Recognition memory: What are the roles of the perirhinal cortex and hippocampus?

Place navigation impaired in rats with hippocampal lesions

Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340

Episodic memory, amnesia, and the hippocampal–anterior thalamic axis

Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879

Differential Effects of Early Hippocampal Pathology on Episodic and Semantic Memory

Vargha-Khadem, F., Gadian, D. G., Watkins, K. E., Connelly, A., Van Paesschen, W., & Mishkin, M. (1997) · Science · doi:10.1126/science.277.5324.376 · Cited by 1,746

Neural mechanisms for visual memory and their role in attention

Desimone, R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13494 · Cited by 1,028

Learning 10000 pictures

Standing, L. (1973) · Quarterly Journal of Experimental Psychology · doi:10.1080/14640747308400340 · Cited by 968

The global record of memory in hippocampal neuronal activity

Wood, E. R., Dudchenko, P. A., & Eichenbaum, H. (1999) · Nature · doi:10.1038/17605 · Cited by 707

Differential cognitive effects of colloid cysts in the third ventricle that spare or compromise the fornix

Aggleton, J. P. (2000) · Brain · doi:10.1093/brain/123.4.800 · Cited by 231

Transient memory impairment in monkeys with bilateral lesions of the entorhinal cortex

Leonard, B., Amaral, D., Squire, L., & Zola-Morgan, S. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-08-05637.1995 · Cited by 174

Role of medial prefrontal cortex serotonin 2A receptors in the control of retrieval of recognition memory in rats

Bekinschtein, P., Renner, M. C., Gonzalez, M. C., & Weisstaub, N. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2087-13.2013 · Cited by 69

Stress Impairs Episodic Retrieval by Disrupting Hippocampal and Cortical Mechanisms of Remembering

Gagnon, S. A., Waskom, M. L., Brown, T. I., & Wagner, A. D. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhy162 · Cited by 69

Episodic-like memory is sensitive to both Alzheimer's-like pathological accumulation and normal ageing processes in mice

Davis, K. E., Eacott, M. J., Easton, A., & Gigg, J. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.03.009 · Cited by 67

Temporary inactivation reveals that the CA1 region of the mouse dorsal hippocampus plays an equivalent role in the retrieval of long-term object memory and spatial memory

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

Synaptic Plasticity from Visual Cortex to Hippocampus: Systems Integration in Spatial Information Processing

Tsanov, M., & Manahan-Vaughan, D. (2008) · The Neuroscientist · doi:10.1177/1073858408315655 · Cited by 65

The hippocampus and exploration: dynamically evolving behavior and neural representations

Johnson, A., Varberg, Z., Benhardus, J., Maahs, A., & Schrater, P. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00216 · Cited by 61

Hippocampal neurotransmitter efflux during one-trial novel object recognition in rats

Stanley, E. M., Wilson, M. A., & Fadel, J. R. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.01.033 · Cited by 57

Evidence that the rat hippocampus has contrasting roles in object recognition memory and object recency memory

Albasser, M. M., Amin, E., Lin, T.-C. E., Iordanova, M. D., & Aggleton, J. P. (2012) · Behavioral Neuroscience · doi:10.1037/a0029754 · Cited by 58

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

Distinct kinds of novelty processing differentially increase extracellular dopamine in different brain regions

De Leonibus, E., Verheij, M. M. M., Mele, A., & Cools, A. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04658.x · Cited by 57

Feedforward inhibition regulates perirhinal transmission of neocortical inputs to the entorhinal cortex: ultrastructural study in guinea pigs

Pinto, A., Fuentes, C., & Paré, D. (2006) · Journal of Comparative Neurology · doi:10.1002/cne.20905 · Cited by 55

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

The effect of catecholaminergic depletion within the prelimbic and infralimbic medial prefrontal cortex on recognition memory for recency, location, and objects

Nelson, A. J. D., Cooper, M. T., Thur, K. E., Marsden, C. A., & Cassaday, H. J. (2011) · Behavioral Neuroscience · doi:10.1037/a0023337 · Cited by 53

The relative contribution of proximal 5′ flanking sequence and microsatellite variation on brain vasopressin 1a receptor (Avpr1a) gene expression and behavior

Donaldson, Z. R., & Young, L. J. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003729 · Cited by 52

Prior knowledge promotes hippocampal separation but cortical assimilation in the left inferior frontal gyrus

Bein, O., Reggev, N., & Maril, A. (2020) · Nature Communications · doi:10.1038/s41467-020-18364-1 · Cited by 52

Dopamine D1 receptor stimulation modulates the formation and retrieval of novel object recognition memory: role of the prelimbic cortex

Pezze, M. A., Marshall, H. J., Fone, K. C. F., & Cassaday, H. J. (2015) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2015.07.018 · Cited by 51

Infusion of protein synthesis inhibitors in the entorhinal cortex blocks consolidation but not reconsolidation of object recognition memory

Lima, R. H., Rossato, J. I., Furini, C. R., Bevilaqua, L. R., Izquierdo, I., & Cammarota, M. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.12.009 · Cited by 49

Spatial and stimulus-type tuning in the LEC, MEC, POR, PrC, CA1, and CA3 during spontaneous item recognition memory: Spatial and Stimulus-Type Tunings in Recognition Memory

Beer, Z., Chwiesko, C., Kitsukawa, T., & Sauvage, M. M. (2013) · Hippocampus · doi:10.1002/hipo.22195 · Cited by 49

Dopamine D1 receptor activity modulates object recognition memory consolidation in the perirhinal cortex but not in the hippocampus

Balderas, I., Moreno‐Castilla, P., & Bermudez‐Rattoni, F. (2013) · Hippocampus · doi:10.1002/hipo.22143 · Cited by 46

The Hippocampus Generalizes across Memories that Share Item and Context Information

Libby, L. A., Reagh, Z. M., Bouffard, N. R., Ragland, J. D., & Ranganath, C. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01345 · Cited by 42

Role of the anterior cingulate cortex in the retrieval of novel object recognition memory after a long delay

Pezze, M. A., Marshall, H. J., Fone, K. C., & Cassaday, H. J. (2017) · Learning & Memory · doi:10.1101/lm.044784.116 · Cited by 35

Distinct roles of the hippocampus and perirhinal cortex in GABAA receptor blockade-induced enhancement of object recognition memory

Kim, J. M., Kim, D. H., Lee, Y., Park, S. J., & Ryu, J. H. (2014) · Brain Research · doi:10.1016/j.brainres.2014.01.024 · Cited by 35

Memory of occasional events in rats: individual episodic memory profiles, flexibility, and neural substrate

Veyrac, A., Allerborn, M., Gros, A., Michon, F., Raguet, L., Kenney, J., Godinot, F., Thevenet, M., Garcia, S., Messaoudi, B., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.3941-14.2015 · Cited by 31

Influx of extracellular Zn2+ into the hippocampal CA1 neurons is required for cognitive performance via long-term potentiation

Takeda, A., Suzuki, M., Tempaku, M., Ohashi, K., & Tamano, H. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.07.042 · Cited by 29

Muscarinic receptors activity in the perirhinal cortex and hippocampus has differential involvement in the formation of recognition memory

Balderas, I., Morin, J.-P., Rodriguez-Ortiz, C. J., & Bermudez-Rattoni, F. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2012.03.006 · Cited by 29

Evolution of the Hippocampus

Manns, J. R., & Eichenbaum, H. (2007) · Evolution of Nervous Systems · doi:10.1016/b0-12-370878-8/00086-0 · Cited by 28

Mapping parahippocampal systems for recognition and recency memory in the absence of the rat hippocampus

Kinnavane, L., Amin, E., Horne, M., & Aggleton, J. P. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12740 · Cited by 21

Sleep deprivation impairs binding of information with its context

Kurinec, C. A., Whitney, P., Hinson, J. M., Hansen, D. A., & Van Dongen, H. P. A. (2021) · SLEEP · doi:10.1093/sleep/zsab113 · Cited by 22

The “Swedish” mutation of the amyloid precursor protein (APPswe) dissociates components of object-location memory in aged Tg2576 mice

Good, M. A., & Hale, G. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.6.1180 · Cited by 22

Atypical evening cortisol profile induces visual recognition memory deficit in healthy human subjects

Gilpin, H., Whitcomb, D., & Cho, K. (2008) · Molecular Brain · doi:10.1186/1756-6606-1-4 · Cited by 20

The neurobiology of dreaming

Pace-Schott, E. F. (2011) · Principles and Practice of Sleep Medicine · doi:10.1016/b978-1-4160-6645-3.00048-7 · Cited by 19

Contrasting networks for recognition memory and recency memory revealed by immediate-early gene imaging in the rat

Olarte-Sánchez, C. M., Kinnavane, L., Amin, E., & Aggleton, J. P. (2014) · Behavioral Neuroscience · doi:10.1037/a0037055 · Cited by 18

Dopamine dysregulation in the prefrontal cortex relates to cognitive deficits in the sub-chronic PCP-model for schizophrenia: a preliminary investigation

McLean, S. L., Harte, M. K., Neill, J. C., & Young, A. M. (2017) · Journal of Psychopharmacology · doi:10.1177/0269881117704988 · Cited by 16

Effects of x-ray radiation on complex visual discrimination learning and social recognition memory in rats

Davis, C. M., Roma, P. G., Armour, E., Gooden, V. L., Brady, J. V., Weed, M. R., & Hienz, R. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104393 · Cited by 15

Perirhinal cortex abnormalities impair hippocampal plasticity and learning in Scn2a , Fmr1 , and Cdkl5 autism mouse models

Keith, R. E., Shen, Y., Janzen-Meza, J. A., Abramovitz, J., Antonello, P. C., Hameed, A., Mohana Krishnan, B., & Antoine, M. W. (2025) · Science Advances · doi:10.1126/sciadv.adt0780 · Cited by 8

Hippocampal infusion of zeta inhibitory peptide impairs recent, but not remote, recognition memory in rats

Hales, J. B., Ocampo, A. C., Broadbent, N. J., & Clark, R. E. (2015) · Neural Plasticity · doi:10.1155/2015/847136 · Cited by 7