The role of hippocampal subregions in detecting spatial novelty
Abstract
Previous literature suggests that the hippocampus subserves processes associated with the encoding of novel information. To investigate the role of different subregions of the hippocampus, the authors made neurotoxic lesions in different subregions of the dorsal hippocampus (i.e., CA1, dentate gyrus [DG], or CA3) of rats, followed by tests using a spontaneous object exploration paradigm. All lesion groups explored normally an object newly introduced in a familiar location. However, when some of the familiar objects were moved to novel locations, both DG and CA3 lesion groups were severely impaired in reexploring the displaced objects, whereas the CA1 lesion group was only mildly impaired in reexploration. The results suggest that the DG-CA3 network is essential in detecting novelty for spatial, but not for individual object, information.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the SNOP test, rodents show preference for exploring a displaced object more than stationary ones, indicating intact spatial recognition.
“Rodents showed preference for exploring the displaced object more than the stationary ones, indicating intact spatial recognition.”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Lee et al., 2005
In the SNOP test, rodents explore a novel object more than familiar ones, indicating object recognition.
“Also, they explored the novel object more than the familiar ones, as an indication for object recognition (Hunsaker et al., 2007a; Lee et al., 2005; Vago and Kesner, 2008).”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Lee et al., 2005
Cites
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 · see citing works
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118 · see citing works
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771 · see citing works
de Nó, R. L. (1934) · Cited by 1,974 · see citing works
Regional dissociations within the hippocampus-memory and anxiety
Bannerman, D. M., Rawlins, J. N. P., McHugh, S. B., Deacon, R. M. J., Yee, B. K., Bast, T., Zhang, W.-N., Pothuizen, H. H. J., & Feldon, J. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.03.004 · Cited by 1,462 · see citing works
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 · see citing works
Computational analysis of the role of the hippocampus in memory
Treves, A., & Rolls, E. T. (1994) · Hippocampus · doi:10.1002/hipo.450040319 · Cited by 1,272 · see citing works
Temporally structured replay of awake hippocampal ensemble activity during rapid eye movement sleep
Louie, K., & Wilson, M. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00186-6 · Cited by 1,148 · see citing works
Hippocampal conjunctive encoding, storage, and recall: Avoiding a trade‐off
O'Reilly, R. C., & McClelland, J. L. (1994) · Hippocampus · doi:10.1002/hipo.450040605 · Cited by 914 · see citing works
Contribution of human hippocampal region to novelty detection
Knight, R. T. (1996) · Nature · doi:10.1038/383256a0 · Cited by 834 · see citing works
Neuromodulation: acetylcholine and memory consolidation
Hasselmo, M. E. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(99)01365-0 · Cited by 809 · see citing works
Contextual cueing of visual attention
Chun, M. M. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01476-5 · Cited by 732 · see citing works
Contextual fear, gestalt memories, and the hippocampus.
Fanselow, M. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00186-2 · Cited by 724 · see citing works
Dissociating hippocampal subregions: A double dissociation between dentate gyrus and CA1
Gilbert, P. E., Kesner, R. P., & Lee, I. (2001) · Hippocampus · doi:10.1002/hipo.1077 · Cited by 641 · see citing works
Self-citationHistology of the nervous system of man and vertebrates
y Cajal, S. R. (1995) · Cited by 553 · see citing works
Vinogradova, O. S. (2001) · Hippocampus · doi:10.1002/hipo.1073 · Cited by 550 · see citing works
NMDA Receptor-Dependent Synaptic Reinforcement as a Crucial Process for Memory Consolidation
Shimizu, E., Tang, Y., Rampon, C., & Tsien, J. Z. (2000) · Science · doi:10.1126/science.290.5494.1170 · Cited by 532 · see citing works
Hippocampal CA3 NMDA Receptors Are Crucial for Memory Acquisition of One-Time Experience
Nakazawa, K., Sun, L. D., Quirk, M. C., Rondi‐Reig, L., Wilson, M. A., & Tonegawa, S. (2003) · Neuron · doi:10.1016/s0896-6273(03)00165-x · Cited by 506 · see citing works
Malleret, G., Haditsch, U., Genoux, D., Jones, M. W., Bliss, T. V. P., Vanhoose, A. M., Weitlauf, C., Kandel, E. R., Winder, D. G., & Mansuy, I. M. (2001) · Cell · doi:10.1016/s0092-8674(01)00264-1 · Cited by 470 · see citing works
Hasselmo, M., & Schnell, E. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03898.1994 · Cited by 466 · see citing works
Different Contributions of the Hippocampus and Perirhinal Cortex to Recognition Memory
Wan, H., Aggleton, J. P., & Brown, M. W. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-03-01142.1999 · Cited by 449 · see citing works
Gothard, K. M., Skaggs, W. E., & McNaughton, B. L. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-24-08027.1996 · Cited by 445 · see citing works
Lisman, J. E., & Otmakhova, N. A. (2001) · Hippocampus · doi:10.1002/hipo.1071 · Cited by 402 · see citing works
Save, É., Poucet, B., Foreman, N., & Buhot, M.-C. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.3.447 · Cited by 383 · see citing works
Distribution of spatial and nonspatial information in dorsal hippocampus
Hampson, R. E., Simeral, J. D., & Deadwyler, S. A. (1999) · Nature · doi:10.1038/45154 · Cited by 303 · see citing works
Knierim, J. J., Kudrimoti, H. S., & McNaughton, B. L. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.425 · Cited by 297 · see citing works
On the use of ibotenic acid to lesion selectively different components of the hippocampal formation
Jarrard, L. E. (1989) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(89)90149-0 · Cited by 295 · see citing works
Lee, I., & Kesner, R. P. (2004) · Hippocampus · doi:10.1002/hipo.10177 · Cited by 268 · see citing works
Self-citationVann, S. D., Brown, M. W., Erichsen, J. T., & Aggleton, J. P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02711.2000 · Cited by 260 · see citing works
Lee, I., & Kesner, R. P. (2004) · Hippocampus · doi:10.1002/hipo.10167 · Cited by 253 · see citing works
Self-citationLocation and identification of excitatory synapses on hippoeampal pyramidal cells
Andersen, P. N., Blackstad, T. W., & L�mo, T. (1966) · Experimental Brain Research · doi:10.1007/bf00234344 · Cited by 245 · see citing works
Differential contribution of NMDA receptors in hippocampal subregions to spatial working memory
Lee, I., & Kesner, R. P. (2002) · Nature Neuroscience · doi:10.1038/nn790 · Cited by 239 · see citing works
Self-citationA Double Dissociation between Hippocampal Subfields
Lee, I., Rao, G., & Knierim, J. J. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.010 · Cited by 236 · see citing works
Self-citationMorris, R. (2001) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2001.0945 · Cited by 221 · see citing works
Hippocampal Neurons Responding to First-Time Dislocation of a Target Object
Fyhn, M., Molden, S., Hollup, S., Moser, M., & Moser, E. I. (2002) · Neuron · doi:10.1016/s0896-6273(02)00784-5 · Cited by 202 · see citing works
Memory for Spatial Location: Role of the Hippocampus in Mediating Spatial Pattern Separation
Gilbert, P. E., Kesner, R. P., & DeCoteau, W. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-02-00804.1998 · Cited by 186 · see citing works
Self-citationXavier, G. F., Oliveira-Filho, F. J. B., & Santos, A. M. G. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:6 · Cited by 175 · see citing works
Hippocampal Lesions Disrupt an Associative Mismatch Process
Honey, R. C., Watt, A. J., & Good, M. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-06-02226.1998 · Cited by 162 · see citing works
Attractor neural network models of spatial maps in hippocampus
Tsodyks, M. V. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:4 · Cited by 147 · see citing works
Lee, I., & Kesner, R. P. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.5.1044 · Cited by 141 · see citing works
Self-citationJenkins, T. A., Amin, E., Pearce, J. M. S., Brown, M. W., & Aggleton, J. P. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.11.024 · Cited by 128 · see citing works
Testing neural network models of memory with behavioral experiments
Kesner, R. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00067-2 · Cited by 124 · see citing works
Self-citationHistology of the Nervous System of Man and Vertebrates
Pestronk, A. (1997) · Neurology · doi:10.1212/wnl.48.1.299-b · Cited by 121 · see citing works
Walsh, T. J., Schulz, D. W., Tilson, H. A., & Schmechel, D. E. (1986) · Brain Research · doi:10.1016/0006-8993(86)91246-1 · Cited by 120 · see citing works
Dynamic Filtering of Recognition Memory Codes in the Hippocampus
Wiebe, S. P., & Staubli, U. V. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-23-10562.1999 · Cited by 87 · see citing works
Roullet, P., Sargolini, F., Oliverio, A., & Mele, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-06-02143.2001 · Cited by 78 · see citing works
The parahippocampal region : implications for neurological and psychiatric diseases
Scharfman, H. E., Witter, M. P., & Schwarcz, R. M. (2000) · Medical Entomology and Zoology · Cited by 72 · see citing works
Computational Modeling of Entorhinal Cortex
Hasselmo, M. E., Fransén, E. A., Dickson, C. T., & Alonso, A. A. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06741.x · Cited by 63 · see citing works
Emerich, D. F., & Walsh, T. J. (1989) · Physiology & Behavior · doi:10.1016/0031-9384(89)90170-4 · Cited by 60 · see citing works
Neurotoxic effects of colchicine.
Mundy, W. R., & Tilson, H. A. (1990) · PubMed · Cited by 57 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
da Luz, A. C. D. D. S., Dias, G. P., Bevilaqua, M. C. D. N., Cocks, G. D., Gardino, P. F., Thuret, S., & Nardi, A. E. (2013) · Neuropsychobiology · doi:10.1159/000353269 · Cited by 4,012 · see citing works
The hippocampal-VTA loop: controlling the entry of information into long-term memory
Lisman, J. E., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.002 · Cited by 1,983 · see citing works
Heldt, S. A., Stanek, L., Chhatwal, J. P., & Ressler, K. J. (2007) · Molecular Psychiatry · doi:10.1038/sj.mp.4001957 · Cited by 684 · see citing works
Messaoudi, E., Kanhema, T., Soule, J. D., Tiron, A., Dagytė, G., da Silva, B., & Bramham, C. R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2883-07.2007 · Cited by 452 · see citing works
Assessment of spatial memory in mice
Sharma, S., Rakoczy, S. G., & Brown‐Borg, H. M. (2010) · Life Sciences · doi:10.1016/j.lfs.2010.09.004 · Cited by 370 · see citing works
Towards a functional organization of episodic memory in the medial temporal lobe
Eichenbaum, H., Sauvage, M., Fortin, N., Komorowski, R., & Lipton, P. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.07.006 · Cited by 354 · see citing works
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 · see citing works
Self-citationHippocampal long-term depression: master or minion in declarative memory processes?
Kemp, A., & Manahan-Vaughan, D. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.01.002 · Cited by 336 · see citing works
An Unexpected Sequence of Events: Mismatch Detection in the Human Hippocampus
Kumaran, D., & Maguire, E. A. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040424 · Cited by 324 · see citing works
Neural circuitry for rat recognition memory
Warburton, E. C., & Brown, M. W. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.09.050 · Cited by 307 · see citing works
The hippocampus supports multiple cognitive processes through relational binding and comparison
Olsen, R. K., Moses, S. N., Riggs, L., & Ryan, J. D. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00146 · Cited by 306 · see citing works
Hippocampal mechanisms for the context-dependent retrieval of episodes
Hasselmo, M. E., & Eichenbaum, H. (2005) · Neural Networks · doi:10.1016/j.neunet.2005.08.007 · Cited by 298 · see citing works
Match–Mismatch Processes Underlie Human Hippocampal Responses to Associative Novelty
Kumaran, D., & Maguire, E. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1677-07.2007 · Cited by 264 · see citing works
Duncan, K. D., Ketz, N., Inati, S., & Davachi, L. (2011) · Hippocampus · doi:10.1002/hipo.20933 · Cited by 263 · see citing works
The role of the dentate gyrus, CA3a,b, and CA3c for detecting spatial and environmental novelty
Hunsaker, M. R., Rosenberg, J. S., & Kesner, R. P. (2008) · Hippocampus · doi:10.1002/hipo.20464 · Cited by 252 · see citing works
Self-citationPattern 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 · see citing works
Distinct roles of medial and lateral entorhinal cortex in spatial cognition
Van Cauter, T., Camon, J., Alvernhe, A., Elduayen, C., Sargolini, F., & Save, E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs033 · Cited by 196 · see citing works
Mustafa, S., Walker, A. J., Bennett, G., & Wigmore, P. M. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06325.x · Cited by 193 · see citing works
Sleep deprivation impairs object recognition in mice
Palchykova, S., Winsky‐Sommerer, R., Meerlo, P., Dürr, R., & Tobler, I. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.11.005 · Cited by 192 · see citing works
Environmental novelty is signaled by reduction of the hippocampal theta frequency
Jeewajee, A., Lever, C., Burton, S., O'Keefe, J. M., & Burgess, N. (2007) · Hippocampus · doi:10.1002/hipo.20394 · Cited by 189 · see citing works
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 183 · see citing works
VanElzakker, M. B., Fevurly, R. D., Breindel, T., & Spencer, R. L. (2008) · Learning & Memory · doi:10.1101/lm.1196508 · Cited by 179 · see citing works
Ito, R., & Lee, A. C. H. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.07.039 · Cited by 173 · see citing works
Kctd13 deletion reduces synaptic transmission via increased RhoA
Escamilla, C. O., Filonova, I., Walker, A. K., Xuan, Z. X., Holehonnur, R., Espinosa, F., Liu, S., Thyme, S. B., López-García, I. A., Mendoza, D. B., et al. (2017) · Nature · doi:10.1038/nature24470 · Cited by 165 · see citing works
Gilbert, P. E., & Brushfield, A. M. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.03.037 · Cited by 164 · see citing works
Karl, T., Duffy, L., Scimone, A., Harvey, R. P., & Schofield, P. R. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00298.x · Cited by 163 · see citing works
Hagena, H., Hansen, N., & Manahan‐Vaughan, D. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv330 · Cited by 163 · see citing works
The role of hippocampal subregions in memory for stimulus associations
Langston, R. F., Stevenson, C. H., Wilson, C. L., Saunders, I., & Wood, E. R. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.07.006 · Cited by 161 · see citing works
Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158 · see citing works
Role of GABAB receptors in learning and memory and neurological disorders
Heaney, C. F., & Kinney, J. W. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.01.007 · Cited by 154 · see citing works
Jaramillo, T. C., Speed, H. E., Xuan, Z., Reimers, J. M., Liu, S., & Powell, C. M. (2015) · Autism Research · doi:10.1002/aur.1529 · Cited by 151 · see citing works
Wigmore, P. M., Mustafa, S., ELBeltagy, M., Lyons, L., Umka, J., & Bennett, G. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-6306-2_20 · Cited by 148 · see citing works
Mueller, S. G., Chao, L. L., Berman, B. D., & Weiner, M. W. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.028 · Cited by 146 · see citing works
Norepinephrine and the dentate gyrus
Harley, C. W. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63018-0 · Cited by 143 · see citing works
Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning
Kaplan, R., Doeller, C. F., Barnes, G. R., Vladimir Litvak, A., Düzel, E., Bandettini, P. A., & Burgess, N. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001267 · Cited by 141 · see citing works
Assessments of dentate gyrus function: discoveries and debates
Borzello, M., Ramirez, S., Treves, A., Lee, I., Scharfman, H. E., Stark, C. E. L., Knierim, J. J., & Rangel, L. M. (2023) · Nature reviews. Neuroscience · doi:10.1038/s41583-023-00710-z · Cited by 138 · see citing works
Self-citationHunsaker, M. R., & Kesner, R. P. (2008) · Hippocampus · doi:10.1002/hipo.20455 · Cited by 133 · see citing works
Self-citationHunsaker, M. R., Mooy, G. G., Swift, J. S., & Kesner, R. P. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.4.742 · Cited by 128 · see citing works
Self-citationHunsaker, M. R., Fieldsted, P. M., Rosenberg, J. S., & Kesner, R. P. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.3.643 · Cited by 127 · see citing works
Self-citationNovel object exploration in mice: Not all objects are created equal
Heyser, C. J., & Chemero, A. (2012) · Behavioural Processes · doi:10.1016/j.beproc.2011.12.004 · Cited by 126 · see citing works
On How the Dentate Gyrus Contributes to Memory Discrimination
van Dijk, M. T., & Fenton, A. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.018 · Cited by 126 · see citing works
BMP Signaling Mediates Effects of Exercise on Hippocampal Neurogenesis and Cognition in Mice
Gobeske, K. T., Das, S., Bonaguidi, M. A., Weiss, C., Radulović, J., Disterhoft, J. F., & Kessler, J. A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007506 · Cited by 120 · see citing works
Rogers, J. L., Santis, S. D., & See, R. E. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1187-7 · Cited by 118 · see citing works
Valproic acid reduces spatial working memory and cell proliferation in the hippocampus
Umka, J., Mustafa, S., ELBeltagy, M., Thorpe, A., Latif, L., Bennett, G., & Wigmore, P. M. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.11.073 · Cited by 118 · see citing works
Spatial Object Recognition Enables Endogenous LTD that Curtails LTP in the Mouse Hippocampus
Goh, J. J., & Manahan‐Vaughan, D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs089 · Cited by 116 · see citing works
Deficient memory acquisition in temporal lobe epilepsy is predicted by hippocampal granule cell loss
Pauli, E., Hildebrandt, M. A. T., Romstöck, J., Stefan, H., & Blümcke, I. (2006) · Neurology · doi:10.1212/01.wnl.0000239828.36651.73 · Cited by 113 · see citing works
Lyons, L., ELBeltagy, M., Umka, J., Markwick, R., Startin, C. M., Bennett, G., & Wigmore, P. M. (2010) · Psychopharmacology · doi:10.1007/s00213-010-2122-2 · Cited by 108 · see citing works
The temporal attributes of episodic memory
Kesner, R. P., & Hunsaker, M. R. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.12.029 · Cited by 102 · see citing works
Self-citationSchumacher, A., Villaruel, F. R., Ussling, A., Riaz, S., Lee, A. C. H., & Ito, R. (2018) · Current Biology · doi:10.1016/j.cub.2018.03.012 · Cited by 101 · see citing works
Evaluating the temporal context of episodic memory: The role of CA3 and CA1
Hunsaker, M. R. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.11.015 · Cited by 101 · see citing works
Self-citationThe roles of the medial prefrontal cortex and hippocampus in a spatial paired-association taskPreprint
Lee, I., & Solivan, F. (2008) · Learning & Memory · doi:10.1101/lm.902708 · Cited by 99 · see citing works
Self-citationKabadi, S. V., Stoica, B. A., Byrnes, K. R., Hanscom, M., Loane, D. J., & Faden, A. I. (2011) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2011.117 · Cited by 94 · see citing works
Vago, D. R., & Kesner, R. P. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.01.002 · Cited by 92 · see citing works
Self-citationHansen, N., & Manahan‐Vaughan, D. (2015) · Hippocampus · doi:10.1002/hipo.22436 · Cited by 92 · see citing works
Hunsaker, M. R., Chen, V., Tran, G. T., & Kesner, R. P. (2013) · Hippocampus · doi:10.1002/hipo.22097 · Cited by 88 · see citing works
Self-citationAdult neurogenesis and the memories of drug addiction
Canales, J. J. (2007) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-007-0730-6 · Cited by 86 · see citing works
Dentate gyrus and spatial behaviour
Xavier, G. F., & Costa, V. C. I. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.03.036 · Cited by 83 · see citing works
Hardt, O., Migues, P. V., Hastings, M., Wong, J., & Nader, K. (2010) · Hippocampus · doi:10.1002/hipo.20708 · Cited by 79 · see citing works
Fast gamma rhythms in the hippocampus promote encoding of novel object-place pairings
Zheng, C., Bieri, K. W., Hwaun, E., & Colgin, L. L. (2016) · eNeuro · doi:10.1523/eneuro.0001-16.2016 · Cited by 79 · see citing works
Aggleton, J. P., Brown, M. W., & Albasser, M. M. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.05.018 · Cited by 79 · see citing works
CA2: A Highly Connected Intrahippocampal Relay
Middleton, S. J., & McHugh, T. J. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-080719-100343 · Cited by 79 · see citing works
O’Tuathaigh, C. M. P., O'Sullivan, G. J., Kinsella, A., Harvey, R. P., Tighe, O., Croke, D. T., & Waddington, J. L. (2005) · Neuroreport · doi:10.1097/01.wnr.0000192738.31029.0a · Cited by 79 · see citing works
Intranetwork and internetwork functional connectivity alterations in post-traumatic stress disorder
Zhang, Y., Liu, F., Chen, H., Li, M., Duan, X., Xie, B., & Chen, H. (2015) · Journal of Affective Disorders · doi:10.1016/j.jad.2015.08.043 · Cited by 79 · see citing works
Hasselmo, M. E. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.1.342 · Cited by 78 · see citing works
Spanswick, S. C., & Sutherland, R. J. (2010) · Learning & Memory · doi:10.1101/lm.1746710 · Cited by 78 · see citing works
Effect of exercise on learning and memory in a rat model of developmental stress
Grace, L. K., Hescham, S., Kellaway, L. A., Bugarith, K., & Russell, V. A. (2009) · Metabolic Brain Disease · doi:10.1007/s11011-009-9162-5 · Cited by 77 · see citing works
Human hippocampal CA3 damage disrupts both recent and remote episodic memories
Miller, T. D., Chong, T. T. ‐., Davies, A. M. A., Johnson, M. R., Irani, S. R., Husain, M., Ng, T. W. C., Jacob, S., Maddison, P., Kennard, C., et al. (2020) · eLife · doi:10.7554/elife.41836 · Cited by 76 · see citing works
Differential impairment of spatial and nonspatial cognition in a mouse model of brain aging
Wang, W., Li, S., Dong, H., Lv, S., & Tang, Y. (2009) · Life Sciences · doi:10.1016/j.lfs.2009.05.003 · Cited by 73 · see citing works
Havekes, R., Bruinenberg, V. M., Tudor, J. C., Ferri, S. L., Baumann, A., Meerlo, P., & Abel, T. G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2403-14.2014 · Cited by 73 · see citing works
Poirier, G. L., Amin, E., & Aggleton, J. P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4607-07.2008 · Cited by 72 · see citing works
Barbosa, F. F., de Oliveira Pontes, I. M., Ribeiro, S., Ribeiro, A. M., & Silva, R. H. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.04.022 · Cited by 71 · see citing works
Deuker, L., Doeller, C. F., Fell, J., & Axmacher, N. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00064 · Cited by 71 · see citing works
Li, S., Fan, Y., Wang, W., & Tang, Y. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.10.007 · Cited by 71 · see citing works
Long, N. M., Lee, H., & Kuhl, B. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1850-16.2016 · Cited by 71 · see citing works
Vouimba, R., Yaniv, D., & Richter‐Levin, G. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.007 · Cited by 70 · see citing works
Bramham, C. R. (2007) · Progress in Brain Research · doi:10.1016/s0079-6123(07)63025-8 · Cited by 69 · see citing works
Cellular, molecular, and genetic substrates underlying the impact of nicotine on learning
Gould, T. J., & Leach, P. T. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.08.004 · Cited by 68 · see citing works
Hunsaker, M. R., & Kesner, R. P. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.11.012 · Cited by 68 · see citing works
Self-citationCyclin D1 Gene Ablation Confers Neuroprotection in Traumatic Brain Injury
Kabadi, S. V., Stoica, B. A., Loane, D. J., Byrnes, K. R., Hanscom, M., Cabatbat, R. M., Tan, M. T., & Faden, A. I. (2011) · Journal of Neurotrauma · doi:10.1089/neu.2011.1980 · Cited by 66 · see citing works
Bath, K. G., Nitenson, A. S., Lichtman, E. S., Lopez, C., Chen, W., Gallo, M. E., Goodwill, H. L., & Manzano-Nieves, G. (2017) · Neurobiology of Stress · doi:10.1016/j.ynstr.2017.04.001 · Cited by 66 · see citing works
Maâroufi, K., Had‐Aissouni, L., Melon, C., Sakly, M., Abdelmelek, H., Poucet, B., & Save, É. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.10.016 · Cited by 64 · see citing works
Nicotinic ACh Receptors in the Hippocampus: Role in Excitability and Plasticity
Yakel, J. L. (2012) · Nicotine & Tobacco Research · doi:10.1093/ntr/nts091 · Cited by 62 · see citing works
Morellini, F., Lepsveridze, E., Kähler, B., Dityatev, A. E., & Schachner, M. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.10.006 · Cited by 61 · see citing works
The role of calsenilin/DREAM/KChIP3 in contextual fear conditioningPreprint
Alexander, J. C., McDermott, C. M., Tunur, T., Rands, V. F., Stelly, C. E., Karhson, D. S., Bowlby, M. R., An, W., Sweatt, J. D., & Schrader, L. A. (2009) · Learning & Memory · doi:10.1101/lm.1261709 · Cited by 61 · see citing works
Behavioral profile of a heterozygous mutant mouse model for EGF-like domain neuregulin 1.
Duffy, L., Cappas, E., Scimone, A., Schofield, P. R., & Karl, T. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.4.748 · Cited by 59 · see citing works
Developmental onset distinguishes three types of spontaneous recognition memory in mice
Cruz-Sanchez, A., Dematagoda, S., Ahmed, R., Mohanathaas, S., Odenwald, N., & Arruda-Carvalho, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-67619-w · Cited by 58 · see citing works
Role of the dorsal hippocampus in object memory load
Sannino, S., Russo, F., Torromino, G., Pendolino, V., Calabresi, P., & De Leonibus, E. (2012) · Learning & Memory · doi:10.1101/lm.025213.111 · Cited by 57 · see citing works
Kabadi, S. V., Stoica, B. A., Hanscom, M., Loane, D. J., Kharebava, G., Murray, M. G., II, Cabatbat, R. M., & Faden, A. I. (2011) · Neurotherapeutics · doi:10.1007/s13311-011-0095-4 · Cited by 57 · see citing works
Pace, T. W. W., Gaylord, R. I., Topczewski, F., Girotti, M., Rubin, B., & Spencer, R. L. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04354.x · Cited by 57 · see citing works
Associative memory deficits in mild cognitive impairment: The role of hippocampal formation
Atienza, M., da Silva, K. C. A., González‐Escamilla, G., Gil-Neciga, E., Gonzalez, A. S., & Cantero, J. L. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.047 · Cited by 57 · see citing works
Circuit-based interventions in the dentate gyrus rescue epilepsy-associated cognitive dysfunction
Kahn, J. B., Port, R. G., Yue, C., Takano, H., & Coulter, D. A. (2019) · Brain · doi:10.1093/brain/awz209 · Cited by 57 · see citing works
Human hippocampal processing of environmental novelty during spatial navigation
Kaplan, R., Horner, A. J., Bandettini, P. A., Doeller, C. F., & Burgess, N. (2014) · Hippocampus · doi:10.1002/hipo.22264 · Cited by 55 · see citing works
c-Fos expression correlates with performance on novel object and novel place recognition tests
Mendez, M., Arias, N., Uceda, S., & Arias, J. L. (2015) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2015.07.004 · Cited by 54 · see citing works
Binder, S., Dere, E., & Zlomuzica, A. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.04.002 · Cited by 53 · see citing works
Mueller, S. G., Laxer, K. D., Scanlon, C., Garcia, P. A., McMullen, W. J., Loring, D. W., Meador, K. J., & Weiner, M. W. (2011) · Human Brain Mapping · doi:10.1002/hbm.21226 · Cited by 53 · see citing works
Zhao, Q., Murakami, Y., Tohda, M., Obi, R., Shimada, Y., & Matsumoto, K. (2007) · Journal of Pharmacological Sciences · doi:10.1254/jphs.fp0061457 · Cited by 51 · see citing works
The role of hippocampal mossy cells in novelty detection
Fredes, F., & Shigemoto, R. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107486 · Cited by 50 · see citing works
Christiansen, K., Dillingham, C. M., Wright, N. F., Saunders, R. C., Vann, S. D., & Aggleton, J. P. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13208 · Cited by 50 · see citing works
The importance of the rat hippocampus for learning the structure of visual arrays
Sanderson, D. J., Pearce, J. M., Kyd, R. J., & Aggleton, J. P. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05035.x · Cited by 49 · see citing works
Brown, T. I., Hasselmo, M. E., & Stern, C. E. (2014) · Hippocampus · doi:10.1002/hipo.22273 · Cited by 48 · see citing works
- Authors
- Lee, I., Hunsaker, M. R., & Kesner, R. P.
- Affiliations
- Boston University (US)
- University of Utah (US)
- Venue
- Behavioral Neuroscience
- Published
- 2005
- Volume
- 119
- Issue
- 1
- Pages
- 145-153
- ISSN
- 0735-7044 (ISSN-L)
- 1939-0084
- OpenAlex
- W2154243350
- Cited by
- 270
- References
- 51
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 10 · 2023: 5 · 2022: 8 · 2021: 11 · 2020: 7 · 2019: 8 · 2018: 13 · 2017: 14 · 2016: 14 · 2015: 15 · 2014: 17 · 2013: 17 · 2012: 19
- FWCI
- 8.57
- 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 › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- hippocampal subfields, dorsal hippocampus, dentate gyrus, CA1, CA3, neurotoxic lesion, spatial memory, novel object recognition
- MeSH terms
- Animals, Cognition, Exploratory Behavior, Hippocampus, Male, Space Perception, Rats, Long-Evans, Rats
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 ›
Are you an author, or do you see a problem with this page? Request a review