the Gap: Binding Experiences across Space and Time in the Human Hippocampus
Staresina, B. P., & Davachi, L. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.024 · Cited by 273
Maren, S. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06485.x · Cited by 280
The Acquisition of Motor Behavior in Vertebrates
Bloedel, J. R., Ebner, T. J., & Wise, S. P. (1996) · The MIT Press eBooks · Cited by 263
Hippocampal lesions prevent trace eyeblink conditioning in the freely moving rat
Weiss, C., Bouwmeester, H., Power, J., & Disterhoft, J. F. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00096-5 · Cited by 262
Structural Synaptic Modifications Associated with Hippocampal LTP and Behavioral Learning
Geinisman, Y. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.952 · Cited by 262
Fiala, J. C., Grossberg, S., & Bullock, D. H. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-11-03760.1996 · Cited by 255
Associative Learning Elicits the Formation of Multiple-Synapse Boutons
Geinisman, Y., Berry, R. W., Disterhoft, J. F., Power, J., & van der Zee, E. A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-15-05568.2001 · Cited by 258
Hasselmo, M. E., Giocomo, L. M., & Zilli, E. A. (2007) · Hippocampus · doi:10.1002/hipo.20374 · Cited by 249
Dorsal hippocampus contributes to model-based planning
Miller, K. J., Botvinick, M., & Brody, C. D. (2017) · Nature Neuroscience · doi:10.1038/nn.4613 · Cited by 252
McEchron, M. D., & Disterhoft, J. F. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.2.1030 · Cited by 252
Classical conditioning, awareness, and brain systems
Clark, R. E., Manns, J. R., & Squire, L. R. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)02041-7 · Cited by 249
Amygdala and hippocampal activity during acquisition and extinction of human fear conditioning
Knight, D. C., Smith, C. N., Cheng, D. T., Stein, E. A., & Helmstetter, F. J. (2004) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.4.3.317 · Cited by 249
Learning During Stressful TimesPreprint
Shors, T. J. (2004) · Learning & Memory · doi:10.1101/lm.66604 · Cited by 245
The Role of the Hippocampus in Trace Conditioning: Temporal Discontinuity or Task Difficulty?
Beylin, A. V., Gandhi, C. C., Wood, G. E., Talk, A. C., Matzel, L. D., & Shors, T. J. (2001) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2001.4039 · Cited by 248
Neural Substrates Mediating Human Delay and Trace Fear Conditioning
Knight, D. C., Cheng, D. T., Smith, C. N., Stein, E. A., & Helmstetter, F. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0433-03.2004 · Cited by 239
Thompson, L. T., Moyer, J. R., & Disterhoft, J. F. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.3.1836 · Cited by 237
Stimulus configuration, classical conditioning, and hippocampal function.
Schmajuk, N. A., & DiCarlo, J. J. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.268 · Cited by 229
Neural substrates underlying human delay and trace eyeblink conditioning
Cheng, D. T., Disterhoft, J. F., Power, J., Ellis, D., & Desmond, J. E. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800374105 · Cited by 215
Intact delay-eyeblink classical conditioning in amnesia.
Gabrieli, J. D. E., McGlinchey, R. E., Carrillo, M. C., Gluck, M. A., Cermak, L. S., & Disterhoft, J. F. (1995) · Behavioral Neuroscience · doi:10.1037/0735-7044.109.5.819 · Cited by 212
Cortical involvement in acquisition and extinction of trace eyeblink conditioning.
Weible, A. P., McEchron, M. D., & Disterhoft, J. F. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.6.1058 · Cited by 212
Is the rodent hippocampus just for ‘place’?
Eichenbaum, H. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80072-9 · Cited by 209
Broglio, C., Gómez, A., Durán, E., Ocaña, F. M., Jiménez-Moya, F., Rodríguez, F., & Salas, C. (2005) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2005.03.021 · Cited by 203
Learning, aging and intrinsic neuronal plasticity
Disterhoft, J. F., & Oh, M. M. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.08.005 · Cited by 207
Hippocampus as a memory map: Synaptic plasticity and memory encoding by hippocampal neurons
Shapiro, M. L., & Eichenbaum, H. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:4 · Cited by 209
On the cerebellum, cutaneomuscular reflexes, movement control and the elusive engrams of memory
Bloedel, J. R., & Bracha, V. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(94)00171-b · Cited by 203
Oscillatory brain states and learning: Impact of hippocampal theta-contingent training
Seager, M. A., Johnson, L. D., Chabot, E. S., Asaka, Y., & Berry, S. D. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.032662099 · Cited by 200
Role of the Serotonin 5-HT2AReceptor in LearningPreprint
Harvey, J. A. (2003) · Learning & Memory · doi:10.1101/lm.60803 · Cited by 201
Wood, G. E., Beylin, A. V., & Shors, T. J. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.1.175 · Cited by 198
Gilmartin, M. R., & Helmstetter, F. J. (2010) · Learning & Memory · doi:10.1101/lm.1597410 · Cited by 208
Impaired trace eyeblink conditioning in bilateral, medial-temporal lobe amnesia.
McGlinchey, R. E., Carrillo, M. C., Gabrieli, J. D. E., Fortier, C. B., & Disterhoft, J. F. (1997) · Behavioral Neuroscience · doi:10.1037/0735-7044.111.5.873 · Cited by 193
Lesions of the Caudal Area of Rabbit Medial Prefrontal Cortex Impair Trace Eyeblink Conditioning
Kronforst-Collins, M. A., & Disterhoft, J. F. (1998) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1997.3818 · Cited by 191
Calcium-dependent afterhyperpolarization and learning in young and aging hippocampus
Disterhoft, J. F., Thompson, L. T., Moyer, J. R., & Mogul, D. J. (1996) · Life Sciences · doi:10.1016/0024-3205(96)00320-7 · Cited by 190
Where is the trace in trace conditioning?
Woodruff‐Pak, D. S., & Disterhoft, J. F. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2007.11.006 · Cited by 188
Trace Conditioning and the Hippocampus: The Importance of Contiguity
Bangasser, D. A., Waxler, D. E., Santollo, J., & Shors, T. J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1742-06.2006 · Cited by 185
A new chapter in the field of memory: adult hippocampal neurogenesis
Koehl, M., & Abrous, D. N. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07609.x · Cited by 198
Gilmartin, M. R., & McEchron, M. D. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.6.1496 · Cited by 183
Hippocampus-dependent learning facilitated by a monoclonal antibody or D-cycloserine
Thompson, L. T., Moskal, J. R., & Disterhoft, J. F. (1992) · Nature · doi:10.1038/359638a0 · Cited by 182
Sears, L. L., & Steinmetz, J. E. (1990) · Behavioral Neuroscience · doi:10.1037/0735-7044.104.5.681 · Cited by 181
Hippocampus, context, and conditioning.
Penick, S., & Solomom, P. R. (1991) · Behavioral Neuroscience · doi:10.1037//0735-7044.105.5.611 · Cited by 180
Cicchese, J. J., & Berry, S. D. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00001 · Cited by 173
Memory for Emotional Words Following Unilateral Temporal Lobectomy
Phelps, E. A., LaBar, K. S., & Spencer, D. D. (1997) · Brain and Cognition · doi:10.1006/brcg.1997.0929 · Cited by 178
Abnormal classical eye-blink conditioning in autism
Sears, L. L., Finn, P., & Steinmetz, J. E. (1994) · Journal of Autism and Developmental Disorders · doi:10.1007/bf02172283 · Cited by 161
Memory traces of trace memories: neurogenesis, synaptogenesis and awareness
Shors, T. J. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.03.007 · Cited by 167
Neuroprotection by two polyphenols following excitotoxicity and experimental ischemia
Gottlieb, M., Leal-Campanario, R., Campos-Esparza, M. R., Sánchez-Gómez, M. V., Alberdi, E., Arranz, A., Delgado-García, J. M., Gruart, A., & Matute, C. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.03.017 · Cited by 141
Hippocampal Contributions to Model-Based Planning and Spatial Memory
Vikbladh, O. M., Meager, M. R., King, J. A., Blackmon, K., Devinsky, O., Shohamy, D., Burgess, N., & Daw, N. D. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.014 · Cited by 159
Chowdhury, N., Quinn, J. J., & Fanselow, M. S. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.5.1396 · Cited by 160
Multiple brain-memory systems: the whole does not equal the sum of its parts
Kim, J. J., & Baxter, M. G. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01818-x · Cited by 172
Spikes, synchrony, and attentive learning by laminar thalamocortical circuits
Grossberg, S., & Massimiliano Versace, A. (2008) · Brain Research · doi:10.1016/j.brainres.2008.04.024 · Cited by 164
Learning to learn – Intrinsic plasticity as a metaplasticity mechanism for memory formation
Sehgal, M., Song, C., Ehlers, V. L., & Moyer, J. R. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.07.008 · Cited by 161
The hippocampus, time, and memory across scales.
Howard, M. W., & Eichenbaum, H. (2013) · Journal of Experimental Psychology General · doi:10.1037/a0033621 · Cited by 163
Thompson, R. F., Bao, S., Chen, L., Cipriano, B. D., Grethe, J. S., Kim, J. J., Thompson, J. K., Tracy, J. A., Weninger, M. S., & Krupa, D. J. (1997) · International review of neurobiology · doi:10.1016/s0074-7742(08)60351-7 · Cited by 151
Self-citationCheung, T. H. C., & Cardinal, R. N. (2005) · BMC Neuroscience · doi:10.1186/1471-2202-6-36 · Cited by 147
Supervised learning in the brain
Knudsen, E. I. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-07-03985.1994 · Cited by 149
Cognitive and emotional functions of the teleost fish cerebellum
Rodrı́guez, F., Durán, E., Gómez, A., Ocaña, F. M., Álvarez, E., Jiménez-Moya, F., Broglio, C., & Salas, C. (2005) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2004.11.026 · Cited by 148
Metadata
- Authors
- Solomon, P. R., Vander Schaaf, E. R., Thompson, R. F., & Weisz, D. J.
- Affiliations
- Williams College (US)
- Venue
- Behavioral Neuroscience
- Published
- 1986
- Volume
- 100
- Issue
- 5
- Pages
- 729-744
- ISSN
- 0735-7044 (ISSN-L)
- 1939-0084
- 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
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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