The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.
Hippocampal Damage and Exploratory Preferences in Rats: Memory for Objects, Places, and Contexts
Open accessAbstract
Rats have a natural tendency to spend more time exploring novel objects than familiar objects, and this preference can be used as an index of object recognition. Rats also show an exploratory preference for objects in locations where they have not previously encountered objects (an index of place memory) and for familiar objects in contexts different from those in which the objects were originally encountered (an index of context memory). In this experiment, rats with cytotoxic lesions of the hippocampal formation were tested on all three versions of the novelty-preference paradigm, with a 5-min retention interval between the familiarization and test phases. Rats with sham lesions displayed a novelty preference on all three trial types, whereas the rats with hippocampal lesions displayed a novelty preference on Object trials but did not discriminate between the objects on Place trials or Context trials. The findings indicate that hippocampal damage impairs memory for contextual or spatial aspects of an experience, whereas memory for objects that were part of the same experience are left relatively intact.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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 citing paper
“The OPP test has been shown to be hippocampus-dependent in rodents (Barker and Warburton, 2011b; Mumby et al., 2002).”
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 Mumby et al., 2002
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
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
Beaton, A. E., & Keppel, G. (1975) · American Educational Research Journal · doi:10.2307/1162588 · Cited by 5,857
A new one-trial test for neurobiological studies of memory in rats. 1: behavioral data
Ennaceur, A., & Delacour, J. (1988) · Behavioural Brain Research · doi:10.1016/0166-4328(88)90157-x · Cited by 3,223
Modality-Specific Retrograde Amnesia of Fear
Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483
Memory consolidation, retrograde amnesia and the hippocampal complex
Nadel, L., & Moscovitch, M. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80010-4 · Cited by 1,924
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
A cortical–hippocampal system for declarative memory
Eichenbaum, H. (2000) · Nature reviews. Neuroscience · doi:10.1038/35036213 · Cited by 1,817
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
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
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–300 of 715
Exercise enhances memory consolidation in the aging brain
Snigdha, S., de Rivera, C., Milgram, N. W., & Cotman, C. W. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00003 · Cited by 69
Wallace, D. G., & Whishaw, I. Q. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02772.x · Cited by 67
Pharmaco-genetic therapeutics targeting parvalbumin neurons attenuate temporal lobe epilepsy
Wang, Y., Liang, J., Chen, L., Shen, Y., Zhao, J., Xu, C., Wu, X., Cheng, H., Ying, X., Guo, Y. C., et al. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.06.006 · Cited by 70
Hale, G., & Good, M. A. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.4.884 · Cited by 71
Hines, D. J., & Whishaw, I. Q. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04412.x · Cited by 67
When is adult hippocampal neurogenesis necessary for learning? Evidence from animal research
Castilla‐Ortega, E., Pedraza, C., Estivill‐Torrús, G., & Santín, L. J. (2011) · Reviews in the Neurosciences · doi:10.1515/rns.2011.027 · Cited by 69
A limited role for the hippocampus in the modulation of novel-object preference by contextual cues
Piterkin, P., Cole, E., Cossette, M.-P., Gaskin, S., & Mumby, D. G. (2008) · Learning & Memory · doi:10.1101/lm.1035508 · Cited by 65
Self-citationStackman, 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
Cognitive and behavioural effects of sugar consumption in rodents. A review
Kendig, M. D. (2014) · Appetite · doi:10.1016/j.appet.2014.04.028 · Cited by 72
Biala, Y. N., Bogoch, Y., Bejar, C., Linial, M., & Weinstock, M. (2010) · Hippocampus · doi:10.1002/hipo.20825 · Cited by 68
Clinical Relevance of Behavior Testing in Animal Models of Traumatic Brain Injury
Shultz, S. R., McDonald, S. J., Corrigan, F., Semple, B. D., Salberg, S., Zamani, A., Jones, N. C., & Mychasiuk, R. (2019) · Journal of Neurotrauma · doi:10.1089/neu.2018.6149 · Cited by 68
Zou, Y., Corniola, R. S., Leu, D., Khan, A., Sahbaie, P., Chakraborti, A., Clark, J. D., Fike, J. R., & Huang, T. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1216913110 · Cited by 66
Sex differences in object recognition are modulated by object similarity
Bettis, T. J., & Jacobs, L. F. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.04.028 · Cited by 64
Haam, J., Zhou, J., Cui, G., & Yakel, J. L. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1712538115 · Cited by 66
Merrer, J. L., Rezaï, X., Scherrer, G., Becker, J. A. J., & Kieffer, B. L. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.1 · Cited by 63
Basal Hippocampal Activity and Its Functional Connectivity Predicts Cocaine Relapse
Adinoff, B. H., Gu, H., Merrick, C., McHugh, M. J., Jeon‐Slaughter, H., Lu, H., Yang, Y., & Stein, E. A. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.12.027 · Cited by 64
Naewla, S., Sirichoat, A., Pannangrong, W., Chaisawang, P., Wigmore, P. M., & Welbat, J. U. (2019) · Nutrients · doi:10.3390/nu11040936 · Cited by 63
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
Winters, B. D., Tucci, M. C., Jacklin, D. L., Reid, J. M., & Newsome, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2968-11.2011 · Cited by 68
Hamm, V., Héraud, C., Bott, J.-B., Herbeaux, K., Strittmatter, C., Mathis, C., & Goutagny, R. (2017) · Science Advances · doi:10.1126/sciadv.1601068 · Cited by 68
Camer, D., Yu, Y., Szabo, A., Fernandez, F., Dinh, C. H. L., & Huang, X. (2015) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2015.01.004 · Cited by 63
Moving beyond standard procedures to assess spontaneous recognition memory
Ameen‐Ali, K. E., Easton, A., & Eacott, M. J. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.03.013 · Cited by 63
Determinants of novel object and location recognition during development
Jablonski, S. A., Schreiber, W. B., Westbrook, S. R., Brennan, L. E., & Stanton, M. E. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.07.055 · Cited by 61
Epigenetic determinants of space radiation-induced cognitive dysfunction
Acharya, M. M., Baddour, A. A. D., Kawashita, T., Allen, B. D., Syage, A. R., Nguyen, T. D., Yoon, N., Giedzinski, E., Yu, L., Parihar, V. K., et al. (2017) · Scientific Reports · doi:10.1038/srep42885 · Cited by 61
Chapter 2.2 Animal episodic memory
Dere, E., Zlomuzica, A., Huston, J. P., & Silva, M. A. D. S. (2008) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(08)00210-5 · Cited by 61
Consolidation and reconsolidation of object recognition memory
Balderas, I., Rodríguez‐Ortiz, C. J., & Bermúdez‐Rattoni, F. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.08.049 · Cited by 62
Rei, D., Mason, X. L., Seo, J., Gräff, J., Rudenko, A., Wang, J., Rueda, R., Siegert, S., Cho, S., Canter, R. G., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1415845112 · Cited by 65
Implications of animal object memory research for human amnesia
Winters, B. D., Saksida, L. M., & Bussey, T. J. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.01.023 · Cited by 63
The Effects of Cyclophosphamide on Hippocampal Cell Proliferation and Spatial Working Memory in Rat
Lyons, L., ELBeltagy, M., Bennett, G., & Wigmore, P. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021445 · Cited by 60
Enhanced context-dependency of object recognition in rats with hippocampal lesions
OBRIEN, N., LEHMANN, H., Lecluse, V., & Mumby, D. G. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.02.008 · Cited by 59
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
Balderas, I., Rodríguez‐Ortiz, C. J., & Bermúdez‐Rattoni, F. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.09.001 · Cited by 64
Albani, S. H., McHail, D. G., & Dumas, T. C. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.04.009 · Cited by 63
Chronic post-traumatic stress disorder-related traits in a rat model of low-level blast exposure
Perez-Garcia, G., Sosa, M. A. G., Gasperi, R. D., Lashof-Sullivan, M. M., Maudlin-Jeronimo, E., Stone, J. R., Haghighi, F. G., Ahlers, S. T., & Elder, G. A. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.09.061 · Cited by 59
Nakazaki, M., Sasaki, M., Kataoka-Sasaki, Y., Oka, S., Suzuki, J., Sasaki, Y., Nagahama, H., Hashi, K., Kocsis, J. D., & Honmou, O. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.04.018 · Cited by 58
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
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
Yang, K., Broussard, J. I., Levine, A. T., Jenson, D., Arenkiel, B. R., & Dani, J. A. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13406 · Cited by 58
Pearson-Smith, J. N., Schulz, K. M., & Patel, M. (2014) · Epilepsy Research · doi:10.1016/j.eplepsyres.2014.04.003 · Cited by 58
Tracelink: A model of consolidation and amnesia
Meeter, M., & Murre, J. M. J. (2005) · Cognitive Neuropsychology · doi:10.1080/02643290442000194 · Cited by 57
Martínez, M. C., Villar, M. E., Ballarini, F., & Viola, H. (2014) · Hippocampus · doi:10.1002/hipo.22328 · Cited by 55
Aggleton, J. P., Poirier, G. L., Aggleton, H. S., Vann, S. D., & Pearce, J. M. (2009) · Behavioral Neuroscience · doi:10.1037/a0015404 · Cited by 57
Travaglia, A., Steinmetz, A. B., Miranda, J. M., & Alberini, C. M. (2018) · Learning & Memory · doi:10.1101/lm.046946.117 · Cited by 63
Llorente‐Berzal, A., Mela, V., Borcel, É., Valero, M., López‐Gallardo, M., Viveros, M., & Marco, E. M. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.07.031 · Cited by 55
Animals lacking endothelin‐converting enzyme‐2 are deficient in learning and memory
Rodriguiz, R. M., Gadnidze, K., Ragnauth, A. K., Dorr, N., Yanagisawa, M., Wetsel, W. C., & Devi, L. A. (2007) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2007.00365.x · Cited by 54
Conrad, C. D., McLaughlin, K. J., Huynh, T. N., El-Ashmawy, M., & Sparks, M. (2011) · Behavioral Neuroscience · doi:10.1037/a0025770 · Cited by 55
In search of a recognition memory engram
Brown, M. W., & Banks, P. J. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.09.016 · Cited by 56
Reversion of age-related recognition memory impairment by iron chelation in rats
de Lima, M. N. M., Dias, C. P., Torres, J. P., Dornelles, A. D. S., Garcia, V. A., Scalco, F. S., Guimarães, M. R., Petry, R. C., Bromberg, E., Constantino, L. D. S., et al. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.02.006 · Cited by 55
Nicotinic receptor activation in perirhinal cortex and hippocampus enhances object memory in rats
Melichercik, A. M., Elliott, K. S., Bianchi, C., Ernst, S. M., & Winters, B. D. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.01.008 · Cited by 54
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
Anterior retrosplenial cortex is required for long-term object recognition memory
de Landeta, A. B., Pereyra, M., Medina, J. H., & Katche, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-60937-z · Cited by 55
The Tagging and Capture Hypothesis from Synapse to Memory
Viola, H., Ballarini, F., Martínez, M. C., & Moncada, D. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00013-1 · Cited by 60
Loi, M., Sarabdjitsingh, R. A., Tsouli, A., Trinh, S., Arp, M., Krugers, H. J., Karst, H., van den Bos, R., & Joëls, M. (2017) · eNeuro · doi:10.1523/eneuro.0253-17.2017 · Cited by 54
Early Exposure to Volatile Anesthetics Impairs Long-Term Associative Learning and Recognition Memory
Lee, B. H., Chan, J. T., Hazarika, O. D., Vutskits, L., & Sall, J. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0105340 · Cited by 53
Neural processes mediating contextual influences on human choice behaviour
Rigoli, F., Friston, K. J., & Dolan, R. J. (2016) · Nature Communications · doi:10.1038/ncomms12416 · Cited by 52
Age-associated gut microbiota impairs hippocampus-dependent memory in a vagus-dependent manner
Rei, D., Saha, S., Haddad, M., Rubio, A. H., Perlaza, B. L., Berard, M., Ungeheuer, M., Sokol, H., & Lledo, P. (2022) · JCI Insight · doi:10.1172/jci.insight.147700 · Cited by 51
Medina, D. X., Orr, M. E., & Oddo, S. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.07.006 · Cited by 50
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
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
Krukowski, K., Grue, K. A., Becker, M., Elizarraras, E., Frias, E. S., Halvorsen, A. T., Koenig-Zanoff, M., Frattini, V., Nimmagadda, H., Feng, X., et al. (2021) · Science Advances · doi:10.1126/sciadv.abg6702 · Cited by 84
Choi, J. Y., Lee, J. M., Lee, D. G., Cho, S., Yoon, Y.-H., Cho, E. J., & Lee, S. (2015) · Journal of Medicinal Food · doi:10.1089/jmf.2014.3292 · Cited by 50
Gasbarri, A., Tavares, M. C. H., Rodrigues, R. C., Tomaz, C. A. B., & Pompili, A. (2012) · Reviews in the Neurosciences · doi:10.1515/revneuro-2012-0051 · Cited by 51
Choi, J. Y., Cho, E. J., Lee, H. S., Lee, J. M., Yoon, Y.-H., & Lee, S. (2012) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.11.002 · Cited by 50
Neonatal exposure to phenobarbital potentiates schizophrenia-like behavioral outcomes in the rat
Bhardwaj, S. K., Forcelli, P. A., Palchik, G. A., Gale, K., Srivastava, L. K., & Kondratyev, A. D. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.02.001 · Cited by 50
Blast-induced "PTSD": Evidence from an animal model
Perez-Garcia, G., Sosa, M. A. G., Gasperi, R. D., Tschiffely, A. E., McCarron, R. M., Hof, P. R., Gandy, S., Ahlers, S. T., & Elder, G. A. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.09.023 · Cited by 53
Distributed interactive brain circuits for object-in-place memory: A place for time?
Aggleton, J. P., & Nelson, A. J. D. (2020) · Brain and Neuroscience Advances · doi:10.1177/2398212820933471 · Cited by 50
Nelson, A. J. D., Thur, K. E., Marsden, C. A., & Cassaday, H. J. (2010) · Behavioral Neuroscience · doi:10.1037/a0021114 · Cited by 50
Evidence of VTA and LC control of protein synthesis required for the behavioral tagging process
Moncada, D. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.003 · Cited by 50
Insulin-like growth factor 2 rescues aging-related memory loss in rats
Steinmetz, A. B., Johnson, S. A., Iannitelli, D. E., Pollonini, G., & Alberini, C. M. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.04.006 · Cited by 49
Movements of exploration intact in rats with hippocampal lesions
Clark, B. J., Hines, D. J., Hamilton, D. A., & Whishaw, I. Q. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.04.007 · Cited by 49
Ozawa, T., Yamada, K., & Ichitani, Y. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.04.022 · Cited by 48
Ontogeny of object versus location recognition in the rat: Acquisition and retention effects
Westbrook, S. R., Brennan, L. E., & Stanton, M. E. (2014) · Developmental Psychobiology · doi:10.1002/dev.21232 · Cited by 54
Manning, E. E., Ransome, M. I., Burrows, E. L., & Hannan, A. J. (2010) · Hippocampus · doi:10.1002/hipo.20900 · Cited by 47
Charles, P. D., Singh, H. K., Jayakumar, P., & Rajan, K. E. (2012) · Journal of Neuroscience Research · doi:10.1002/jnr.23080 · Cited by 48
Deletion of the GluA1 AMPA receptor subunit impairs recency-dependent object recognition memoryPreprint
Sanderson, D. J., Hindley, E., Smeaton, E., Denny, N., Taylor, A., Barkus, C., Sprengel, R., Seeburg, P. H., & Bannerman, D. M. (2011) · Learning & Memory · doi:10.1101/lm.2083411 · Cited by 49
The role of the dorsal dentate gyrus in object and object-context recognition
Dees, R. L., & Kesner, R. P. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.07.013 · Cited by 47
Kanatsou, S., Karst, H., Kortesidou, D., van den Akker, R. A., den Blaauwen, J. L., Harris, A. P., Seckl, J. R., Krugers, H. J., & Joëls, M. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00132 · Cited by 48
Koss, W. A., & Frick, K. M. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.01.002 · Cited by 47
Campolongo, P., Ratano, P., Manduca, A., Scattoni, M. L., Palmery, M., Trezza, V., & Cuomo, V. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00011 · Cited by 52
Cornejo, B. J., Mesches, M. H., & Benke, T. A. (2008) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2008.07.002 · Cited by 47
Caccamo, A., Majumder, S., & Oddo, S. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.09.022 · Cited by 48
Pillai, A. G., Arp, M., Velzing, E. H., Lesuis, S. L., Schmidt, M. V., Holsboer, F., Joëls, M., & Krugers, H. J. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.02.001 · Cited by 44
Brancato, A., Castelli, V., Lavanco, G., Marino, R. A. M., & Cannizzaro, C. (2020) · Journal of Psychopharmacology · doi:10.1177/0269881120916135 · Cited by 47
Wang, L., Ling, H., He, H., Hu, N., Xiao, L., Zhang, Y., Xie, L., & You, Z. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100553 · Cited by 47
Repetitive fluoxetine treatment affects long-term memories but not learning
Ampuero, E., Stehberg, J., Gonzalez, D., Besser, N., Ferrero, M., Díaz‐Véliz, G., Wyneken, Ú., & Rubio, F. J. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.03.011 · Cited by 44
Tryptophan depletion impairs object-recognition memory in the rat: Reversal by risperidone
Jenkins, T. A., Elliott, J. J., Ardis, T. C., Cahir, M., Reynolds, G. P., Bell, R., & Cooper, S. J. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.12.030 · Cited by 44
Hendriksen, H., Meulendijks, D., Douma, T. N., Bink, D. I., Breuer, M. E., Westphal, K. G. C., Olivier, B., & Oosting, R. S. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.07.018 · Cited by 45
Moriarty, O., Gorman, C. L., McGowan, F., Ford, G. K., Roche, M., Thompson, K., Dockery, P., McGuire, B. E., & Finn, D. P. (2015) · Scandinavian Journal of Pain · doi:10.1016/j.sjpain.2015.09.008 · Cited by 44
Tran, D. M. D., & Westbrook, R. F. (2016) · Appetite · doi:10.1016/j.appet.2016.12.010 · Cited by 44
Peay, D. N., Saribekyan, H. M., Parada, P. A., Hanson, E. M., Badaruddin, B. S., Judd, J. M., Donnay, M. E., Padilla-Garcia, D., & Conrad, C. D. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112519 · Cited by 46
Bredy, T. W., Brown, R. E., & Meaney, M. J. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05266.x · Cited by 44
NMDA receptor modulation by d-cycloserine promotes episodic-like memory in mice
Zlomuzica, A., Silva, M. A. D. S., Huston, J. P., & Dere, E. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0816-x · Cited by 44
Enhanced recognition memory following glycine transporter 1 deletion in forebrain neurons.
Singer, P., Boison, D., Möhler, H., Feldon, J., & Yee, B. K. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.5.815 · Cited by 44
Fimbria-Fornix Lesions Disrupt the Dead Reckoning (Homing) Component of Exploratory Behavior in MicePreprint
Gorny, J. H., Gorny, B., Wallace, D. G., & Whishaw, I. Q. (2002) · Learning & Memory · doi:10.1101/lm.53002 · Cited by 44
Kelemen, E., Bahrendt, M., Born, J., & Inostroza, M. (2014) · Hippocampus · doi:10.1002/hipo.22266 · Cited by 43
Choi, J. R., Kim, J. H., Lee, S., Cho, E. J., & Kim, H. Y. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111571 · Cited by 43
On familiarity and recall of events by rats
Eacott, M. J., & Easton, A. (2007) · Hippocampus · doi:10.1002/hipo.20325 · Cited by 45
Novelty and Novel Objects Increase c-Fos Immunoreactivity in Mossy Cells in the Mouse Dentate Gyrus
Bernstein, H. L., Lu, Y.-L., Botterill, J. J., & Scharfman, H. E. (2019) · Neural Plasticity · doi:10.1155/2019/1815371 · Cited by 44
Yuan, R. K., Lopez, M. R., Ramos‐Álvarez, M. M., Normandin, M. E., Thomas, A. S., Uygun, D. S., Cerda, V. R., Grenier, A. E., Wood, M. T., Gagliardi, C. M., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109234 · Cited by 41
Spatial memory and hippocampal function: Where are we now?
Good, M. A. (2002) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 41
Metadata
- Authors
- Mumby, D. G., Gaskin, S., Glenn, M. J., Schramek, T. E., & Lehmann, H.
- Affiliations
- Concordia University (CA)
- Venue
- Learning & Memory
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2002-03-01
- Volume
- 9
- Issue
- 2
- Pages
- 49-57
- ISSN
- 1072-0502 (ISSN-L)
- 1549-5485
- PMC
- PMC155935
- OpenAlex
- W2024032885
- Cited by
- 714
- References
- 44
- Citations by year
- 2026: 11 · 2025: 17 · 2024: 19 · 2023: 24 · 2022: 28 · 2021: 26 · 2020: 36 · 2019: 34 · 2018: 37 · 2017: 28 · 2016: 36 · 2015: 30 · 2014: 49 · 2013: 43 · 2012: 55
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Learning & Memory (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
- Keywords
- hippocampal lesions, novelty preference, object recognition memory, place memory, contextual memory, spatial memory, hippocampal formation, rats, cytotoxic lesions, memory impairment
- MeSH terms
- Animals, Behavior, Animal, Choice Behavior, Exploratory Behavior, Hippocampus, Male, Memory, Pattern Recognition, Visual, 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