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Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
Open accessAbstract
One literature treats the hippocampus as a purely cognitive structure involved in memory; another treats it as a regulator of emotion whose dysfunction leads to psychopathology. We review behavioral, anatomical, and gene expression studies that together support a functional segmentation into three hippocampal compartments: dorsal, intermediate, and ventral. The dorsal hippocampus, which corresponds to the posterior hippocampus in primates, performs primarily cognitive functions. The ventral (anterior in primates) relates to stress, emotion, and affect. Strikingly, gene expression in the dorsal hippocampus correlates with cortical regions involved in information processing, while genes expressed in the ventral hippocampus correlate with regions involved in emotion and stress (amygdala and hypothalamus).
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In the citing paper
“The hippocampus is an important brain region involved in the consolidation and storage of long-term memories, cognition and emotional processing [54, 55].”
From Sex chromosomes and sex hormones differently shape microglial properties during normal physiological conditions in the adult mouse hippocampus (2025) · cites this paper as [54]
Experimental — accuracy not yet measuredIn the citing paper
“processing of sensory signals into memories in rodents involves dorsal hippocampus networks.9,10”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
In the citing paper
“In contrast, ventral hippocampus is endowed with distinct afferent/efferent connections9,11 including robust pathways to amygdala,12,13 which may enhance the emotional salience of memories.9,14”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
In the citing paper
“dorsal hippocampus primarily projects to cortical structures, whereas outflow from ventral hippocampus targets subcortical regions including amygdala and hypothalamus.9,11,13”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
In the citing paper
“Dorsal hippocampus in the rodent, and primarily CA1, has emerged as the principal location of memory encoding and processing”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
In the citing paper
“ventral hippocampus contributes to a network involved in salience and emotionality.9,10,25,117”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
In the citing paper
“Studies have shown that different parts of the hippocampus serve these different functions, with the dorsal hippocampus supporting spatial navigation learning and memory, and the ventral hippocampus as important for anxiety and stress regulation (Fanselow and Dong, 2010; Kheirbek et al., 2013).”
From Adult neurogenesis, glia, and the extracellular matrix (2019) · cites this paper as Fanselow and Dong, 2010
In the citing paper
“a region that is considered analogous to the vHIP in rodents (22).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [22]
In the citing paper
“The vHIP was analyzed separately as it is functionally distinct from the dHIP and has been implicated in anxiety regulation (22).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [22]
In the citing paper
“We observed selective and robust YFP expression in CA2 PNs throughout dorsal hippocampus9-11”
From The hippocampal CA2 region is essential for social memory (2014) · cites this paper as [11]
In the citing paper
“with ventral/temporal portions more involved in anxiety and emotional processing, and dorsal/septal portions more involved in learning and memory [41].”
From An emerging circuit pharmacology of GABAA receptors (2018) · cites this paper as [41]
In the citing paper
“The dorsal and ventral hippocampus exhibit functional heterogeneity”
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 Fanselow and Dong, 2010
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Citations
Cites
LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS
Scoville, W. B., & Milner, B. (1957) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.20.1.11 · Cited by 7,322
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
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376
Gray, J. A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00013066 · Cited by 4,477
Paxinos, G. (1985) · Cited by 3,715
The psychology of fear and stress
(1988) · Choice Reviews Online · doi:10.5860/choice.26-2399 · Cited by 3,133
Hypothalamic regulation of sleep and circadian rhythms
Saper, C. B., Scammell, T. E., & Lu, J. (2005) · Nature · doi:10.1038/nature04284 · Cited by 2,804
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
Self-citationRemembrance of places passed: Spatial memory in rats.
Olton, D. S., & Samuelson, R. J. (1976) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.2.2.97 · Cited by 1,993
de Nó, R. L. (1934) · Cited by 1,974
Taube, J., Muller, R., & Ranck, J. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00420.1990 · Cited by 1,809
JACOBSON, L., & SAPOLSKY, R. (1991) · Endocrine Reviews · doi:10.1210/edrv-12-2-118 · Cited by 1,739
Swanson, L. W., & Cowan, W. M. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901720104 · Cited by 1,592
Anatomical analysis of afferent projections to the medial prefrontal cortex in the rat
Hoover, W. B., & Vertes, R. P. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0150-4 · Cited by 1,365
Limbic system mechanisms of stress regulation: Hypothalamo-pituitary-adrenocortical axis
Herman, J. P., Ostrander, M. M., Mueller, N. K., & Figueiredo, H. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.08.006 · Cited by 1,322
Knowing Where and Getting There: A Human Navigation Network
Maguire, E. A., Burgess, N., Donnett, J. G., Frackowiak, R. S. J., Frith, C. D., & O'Keefe, J. (1998) · Science · doi:10.1126/science.280.5365.921 · Cited by 1,303
Theta rhythms coordinate hippocampal-prefrontal interactions in a spatial memory task
Jones, M. W., & Wilson, M. A. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030402 · Cited by 1,036
Pitkänen, A., Pikkarainen, M., Nurminen, N., & Ylinen, A. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06738.x · Cited by 1,001
The Involvement of the Anterior Cingulate Cortex in Remote Contextual Fear Memory
Frankland, P. W., Bontempi, B., Talton, L. E., Kaczmarek, L., & Silva, A. J. (2004) · Science · doi:10.1126/science.1094804 · Cited by 1,001
The Head Direction Signal: Origins and Sensory-Motor Integration
Taube, J. S. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112854 · Cited by 969
Spatial learning with a minislab in the dorsal hippocampus.
Moser, M., Moser, E. I., Forrest, E., Andersen, P. N., & Morris, R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.21.9697 · Cited by 944
Reduced fear expression after lesions of the ventral hippocampus
Kjelstrup, K. G., Tuvnes, F. A., Steffenach, H.-A., Murison, R., Moser, E. I., & Moser, M.-B. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152112399 · Cited by 912
Organization of intrahippocampal projections originating from CA3 pyramidal cells in the rat
Ishizuka, N., Weber, J., & Amaral, D. G. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902950407 · Cited by 899
Cerebral hemisphere regulation of motivated behavior
Swanson, L. W. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02905-x · Cited by 846
Comparison of spatial firing characteristics of units in dorsal and ventral hippocampus of the rat
Jung, M. W., Wiener, S. I., & McNaughton, B. L. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07347.1994 · Cited by 844
Hikosaka, O., & Wurtz, R. H. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1285 · Cited by 811
Finite scale of spatial representation in the hippocampus
Kjelstrup, K. B., Solstad, T., Brun, V. H., Hafting, T., Leutgeb, S., Witter, M. P., Moser, E. I., & Moser, M.-B. (2008) · Science · doi:10.1126/science.1157086 · Cited by 760
Contextual fear, gestalt memories, and the hippocampus
Fanselow, M. S. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00186-2 · Cited by 752
Self-citationCorticostriatal-hypothalamic circuitry and food motivation: Integration of energy, action and reward
Kelley, A. E., Baldo, B. A., Pratt, W. E., & Will, M. J. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.08.066 · Cited by 752
The olfactory bulbectomised rat as a model of depression
Song, C., & Leonard, B. E. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.03.010 · Cited by 730
Topography of projections from amygdala to bed nuclei of the stria terminalis
Dong, H.-W., Petrovich, G. D., & Swanson, L. W. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00079-0 · Cited by 714
Self-citation(1997) · Neuroscience · doi:10.1016/s0306-4522(97)00239-x · Cited by 707
An autoradiographic study of the organization of intrahippocampal association pathways in the rat
Swanson, L. W., Wyss, J. M., & Cowan, W. M. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901810402 · Cited by 704
The brain and the stress axis: the neural correlates of cortisol regulation in response to stress
Dedovic, K., Duchesne, A., Andrews, J., Engert, V., & Pruessner, J. C. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.074 · Cited by 699
The Neuroscience of Mammalian Associative Learning
Fanselow, M. S., & Poulos, A. M. (2005) · Annual Review of Psychology · doi:10.1146/annurev.psych.56.091103.070213 · Cited by 683
Self-citationWatts, A. G., Swanson, L. W., & Sanchez‐Watts, G. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902580204 · Cited by 678
Combinatorial amygdalar inputs to hippocampal domains and hypothalamic behavior systems
Petrovich, G. D., Canteras, N. S., & Swanson, L. W. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00080-7 · Cited by 662
Recalling Routes around London: Activation of the Right Hippocampus in Taxi Drivers
Maguire, E. A., Frackowiak, R. S. J., & Frith, C. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-18-07103.1997 · Cited by 655
Cenquizca, L. A., & Swanson, L. W. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.05.002 · Cited by 640
Factors governing one-trial contextual conditioning
Fanselow, M. S. (1990) · Animal Learning & Behavior · doi:10.3758/bf03205285 · Cited by 564
Self-citationThe Influence of Stress Hormones on Fear Circuitry
Rodrigues, S. M., LeDoux, J. E., & Sapolsky, R. M. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135620 · Cited by 556
Do septal neurons pace the hippocampal theta rhythm?
Stewart, M., & Fox, S. E. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90040-h · Cited by 552
"Psychic blindness" and other symptoms following bilateral temporal lobectomy in Rhesus monkeys.
Klüver, H., & Bucy, P. C. (1937) · American Journal of Physiology-Legacy Content · Cited by 545
Cullinan, W. E., Herman, J. P., & Watson, S. J. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903320102 · Cited by 541
Cortical connections between rat cingulate cortex and visual, motor, and postsubicular cortices
Vogt, B. A., & Miller, M. W. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902160207 · Cited by 528
Dong, H., Petrovich, G. D., Watts, A. G., & Swanson, L. W. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1079 · Cited by 521 · cited 5×
“…disorders (such as depression, anxiety, and PTSD), because the latter is the only known cerebral structure that sends direct projections to innervate CRH neuroendocrine neurons in the hypothalamic paraventricular nucleus (PVH) (Cullinan et al., 1993; Dong et al., 2001b; Dong and Swanson, 2006).”
BackgroundInfluentialSelf-citationThe Parahippocampal Region: Corticocortical Connectivity
Burwell, R. D. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06717.x · Cited by 513
Synaptic plasticity in the basolateral amygdala induced by hippocampal formation stimulation in vivo
Maren, S., & Fanselow (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-11-07548.1995 · Cited by 499
Macaque monkey retrosplenial cortex: III. Cortical efferents
Kobayashi, Y., & Amaral, D. G. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21346 · Cited by 487
Witter, M. P., & Amaral, D. G. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903070308 · Cited by 480
Structural Evidence for Functional Domains in the Rat Hippocampus
Risold, P., & Swanson, L. W. (1996) · Science · doi:10.1126/science.272.5267.1484 · Cited by 451
Groenewegen, H. J., & Russchen, F. T. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902230303 · Cited by 447
Connections of the retrosplenial granular a cortex in the rat
van Groen, T., & Wyss, J. M. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903000412 · Cited by 419
Bernard, J. F., Alden, M., & Besson, J. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903290205 · Cited by 411
Mogenson, G. J., Swanson, L. W., & Wu, M. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-01-00189.1983 · Cited by 410
Genomic anatomy of the hippocampus
Thompson, C. L., Pathak, S. D., Jeromin, A., Ng, L. L., MacPherson, C. R., Mortrud, M. T., Cusick, A., Riley, Z. L., Sunkin, S. M., Bernard, A., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.12.008 · Cited by 403
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 · Cited by 397
Choi, D. C., Furay, A. R., Evanson, N. K., Ostrander, M. M., Ulrich-Lai, Y. M., & Herman, J. P. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4301-06.2007 · Cited by 392
The Temporal Lobe and Limbic System
GLOOR, P. (1997) · Medical Entomology and Zoology · Cited by 391
The hippocampus as a cognitive graph.
Muller, R. U., Stead, M., & Pach, J. (1996) · The Journal of general physiology · doi:10.1085/jgp.107.6.663 · Cited by 391
Connections between the retrosplenial cortex and the hippocampal formation in the rat: A review
Wyss, J. M., & van Groen, T. (1992) · Hippocampus · doi:10.1002/hipo.450020102 · Cited by 382
Topographical organization of the entorhinal projection to the dentate gyrus of the monkey
Witter, M., Hoesen, G. W. V., & Amaral, D. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-01-00216.1989 · Cited by 380
Thoughts, behaviour, and brain dynamics during navigation in the real world
Spiers, H. J., & Maguire, E. A. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.037 · Cited by 371
Genomic–anatomic evidence for distinct functional domains in hippocampal field CA1
Dong, H., Swanson, L. W., Chen, L., Fanselow, M. S., & Toga, A. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812608106 · Cited by 361
Self-citationWitter, M. P., & Amaral, D. G. (2004) · Elsevier eBooks · doi:10.1016/b978-012547638-6/50022-5 · Cited by 361
Risold, P., Thompson, R. H., & Swanson, L. W. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00007-6 · Cited by 356
Kelley, A. E., Baldo, B. A., & Pratt, W. E. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20769 · Cited by 352
Vertes, R. P., Hoover, W. B., Szigeti‐Buck, K., & Léránth, C. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.12.002 · Cited by 345
Chapter 29 The nucleus accumbens: gateway for limbic structures to reach the motor system?
Groenewegen, H. J., Wright, C. I., & Beijer, A. V. J. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)61883-x · Cited by 344
Swanson, L. W., & Köhler, C. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-10-03010.1986 · Cited by 340
Navigation around London by a taxi driver with bilateral hippocampal lesions
Maguire, E. A., Nannery, R., & Spiers, H. J. (2006) · Brain · doi:10.1093/brain/awl286 · Cited by 335
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 334
Walker, D. L., Miles, L. A., & Davis, M. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.06.022 · Cited by 331
Fanselow, M. S. (1986) · Learning and Motivation · doi:10.1016/0023-9690(86)90018-4 · Cited by 326
Self-citationNeural connections of the posteromedial cortex in the macaque
Parvizi, J., Hoesen, G. W. V., Buckwalter, J. A., V, & Damásio, A. R. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507729103 · Cited by 312
Hippocampo-Hypothalamic Connections: Origin in Subicular Cortex, Not Ammon's Horn
Swanson, L. W., & Cowan, W. M. (1975) · Science · doi:10.1126/science.49928 · Cited by 305
Neuronal Mechanisms of the Orienting Reflex
Stern, J. A. (1976) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-197611000-00016 · Cited by 305
Trace but not delay fear conditioning requires attention and the anterior cingulate cortex
Han, C. J., O'Tuathaigh, C. M., van Trigt, L., Quinn, J. J., Fanselow, M. S., Mongeau, R., Koch, C., & Anderson, D. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2132313100 · Cited by 302
Self-citationConnections of the retrosplenial granular b cortex in the rat
van Groen, T., & Wyss, J. M. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10757 · Cited by 297
Dong, H.-W., & Swanson, L. W. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20788 · Cited by 290
Self-citationNaber, P. A., Lopes, F. H. D. S., & Witter, M. P. (2001) · Hippocampus · doi:10.1002/hipo.1028 · Cited by 286
Maren, S., & Holt, W. G. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.97 · Cited by 280
Pothuizen, H. H. J., Zhang, W., Jongen‐Rêlo, A. L., Feldon, J., & Yee, B. K. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03170.x · Cited by 274
Connections of the posterior nucleus of the amygdala
Canteras, N. S., Simerly, R. B., & Swanson, L. W. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903240203 · Cited by 273
Organization of CA1 projections to the subiculum: A PHA‐L analysis in the rat
Amaral, D. G., Dolorfo, C. L., & Alvarez‐Royo, P. (1991) · Hippocampus · doi:10.1002/hipo.450010410 · Cited by 272
The connections of presubiculum and parasubiculum in the rat
van Groen, T., & Wyss, J. M. (1990) · Brain Research · doi:10.1016/0006-8993(90)90976-i · Cited by 269
Haglund, L., Swanson, L. W., & Köhler, C. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902290204 · Cited by 264
Tracking the emergence of conceptual knowledge during human decision making
Kumaran, D., Summerfield, J. J., Hassabis, D., & Maguire, E. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.030 · Cited by 260
(1975) · Medical Entomology and Zoology · Cited by 252
Regional analysis of hippocampal activation during memory encoding and retrieval: fMRI study
Greicius, M. D., Krasnow, B., Anderson, J. M. B., D, S. E. M., Schatzberg, A. F., Reiss, A. L., & Menon, V. (2002) · Hippocampus · doi:10.1002/hipo.10064 · Cited by 229
Allen reference atlas : a digital color brain atlas of the C57Black/6J male mouse
Dong, H. (2008) · Wiley eBooks · Cited by 228
Self-citationTamamaki, N., & Nojyo, Y. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903530306 · Cited by 225
Saunders, R. C., Rosene, D. L., & Hoesen, G. W. V. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902710203 · Cited by 206
Dorsal/ventral hippocampus, fornix, and conditioned place preference
Ferbinteanu, J., & McDonald, R. J. (2001) · Hippocampus · doi:10.1002/hipo.1036 · Cited by 204
From Rapid Place Learning to Behavioral Performance: A Key Role for the Intermediate Hippocampus
Bast, T., Wilson, I. A., Witter, M. P., & Morris, R. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000089 · Cited by 204
Roberts, A., Tomic, D. L., Parkinson, C. H., Roeling, T. A. P., Cutter, D. J., Robbins, T. W., & Everitt, B. J. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21300 · Cited by 188
Distinct opioid circuits determine the palatability and the desirability of rewarding events
Wassum, K. M., Ostlund, S. B., Maidment, N. T., & Balleine, B. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905874106 · Cited by 182
Witter, M. P., & Groenewegen, H. J. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902240305 · Cited by 178
Sutherland, R. J., McDonald, R. J., & Savage, D. D. (1997) · Hippocampus · doi:10.1002/(sici)1098-1063(1997)7:2 · Cited by 178
Dorsal hippocampus NMDA receptors differentially mediate trace and contextual fear conditioning
Quinn, J. J., Loya, F., Ma, Q. D., & Fanselow, M. S. (2005) · Hippocampus · doi:10.1002/hipo.20088 · Cited by 175
Self-citationSultan, F. R., & Bower, J. M. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980413)393:3 · Cited by 170
The role of hippocampus in the pathophysiology of bipolar disorder
Frey, B. N., Andreazza, A. C., Nery, F. G., Martins, M. R., Quevedo, J., Soares, J. C., & Kapczinski, F. (2007) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e3282df3cde · Cited by 162
Bast, T. (2007) · Reviews in the Neurosciences · doi:10.1515/revneuro.2007.18.3-4.253 · Cited by 159
Analysis of direct hippocampal cortical field CA1 axonal projections to diencephalon in the rat
Cenquizca, L. A., & Swanson, L. W. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20985 · Cited by 157
Reduced posterior hippocampal volume in posttraumatic stress disorder
Bonne, O., Vythilingam, M., Inagaki, M., Wood, S., Neumeister, A., Nugent, A. C., Snow, J., Luckenbaugh, D. A., Bain, E. E., Drevets, W. C., et al. (2008) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v69n0707 · Cited by 156
Hunsaker, M. R., & Kesner, R. P. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.08.016 · Cited by 156
Contributions of postrhinal and perirhinal cortex to contextual information processing.
Bucci, D. J., Phillips, R. G., & Burwell, R. D. (2021) · Behavioral Neuroscience · doi:10.1037/bne0000436 · Cited by 154
Hippocampal pathway to the amygdala and stress ulcer development.
Henke, P. G. (1990) · Brain Research Bulletin · doi:10.1016/0361-9230(90)90044-z · Cited by 153
Rudy, J. W., & Matus-Amat, P. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.1.154 · Cited by 153
Hippocampal Lesion Prevents Spatial Relational Learning in Adult Macaque Monkeys
Lavenex, P. B., Amaral, D. G., & Lavenex, P. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5412-05.2006 · Cited by 153
Malin, E. L., & McGaugh, J. L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510890103 · Cited by 151
Kishi, T., Tsumori, T., Yokota, S., & Yasui, Y. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20919 · Cited by 150
Barrientos, R. M., O’Reilly, R. C., & Rudy, J. W. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00045-1 · Cited by 147
Contributions of postrhinal and perirhinal cortex to contextual information processing.
Bucci, D. J., Phillips, R. G., & Burwell, R. D. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.5.882 · Cited by 147
Chapter 4 The subiculum: cytoarchitectonically a simple structure, but hodologically complex
Witter, M. P., & Groenewegen, H. J. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61240-6 · Cited by 145
Laminar organization of the pyramidal cell layer of the subiculum in the rat
Ishizuka, N. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1195 · Cited by 144
Zhang, W. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00256-x · Cited by 137
Prevention of stress-induced morphological and cognitive consequences
McEwen, B. S., Conrad, C. D., Kuroda, Y., Frankfurt, M., Magariños, A. M., & McKittrick, C. R. (1997) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(97)00064-3 · Cited by 137
Contributions of postrhinal and perirhinal cortex to contextual information processing.
Bucci, D. J., Phillips, R. G., & Burwell, R. D. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.5.882 · Cited by 136
Pandi-Perumal, S. R., Moscovitch, A., Srinivasan, V., Spence, D. W., Cardinali, D. P., & Brown, G. M. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.04.007 · Cited by 132
Gaykema, R. P. A., van der Kuil, J., Hersh, L. B., & Luiten, P. G. M. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90299-4 · Cited by 131
SUZUKI, W. A., & Amaral, D. G. (1990) · Neuroscience Letters · doi:10.1016/0304-3940(90)90515-b · Cited by 127
Hunsaker, M. R., Fieldsted, P. M., Rosenberg, J. S., & Kesner, R. P. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.3.643 · Cited by 127
Both dorsal and ventral hippocampus contribute to spatial learning in Long–Evans rats
Ferbinteanu, J., Ray, C. A., & McDonald, R. J. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00473-7 · Cited by 127
Klur, S., Muller, C., de Vasconcelos, A. P., Ballard, T. M., Lopez, J., Galani, R., Certa, U., & Cassel, J. (2009) · Hippocampus · doi:10.1002/hipo.20562 · Cited by 126
Perirhinal and Postrhinal Contributions to Remote Memory for Context
Burwell, R. D., Bucci, D. J., Sanborn, M. R., & Jutras, M. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3781-04.2004 · Cited by 124
Groen, T. V., van Haren, F. J., Witter, M. P., & Groenewegen, H. J. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902500407 · Cited by 109
The Temporal Lobe and Limbic System.
MacLean, P. D. (1998) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-199811000-00015 · Cited by 108
Swanson, C. J., & Kalivas, P. W. (2000) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)35306-6 · Cited by 108
Choi, D. C., Evanson, N. K., Furay, A. R., Ulrich‐Lai, Y. M., Ostrander, M. M., & Herman, J. P. (2007) · Endocrinology · doi:10.1210/en.2007-0883 · Cited by 106
Kloosterman, F., van Haeften, T., Witter, M. P., & Lopes, F. H. D. S. (2003) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2003.03046.x · Cited by 105
Exploration and visualization of gene expression with neuroanatomy in the adult mouse brain
Lau, C. C., Ng, L., Thompson, C. L., Pathak, D. S., Kuan, L., Jones, A., & Hawrylycz, M. (2008) · BMC Bioinformatics · doi:10.1186/1471-2105-9-153 · Cited by 102
Integration of the sensory inputs to place cells: What, where, why, and how?
Jeffery, K. J. (2007) · Hippocampus · doi:10.1002/hipo.20322 · Cited by 95
Werner, W., Hoffmann, K.-P., & Dannenberg, S. (1997) · Experimental Brain Research · doi:10.1007/pl00005691 · Cited by 94
Nadel, L., & Bohbot, V. D. (2001) · Hippocampus · doi:10.1002/1098-1063(2001)11:1 · Cited by 92
Wang, D., Noda, Y., Tsunekawa, H., Zhou, Y., Miyazaki, M., Senzaki, K., & Nabeshima, T. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.01.003 · Cited by 89
Rogers, J. L., & Kesner, R. P. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.4.852 · Cited by 65
Entorhinal cortex of the monkey: VII. Intrinsic connections
Chrobak, J. J., & Amaral, D. G. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21200 · Cited by 64
Antidepressants and Sleep: A Review
Holshoe, J. M. (2009) · Perspectives In Psychiatric Care · doi:10.1111/j.1744-6163.2009.00221.x · Cited by 55
NMDA Receptor Modulation of Incidental Learning in Pavlovian Context Conditioning.
Stote, D. L., & Fanselow, M. S. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.253 · Cited by 54
Self-citationHarker, K. T., & Whishaw, I. Q. (2004) · Hippocampus · doi:10.1002/hipo.10159 · Cited by 51
Spatial relational learning persists following neonatal hippocampal lesions in macaque monkeys
Lavenex, P., Lavenex, P. B., & Amaral, D. G. (2006) · Nature Neuroscience · doi:10.1038/nn1820 · Cited by 51
Hippocampal lesions interfere with long-trace taste aversion conditioning
Koh, M. T., Wheeler, D. S., & Gallagher, M. (2009) · Physiology & Behavior · doi:10.1016/j.physbeh.2009.04.017 · Cited by 46
McGaugh, J. L. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.5.1140 · Cited by 43
The hippocampus and Pavlovian fear conditioning: Reply to Bast et al.
Anagnostaras, S., Gale, G. D., & Fanselow, M. S. (2002) · Hippocampus · doi:10.1002/hipo.10071 · Cited by 42
Self-citationGuinard, D., Usson, Y., Guillermet, C., & Saxod, R. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980817)398:1 · Cited by 41
Chiba, T. (2000) · Neuroscience Research · doi:10.1016/s0168-0102(00)00183-8 · Cited by 37
Tokita, K., Shimura, T., Nakamura, S., Inoue, T., & Yamamoto, T. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.023 · Cited by 29
Clark, E. W., & Bernstein, I. L. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.030 · Cited by 13
Hoshino, K., Hicks, T. P., Hirano, S., & Norita, M. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000403)419:2 · Cited by 8
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
Fashena, D. (1999) · doi:10.1002/(sici)1096-9861(19990412)406:3
Research works printed but not linked: 3
- Cajal, 1901, Significación probable de las células de axón corto, Trab. Lab. Investig. Biol., 1, 151
- Kocsis, 1997, Phase relations of rhythmic neuronal firing in the supramammillary nucleus and mammillary body to the hippocampal theta activity in urethane anesthetized rats, Hippocampus, 7, 204, 10.1002/(SICI)1098-1063(1997)7:2<204::AID-HIPO7>3.0.CO;2-M · DOI
- Vertes, 1997, Brainstem-diencephalo-septohippocampal systems controlling the theta rhythm of the hippocampus, Neuroscience, 81, 893
Cited by
Sorted by citations
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Neuronal circuits for fear and anxiety
Tovote, P., Fadok, J. P., & Lüthi, A. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3945 · Cited by 1,786
Functional organization of the hippocampal longitudinal axis
Strange, B. A., Witter, M. P., Lein, E. S., & Moser, E. I. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3785 · Cited by 1,738
The contextual brain: implications for fear conditioning, extinction and psychopathology
Maren, S., Phan, K. L., & Liberzon, I. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3492 · Cited by 1,547
Long-axis specialization of the human hippocampus
Poppenk, J., Evensmoen, H. R., Moscovitch, M., & Nadel, L. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.03.005 · Cited by 1,100
Metadata
- Authors
- Fanselow, M. S., & Dong, H.-W.
- Affiliations
- University of California, Los Angeles (US)
- Corresponding author
- Fanselow, Michael S.
- Dong, Hong-Wei
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2010-01
- Volume
- 65
- Issue
- 1
- Pages
- 7-19
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC2822727
- OpenAlex
- W2051005796
- Cited by
- 3,358
- References
- 148
- Citations by year
- 2026: 187 · 2025: 215 · 2024: 220 · 2023: 242 · 2022: 246 · 2021: 286 · 2020: 248 · 2019: 235 · 2018: 234 · 2017: 202 · 2016: 193 · 2015: 196 · 2014: 210 · 2013: 165 · 2012: 141
- FWCI
- 10.23
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1293 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (MH083180, MH62122)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- hippocampus, dorsal hippocampus, ventral hippocampus, cognitive function, emotion regulation, stress, gene expression, amygdala, hypothalamus, memory, psychopathology
- MeSH terms
- Animals, Behavior, Animal, Cognition, Emotions, Gene Expression Regulation, Hippocampus, Humans, Memory, Nerve Net, Neural Pathways, Primates
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