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A comparison of the effects of medial prefrontal, cingulate cortex, and cingulum bundle lesions on tests of spatial memory: evidence of a double dissociation between frontal and cingulum bundle contributions
Open accessAbstract
Rats were trained on an automated delayed nonmatching-to-position (DNMP) task. They then received cytotoxic lesions in either the medial prefrontal cortex (n = 13) or the cingulate and retrosplenial cortices (n = 8), or radiofrequency lesions in either the fornix (n = 6) or the cingulum bundle (n = 8). Twelve animals served as surgical controls. Only the fornical and medial prefrontal lesions disrupted DNMP performance, both groups showing a loss of accuracy and an increase in bias. The rats were then trained on a lever discrimination and reversal task, the medial prefrontal and fornical groups showing evidence of an increase in bias when compared with the cingulate cortex group. Finally, the rats were trained on a forced alternation task in a T- maze. Marked deficits were observed in the fornix and cingulum bundle groups, but the medial prefrontal and cingulate groups were unimpaired. The double dissociation between the effects of the prefrontal and cingulum bundle lesions highlights the very different nature of the two spatial tasks (DNMP and T-maze alternation), even though both involved a nonmatching rule. These findings may reflect the involvement of divergent outputs from the fornix-anterior thalamic pathway. One possibility is that anterior thalamic projections to the medial prefrontal cortex are concerned with processing egocentric information, while anterior thalamic projections to temporal regions via the cingulum bundle are concerned with allocentric information. The results also indicate that the effects of conventional lesions in the cingulate cortex and medial prefrontal cortex may be compromised by additional damage to the cingulum bundle.
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“In contrast, both fornix and anterior thalamic lesions, as well as hippocampal and medial prefrontal lesions (Aggleton et al., 1992, 1995), persistently impair this task.”
From The cingulum bundle: Anatomy, function, and dysfunction (2018) · cites this paper as Aggleton et al., 1995
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Citations
Cites
Statistical principles in experimental design.
Winer, B. J. (1962) · McGraw-Hill Book Company · doi:10.1037/11774-000 · Cited by 27,137
Brain Maps: Structure of the Rat Brain
Swanson, L. W. (1992) · Medical Entomology and Zoology · Cited by 1,878
Taube, J., Muller, R., & Ranck, J. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00420.1990 · Cited by 1,809
Functions of the frontal cortex of the rat: A comparative review
Kolb, B. E. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90018-3 · Cited by 897
The effects of hippocampal lesions upon spatial and non-spatial tests of working memory
Aggleton, J. P., Hunt, P. R., & Rawlins, J. N. P. (1986) · Behavioural Brain Research · doi:10.1016/0166-4328(86)90011-2 · Cited by 500
Self-citationContributions of cingulate cortex to two forms of spatial learning and memory
Sutherland, R., Whishaw, I., & Kolb, B. E. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-06-01863.1988 · Cited by 415
Mizumori, S., & Williams, J. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-09-04015.1993 · Cited by 369
The role of the fornix/fimbria and some related subcortical structures in place learning and memory
Sutherland, R. J., & Rodríguez, A. J. (1989) · Behavioural Brain Research · doi:10.1016/s0166-4328(89)80059-2 · Cited by 355
Selectivity of the hippocampal projection to the prelimbic area of the prefrontal cortex in the rat
Jay, T. M., Glowinski, J., & Thierry, A. M. (1989) · Brain Research · doi:10.1016/0006-8993(89)91464-9 · Cited by 311
Connections of the retrosplenial dysgranular cortex in the rat
van Groen, T., & Wyss, J. M. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903150207 · Cited by 308
Cited by
Sorted by citations
Items 101–195 of 195
Cassaday, H. J. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00160 · Cited by 54
Effects of selective granular retrosplenial cortex lesions on spatial working memory in rats
Pothuizen, H. H. J., Davies, M., Aggleton, J. P., & Vann, S. D. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.01.001 · Cited by 53
Self-citationEffects of rat ventral and dorsal hippocampus temporal inactivation on delayed alternation task
Maruki, K., Izaki, Y., Hori, K., Nomura, M., & Yamauchi, T. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02084-4 · Cited by 51
Evidence for two distinct thalamocortical circuits in retrosplenial cortex
Lomi, E., Mathiasen, M. L., Cheng, H. Y., Zhang, N., Aggleton, J. P., Mitchell, A. S., & Jeffery, K. J. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107525 · Cited by 51
Self-citationThe retrosplenial cortex and object recency memory in the rat
Powell, A. L., Vann, S. D., Olarte‐Sánchez, C. M., Kinnavane, L., Davies, M., Amin, E., Aggleton, J. P., & Nelson, A. J. D. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13577 · Cited by 50
Self-citationShires, K. L., & Aggleton, J. P. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06402.x · Cited by 48
Self-citationSchiller, D., & Weiner, I. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.06.020 · Cited by 48
Miner, L. A. H., Ostrander, M. M., & Sarter, M. F. (1997) · Journal of Psychopharmacology · doi:10.1177/026988119701100210 · Cited by 47
Impaired structural correlates of memory in Alzheimer's disease mice
Badhwar, A., Lerch, J. P., Hamel, É., & Sled, J. G. (2013) · NeuroImage Clinical · doi:10.1016/j.nicl.2013.08.017 · Cited by 50
Hernádi, I., Karádi, Z., Vı́gh, J., Petykó, Z., Egyed, R., Berta, B., & Lénárd, L. (2000) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00361-0 · Cited by 45
Harker, K. T., & Whishaw, I. Q. (2004) · Hippocampus · doi:10.1002/hipo.10159 · Cited by 51
Antonelli, T., Tanganelli, S., Tomasini, M. C., Finetti, S., Trabace, L., Steardo, L., Sabino, V., Carratù, M. R., Cuomo, V., & Ferraro, L. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.10.034 · Cited by 44
A comparison of egocentric and allocentric age-dependent spatial learning in the beagle dog
Christie, L., Studzinski, C. M., Araujo, J. A., Leung, C. S. K., Ikeda-Douglas, C. J., Head, E., Cotman, C. W., & Milgram, N. W. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2004.12.002 · Cited by 43
Aujla, H., & Beninger, R. J. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.6.1204 · Cited by 46
What does spatial alternation tell us about retrosplenial cortex function?
Nelson, A. J. D., Powell, A. L., Holmes, J. D., Vann, S. D., & Aggleton, J. P. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00126 · Cited by 41
Self-citationAggleton, J. P., & Vann, S. D. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.08.003 · Cited by 41
Self-citationKahn, J. B., Ward, R. D., Kahn, L. W., Rudy, N. M., Kandel, E. R., Balsam, P. D., & Simpson, E. H. (2012) · Learning & Memory · doi:10.1101/lm.026302.112 · Cited by 39
The anterior thalamic nuclei and nucleus reuniens: So similar but so different
Mathiasen, M. L., O’Mara, S. M., & Aggleton, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.10.006 · Cited by 41
Self-citationRetrosplenial cortex in spatial memory: focus on immediate early genes mapping
Balcerek, E., Włodkowska, U., & Czajkowski, R. (2021) · Molecular Brain · doi:10.1186/s13041-021-00880-w · Cited by 39
Neave, N., Nagle, S., Sahgal, A., & Aggleton, J. P. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(96)00022-8 · Cited by 36
Self-citationRytter, H. M., Andersen, L. G., Christensen, R. F., Felbinger, A., Hagstrøm, J., Meder, D., Pearce, H. L., & Mogensen, J. (2015) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2015.05.006 · Cited by 37
Vakalopoulos, C. (2005) · Medical Hypotheses · doi:10.1016/j.mehy.2005.09.037 · Cited by 36
Sircar, R., & BASAK, A. (2004) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2004.09.022 · Cited by 34
Cain, D. P., Humpartzoomian, R., & Boon, F. H. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.03.003 · Cited by 34
Laatikainen, L. M., Sharp, T., Bannerman, D. M., Harrison, P. J., & Tunbridge, E. M. (2012) · Journal of Psychopharmacology · doi:10.1177/0269881112454228 · Cited by 33
Ruotsalainen, S., Miettinen, R. A., MacDonald, E., Riekkinen, M., & Sirviö, J. (1997) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(96)00065-6 · Cited by 32
Repeated ethanol treatment in adolescent rats alters cortical NMDA receptor
Sircar, R., & Sircar, D. (2006) · Alcohol · doi:10.1016/j.alcohol.2006.07.002 · Cited by 32
Structural correlates of subjective and objective memory performance in multiple sclerosis
Pardini, M., Bergamino, M., Bommarito, G., Bonzano, L., Mancardi, G., & Roccatagliata, L. (2013) · Hippocampus · doi:10.1002/hipo.22237 · Cited by 31
Limbic system structures differentially contribute to exploratory trip organization of the rat
Winter, S. S., Köppen, J. R., Ebert, T. B. N., & Wallace, D. G. (2012) · Hippocampus · doi:10.1002/hipo.22075 · Cited by 30
Watson, D. J., & Stanton, M. E. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.07.026 · Cited by 29
Durkee, C. A., Sarlls, J. E., Hommer, D. W., & Momenan, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080952 · Cited by 27
Ruotsalainen, S., MacDonald, E., Koivisto, E., Stefański, R., Haapalinna, A., Riekkinen, P. J., & Sirviö, J. (1998) · Journal of Psychopharmacology · doi:10.1177/026988119801200210 · Cited by 28
Machin, P. E., Vann, S. D., Muir, J. L., & Aggleton, J. P. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.2.232 · Cited by 27
Self-citationFunctional dissociation between dorsal and ventral regions of the medial prefrontal cortex in rats
Gisquet-Verrier, P., Winocur, G., & Delatour, B. (2000) · Psychobiology · doi:10.3758/bf03331983 · Cited by 27
Souza, T. M. E., Roesler, R., Madruga, M. P., de-Paris, F., Quevedo, J., Rodrigues, C. A., Kauer‐Sant’Anna, M., Medina, J. H., & Izquierdo, I. (1999) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3892 · Cited by 27
Johnson, A. W., Bannerman, D. M., Rawlins, N. P., Sprengel, R., & Good, M. A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4146-04.2005 · Cited by 26
The rat retrosplenial cortex as a link for frontal functions: A lesion analysis
Powell, A. L., Nelson, A. J. D., Hindley, E. L., Davies, M., Aggleton, J. P., & Vann, S. D. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.08.010 · Cited by 24
Self-citationOrtega‐Legaspi, J. M., López-Ávila, A., Coffeen, U., del Ángel, R., & Pellicer, F. (2003) · European Journal of Pain · doi:10.1016/s1090-3801(02)00147-7 · Cited by 25
Estapé, N., & Steckler, T. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00379-x · Cited by 24
Catecholaminergic depletion within the prelimbic medial prefrontal cortex enhances latent inhibition
Nelson, A. J. D., Thur, K. E., Marsden, C. A., & Cassaday, H. J. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.06.066 · Cited by 23
Yee, B. K., & Rawlins, J. N. P. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00163-0 · Cited by 22
Zheng, Y., Pearce, J., Vann, S. D., Good, M. A., Jenkins, T. A., Smith, P. F., & Aggleton, J. P. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.6.1363 · Cited by 21
Self-citationSkelton, R. W. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00199-x · Cited by 21
Parallel Recovery of MK-801–Induced Spatial Learning Impairment and Neuronal Injury in Male Mice
Brosnan-Watters, G., Wozniak, D. F., Nardi, A. M. D., & Olney, J. W. (1999) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(98)00149-x · Cited by 21
Keith, G. P., DeSouza, J. F. X., Yan, X., Wang, H., & Crawford, J. D. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.03.004 · Cited by 20
Loukavenko, E. A., Wolff, M., Poirier, G. L., & Dalrymple‐Alford, J. C. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1015-x · Cited by 19
Rule shift under long-term PCP challenge in rats
Deschênes, A., Goulet, S., & Doré, F. Y. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.08.013 · Cited by 19
Kinoshita, S., Yokoyama, C., Masaki, D., Yamashita, T., Tsuchida, H., Nakatomi, Y., & Fukui, K. (2007) · Neuroscience Research · doi:10.1016/j.neures.2007.10.012 · Cited by 19
Tomasini, M. C., Beggiato, S., Ferraro, L., Tanganelli, S., Marani, L., Lorenzini, L., & Antonelli, T. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.07.004 · Cited by 18
Berardino, B. G., Chertoff, M., Gianatiempo, O., Alberca, C. D., Priegue, R., Fiszbein, A., Long, P. T., Corfas, G., & Cánepa, E. T. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.03.027 · Cited by 17
Mogensen, J., Boyd, M., Nielsen, M. D., Kristensen, R. S., & Rytter, H. M. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.05.005 · Cited by 17
Rosenbloom, M. J., Sassoon, S. A., Pfefferbaum, A., & Sullivan, E. V. (2009) · Brain Imaging and Behavior · doi:10.1007/s11682-009-9080-5 · Cited by 16
Telencephalic neurocircuitry and synaptic plasticity in rodent spatial learning and memory
Pooters, T., der Jeugd, A. V., Callaerts‐Vegh, Z., & D’Hooge, R. (2015) · Brain Research · doi:10.1016/j.brainres.2015.01.015 · Cited by 15
Onos, K. D., Francoeur, M. J., Wormwood, B. A., Miller, R. L. A., Gibson, B. M., & Mair, R. G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149019 · Cited by 14
Context-specific adaptation of pursuit initiation in humans.
Takagi, M., Abe, H., Hasegawa, S., Usui, T., Hasebe, H., Miki, A., & Zee, D. S. (2000) · PubMed · Cited by 14
Griffin, A. L., & Berry, S. D. (2004) · Learning & Memory · doi:10.1101/lm.78404 · Cited by 14
Testosterone impairs the acquisition of an operant delayed alternation task in male rats
Neese, S. L., & Schantz, S. L. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.10.003 · Cited by 13
Saha, R., Shrivastava, K., Jing, L., Schayek, R., Maroun, M., Kriebel, M., Volkmer, H., & Richter‐Levin, G. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx300 · Cited by 13
Behavioural effects of extracellular matrix protein Fras1 depletion in the mouse
Kalpachidou, T., Makrygiannis, A. K., Pavlakis, E., Stylianopoulou, F., Chalepakis, G., & Stamatakis, A. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14759 · Cited by 12
Bubb, E. J., Nelson, A. J. D., Cozens, T. C., & Aggleton, J. P. (2020) · Brain and Neuroscience Advances · doi:10.1177/2398212820957160 · Cited by 10
Self-citation[Erysipelas: evolution under treatment, complications].
Crickx, B. (2001) · PubMed · Cited by 10
Closed-loop modulation of remote hippocampal representations with neurofeedback
Coulter, M. E., Gillespie, A. K., Chu, J. P., Denovellis, E. L., Nguyen, T. T. K., Liu, D. F., Wadhwani, K., Sharma, B., Wang, K. X.-L., Deng, X., et al. (2025) · Neuron · doi:10.1016/j.neuron.2024.12.023 · Cited by 14
Yanakieva, S., Frost, B. E., Amin, E., Nelson, A. J. D., & Aggleton, J. P. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16303 · Cited by 8
Self-citationBlokland, A., Broersen, L. M., Uylings, H. B. M., & Jolles, J. (2003) · Neuroscience Research Communications · doi:10.1002/nrc.10076 · Cited by 8
Delayed effects of prenatal low-dose irradiation in the white matter of the rat brain
H. Reyners, E. G. D. R. (1999) · International Journal of Radiation Biology · doi:10.1080/095530099139494 · Cited by 7
Weiner, I. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511730184.017 · Cited by 5
Clarke, H. A., Skinner, D. M., & van der Kooy, D. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.2.341 · Cited by 5
Thanks for the memories: Extending the hippocampal-diencephalic mnemonic system
Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99482032 · Cited by 5
Self-citationChapter 5.2 Using hippocampal amnesia to understand the neural basis of diencephalic amnesia
Aggleton, J. P., Saunders, R. C., & Vann, S. D. (2008) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(08)00227-0 · Cited by 4
Self-citationSavage, L. M., & Guarino, S. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.09.008 · Cited by 4
Baxter, M. G. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-422-3_3 · Cited by 4
Jung, Y., & Hong, S. J. (2003) · Korean Journal of Biological Sciences · doi:10.1080/12265071.2003.9647710 · Cited by 4
Sheppard, P. A. S., Oomen, C. A., Bussey, T. J., & Saksida, L. M. (2024) · eNeuro · doi:10.1523/eneuro.0120-24.2024 · Cited by 3
Neese, S. L., Korol, D. L., & Schantz, S. L. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.08.008 · Cited by 3
Investigating the role of the hippocampal formation in episodic and spatial memory
Stevenson, C. H. (2011) · ERA · Cited by 4
Grancha, M. L., Crespo, G. A. L., & Flores, P. (2006) · Revista internacional de psicología y terapia psicológica/Revista internacional de psicología y terapia psicológica · Cited by 3
Bauer, R. M., & Asken, B. M. (2017) · Taylor & Francis eBooks · doi:10.4324/9781315271743-28 · Cited by 2
Cortico-hippocampal communication by way of parallel parahippocampal-subicular pathways.
Lavenex (2000) · Pure Amsterdam UMC · doi:10.1002/1098-1063(2000)10:4 · Cited by 1
Self-citationFaridi, F., Alvand, A., & Khosrowabadi, R. (2021) · Basic and Clinical Neuroscience Journal · doi:10.32598/bcn.2021.2244.1 · Cited by 1
Konaç, A., & Ünal, Ç. T. (2022) · Ayna Klinik Psikoloji Dergisi · doi:10.31682/ayna.777249 · Cited by 1
Graham, K. S., & Hodges, J. R. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99292035 · Cited by 1
Influences of self-motion signals on the hippocampal neural code for space
Terrazas, A. (2003) · UA Campus Repository (The University of Arizona) · Cited by 1
Executive function and prefrontal cortex in rats
Duffaud, A. M. (2008) · ORCA Online Research @Cardiff (Cardiff University)
Meunier, M., & Destrade, C. (1997)
Nusrat, L. (2017) · TSpace (University of Toronto)
Neural correlates of sensation and navigation in the retrosplenial cortex
Mao, D. (2017) · Open ULeth Scholarship (OPUS) (University of Lethbridge)
The Development of Spatial Memory Processes and Associated Cellular Correlates in Juvenile Rats
Tzakis, N. (2020) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2020-13967
Fuster, J. M. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-373644-4.00004-9
Fuster, J. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-407815-4.00004-0
Effect of Lesions of the Retrosplenial Cortex on Spatial Tasks in the Rat
HAYASHI, T., & Sato, N. (2020) · Japanese Journal of Physiological Psychology and Psychophysiology · doi:10.5674/jjppp.2002si
Effects of experimental brain lesions on spatial navigation
Vann, S. D. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00008-5
Stable and flexible representations in mouse mPFC across different behaviors
Hahn, J. (2024) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.85685
A re-examination of the retrosplenial contribution to place navigation in the rat
Harker, K. T. (2002) · Open ULeth Scholarship (OPUS) (University of Lethbridge)
Finch (1996) · doi:10.1002/(sici)1098-1063(1996)6:5
Metadata
- Authors
- Aggleton, J., Neave, N., Nagle, S., & Sahgal, A.
- Affiliations
- Durham University (GB)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1995-11-01
- Volume
- 15
- Issue
- 11
- Pages
- 7270-7281
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6578066
- OpenAlex
- W2129684141
- Cited by
- 196
- References
- 34
- Citations by year
- 2025: 1 · 2024: 3 · 2023: 1 · 2022: 1 · 2021: 4 · 2020: 5 · 2019: 1 · 2018: 2 · 2017: 8 · 2016: 2 · 2015: 7 · 2014: 4 · 2013: 6 · 2012: 5
- FWCI
- 5.59
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (acceptedVersion)
- Northumbria Research Link (Northumbria University) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Keywords
- spatial memory, medial prefrontal cortex, cingulate cortex, cingulum, fornix, double dissociation, reversal learning, T-maze, retrosplenial cortex
- MeSH terms
- Animals, Discrimination, Psychological, Gyrus Cinguli, Hippocampus, Male, Memory, Rats, Inbred Strains, Space Perception, Prefrontal Cortex, Maze Learning, Rats
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