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Differential contributions of dorsal hippocampal subregions to memory acquisition and retrieval in contextual fear‐conditioning
Abstract
The hippocampus is an essential neural structure in developing contextual memory in a situation in which rapid development of associative learning should occur. We tested a subregion‐specific contribution in the hippocampus to memory acquisition and retrieval, using the contextual fear‐conditioning paradigm. The current results suggest that all three subregions (i.e., CA3, CA1, and dentate gyrus) of the hippocampus contribute to rapid acquisition of contextual memory in the initial phase of acquisition. The involvement of CA3 seems to be important at the earliest stage of acquisition, presumably for developing instant representation of a context. The role of CA3, however, was minimal in retrieving contextual memory after a long time period (i.e., 24 h), whereas the other subregions (i.e., CA1 and dentate gyrus) were critically involved. The results indicate time‐dependent differential contributions of the hippocampal subregions to memory acquisition and retrieval in contextual fear‐conditioning. © 2004 Wiley‐Liss, Inc.
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McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256
Gray, J. A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00013066 · Cited by 4,477
Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.
Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.2.274 · Cited by 3,292
Modality-Specific Retrograde Amnesia of Fear
Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483
Hippocampal synaptic enhancement and information storage within a distributed memory system
McNaughton, B. L., & Morris, R. G. M. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90011-7 · Cited by 1,304
Memory deficits for implicit contextual information in amnesic subjects with hippocampal damage
Chun, M. M., & Phelps, E. A. (1999) · Nature Neuroscience · doi:10.1038/12222 · Cited by 554
Phillips, R. G., & LeDoux, J. E. (1994) · Learning & Memory · doi:10.1101/lm.1.1.34 · Cited by 528
Cited by
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Kheirbek, M. A., Drew, L. J., Burghardt, N. S., Costantini, D. O., Tannenholz, L., Ahmari, S. E., Zeng, H., Fenton, A. A., & Hen, R. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.038 · Cited by 713
A computational theory of hippocampal function, and empirical tests of the theory
Rolls, E. T., & Kesner, R. P. (2006) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2006.04.005 · Cited by 608
Self-citationCaspase-3 triggers early synaptic dysfunction in a mouse model of Alzheimer's disease
D'Amelio, M., Cavallucci, V., Middei, S., Marchetti, C., Pacioni, S., Ferri, A., Diamantini, A., De Zio, D., Carrara, P., Battistini, L., et al. (2011) · Nature Neuroscience · doi:10.1038/nn.2709 · Cited by 572
A computational theory of hippocampal function, and tests of the theory: New developments
Kesner, R. P., & Rolls, E. T. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.11.009 · Cited by 347
Self-citationEvolution of declarative memory
Manns, J. R., & Eichenbaum, H. (2006) · Hippocampus · doi:10.1002/hipo.20205 · Cited by 345
The role of hippocampal subregions in detecting spatial novelty
Lee, I., Hunsaker, M. R., & Kesner, R. P. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.1.145 · Cited by 270
Self-citationBarrett, R. M., Malvaez, M., Kramar, E., Matheos, D. P., Arrizon, A., Cabrera, S. M., Lynch, G., Greene, R. W., & Wood, M. A. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.61 · Cited by 243
Pattern separation, pattern completion, and new neuronal codes within a continuous CA3 map
Leutgeb, S., & Leutgeb, J. K. (2007) · Learning & Memory · doi:10.1101/lm.703907 · Cited by 234
The temporal paradox of Hebbian learning and homeostatic plasticity
Zenke, F., Gerstner, W., & Ganguli, S. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.015 · Cited by 201
BERLAU, D., & MCGAUGH, J. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.12.008 · Cited by 220
Bernier, B. E., Lacagnina, A. F., Ayoub, A., Shue, F., Zemelman, B. V., Krasne, F. B., & Drew, M. R. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3029-16.2017 · Cited by 168
Immature Dentate Gyrus: An Endophenotype of Neuropsychiatric Disorders
Hagihara, H., Takao, K., Walton, N. M., Matsumoto, M., & Miyakawa, T. (2013) · Neural Plasticity · doi:10.1155/2013/318596 · Cited by 123
Hernández-Rabaza, V., Hontecillas-Prieto, L., Velázquez-Sánchez, C., Ferragud, A., Pérez-Villaba, A., Arcusa, A., Barcia, J. A., Trejo, J. L., & Canales, J. J. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.06.008 · Cited by 114
Connor, S. A., Ammendrup-Johnsen, I., Chan, A. W., Kishimoto, Y., Murayama, C., Kurihara, N., Tada, A., Ge, Y., Lu, H., Yan, R., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.016 · Cited by 100
Vago, D. R., Bevan, A., & Kesner, R. P. (2007) · Hippocampus · doi:10.1002/hipo.20329 · Cited by 94
Self-citationAdult hippocampal neurogenesis and its role in cognition.
Oomen, C. A., Bekinschtein, P., Kent, B. A., Saksida, L. M., & Bussey, T. J. (2014) · WIREs Cognitive Science · doi:10.1002/wcs.1304 · Cited by 93
The role of the ventral dentate gyrus in anxiety-based behaviors
Weeden, C. S. S., Roberts, J. M., Kamm, A. M., & Kesner, R. P. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.12.002 · Cited by 80
Stackman, R. W., Cohen, S. J., Lora, J. C., & Rios, L. M. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.016 · Cited by 66
Patten, A. R., Yau, S. Y., Fontaine, C. J., Meconi, A., Wortman, R. C., & Christie, B. R. (2015) · Brain Plasticity · doi:10.3233/bpl-150016 · Cited by 64
Ballesteros, C. I., de Oliveira Galvão, B., Maisonette, S., & Landeira-Fernandez, J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0083342 · Cited by 39
“These results are consistent with previous reports [6–10,20] and corroborate the fact that the hippocampus is a complex brain structure involved in different aspects of contextual fear conditioning.”
BackgroundResultA microRNA negative feedback loop downregulates vesicle transport and inhibits fear memory
Mathew, R. S., Tatarakis, A., Rudenko, A., Johnson-Venkatesh, E. M., Yang, Y. J., Murphy, E. A., Todd, T. P., Schepers, S. T., Siuti, N., Martorell, A. J., et al. (2016) · eLife · doi:10.7554/elife.22467 · Cited by 39
Holliday, E. D., Nucero, P., Kutlu, M. G., Oliver, C., Connelly, K. L., Gould, T. J., & Unterwald, E. M. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13398 · Cited by 38
Tewari, S., & Parpura, V. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00145 · Cited by 35
Primary cilia are required for the persistence of memory and stabilization of perineuronal nets
Jovasevic, V., Zhang, H., Sananbenesi, F., Guedea, A. L., Soman, K. V., Wiktorowicz, J. E., Fischer, A., & Radulovic, J. (2021) · iScience · doi:10.1016/j.isci.2021.102617 · Cited by 32
Learned together, extinguished apart: reducing fear to complex stimuli
Jones, C. E., Ringuet, S., & Monfils, M.-H. (2013) · Learning & Memory · doi:10.1101/lm.031740.113 · Cited by 30
Gitik, M., Holliday, E. D., Leung, M., Yuan, Q., Logue, S. F., Tikkanen, R., Goldman, D., & Gould, T. J. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.08.009 · Cited by 21
Metadata
- Authors
- Lee, I., & Kesner, R. P.
- Venue
- Hippocampus
- Publisher
- Wiley
- Published
- 2004-01
- Volume
- 14
- Issue
- 3
- Pages
- 301-310
- ISSN
- 1050-9631 (ISSN-L)
- 1098-1063
- OpenAlex
- W2054982643
- Cited by
- 266
- References
- 7
- FWCI
- 8.32
- Type
- journal article
- Language
- en
- Open access
- closed
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