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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-citation
Flagged first, then by citations
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
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Viard, A., Doeller, C. F., Hartley, T., Bird, C. M., & Burgess, N. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4640-10.2011 · Cited by 144
Agster, K. L., & Burwell, R. D. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.07.005 · Cited by 143
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Shi, H., Wang, S., Wang, X., Zhang, R.-X., & Zhu, L. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01020-1 · Cited by 151
Levy‐Gigi, E., Szabó, C., Kelemen, O., & Kéri, S. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.017 · Cited by 149
Maruszak, A., & Thuret, S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00095 · Cited by 147
The vagus nerve modulates BDNF expression and neurogenesis in the hippocampus
O’Leary, O. F., Ogbonnaya, E. S., Felice, D., Levone, B. R., C. Conroy, L., Fitzgerald, P., Bravo, J. A., Forsythe, P., Bienenstock, J., Dinan, T. G., et al. (2018) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2017.12.004 · Cited by 151
Morley‐Fletcher, S., Mairesse, J., Soumier, A., Banasr, M., Fagioli, F., Gabriel, C., Mocaër, E., Daszuta, A., McEwen, B. S., Nicoletti, F., et al. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2280-x · Cited by 149
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Malik, R., Li, Y., Schamiloglu, S., & Sohal, V. S. (2022) · Cell · doi:10.1016/j.cell.2022.04.001 · Cited by 142
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Murty, V. P., Tompary, A., Adcock, R. A., & Davachi, L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4032-15.2016 · Cited by 141
Floriou‐Servou, A., von Ziegler, L., Stalder, L., Sturman, O., Privitera, M., Rassi, A., Cremonesi, A., Thöny, B., & Bohacek, J. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.02.003 · Cited by 129
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Fares, J., Diab, Z. B., Nabha, S. M., & Fares, Y. (2018) · International Journal of Neuroscience · doi:10.1080/00207454.2018.1545771 · Cited by 145
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Nollet, M., Gaillard, P., Tanti, A., Girault, V., Belzung, C., & Leman, S. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.70 · Cited by 146
Schoenfeld, T. J., Rada, P., Pieruzzini, P. R., Hsueh, B., & Gould, E. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.5352-12.2013 · Cited by 138
Czéh, B., Varga, Z., Henningsen, K., Kovács, G. L., Miseta, A., & Wiborg, O. (2014) · Hippocampus · doi:10.1002/hipo.22382 · Cited by 145
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Holm, T. H., & Lykke‐Hartmann, K. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00209 · Cited by 134
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Nilakantan, A. S., Bridge, D. J., Gagnon, E. P., VanHaerents, S. A., & Voss, J. L. (2017) · Current Biology · doi:10.1016/j.cub.2016.12.042 · Cited by 136
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Aggleton, J. P., Wright, N. F., Rosene, D. L., & Saunders, R. C. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv019 · Cited by 133
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Yun, S., Reynolds, R. P., Masiulis, I., & Eisch, A. J. (2016) · Nature Medicine · doi:10.1038/nm.4218 · Cited by 136
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Chiang, M.-C., Huang, A. J. Y., Wintzer, M. E., Ohshima, T., & McHugh, T. J. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.01.019 · Cited by 133
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Initiative, A. D. N., van der Meer, D., for the Pediatric Imaging, N. A. G. S., Rokicki, J., Kaufmann, T., Córdova‐Palomera, A., Moberget, T., Alnæs, D., Bettella, F., Frei, O., et al. (2018) · Molecular Psychiatry · doi:10.1038/s41380-018-0262-7 · Cited by 126
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Barker, G. R. I., Banks, P. J., Scott, H., Ralph, G. S., Mitrophanous, K. A., Wong, L.-F., Bashir, Z. I., Uney, J. B., & Warburton, E. C. (2017) · Nature Neuroscience · doi:10.1038/nn.4472 · Cited by 124
Kim, H. (2014) · Hippocampus · doi:10.1002/hipo.22387 · Cited by 133
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Monteiro, S., Ferreira, F. M., Pinto, V., Roque, S., Morais, M., Calçada, D. D. S., Mota, C., Correia‐Neves, M., & Cerqueira, J. (2016) · Translational Psychiatry · doi:10.1038/tp.2015.194 · Cited by 133
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Kim, E. J., & Kim, J. J. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-01986-4 · Cited by 154
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Tanaka, K. F., Samuels, B. A., & Hen, R. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0038 · Cited by 124
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Gourley, S. L., Lee, A. S., Howell, J. L., Pittenger, C., & Taylor, J. R. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07438.x · Cited by 117
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Rainer, Q., Xia, L., Guilloux, J., Gabriel, C., Mocaër, E., Hen, R., Enhamre, E., Gardier, A. M., & David, D. J. P. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145711000356 · Cited by 139
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Genon, S., Bernhardt, B. C., Joie, R. L., Amunts, K., & Eickhoff, S. B. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.10.003 · Cited by 119
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Konradi, C., Zimmerman, E. I., Yang, C. K., Lohmann, K. M., Gresch, P., Pantazopoulos, H., Berretta, S., & Heckers, S. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.175 · Cited by 115
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Wells, C. E., Amos, D. P., Jeewajee, A., Douchamps, V., Rodgers, J., O'Keefe, J. M., Burgess, N., & Lever, C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5040-12.2013 · Cited by 120
Zhao, Z., Loane, D. J., Murray, M. G., Stoica, B. A., & Faden, A. I. (2012) · Journal of Neurotrauma · doi:10.1089/neu.2012.2511 · Cited by 119
Hartmann, J., Bajaj, T., Klengel, C., Chatzinakos, C., Ebert, T., Dedic, N., McCullough, K. M., Lardenoije, R., Joëls, M., Meijer, O. C., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109185 · Cited by 119
Medina, A. M., Seasholtz, A. F., Sharma, V., Burke, S., Bunney, W. E., Myers, R., Schatzberg, A. F., Akil, H., & Watson, S. J. (2012) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2012.11.002 · Cited by 125
Grady, C. L. (2019) · Hippocampus · doi:10.1002/hipo.23164 · Cited by 127
Malik, R., Dougherty, K. A., Parikh, K., Byrne, C. T., & Johnston, D. (2015) · Hippocampus · doi:10.1002/hipo.22526 · Cited by 114
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Maras, P. M., Molet, J., Chen, Y., Rice, C., Ji, S. G., Solodkin, A., & Baram, T. Z. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.12 · Cited by 118
Murthy, S., Kane, G. A., Katchur, N. J., Lara Mejia, P. S., Obiofuma, G., Buschman, T. J., McEwen, B. S., & Gould, E. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.02.021 · Cited by 118
McCormick, C. M., Thomas, C. M., Sheridan, C. S., Nixon, F., Flynn, J. A., & Zovkic, I. B. (2011) · Hippocampus · doi:10.1002/hipo.20966 · Cited by 118
Sun, Q., Li, X., Li, A., Zhang, J., Ding, Z., Gong, H., & Luo, Q. (2020) · iScience · doi:10.1016/j.isci.2020.100894 · Cited by 105
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Bravo‐Zehnder, M., Toledo, E. M., Segovia‐Miranda, F., Serrano, F. G., Benito, M. J., Metz, C., Retamal, C., Alvarez, A. R., Massardo, L., Inestrosa, N. C., et al. (2014) · Arthritis & Rheumatology · doi:10.1002/art.38900 · Cited by 116
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Aleksandrova, L. R., Wang, Y. T., & Phillips, A. G. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.07.007 · Cited by 114
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Raybuck, J. D., & Lattal, K. M. (2014) · Behavioural Processes · doi:10.1016/j.beproc.2013.08.016 · Cited by 114
Nollet, M., Gaillard, P., Minier, F., Tanti, A., Belzung, C., & Leman, S. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.04.022 · Cited by 120
Cappaert, N. L. M., van Strien, N. M., & Witter, M. P. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00020-6 · Cited by 120
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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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