Processing of spatial and non-spatial information in rats with lesions of the medial and lateral entorhinal cortex: environmental complexity matters
Abstract
The entorhinal-hippocampal circuitry has been suggested to play an important role in episodic memory but the contribution of the entorhinal cortex remains elusive. Predominant theories propose that the medial entorhinal cortex (MEC) processes spatial information whereas the lateral entorhinal cortex (LEC) processes non spatial information. A recent study using an object exploration task has suggested that the involvement of the MEC and LEC spatial and non-spatial information processing could be modulated by the amount of information to be processed, i.e. environmental complexity. To address this hypothesis we used an object exploration task in which rats with excitotoxic lesions of the MEC and LEC had to detect spatial and non-spatial novelty among a set of objects and we varied environmental complexity by decreasing the number of objects or amount of object diversity. Reducing diversity resulted in restored ability to process spatial and non-spatial information in MEC and LEC groups, respectively. Reducing the number of objects yielded restored ability to process non-spatial information in the LEC group but not the ability to process spatial information in the MEC group. The findings indicate that the MEC and LEC are not strictly necessary for spatial and non-spatial processing but that their involvement depends on the complexity of the information to be processed.
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?
Recognition memory for identical objects is not the same as memory for distinct objects.
“This suggests that the recognition memory for identical objects is not as the same as the memory for distinct objects.”
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 Rodo et al., 2017
In the SNOP test, object recognition was compromised when four distinct, but not identical, objects were required to be remembered by LEC-lesioned rats.
“Evidence from the SNOP test has supported this perspective, as object recognition was compromised when four distinct, but not identical, objects were required to be remembered by LEC lesioned rats (Rodo et al., 2017; Van Cauter et al., 2013).”
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 Rodo et al., 2017
MEC-lesioned animals exhibited deficits in spatial recognition when three or four distinct, but not identical, objects were used in the sample trial of the SNOP test.
“The MEC-lesioned animals exhibited deficits in spatial recognition when three or four distinct, but not identical, objects were used in the sample trial of the SNOP test (Rodo et al., 2017).”
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 Rodo et al., 2017
When reducing the diversity of objects to three distinct objects, the LEC-lesioned animals were able to show intact object recognition in the SNOP test.
“When reducing the diversity of objects to three distinct objects, the LEC-lesioned animals were able to show intact object recognition in the SNOP test (Rodo et al., 2017).”
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 Rodo et al., 2017
In the SNOP test, impaired spatial recognition was found after lesion of the MEC.
“In the SNOP test, impaired spatial recognition was found after lesion of the MEC (Rodo et al., 2017; Van Cauter et al., 2013).”
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 Rodo et al., 2017
Cites
The rat brain in stereotaxic coordinates
Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959 · see citing works
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works
Conflict, arousal, and curiosity.
Berlyne, D. E. (1960) · McGraw-Hill Book Company · doi:10.1037/11164-000 · Cited by 6,018 · see citing works
Microstructure of a spatial map in the entorhinal cortex
Hafting, T., Fyhn, M., Molden, S., Moser, M.-B., & Moser, E. I. (2005) · Nature · doi:10.1038/nature03721 · Cited by 4,068 · see citing works
Object vision and spatial vision: Two cortical pathways
Mishkin, M., Ungerleider, L. G., & Macko, K. A. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90190-x · Cited by 2,947 · cited 1× · see citing works
“In the frame of the nfluential conceptualization of two distinct processing pathways n the brain, a dorsal (processing “where” information) and a ventral processing “what” information) pathway [5], it has been proposed”
A purely geometric module in the rat's spatial representation
Cheng, K. (1986) · Cognition · doi:10.1016/0010-0277(86)90041-7 · Cited by 1,182 · see citing works
The anatomy of memory: an interactive overview of the parahippocampal–hippocampal network
van Strien, N. M., Cappaert, N. L. M., & Witter, M. P. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2614 · Cited by 1,041 · see citing works
Major Dissociation Between Medial and Lateral Entorhinal Input to Dorsal Hippocampus
Hargreaves, E. L., Rao, G., Lee, I., & Knierim, J. J. (2005) · Science · doi:10.1126/science.1110449 · Cited by 685 · see citing works
Assessing rodent hippocampal involvement in the novel object recognition task. A review
Cohen, S. J., & Stackman, R. W. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.08.002 · Cited by 595 · see citing works
Interleaving brain systems for episodic and recognition memory.
Aggleton, J., & Brown, M. W. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.08.003 · Cited by 465 · see citing works
Representation of Non-Spatial and Spatial Information in the Lateral Entorhinal Cortex
Deshmukh, S. S., & Knierim, J. J. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00069 · Cited by 454 · see citing works
Functional neuroanatomy of the parahippocampal region: The lateral and medial entorhinal areas
Kerr, K. M., Agster, K. L., Furtak, S. C., & Burwell, R. D. (2007) · Hippocampus · doi:10.1002/hipo.20315 · Cited by 433 · see citing works
Spatial Memory in the Rat Requires the Dorsolateral Band of the Entorhinal Cortex
Steffenach, H.-A., Witter, M. P., Moser, M., & Moser, E. I. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.044 · Cited by 321 · see citing works
Traces of experience in the lateral entorhinal cortex
Tsao, A., Moser, M.-B., & Moser, E. I. (2013) · Current Biology · doi:10.1016/j.cub.2013.01.036 · Cited by 290 · see citing works
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 · see citing works
Entorhinal cortex of the rat: Organization of intrinsic connections
Dolorfo, C. L., & Amaral, D. G. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980817)398:1 · Cited by 268 · see citing works
Lateral entorhinal cortex is critical for novel object‐context recognition
Wilson, D. I. G., Langston, R. F., Schlesiger, M. I., Wagner, M. A., Watanabe, S., & Ainge, J. A. (2013) · Hippocampus · doi:10.1002/hipo.22095 · Cited by 232 · see citing works
Influence of local objects on hippocampal representations: Landmark vectors and memory
Deshmukh, S. S., & Knierim, J. J. (2013) · Hippocampus · doi:10.1002/hipo.22101 · Cited by 217 · see citing works
Failure of Centrally Placed Objects to Control the Firing Fields of Hippocampal Place Cells
Cressant, A., Muller, R. U., & Poucet, B. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-07-02531.1997 · Cited by 210 · see citing works
Intrinsic exploration in animals: motives and measurement
Hughes, R. N. (1997) · Behavioural Processes · doi:10.1016/s0376-6357(97)00055-7 · Cited by 197 · 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
Self-citationNeotic preferences in laboratory rodents: Issues, assessment and substrates
Hughes, R. N. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.11.004 · Cited by 160 · see citing works
Galani, R., Weiss, I. C., Cassel, J., & Kelche, C. R. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00197-6 · Cited by 135 · see citing works
Keene, C. S., Bladon, J. H., McKenzie, S., Liu, C. D., O'Keefe, J., & Eichenbaum, H. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4368-15.2016 · Cited by 131 · see citing works
Hunsaker, 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
Pyapali, G. K., Attila Gabor, S. I. K., Penttonen, M., Buzsáki, G., & Turner, D. A. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980216)391:3 · Cited by 128 · see citing works
Sharp, P. E. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:4 · Cited by 125 · see citing works
Lateral entorhinal neurons are not spatially selective in cue‐rich environments
Yoganarasimha, D., Rao, G., & Knierim, J. J. (2010) · Hippocampus · doi:10.1002/hipo.20839 · Cited by 122 · see citing works
Landmark use by navigating rats (Rattus norvegicus) contrasting geometric and featural information.
Benhamou, S., & Poucet, B. (1998) · Journal of comparative psychology · doi:10.1037/0735-7036.112.3.317 · Cited by 111 · see citing works
Chao, O. Y.-H., Huston, J. P., Li, J., Wang, A., & Silva, M. A. D. S. (2015) · Hippocampus · doi:10.1002/hipo.22547 · Cited by 110 · see citing works
Selective immunolesions of hippocampal cholinergic input fail to impair spatial working memory
McMahan, R. W., Sobel, T. J., & Baxter, M. G. (1997) · Hippocampus · doi:10.1002/(sici)1098-1063(1997)7:2 · Cited by 109 · see citing works
Save, É., Buhot, M.-C., Foreman, N., & Thinus‐Blanc, C. (1992) · Behavioural Brain Research · doi:10.1016/s0166-4328(05)80118-4 · Cited by 106 · see citing works
Unstable CA1 place cell representation in rats with entorhinal cortex lesions
Cauter, T. V., Poucet, B., & Save, É. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06158.x · Cited by 103 · see citing works
Cho, Y. H., & Kesner, R. P. (1996) · Behavioral Neuroscience · doi:10.1037//0735-7044.110.3.436 · Cited by 100 · see citing works
Ferbinteanu, J., Holsinger, R. M. D., & McDonald, R. J. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00144-2 · 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
Cho, Y. H., & Kesner, R. P. (1996) · Behavioral Neuroscience · doi:10.1037/0735-7044.110.3.436 · Cited by 83 · see citing works
Parron, C., & Save, É. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.03.004 · Cited by 76 · see citing works
Entorhinal cortex and cognition
Coutureau, É., & Scala, G. D. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.03.038 · Cited by 72 · see citing works
Sewards, T. V., & Sewards, M. A. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00175-9 · Cited by 59 · see citing works
Granon, S., Save, É., Buhot, M.-C., & Poucet, B. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00242-1 · Cited by 58 · see citing works
Landmark geometry and identity controls spatial navigation in rats
Greene, C. M., & Cook, R. G. (1997) · Animal Learning & Behavior · doi:10.3758/bf03199089 · Cited by 52 · see citing works
Parron, C., Poucet, B., & Save, É. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.02.006 · Cited by 51 · see citing works
Beer, Z., Chwiesko, C., Kitsukawa, T., & Sauvage, M. M. (2013) · Hippocampus · doi:10.1002/hipo.22195 · Cited by 49 · see citing works
Morrissey, M. D., & Takehara‐Nishiuchi, K. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.08.006 · Cited by 39 · see citing works
Delay-dependent involvement of the rat entorhinal cortex in habituation to a novel environment
Cauter, T. V., Poucet, B., & Save, É. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.03.001 · Cited by 16 · see citing works
Craig, S., Cunningham, L., Kelly, L., & Commins, S. (2005) · Behavioural Processes · doi:10.1016/j.beproc.2004.12.001 · Cited by 6 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
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
Neuronal circuitry for recognition memory of object and place in rodent models
Chao, O. Y.-H., Nikolaus, S., Yang, Y., & Huston, J. P. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104855 · Cited by 157 · see citing works
Integration of objects and space in perception and memory
Connor, C. E., & Knierim, J. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4657 · Cited by 132 · see citing works
Durante, V., de Iure, A., Loffredo, V., Vaikath, N. N., Risi, M. D., Paciotti, S., Quiroga‐Varela, A., Chiasserini, D., Mellone, M., Mazzocchetti, P., et al. (2019) · Brain · doi:10.1093/brain/awz065 · Cited by 117 · see citing works
Doan, T. P., Lagartos-Donate, M. J., Nilssen, E. S., Ohara, S., & Witter, M. P. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.005 · Cited by 91 · see citing works
Marino, G., Campanelli, F., Natale, G., Carluccio, M. D., Servillo, F., Ferrari, E. S., Gardoni, F., Caristo, M. E., Picconi, B., Cardinale, A., et al. (2023) · Science Advances · doi:10.1126/sciadv.adh1403 · Cited by 75 · see citing works
Save, É., & Sargolini, F. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00081 · Cited by 53 · see citing works
Self-citationOhara, S., Gianatti, M., Itou, K., Berndtsson, C. H., Doan, T. P., Kitanishi, T., Mizuseki, K., Iijima, T., Tsutsui, K., & Witter, M. P. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00054 · Cited by 42 · see citing works
Lateral Entorhinal Cortex Lesions Impair Local Spatial Frameworks
Kuruvilla, M. V., & Ainge, J. A. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00030 · Cited by 39 · see citing works
Yoo, S., & Lee, I. (2017) · eLife · doi:10.7554/elife.21543 · Cited by 31 · see citing works
Grid coding, spatial representation, and navigation: Should we assume an isomorphism?
Ekstrom, A. D., Harootonian, S. K., & Huffman, D. J. (2019) · Hippocampus · doi:10.1002/hipo.23175 · Cited by 30 · see citing works
Object and object‐memory representations across the proximodistal axis of CA1
Vandrey, B., Duncan, S., & Ainge, J. A. (2021) · Hippocampus · doi:10.1002/hipo.23331 · Cited by 28 · see citing works
Thalamo-hippocampal pathway regulates incidental memory capacity in mice
Torromino, G., Loffredo, V., Cavezza, D., Sonsini, G., Esposito, F., Crevenna, Á. H., Gioffrè, M., Risi, M. D., Treves, A., Griguoli, M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31781-8 · Cited by 25 · see citing works
Lateral entorhinal cortex lesions impair odor‐context associative memory in male rats
Persson, B. M., Ambrozova, V., Duncan, S., Wood, E. R., O’Connor, A. R., & Ainge, J. A. (2022) · Journal of Neuroscience Research · doi:10.1002/jnr.25027 · Cited by 23 · see citing works
Distinct spatial maps and multiple object codes in the lateral entorhinal cortex
Huang, X., Schlesiger, M. I., Barriuso-Ortega, I., Leibold, C., MacLaren, D. A. A., Bieber, N., & Monyer, H. (2023) · Neuron · doi:10.1016/j.neuron.2023.06.020 · Cited by 20 · see citing works
Goal‐directed interaction of stimulus and task demand in the parahippocampal region
Lee, S., Jin, S., Park, S., Park, E., Lee, C., Lee, H., Lim, H., Yoo, S., Ahn, J. R., Shin, J., et al. (2021) · Hippocampus · doi:10.1002/hipo.23295 · Cited by 20 · see citing works
Schlecht, M., Jayachandran, M., Rasch, G. E., & Allen, T. A. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2022.107586 · Cited by 19 · see citing works
Lateral entorhinal cortex lesions impair both egocentric and allocentric object–place associations
Kuruvilla, M. V., Wilson, D. I. G., & Ainge, J. A. (2020) · Brain and Neuroscience Advances · doi:10.1177/2398212820939463 · Cited by 18 · see citing works
Mahmoudi, N. E., Laurent, C., Péricat, D., Watabe, I., Lapôtre, A., Jacob, P.-Y., Tonetto, A., Tighilet, B., & Sargolini, F. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2023.102403 · Cited by 17 · see citing works
Self-citationCaputi, A., Liu, X., Fuchs, E. C., Liu, Y., & Monyer, H. (2022) · Neuron · doi:10.1016/j.neuron.2022.08.013 · Cited by 15 · see citing works
Poitreau, J., Buttet, M., Manrique, C., Poucet, B., Sargolini, F., & Save, E. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113448 · Cited by 10 · see citing works
Self-citationNilssen, E. S., Jacobsen, B., Doan, T. P., Girão, P. J., & Witter, M. P. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.29.518323 · Cited by 4 · see citing works
Hales, J. B., Olivas, L., Abouchedid, D., & Blaser, R. E. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.114883 · Cited by 3 · see citing works
Maâroufi, K., Khadhraoui, Y., Moulahi, A., Ouarghi, A., Poirot, K., Save, É., & Sebaï, H. (2025) · Biological Trace Element Research · doi:10.1007/s12011-024-04511-y · Cited by 3 · see citing works
Revising the Parallel-Pathways Hypothesis with Time
Tsao, A. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00059 · Cited by 3 · see citing works
The entorhinal spatial map integrates visual identity information of landmarks
Wang, G., Shahid, F., Malone, T. J., Tyan, J., Cekada, K., Chen, L., & Gu, Y. Z. (2026) · Nature Communications · doi:10.1038/s41467-026-72453-1 · Cited by 3 · see citing works
Backtracking α-synuclein pathology: social deficits precede motor symptoms in Parkinson’s disease
Marino, G., Campanelli, F., Natale, G., Carluccio, M. D., Servillo, F., Nutarelli, S., Caristo, M. E., Viscomi, M. T., Ghiglieri, V., & Calabresi, P. (2025) · npj Parkinson s Disease · doi:10.1038/s41531-025-01225-3 · Cited by 2 · see citing works
Object-translocation induces event coding in the rat hippocampus
Duan, Y., Hu, S.-Y., Ge, X.-F., Long, J.-L., Deng, C., Sun, Y.-M., Li, C.-J., Zhang, R., Cai, X., & Lu, L. (2025) · Communications Biology · doi:10.1038/s42003-025-08241-2 · Cited by 2 · see citing works
How Does Aging Impact the Structure and Function of Parallel Navigation Circuits across Mammals?
Barnes, C. A., Srivathsa, S., Hill, P. F., Srokova, S., & Ekstrom, A. D. (2026) · Springer eBooks · doi:10.1007/978-3-032-20563-6_13 · Cited by 1 · see citing works
Woodward, M. L., Ker, A. H., Barr, A. M., Beasley, C. L., Hercher, C., Boyda, H. N., Procyshyn, R. M., Honer, W. G., & Lang, D. J. (2019) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2019.172834 · Cited by 1 · see citing works
Nilssen, E. S., Jacobsen, B., Doan, T. P., Girão, P. J., & Witter, M. P. (2025) · eLife · doi:10.7554/elife.109082.1 · Cited by 1 · see citing works
Borcuk, C. (2021) · theses.fr (ABES) · doi:10.70675/c316f2dcz54d3z41cfzb3f5z99c7b2d3cd95 · Cited by 1 · see citing works
Tanninen, S. E. (2018) · TSpace (University of Toronto)
Age-related Changes in Memory for Object and Position-In-ContextPreprint
Tran, T., Tobin, K. E., Block, S. H., Puliyadi, V., Gallagher, M., & Bakker, A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.22.393355
Effects of experimental brain lesions on spatial navigation
Vann, S. D. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00008-5
Nilssen, E. S., Jacobsen, B., Doan, T. P., Girão, P. J., & Witter, M. P. (2025) · eLife · doi:10.7554/elife.109082
Srbovan, M., Potrebić, M., Dubljević, O., & Pavković, Ž. (2025) · Animals · doi:10.3390/ani15243552
Hopkins, M. D., Rahal, P., Robert, V., Kim, E., & Basu, J. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.23.711409
Nilssen, E. S., Jacobsen, B., Doan, T. P., Girão, P. J., & Witter, M. P. (2026) · eLife · doi:10.7554/elife.109082.2.sa0
Nilssen, E. S., Jacobsen, B., Doan, T. P., Girão, P. J., & Witter, M. P. (2026) · eLife · doi:10.7554/elife.109082.2
- Authors
- Rodo, C., Sargolini, F., & Save, E.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- ORCID
- Sargolini, Francesca
- Venue
- Behavioural Brain Research
- Publisher
- Elsevier BV
- Published
- 2017-03
- Volume
- 320
- Pages
- 200-209
- ISSN
- 0166-4328 (ISSN-L)
- OpenAlex
- W2560576377
- Cited by
- 42
- References
- 46
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 2 · 2023: 3 · 2022: 7 · 2021: 6 · 2020: 3 · 2019: 5 · 2018: 1 · 2017: 5
- FWCI
- 2.33
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Behavioural Brain Research (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Physical Sciences › Engineering › Automotive Engineering › Spatial Cognition and Navigation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- medial entorhinal cortex, lateral entorhinal cortex, spatial data processing, environmental complexity, object exploration, novelty detection, excitotoxic lesions, episodic memory, rats
- MeSH terms
- Animals, Environment, Exploratory Behavior, Hippocampus, Locomotion, Male, Neural Pathways, Spatial Behavior, Time Factors, Statistics, Nonparametric, Entorhinal Cortex, 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