Cited by 397Memory and Neural MechanismsMemory Processes and InfluencesNeuroscience and Neuropharmacology Research

The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.

Double dissociation of function within the hippocampus: A comparison of dorsal, ventral, and complete hippocampal cytotoxic lesions

Bannerman, D. M., Yee, B. K., Good, M. A., Heupel, M. J., Iversen, S. D., Rawlins, J. N. P.·1999·Behavioral Neuroscience

DOI 10.1037/0735-7044.113.6.1170

Open this paper in CoChat — free account

Abstract

Rats with complete cytotoxic hippocampal lesions exhibited spatial memory impairments in both the water maze and elevated T maze. They were hyperactive in photocell cages; swam faster in the water maze; and were less efficient on a nonspatial, differential reinforcement of low rates (DRL) task. Performance on both spatial tasks was also impaired by selective dorsal but not ventral lesions; swim speed was increased by ventral but not dorsal lesions. Both partial lesions caused a comparable reduction in DRL efficiency, although these effects were smaller than those of complete lesions. Neither partial lesion induced hyperactivity when rats were tested in photocell cages, although both complete and ventral lesion groups showed increased activity after footshock in other studies (Richmond et al., 1999). These results demonstrate possible functional dissociations along the septotemporal axis of the hippocampus.

Integrity signals

Registry

Crossref · 10.1037/0735-7044.113.6.1170

Cites

50 of 50 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Statistical power analysis for the behavioral sciences
Cohen, J. (1990) · Computers Environment and Urban Systems · doi:10.1016/0198-9715(90)90050-4 · Cited by 65,417
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Untitled work
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
Developments of a water-maze procedure for studying spatial learning in the rat
Morris, R. (1984) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(84)90007-4 · Cited by 7,180
Spatial localization does not require the presence of local cues
Morris, R. G. M. (1981) · Learning and Motivation · doi:10.1016/0023-9690(81)90020-5 · Cited by 2,699
Modality-Specific Retrograde Amnesia of Fear
Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483
Hippocampus, space, and memory
Olton, D. S., Becker, J. T., & Handelmann, G. E. (1979) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00062713 · Cited by 2,018
The Role of the Hippocampus in Feedback Regulation of the Hypothalamic-Pituitary-Adrenocortical Axis*
JACOBSON, L., & SAPOLSKY, R. (1991) · Endocrine Reviews · doi:10.1210/edrv-12-2-118 · Cited by 1,739
On the role of the hippocampus in learning and memory in the rat.
Jarrard, L. E. (1993) · Behavioral and Neural Biology · doi:10.1016/0163-1047(93)90664-4 · Cited by 1,125
The patterns of afferent innervation of the core and shell in the “Accumbens” part of the rat ventral striatum: Immunohistochemical detection of retrogradely transported fluoro‐gold
Brog, J. S., Salyapongse, A., Deutch, A. Y., & Zahm, D. S. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903380209 · Cited by 1,102

Show all 50 references

Sorted by citations

Items 201–300 of 396

Dorsal hippocampus cannabinoid type 1 receptors modulate the expression of contextual fear conditioning in rats: Involvement of local glutamatergic/nitrergic and GABAergic neurotransmissions
Spiacci, G. B. L., Antero, L. S., dos Reis, D. G., Lisboa, S. F. D. S., & Resstel, L. B. M. (2016) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2016.08.010 · Cited by 34
Evaluating spatial memory function in mice: A within-subjects comparison between the water maze test and its adaptation to dry land
López, L., Hauser, J., Feldon, J., Gargiulo, P. Á., & Yee, B. K. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.01.020 · Cited by 33
α2 GABAA receptor sub-units in the ventral hippocampus and α5 GABAA receptor sub-units in the dorsal hippocampus mediate anxiety and fear memory
McEown, K., & Treit, D. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.012 · Cited by 34
Emergence of synaptic and cognitive impairment in a mature-onset APP mouse model of Alzheimer’s disease
Sri, S., Pegasiou, C.-M., Cave, C. A., Hough, K., Wood, N. J., Gómez‐Nicola, D., Deinhardt, K., Bannerman, D. M., Perry, V. H., & Vargas‐Caballero, M. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0670-1 · Cited by 35
Modulation of hippocampal dopamine metabolism and hippocampal-dependent cognitive function by catechol-O-methyltransferase inhibition
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
Amphetamine-induced hyperlocomotion in rats: Hippocampal modulation of the nucleus accumbens
White, I. M., Whitaker, C., & White, W. O. (2006) · Hippocampus · doi:10.1002/hipo.20189 · Cited by 33
Unpredictable Chronic Mild Stress Suppresses the Incorporation of New Neurons at the Caudal Pole of the Chicken Hippocampal Formation
Gualtieri, F., Armstrong, E. A., Longmoor, G., D’Eath, R. B., Sandilands, V., Boswell, T., & Smulders, T. V. (2019) · Scientific Reports · doi:10.1038/s41598-019-43584-x · Cited by 31
Acetylcholine Muscarinic Receptors in Ventral Hippocampus Modulate Stress-Induced Anxiety-Like Behaviors in Mice
Mei, L., Zhou, Y., Sun, Y., Liu, H. S., Zhang, D., Liu, P., & Shu, H. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.598811 · Cited by 32
Time-based reward maximization
Çavdaroğlu, B., Zeki, M., & Balcı, F. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0461 · Cited by 32
Estradiol's effects on learning and neuronal morphology vary with route of administration.
Garza-Meilandt, A., Cantu, R. E., & Claiborne, B. J. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.4.905 · Cited by 32
Transient overexpression of the 5-HT1A receptor impairs water-maze but not hole-board performance
Bert, B., Dere, E., Wilhelmi, N., Kusserow, H., Theuring, F., Huston, J. P., & Fink, H. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.03.005 · Cited by 32
Chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with NF-κB
Snow, W. M., Cadonic, C., Cortes-Perez, C., Roy Chowdhury, S. K., Djordjevic, J., Thomson, E., Bernstein, M. J., Suh, M., Fernyhough, P., & Albensi, B. C. (2018) · Learning & Memory · doi:10.1101/lm.046284.117 · Cited by 31
Rats with ventral hippocampal damage are impaired at various forms of learning including conditioned inhibition, spatial navigation, and discriminative fear conditioning to similar contexts
McDonald, R. J., Balog, R. J., Lee, J. Q., Stuart, E. A., Carrels, B. B., & Hong, N. S. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.06.003 · Cited by 31
Intact spatial learning in adult Tg2576 mice
Bizon, J., Prescott, S., & Nicolle, M. M. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.01.004 · Cited by 23
Linked networks for learning and expressing location-specific threat
Suarez‐Jimenez, B., Bisby, J. A., Horner, A. J., King, J. A., Pine, D. S., & Burgess, N. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714691115 · Cited by 31
The homogenous hippocampus: How hippocampal cells process available and potential goals
McNaughton, N., & Bannerman, D. M. (2024) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2024.102653 · Cited by 33
Alterations in spatial memory and anxiety in the MAM E17 rat model of hippocampal pathology in schizophrenia
Gastambide, F., Taylor, A. M., Palmer, C. E., Svärd, H., Karjalainen, M., Janhunen, S. K., Tricklebank, M. D., & Bannerman, D. M. (2015) · Psychopharmacology · doi:10.1007/s00213-014-3862-1 · Cited by 31
Anxiolytic Actions of Exercise in Absence of New Neurons
Schoenfeld, T. J., McCausland, H. C., Sonti, A. N., & Cameron, H. A. (2016) · Hippocampus · doi:10.1002/hipo.22649 · Cited by 29
Adenosine A2A receptor and ERK-driven impulsivity potentiates hippocampal neuroblast proliferation
Oliveros, A., Cho, C. H., Cui, A., Choi, S. H., Lindberg, D. M., Hinton, D. R., Jang, M.-H., & Choi, D.-S. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.64 · Cited by 29
The GABAA receptor-mediated recurrent inhibition in ventral compared with dorsal CA1 hippocampal region is weaker, decays faster and lasts less
Petrides, T., Georgopoulos, P., Kostopoulos, G., & Papatheodoropoulos, C. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0681-6 · Cited by 29
Hippocampal GABAB(1a) Receptors Constrain Generalized Contextual Fear
Lynch, J. F., Winiecki, P., Gilman, T. L., Adkins, J. M., & Jasnow, A. M. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.255 · Cited by 29
Delta Opioid Receptors: Learning and Motivation
Pellissier, L. P., Pujol, C., Becker, J. A. J., & Merrer, J. L. (2016) · Handbook of experimental pharmacology · doi:10.1007/164_2016_89 · Cited by 30
Hippocampal mossy fiber sprouting induced by forced and voluntary physical exercise
Toscano-Silva, M., da Silva, S. G., Scorza, F. A., Bonvent, J. J., Cavalheiro, E. A., & Arida, R. M. (2010) · Physiology & Behavior · doi:10.1016/j.physbeh.2010.05.012 · Cited by 27
Learning‐dependent plasticity of hippocampal CA1 pyramidal neuron postburst afterhyperpolarizations and increased excitability after inhibitory avoidance learning depend upon basolateral amygdala inputs
Farmer, G. E., & Thompson, L. T. (2012) · Hippocampus · doi:10.1002/hipo.22005 · Cited by 28
Small lesions of the dorsal or ventral hippocampus subregions are associated with distinct impairments in working memory and reference memory retrieval, and combining them attenuates the acquisition rate of spatial reference memory
Hauser, J., López, L. H. L., Feldon, J., Gargiulo, P. Á., & Yee, B. K. (2020) · Hippocampus · doi:10.1002/hipo.23207 · Cited by 27
Timing and space usage are disrupted by amphetamine in rats maintained on DRL 24-s and DRL 72-s schedules of reinforcement
Fowler, S. C., Pinkston, J. W., & Vorontsova, E. (2009) · Psychopharmacology · doi:10.1007/s00213-008-1451-x · Cited by 27
Alteration of conditioned emotional response and conditioned taste aversion after neonatal ventral hippocampus lesions in rats
Angst, M.-J., de Macedo, C. E. A., Guiberteau, T., & Sandner, G. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.093 · Cited by 29
The complexity of ventral CA1 and its multiple functionalities
Hong, I., & Kaang, B. (2022) · Genes Brain & Behavior · doi:10.1111/gbb.12826 · Cited by 27
The impact of fornix lesions in rats on spatial learning tasks sensitive to anterior thalamic and hippocampal damage
Dumont, J. R., Amin, E., Wright, N. F., Dillingham, C. M., & Aggleton, J. P. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.10.016 · Cited by 26
Hippocampal GluA1 expression in Gria1 −/− mice only partially restores spatial memory performance deficits
Freudenberg, F., Resnik, E., Kolleker, A., Celikel, T., Sprengel, R., & Seeburg, P. H. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.005 · Cited by 26
The Projection From Ventral CA1, Not Prefrontal Cortex, to Nucleus Accumbens Core Mediates Recent Memory Retrieval of Cocaine-Conditioned Place Preference
Zhou, Y., Yan, E., Cheng, D., Zhu, H., Liu, Z., Chen, X., Ma, L., & Liu, X. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.558074 · Cited by 25
Global State Measures of the Dentate Gyrus Gene Expression System Predict Antidepressant-Sensitive Behaviors
Samuels, B. A., Leonardo, E. D., Dranovsky, A., Williams, A., Wong, E. H. F., Nesbitt, A. M. I., McCurdy, R. D., Hen, R., & Alter, M. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085136 · Cited by 27
Rapid encoding of new information alters the profile of plasticity-related mRNA transcripts in the hippocampal CA3 region
Haberman, R. P., Lee, H. J., Colantuoni, C., Koh, M. T., & Gallagher, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804292105 · Cited by 25
Circuit mechanisms of GluA1-dependent spatial working memory
Freudenberg, F., Marx, V., Seeburg, P. H., Sprengel, R., & Celikel, T. (2013) · Hippocampus · doi:10.1002/hipo.22184 · Cited by 26
Ischemic LTP : NMDA ‐dependency and dorso/ventral distribution within the hippocampus
Maggio, N., Stein, E. S., & Segal, M. (2015) · Hippocampus · doi:10.1002/hipo.22467 · Cited by 26
Hippocampal scrapie infection impairs operant DRL performance in mice
Deacon, R. M. J., Reisel, D., Perry, V. H., Nicholas, J., & Rawlins, P. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.06.013 · Cited by 25
Association rules for rat spatial learning: The importance of the hippocampus for binding item identity with item location
Albasser, M. M., Dumont, J. R., Amin, E., Holmes, J. D., Horne, M. R., Pearce, J. M., & Aggleton, J. P. (2013) · Hippocampus · doi:10.1002/hipo.22154 · Cited by 24
Midline thalamic reuniens lesions improve executive behaviors
Prasad, J. A., Abela, A. R., & Chudasama, Y. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.01.071 · Cited by 24
Deciphering Memory Function with Optogenetics
Beyeler, A., Eckhardt, C. A., & Tye, K. M. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00012-x · Cited by 24
Dissociating ventral and dorsal subicular dopamine D₁ receptor involvement in instrumental learning, spontaneous motor behavior, and motivation.
Andrzejewski, M. E., Spencer, R. C., & Kelley, A. E. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.3.542 · Cited by 24
MicroRNA Expression Profiling in the Prefrontal Cortex: Putative Mechanisms for the Cognitive Effects of Adolescent High Fat Feeding
Labouesse, M. A., Polesel, M., Clementi, E., Müller, F., Markkanen, E., Mouttet, F., Cattaneo, A., & Richetto, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-26631-x · Cited by 24
Rats with hippocampal lesion show impaired learning and memory in the ziggurat task: A new task to evaluate spatial behavior
Faraji, J., Lehmann, H., Metz, G. A. S., & Sutherland, R. J. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.12.002 · Cited by 23
Morris Water Maze Training in Mice Elevates Hippocampal Levels of Transcription Factors Nuclear Factor (Erythroid-derived 2)-like 2 and Nuclear Factor Kappa B p65
Snow, W. M., Pahlavan, P. S., Djordjevic, J., McAllister, D., Platt, E. E., Alashmali, S. M., Bernstein, M. J., Suh, M., & Albensi, B. C. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00070 · Cited by 23
Topographic separation of fornical fibers associated with the anterior and posterior hippocampus in the human brain: An MRI ‐diffusion study
Christiansen, K., Metzler‐Baddeley, C., Parker, G. D., Muhlert, N., Jones, D. K., Aggleton, J. P., & Vann, S. D. (2016) · Brain and Behavior · doi:10.1002/brb3.604 · Cited by 24
Hippocampal lesions impair performance on a conditional delayed matching and non-matching to position task in the rat
Sloan, H. L., Döbrössy, M. D., & Dunnett, S. B. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.03.042 · Cited by 22
Dramatic impacts on brain pathology, anxiety, and cognitive function in the knock-in APPNL-G-F mouse model of Alzheimer disease following long-term voluntary exercise
Mehla, J., Deibel, S. H., Karem, H., Hossain, S., Lacoursiere, S. G., Sutherland, R. J., Mohajerani, M. H., & McDonald, R. J. (2022) · Alzheimer s Research & Therapy · doi:10.1186/s13195-022-01085-6 · Cited by 22
Home-cage odors spatial cues elicit theta phase/gamma amplitude coupling between olfactory bulb and dorsal hippocampus
Pena, R. R., Medeiros, D. D. C., Guarnieri, L. D. O., GUERRA, J. B., Carvalho, V. R., Mendes, E. M. A. M., Pereira, G. S., & Moraes, M. F. D. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.08.058 · Cited by 21
Dentate spikes and learning: disrupting hippocampal function during memory consolidation can improve pattern separation
Lensu, S., Waselius, T., Penttonen, M., & Nokia, M. S. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00696.2018 · Cited by 20
Cyto-, axo- and dendro-architectonic changes of neurons in the limbic system in the mouse pilocarpine model of temporal lobe epilepsy
Tang, F. R., & Loke, W. K. (2009) · Epilepsy Research · doi:10.1016/j.eplepsyres.2009.10.015 · Cited by 20
Anxiogenic-like profile of Wistar adult rats based on the pilocarpine model: an animal model for trait anxiety?
Duarte, F. S., Duzzioni, M., Hoeller, A. A., Silva, N. M., Ern, A. L., Piermartiri, T., Tasca, C. I., Gavioli, E. C., Lemos, T., Carobrez, A. P., et al. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2951-2 · Cited by 20
Scalar timing in memory: A temporal map in the hippocampus
Oprisan, S. A., Aft, T., Buhusi, M. C., & Buhusi, C. V. (2017) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2017.11.012 · Cited by 22
Behavioral, cognitive and histological changes following neonatal anoxia: Male and female rats' differences at adolescent age
Kumar, A. J., Motta‐Teixeira, L. C., Takada, S. H., Lee, V. Y., Machado‐Nils, A. V., Xavier, G. F., & Nogueira, M. I. (2018) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2018.12.002 · Cited by 20
Grafts of fetal septal cells after cholinergic immunotoxic denervation of the hippocampus: a functional dissociation between dorsal and ventral implantation sites
Cassel, J., Gaurivaud, M., Lazarus, C., Bertrand, F., Galani, R., & Jeltsch‐David, H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00226-9 · Cited by 20
Modulation by the dorsal, but not the ventral, hippocampus of the expression of behavioural sensitization to amphetamine
Degoulet, M., Rouillon, C., Rostain, J., David, H., & Abraini, J. H. (2007) · The International Journal of Neuropsychopharmacology · doi:10.1017/s146114570700822x · Cited by 20
The time course of the hyperactivity that follows lesions or temporary inactivation of the fimbria-fornix
Bannerman, D. M., Gilmour, G., Norman, G., Lemaire, M., Iversen, S. D., & Rawlins, J. N. P. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00354-5 · Cited by 20
The neuroprotective effects of N1-dansyl-spermine in the gerbil model of cerebral ischaemia
Kirby, B. P., & Shaw, G. G. (2004) · Brain Research · doi:10.1016/j.brainres.2004.02.074 · Cited by 20
Region-specific expression of circular RNAs in the mouse brain
Chen, B. J., Yang, B., & Janitz, M. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.12.022 · Cited by 19
Cognitive demands induce selective hippocampal reorganization: Arc expression in a place and response task
Schmidt, B., Satvat, E., Argraves, M., Markus, E. J., & Marrone, D. F. (2012) · Hippocampus · doi:10.1002/hipo.22031 · Cited by 19
Simultaneous training on two hippocampus-dependent tasks facilitates acquisition of trace eyeblink conditioningPreprint
Kuo, A. G., Lee, G., & Disterhoft, J. F. (2006) · Learning & Memory · doi:10.1101/lm.98406 · Cited by 19
Dissociable contributions of the amygdala and ventral hippocampus to stress-induced changes in defensive behavior
Pennington, Z. T., LaBanca, A. R., Sompolpong, P., Abdel-Raheim, S. D., Ko, B., Wick, Z. C., Feng, Y., Dong, Z., Francisco, T. R., Bacon, M. E., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114871 · Cited by 23
Medial prefrontal and ventral hippocampal contributions to incidental context learning and memory in adolescent rats
Heroux, N. A., Horgan, C. J., Pinizzotto, C. C., Rosen, J. B., & Stanton, M. E. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.107091 · Cited by 18
Endothelin-1-induced mini-stroke in the dorsal hippocampus or lateral amygdala results in deficits in learning and memory
Sheng, T., Xueting, Z., Shaoli, W., Jingyun, Z., Lu, W., & Yifan, D. (2015) · Journal of Biomedical Research · doi:10.7555/jbr.29.20150008 · Cited by 18
Effects of Strain and Species on the Septo-Temporal Distribution of Adult Neurogenesis in Rodents
Wiget, F., van Dijk, R. M., Louet, E. R., Slomianka, L., & Amrein, I. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00719 · Cited by 18
Eternal sunshine of the neuromodulated mind: Altering fear memories through neuromodulation
Tan, S. Z. K., Sheng, V., Chan, Y., & Lim, L. W. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.01.004 · Cited by 18
Role of dCA3 efferents via the fimbria in the acquisition of a delay nonmatch to place task
Hunsaker, M. R., Allan, K. D., & Kesner, R. P. (2007) · Hippocampus · doi:10.1002/hipo.20288 · Cited by 16
Regional differences in dopamine receptor blockade affect timing impulsivity that is altered by d-amphetamine on differential reinforcement of low-rate responding (DRL) behavior in rats
Cheng, R., & Liao, R. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.05.020 · Cited by 16
Chronic infection with Mycobacterium lepraemurium induces alterations in the hippocampus associated with memory loss
Becerril‐Villanueva, E., Ponce-Regalado, M. D., Pérez‐Sánchez, G., Salazar‐Juárez, A., Arreola, R., Álvarez-Sánchez, M. E., Juarez‐Ortega, M., Falfán‐Valencia, R., Hernández‐Pando, R., Morales‐Montor, J., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-27352-x · Cited by 16
GSA: behavioral, histological, electrophysiological and neurochemical effects
Torremans, A., Marescau, B., Dam, D. V., Ginneken, C. J. V., Meir, F. V., van Bogaert, P., D’Hooge, R., de Vente, J., & Deyn, P. P. D. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.12.001 · Cited by 16
Appetitively motivated instrumental learning in SynGAP heterozygous knockout mice.
Muhia, M., Feldon, J., Knuesel, I., & Yee, B. K. (2009) · Behavioral Neuroscience · doi:10.1037/a0017118 · Cited by 18
Dorsal hippocampus represents locations to avoid as well as locations to approach during approach-avoidance conflict
Calvin, O. L., Erickson, M. T., Walters, C. J., & Redish, A. D. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3002954 · Cited by 24
Does the dorsal hippocampus process navigational routes or behavioral context? A single‐unit analysis
Oler, J. A., Penley, S. C., Sava, S., & Markus, E. J. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06375.x · Cited by 14
Adult neurogenesis affects motivation to obtain weak, but not strong, reward in operant tasks
Karlsson, R., Wang, A. S., Sonti, A. N., & Cameron, H. A. (2018) · Hippocampus · doi:10.1002/hipo.22950 · Cited by 16
Ventral hippocampus lesions and allocentric spatial memory in the radial maze: Anterograde and retrograde deficits
Ramos, J. M. J., & Morón, I. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113620 · Cited by 15
Medial Entorhinal Cortex Excitatory Neurons Are Necessary for Accurate Timing
Dias, M., Ferreira, R., & Remondes, M. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0750-21.2021 · Cited by 15
NMDA-Dependent Phase Synchronization between Septal and Temporal CA3 Hippocampal Networks
Gu, N., Jackson, J., Goutagny, R., Lowe, G. C., Manseau, F., & Williams, S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0179-13.2013 · Cited by 17
Normal behavioral responses to light and darkness and the pupillary light reflex are dependent upon the olivary pretectal nucleus in the diurnal Nile grass rat
Gall, A. J., Khacherian, O. S., Ledbetter, B., Deats, S., Luck, M., Smale, L., Yan, L., & Núñez, A. A. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.002 · Cited by 14
Recording Field Potentials and Synaptic Plasticity From Freely Behaving Rodents
Manahan‐Vaughan, D. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812028-6.00001-x · Cited by 14
Differential behavioral profile induced by the injection of dipotassium chlorazepate within brain areas that project to the nucleus accumbens septi
López, L., Caif, F., Fraile, M., Tinnirello, B., de Gargiulo, A. I. L., Lafuente, J. V., Baiardi, G., & Gargiulo, P. Á. (2013) · Pharmacological Reports · doi:10.1016/s1734-1140(13)71034-x · Cited by 14
Functional interaction of ventral hippocampal CA1 region and prelimbic cortex contributes to the encoding of contextual fear association of stimuli separated in time
Santos, T. B., Wallau, A. E., Soares, J. C. K., & Oliveira, M. G. M. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107216 · Cited by 14
Loss of hippocampal function impairs pattern separation on a mouse touch-screen operant paradigm
Josey, M., & Brigman, J. L. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.08.002 · Cited by 13
The Successive Alleys Test of Anxiety in Mice and Rats
Deacon, R. M. J. (2013) · Journal of Visualized Experiments · doi:10.3791/2705-v · Cited by 13
Differential expression of genes encoding neurotrophic factors and their receptors along the septal‐temporal axis of the rat hippocampus
Toyoda, A., Iio, W., Goto, T., Koike, H., & Tsukahara, T. (2014) · Animal Science Journal · doi:10.1111/asj.12268 · Cited by 12
Vortioxetine Improves Context Discrimination in Mice Through a Neurogenesis Independent Mechanism
Felice, D., Guilloux, J., Pehrson, A. L., Li, Y., Mendez‐David, I., Gardier, A. M., Sánchez, C., & David, D. J. P. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00204 · Cited by 12
Adolescent Δ-9-tetrahydrocannabinol exposure induces differential acute and long-term neuronal and molecular disturbances in dorsal vs. ventral hippocampal subregions
Felice, M. D., Chen, C., Rodríguez-Ruiz, M., Szkudlarek, H. J., Lam, M., Sert, S., Whitehead, S. N., Yeung, K. K. ‐., Rushlow, W. J., & Laviolette, S. R. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01496-x · Cited by 11
Inhibition, the final frontier: The impact of hippocampal lesions on behavioral inhibition and spatial processing in pigeons.
Scarf, D., Millar, J., Pow, N., & Colombo, M. (2014) · Behavioral Neuroscience · doi:10.1037/a0035487 · Cited by 11
Adult brain cytogenesis in the context of mood disorders: From neurogenesis to the emergent role of gliogenesis
Martins‐Macedo, J., Salgado, A. J., Gomes, E. D., & Pinto, L. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.09.030 · Cited by 11
Adolescent intermittent ethanol exposure enhances adult stress effects in male rats
Healey, K. L., Kibble, S., Dubester, K., Bell, A., & Swartzwelder, H. S. (2023) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2022.173513 · Cited by 14
The ventral hippocampus is necessary for cue-elicited, but not outcome driven approach-avoidance conflict decisions: a novel operant choice decision-making task
Çavdaroğlu, B., Riaz, S., Yeung, E., Lee, A. C. H., & Ito, R. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-00898-z · Cited by 11
Topographical disorientation after ischemic mini infarct in the dorsal hippocampus: whispers in silence
Faraji, J., Soltanpour, N., Moeeini, R., Roudaki, S., Soltanpour, N., Abdollahi, A. A., & Metz, G. A. S. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00261 · Cited by 10
Regional dissociation of paradigm-specific synapse remodeling during memory consolidation in the adult rat dentate gyrus
Scully, D., Fedriani, R., DeSouza, I. E. J., Murphy, K. J., & Regan, C. M. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.01.020 · Cited by 11
Schizophrenia pathology reverse-translated into mouse shows hippocampal hyperactivity, psychosis behaviors and hyper-synchronous events
Scott, D. S., Subramanian, M., Yamamoto, J., & Tamminga, C. A. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02781-5 · Cited by 9
Neural basis of operant behaviors maintained on the differential-reinforcement-of-low-rate (DRL) schedule in rodents
Liao, R., & Pattij, T. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.04.003 · Cited by 9
Integration and segregation of functional segmented anterior and posterior hippocampal networks in memory performance
Xu, J., Guan, X., Li, H., Xu, X., & Zhang, M. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.02.019 · Cited by 9
Transient oligemia is associated with long-term changes in binding densities of cortical inhibitory GABAA receptors in the rat brain
Frauenknecht, K. B. M., Plaschke, K., & Sommer, C. (2009) · Brain Research · doi:10.1016/j.brainres.2009.03.028 · Cited by 9
Hippocampal and amygdalar involvement in discriminatory place learning
Oler, J. A., Ramos, R. L., Penley, S. C., & Markus, E. J. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.11.051 · Cited by 9
Hippocampal plasticity mechanisms mediating experience-dependent learning change over time
Crestani, A. P., Sierra, R. O., Machado, A. E., Haubrich, J., Scienza-Martin, K., Alvares, L. D. O., & Quillfeldt, J. A. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.02.020 · Cited by 11
Deep brain stimulation of the prelimbic cortex disrupts consolidation of fear memories
Tan, S. Z. K., Poon, C. H., Chan, Y., & Lim, L. W. (2019) · IBRO Reports · doi:10.1016/j.ibror.2019.07.217 · Cited by 9
Fronto-temporal galanin modulates impulse control
Messanvi, F., Perkins, A., du Hoffmann, J., & Chudasama, Y. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05365-2 · Cited by 8
Neural circuits mediating latent learning and conditioning for salt in the rat
Stouffer, E. M., & White, N. M. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.12.006 · Cited by 8
A Direct Comparison of Afferents to the Rat Anterior Thalamic Nuclei and Nucleus Reuniens: Overlapping But Different
Mathiasen, M. L., Nelson, A. J. D., Amin, E., O’Mara, S. M., & Aggleton, J. P. (2021) · eNeuro · doi:10.1523/eneuro.0103-20.2021 · Cited by 11

Authors: Bannerman, D. M., Yee, B. K., Good, M. A., Heupel, M. J., Iversen, S. D., & Rawlins, J. N. P.
Affiliations: University of Oxford (GB)
ORCID: Bannerman, D. M.
Yee, B. K.
Good, M. A.
Venue: Behavioral Neuroscience
Publisher: American Psychological Association (APA)
Published: 1999
Volume: 113
Issue: 6
Pages: 1170-1188
ISSN: 0735-7044 (ISSN-L)
1939-0084
DOI: 10.1037/0735-7044.113.6.1170
OpenAlex: W2037522799
Cited by: 397
References: 50
Citations by year: 2026: 3 · 2025: 5 · 2024: 5 · 2023: 6 · 2022: 10 · 2021: 11 · 2020: 12 · 2019: 17 · 2018: 19 · 2017: 18 · 2016: 15 · 2015: 16 · 2014: 24 · 2013: 22 · 2012: 20
FWCI: 5.36
Type: journal article
Language: en
Open access: closed
Locations: Behavioral Neuroscience (publishedVersion)
PubMed (publishedVersion)
Funders: Wellcome Trust
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: hippocampus, double dissociation, dorsal hippocampus, ventral hippocampus, cytotoxic lesions, spatial memory, water maze, elevated T-maze, hyperactivity, differential reinforcement of low rates, footshock, septotemporal axis, rats
MeSH terms: Analysis of Variance, Animals, Hippocampus, Hyperkinesis, Locomotion, Male, Microinjections, Rats, Inbred Strains, Space Perception, N-Methylaspartate, Excitatory Amino Acid Antagonists, Maze Learning, 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

Double dissociation of function within the hippocampus: A comparison of dorsal, ventral, and complete hippocampal cytotoxic lesions

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks