The three-dimensional organization of the hippocampal formation: A review of anatomical data
Abstract
In the early 1970s, Andersen and colleagues proposed that the principal excitatory pathways of the hippocampal formation were organized in a lamellar fashion. This proposition, based heavily on the physiological studies of the proponents, indicated that "a point source of entorhinal activity projects its impulses through the four membered pathway (of the hippocampal formation) along a slice or lamella, of hippocampal tissue oriented normally to the alvear surface" [Anderson P., Bliss V.P. and Skrede K. K. (1971) Expl Brain Res. 13, 222-238] and perpendicular to the long axis of the hippocampus. Andersen et al. further suggested that, "By means of this lamellar organization, small strips of the hippocampal cortex may operate as independent functional units, although excitatory and inhibitory transverse connections may modify the behavior of neighboring lamellae." The "lamellar hypothesis" of hippocampal anatomical organization has had tremendous influence on the conceptualization of hippocampal information processing and was largely responsible for prompting the establishment of the in vitro hippocampal slice technology. While the "lamellar hypothesis" was consistent with the known neuroanatomy, subsequent neuroanatomical investigations, using a variety of modern tracing techniques, have invariably demonstrated that all of the major hippocampal projections, except for those arising from the granule cells of the dentate gyrus, are much more divergent than would be consistent with a strict interpretation of the lamellar hypothesis. This has become particularly clear in ongoing studies of the intrinsic hippocampal projections using the recently introduced anterograde tracer, Phaseolus vulgaris leucoagglutinin. Citing the conclusions from several papers dealing with the anatomical organization of the hippocampal formation and using examples from recent Phaseolus vulgaris leucoagglutinin mapping studies, the following are demonstrated. (1) That the major hippocampal projections are as extensive and highly organized in the long or septotemporal axis of the hippocampus as in the transverse axis. (2) That at least some of the hippocampal projections, such as the associational projections arising from the dentate gyrus, appear to be specifically organized to integrate distant levels of the hippocampal formation. (3) That the physiological data of Anderson et al. can be re-interpreted in the light of these new anatomical data to show how the stimulation and recording protocols used at the time would, in fact, generate the appearance of a lamellar organization. It is concluded that it is heuristically most reasonable to consider the hippocampal formation as a three-dimensional cortical region with important information processing taking place in both the transverse and long axes.(ABSTRACT TRUNCATED AT 400 WORDS)
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In rodents, the hippocampal formation system consists of several structures connected within a loop: entorhinal cortex, dentate gyrus, CA3, CA1, and subiculum, with specified inputs and outputs.
“In rodents, this system consists of several structures connected within a loop that encompasses (Figure 9) the entorhinal cortex (EC), with inputs from higher sensory cortices; dentate gyrus (DG), with inputs from EC; CA3, with 'external' inputs from EC and DG and 'internal' inputs from CA3; CA1, with inputs from CA3 and EC; and subiculum(SUB), with inputs from CA1 and outputs to EC (Lorente de No”
From The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory. (1996) · cites this paper as Amaral and Witter, 1989
Evidence from neuroanatomical studies of individuals with depression and suicidal behaviour have demonstrated changes in density of glutamatergic neurons and glial cells, and the volume of the hippocampus.
“Evidence from neuroanatomical studies of individuals with depression and suicidal behaviour have demonstrated changes in density of glutamatergic neurons and glial cells 161,162 , and the volume 163 of the hippocampus, which relies on excitatory neurotransmission via glutamatergic signalling and is involved in learning and memory 164 .”
From Suicide and suicide risk (2019) · cites this paper as [164]
Cited by
Sorted by citations
Genome-wide atlas of gene expression in the adult mouse brain
Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A., Boe, A. F., Boguski, M. S., Brockway, K. S., Byrnes, E. J., et al. (2007) · Nature · doi:10.1038/nature05453 · Cited by 5,572 · see citing works
Theta oscillations in the hippocampus
Buzsáki, G. (2002) · Neuron · doi:10.1016/s0896-6273(02)00586-x · Cited by 3,332 · see citing works
Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning
Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759 · see citing works
The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory.
Tsien, J. Z., Huerta, P. T., & Tonegawa, S. (1996) · Cell · doi:10.1016/s0092-8674(00)81827-9 · Cited by 1,782 · see citing works
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 · see citing works
Self-citationRegional dissociations within the hippocampus-memory and anxiety
Bannerman, D. M., Rawlins, J. N. P., McHugh, S. B., Deacon, R. M. J., Yee, B. K., Bast, T., Zhang, W.-N., Pothuizen, H. H. J., & Feldon, J. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.03.004 · Cited by 1,462 · see citing works
Hippocampal BDNF mediates the efficacy of exercise on synaptic plasticity and cognition
Vaynman, S., Ying, Z., & Gomez‐Pinilla, F. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03720.x · Cited by 1,460 · see citing works
Life and Death of Neurons in the Aging Brain
Morrison, J. H., & Hof, P. R. (1997) · Science · doi:10.1126/science.278.5337.412 · Cited by 1,344 · see citing works
Adult hippocampal neurogenesis in depression
Sahay, A., & Hen, R. (2007) · Nature Neuroscience · doi:10.1038/nn1969 · Cited by 1,206 · see citing works
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 · see citing works
The Hippocampus, Memory, and Place Cells
Eichenbaum, H., Dudchenko, P., Wood, E., Shapiro, M., & Tanila, H. (1999) · Neuron · doi:10.1016/s0896-6273(00)80773-4 · Cited by 1,064 · see citing works
Turecki, G., Brent, D. A., Gunnell, D., O’Connor, R. C., Oquendo, M. A., Pirkis, J., & Stanley, B. H. (2019) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0121-0 · Cited by 1,074 · see citing works
Megı́as, M., Emri, Z., Freund, T. F., & Gulyás, A. I. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00496-6 · Cited by 950 · see citing works
Adult neurogenesis: from precursors to network and physiology
Abrous, D. N., Koehl, M., & Le Moal, M. (2005) · Physiological Reviews · doi:10.1152/physrev.00055.2003 · Cited by 971 · see citing works
The dentate gyrus: fundamental neuroanatomical organization (dentate gyrus for dummies)
Amaral, D. G., Scharfman, H. E., & Lavenex, P. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63001-5 · Cited by 888 · see citing works
Self-citationThe hippocampus—what does it do?
Eichenbaum, H., Otto, T., & Cohen, N. J. (1992) · Behavioral and Neural Biology · doi:10.1016/0163-1047(92)90724-i · Cited by 867 · see citing works
Synaptic alterations in CA1 in mild Alzheimer disease and mild cognitive impairment
Scheff, S. W., Price, D. A., Schmitt, F. A., DeKosky, S. T., & Mufson, E. J. (2007) · Neurology · doi:10.1212/01.wnl.0000260698.46517.8f · Cited by 824 · see citing works
GABAergic Cells Are the Major Postsynaptic Targets of Mossy Fibers in the Rat Hippocampus
Acsády, L., Kamondi, A., Sı́k, A., Freund, T., & Buzsáki, G. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-09-03386.1998 · Cited by 741 · see citing works
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 · see citing works
Self-citationMizuseki, K., Sirota, A., Pastalkova, E., & Buzsáki, G. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.037 · Cited by 718 · see citing works
Connections of the rat lateral septal complex 1Published on the World Wide Web on 2 June 1997. 1
Risold, P. Y., & Swanson, L. W. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00009-x · Cited by 671 · see citing works
Antidepressants increase neural progenitor cells in the human hippocampus
Boldrini, M., Underwood, M. D., Hen, R., Rosoklija, G. B., Dwork, A. J., John Mann, J., & Arango, V. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.75 · Cited by 686 · see citing works
Hippocampal CA1 interneurons: an in vivo intracellular labeling study
Sik, A., Penttonen, M., Ylinen, A., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06651.1995 · Cited by 669 · see citing works
NMDA receptors, place cells and hippocampal spatial memory
Nakazawa, K., McHugh, T. J., Wilson, M. A., & Tonegawa, S. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1385 · Cited by 619 · see citing works
Place cells and place recognition maintained by direct entorhinal-hippocampal circuitry
Brun, V. H., Otnæss, M. K., Molden, S., Steffenach, H.-A., Witter, M. P., Moser, M.-B., & Moser, E. I. (2002) · Science · doi:10.1126/science.1071089 · Cited by 606 · see citing works
Self-citationAnatomical organization of the parahippocampal-hippocampal network
WITTER, M. P., WOUTERLOOD, F. G., NABER, P. A., & VAN HAEFTEN, T. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06716.x · Cited by 567 · see citing works
Self-citationThe mechanisms for pattern completion and pattern separation in the hippocampus
Rolls, E. T. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00074 · Cited by 545 · see citing works
Cell type–specific genetic and optogenetic tools reveal hippocampal CA2 circuits
Kohara, K., Pignatelli, M., Rivest, A. J., Jung, H.-Y., Kitamura, T., Suh, J., Frank, D., Kajikawa, K., Mise, N., Obata, Y., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3614 · Cited by 528 · see citing works
Space in the brain: How the hippocampal formation supports spatial cognition
Hartley, T., Lever, C., Burgess, N., & O'Keefe, J. (2014) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2012.0510 · Cited by 495 · see citing works
Space and Time: The Hippocampus as a Sequence Generator
Buzsáki, G., & Tingley, D. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.07.006 · Cited by 461 · see citing works
The hippocampal sharp wave-ripple in memory retrieval for immediate use and consolidation
Joo, H. R., & Frank, L. M. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0077-1 · Cited by 430 · see citing works
NMDA-dependent modulation of CA1 local circuit inhibition
Grunze, H., Rainnie, D., Hasselmo, M., Barkai, E., Hearn, E., McCarley, R., & Greene, R. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-06-02034.1996 · Cited by 467 · see citing works
Antidepressants recruit new neurons to improve stress response regulation
Surget, A., Tanti, A., Leonardo, E. D., Laugeray, A., Rainer, Q., Touma, C., Palme, R., Griebel, G., Ibarguen-Vargas, Y., Hen, R., et al. (2011) · Molecular Psychiatry · doi:10.1038/mp.2011.48 · Cited by 471 · see citing works
Gulyás, A. I., Megı́as, M., Emri, Z., & Freund, T. F. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-22-10082.1999 · Cited by 476 · see citing works
Theta Phase Segregation of Input-Specific Gamma Patterns in Entorhinal-Hippocampal Networks
Schomburg, E. W., Fernández-Ruiz, A., Mizuseki, K., Berényi, A., Anastassiou, C. A., Koch, C., & Buzsáki, G. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.051 · Cited by 465 · see citing works
Hasselmo, M., & Schnell, E. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03898.1994 · Cited by 466 · see citing works
Knierim, J. J., Neunuebel, J. P., & Deshmukh, S. S. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0369 · Cited by 425 · see citing works
Memory and MRI-based hippocampal volumes in aging and AD
Petersen, R. C., Jack, C. R., Xu, Y.-C., Waring, S. C., O’Brien, P. C., Smith, G. E., Ivnik, R. J., Tangalos, E. G., Boeve, B. F., & Kokmen, E. (2000) · Neurology · doi:10.1212/wnl.54.3.581 · Cited by 426 · see citing works
Bezaire, M. J., & Soltesz, I. (2013) · Hippocampus · doi:10.1002/hipo.22141 · Cited by 373 · see citing works
Han, Z., Buhl, E. H., Lörinczi, Z., & Somogyi, P. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00507.x · Cited by 411 · see citing works
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 · see citing works
Neuronal Diversity in GABAergic Long-Range Projections from the Hippocampus
Jinno, S., Klausberger, T., Marton, L. F., Dalezios, Y., Roberts, J. D. B., Fuentealba, P., Bushong, E. A., Henze, D., Buzsáki, G., & Somogyi, P. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1847-07.2007 · Cited by 369 · see citing works
Spatial Gene-Expression Gradients Underlie Prominent Heterogeneity of CA1 Pyramidal Neurons
Cembrowski, M. S., Bachman, J. L., Wang, L., Sugino, K., Shields, B. C., & Spruston, N. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.013 · Cited by 328 · see citing works
The evolution of episodic memory
Allen, T. A., & Fortin, N. J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301199110 · Cited by 350 · see citing works
Microglial cell population dynamics in the injured adult central nervous system
Ladeby, R., Wirenfeldt, M., Garcia-Ovejero, D., Fenger, C., Dissing-Olesen, L., Dalmau, I., & Finsen, B. (2005) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.12.009 · Cited by 334 · see citing works
Gating of hippocampal activity, plasticity, and memory by entorhinal cortex long-range inhibition
Basu, J., Zaremba, J. D., Cheung, S. K., Hitti, F. L., Zemelman, B. V., Losonczy, A., & Siegelbaum, S. A. (2016) · Science · doi:10.1126/science.aaa5694 · Cited by 274 · see citing works
Self-generated theta oscillations in the hippocampus
Goutagny, R., Jackson, J., & Williams, S. (2009) · Nature Neuroscience · doi:10.1038/nn.2440 · Cited by 301 · see citing works
Interaction between neocortical and hippocampal networks via slow oscillations
Sirota, A., & Buzsáki, G. (2005) · Thalamus and Related Systems · doi:10.1017/s1472928807000258 · Cited by 270 · see citing works
Huang, Y.-Y., Kandel, E. R., Varshavsky, L., Brandont, E. P., Qi, M., Idzerda, R. L., Stanley McKnight, G., & Bourtchouladz, R. (1995) · Cell · doi:10.1016/0092-8674(95)90146-9 · Cited by 267 · see citing works
Heterogeneity within classical cell types is the rule: lessons from hippocampal pyramidal neurons
Cembrowski, M. S., & Spruston, N. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0125-5 · Cited by 258 · see citing works
Porta, S., Xu, Y., Restrepo, C. R., Kwong, L. K., Zhang, B., Brown, H. J., Lee, E. B., Trojanowski, J. Q., & Lee, V. M.-Y. (2018) · Nature Communications · doi:10.1038/s41467-018-06548-9 · Cited by 248 · see citing works
Popov, V. I., Bocharova, L. S., & Bragin, A. G. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90336-z · Cited by 241 · see citing works
Sun, Y., Nguyen, A. Q., Nguyen, J. P., Le, L., Saur, D., Choi, J., Callaway, E. M., & Xu, X. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.02.030 · Cited by 218 · see citing works
Otto, T., & Eichenbaum, H. (1992) · Hippocampus · doi:10.1002/hipo.450020310 · Cited by 232 · see citing works
Exercise and Hippocampal Memory Systems
Voss, M. W., Soto, C., Yoo, S., Sodoma, M., Vivar, C., & van Praag, H. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.01.006 · Cited by 235 · see citing works
Pattern separation, completion, and categorisation in the hippocampus and neocortex
Rolls, E. T. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.07.008 · Cited by 234 · see citing works
Hypothalamic and other connections with dorsal CA2 area of the mouse hippocampus
Cui, Z., Gerfen, C. R., & Young, W. S. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23263 · Cited by 214 · see citing works
Morphological diversity and connectivity of hippocampal interneurons
Booker, S. A., & Vida, I. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2882-2 · Cited by 210 · see citing works
Imaging hippocampal function across the human life span: Is memory decline normal or not?
Small, S. A., Tsai, W. Y., DeLaPaz, R., Mayeux, R., & Stern, Y. (2002) · Annals of Neurology · doi:10.1002/ana.10105 · Cited by 205 · see citing works
Exercise induces BDNF and synapsin I to specific hippocampal subfields
Vaynman, S., Ying, Z., & Gómez‐Pinilla, F. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20077 · Cited by 203 · see citing works
Vida, I., Halasy, K., Szinyei, C., Somogyi, P., & Buhl, E. H. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.755bv.x · Cited by 190 · see citing works
Dudman, J. T., Tsay, D., & Siegelbaum, S. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.020 · Cited by 192 · see citing works
Spatial long-term memory is related to mossy fiber synaptogenesis
Ramı́rez-Amaya, V., Balderas, I., Sandoval, J., Escobar, M. L., & Bermúdez-Rattoni, F. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-18-07340.2001 · Cited by 177 · see citing works
Gruber, A. J., & McDonald, R. J. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00050 · Cited by 173 · see citing works
Cloning and localization of a conventional kinesin motor expressed exclusively in neurons
Niclas, J., Navone, F., Hom-Booker, N., & Vale, R. D. (1994) · Neuron · doi:10.1016/0896-6273(94)90314-x · Cited by 153 · see citing works
Running rewires the neuronal network of adult-born dentate granule cells
Vivar, C., Peterson, B. D., & van Praag, H. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.031 · Cited by 143 · see citing works
Cholinergic modulation of excitatory synaptic transmission in the CA3 area of the hippocampus
Vogt, K. E., & Regehr, W. G. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-01-00075.2001 · Cited by 149 · see citing works
Jensen, C. B., Pyke, C., Rasch, M. G., Dahl, A. B., Knudsen, L. B., & Secher, A. (2018) · Endocrinology · doi:10.1210/en.2017-00812 · Cited by 145 · see citing works
Narboux-Nême, N., Pavone, L. M., Avallone, L., Zhuang, X., & Gaspar, P. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.08.020 · Cited by 148 · see citing works
Ferraguti, F., Klausberger, T., Cobden, P., Baude, A., Roberts, J. D. B., Szucs, P., Kinoshita, A., Shigemoto, R., Somogyi, P., & Dalezios, Y. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2547-05.2005 · Cited by 137 · see citing works
Distinct roles for dorsal CA3 and CA1 in memory for sequential nonspatial events
Farovik, A., Dupont, L. M., & Eichenbaum, H. (2010) · Learning & Memory · doi:10.1101/lm.1616209 · Cited by 140 · see citing works
Donohue, H. S., Gabbott, P. L. A., Davies, H. A., Rodríguez, J. J., Cordero, M. I., Sandi, C., Medvedev, N. I., Popov, V. I., Colyer, F. M., Peddie, C. J., et al. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.02.072 · Cited by 139 · see citing works
Yang, X., Yao, C., Tian, T., Li, X., Yan, H., Wu, J., Li, H., Pei, L., Liu, D., Tian, Q., et al. (2018) · Molecular Psychiatry · doi:10.1038/mp.2016.151 · Cited by 136 · see citing works
Vervaeke, K., Gu, N., Agdestein, C., Hu, H., & Storm, J. F. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.111336 · Cited by 135 · see citing works
Basu, J., Srinivas, K. V., Cheung, S. K., Taniguchi, H., Huang, Z. J., & Siegelbaum, S. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.001 · Cited by 122 · see citing works
Patch-clamp recordings reveal powerful GABAergic inhibition in dentate hilar neurons
Soltesz, I., & Mody, I. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-04-02365.1994 · Cited by 114 · see citing works
Sharif, F., Tayebi, B., Buzsáki, G., Royer, S., & Fernandez-Ruiz, A. (2021) · Neuron · doi:10.1016/j.neuron.2020.10.034 · Cited by 111 · see citing works
Yuan, M., Meyer, T., Benkowitz, C., Savanthrapadian, S., Ansel-Bollepalli, L., Foggetti, A., Wulff, P., Alcami, P., Elgueta, C., & Bartos, M. (2017) · eLife · doi:10.7554/elife.21105 · Cited by 93 · see citing works
Hashimotodani, Y., Nasrallah, K., Jensen, K. R., Chávez, A. E., Carrera, D., & Castillo, P. E. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.028 · Cited by 104 · see citing works
Korol, S. V., Jin, Z., Babateen, O., & Birnir, B. (2015) · Diabetes · doi:10.2337/db14-0668 · Cited by 101 · see citing works
Mohandas Rao, K. G., Muddanna Rao, S., & Gurumadhva Rao, S. (2006) · Evidence-Based Complementary and Alternative Medicine · doi:10.1093/ecam/nel024 · Cited by 103 · see citing works
“The CA3 neurons also receive a significant number of intrinsic afferents from the axons of dentate granule cells and the contralateral CA3 regions (35,36).”
BackgroundMultiple Maps of the Same Spatial Context Can Stably Coexist in the Mouse Hippocampus
Sheintuch, L., Geva, N., Baumer, H., Rechavi, Y., Rubin, A., & Ziv, Y. (2020) · Current Biology · doi:10.1016/j.cub.2020.02.018 · Cited by 88 · see citing works
Hashimotodani, Y., Karube, F., Yanagawa, Y., Fujiyama, F., & Kano, M. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.11.016 · Cited by 92 · see citing works
Hagiwara, A., Fukazawa, Y., Deguchi‐Tawarada, M., Ohtsuka, T., & Shigemoto, R. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20633 · Cited by 90 · see citing works
Herold, C., Coppola, V. J., & Bingman, V. P. (2015) · Hippocampus · doi:10.1002/hipo.22463 · Cited by 84 · see citing works
Lenck-Santini, P.-P., Rivard, B., Muller, R. U., & Poucet, B. (2005) · Hippocampus · doi:10.1002/hipo.20060 · Cited by 81 · see citing works
Wang, J. X., Cohen, N. J., & Voss, J. L. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.04.003 · Cited by 75 · see citing works
Trongnetrpunya, A., Nandi, B., Kang, D., Kocsis, B., Schroeder, C. E., & Ding, M. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00189 · Cited by 75 · see citing works
Effects of repeated stress on excitatory drive of basal amygdala neurons in vivo
Padival, M., Quinette, D., & Rosenkranz, J. A. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.74 · Cited by 75 · see citing works
Hippocampal volume reduction in 22q11.2 deletion syndrome
Debbané, M., Schaer, M., Farhoumand, R., Glaser, B., & Eliez, S. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.05.006 · Cited by 69 · see citing works
Plasticity in the Hippocampus, Neurogenesis and Drugs of Abuse
Avchalumov, Y., & Mandyam, C. D. (2021) · Brain Sciences · doi:10.3390/brainsci11030404 · Cited by 49 · see citing works
Katona, L., Micklem, B., Borhegyi, Z., Swiejkowski, D. A., Valenti, O., Viney, T. J., Kotzadimitriou, D., Klausberger, T., & Somogyi, P. (2017) · Hippocampus · doi:10.1002/hipo.22696 · Cited by 50 · see citing works
Chawla, M. K., Sutherland, V. L., Olson, K., McNaughton, B. L., & Barnes, C. A. (2018) · Hippocampus · doi:10.1002/hipo.22820 · Cited by 49 · see citing works
Beer, Z., Vavra, P., Atucha, E., Rentzing, K., Heinze, H.-J., & Sauvage, M. M. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2006100 · Cited by 44 · see citing works
Pennartz, C. M. A., Oude Lohuis, M. N., & Olcese, U. (2023) · Philosophical Transactions of the Royal Society B · doi:10.1098/rstb.2022.0336 · Cited by 38 · see citing works
Hoang, T., Aliane, V., & Manahan‐Vaughan, D. (2018) · Hippocampus · doi:10.1002/hipo.22833 · Cited by 37 · see citing works
Fujisawa, S., Matsuki, N., & Ikegaya, Y. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.066639 · Cited by 36 · see citing works
Eagleson, K. L., Milner, T. A., Xie, Z., & Levitt, P. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23343 · Cited by 32 · see citing works
Romani, A., Antonietti, A., Bella, D., Budd, J., Giacalone, E., Kurban, K., Sáray, S., Abdellah, M., Arnaudon, A., Boci, E., et al. (2024) · PLOS Biology · doi:10.1371/journal.pbio.3002861 · Cited by 39 · see citing works
Bello-Medina, P. C., Prado-Alcalá, R. A., & Rivas-Arancibia, S. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.01.018 · Cited by 29 · see citing works
- Authors
- Amaral, D. G., & Witter, M. P.
- Affiliations
- Salk Institute for Biological Studies (US)
- Vrije Universiteit Amsterdam (NL)
- Corresponding author
- Amaral, D.G.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 1989-01
- Volume
- 31
- Issue
- 3
- Pages
- 571-591
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W2142925815
- Cited by
- 2,180
- References
- 0
- Citations by year
- 2026: 49 · 2025: 64 · 2024: 56 · 2023: 52 · 2022: 69 · 2021: 92 · 2020: 57 · 2019: 81 · 2018: 80 · 2017: 69 · 2016: 57 · 2015: 76 · 2014: 82 · 2013: 80 · 2012: 61
- FWCI
- 5.75
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (NS 16980)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- hippocampal formation, hippocampal projections, entorhinal cortex, dentate gyrus, Phaseolus vulgaris leucoagglutinin, anterograde tracing, septotemporal axis, hippocampal slices
- MeSH terms
- Animals, Hippocampus, 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