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The three-dimensional organization of the hippocampal formation: A review of anatomical data

Amaral, D.G., Witter, M.P.·1989·Neuroscience

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)

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  1. Amaral, 1978, A Golgi study of the cell types in the hilar region of the hippocampus in the rat, J. comp. Neurol., 182, 851, 10.1002/cne.901820508 · DOI
  2. Andersen, 1971, Lamellar organization of hippocampal excitatory pathways, Expl Brain Res., 13, 222, 10.1007/BF00234087 · DOI
  3. Bakst, 1986, An experimental analysis of the origins of the somatostatin immunoreactive fibers in the dentate gyrus of the rat, J. Neurosci., 6, 1452, 10.1523/JNEUROSCI.06-05-01452.1986 · DOI
  4. Beckstead, 1978, Afferent connections of the entorhinal area in the rat as demonstrated by retrograde cell-labeling with horseradish peroxidase, Brain Res., 152, 249, 10.1016/0006-8993(78)90254-8 · DOI
  5. Blackstad, 1956, Commissural connections of the hippocampal region in the rat, with special reference to their mode of termination, J. comp. Neurol., 105, 417, 10.1002/cne.901050305 · DOI
  6. Blackstad, 1958, On the termination of some afferents to the hippocampus and fascia dentata. An experimental study in the rat, Acta Anat., 35, 202, 10.1159/000141409 · DOI
  7. Blackstad, 1970, Distribution of hippocampal mossy fibers in the rat. An experimental study with silver impregnation methods, J. comp. Neurol., 138, 433, 10.1002/cne.901380404 · DOI
  8. Claiborne, 1986, A light and electron microscopic analysis of the mossy fibers of the rat dentate gyrus, J. comp. Neurol., 246, 435, 10.1002/cne.902460403 · DOI
  9. Cowan, 1972, The autoradiographic demonstration of axonal connections in the central nervous system, Brain Res., 37, 21, 10.1016/0006-8993(72)90344-7 · DOI
  10. Finch, 1981, Demonstration of caudally directed hippocampal efferents in the rat by intracellular injection of horseradish peroxidase, Brain Res., 214, 405, 10.1016/0006-8993(81)91203-8 · DOI
  11. Finch, 1983, Demonstration of axonal projections of neurons in the rat hippocampus and subiculum by intracellular injection by HRP, Brain Res., 271, 201, 10.1016/0006-8993(83)90283-4 · DOI
  12. Gaarskjaer, 1978, Organization of the mossy fiber system of the rat studied in extended hippocampi. I. Terminal area related to number of granule and pyramidal cells, J. comp. Neurol., 178, 49, 10.1002/cne.901780104 · DOI
  13. Gaarskjaer, 1986, The organization and development of the hippocampal mossy fiber system, Brain Res., 396, 335, 10.1016/0165-0173(86)90004-4 · DOI
  14. Gerfen, 1984, An anterograde neuroanatomical tracing method that shows the detailed morphology of neurons, their axons and terminals: immunohistochemical localization of an axonally transported plant lectin,Phaseolus vulgaris Leucoagglutinin (PHA-L), Brain Res., 290, 219, 10.1016/0006-8993(84)90940-5 · DOI
  15. Hjorth-Simonsen, 1973, Some intrinsic connections of the hippocampus in the rat: an experimental analysis, J. comp. Neurol., 147, 145, 10.1002/cne.901470202 · DOI
  16. Hjorth-Simonsen, 1972, Origin and termination of the hippocampal perforant path in the rat studied by silver impregnation, J. comp. Neurol., 144, 215, 10.1002/cne.901440206 · DOI
  17. Hjorth-Simonsen, 1977, Commissural connections of the dentate area of the rat, J. comp. Neurol., 174, 591, 10.1002/cne.901740404 · DOI
  18. Kohler, 1985, Intrinsic projections of the retrohippocampal region in the rat brain. I. The subicular complex, J. comp. Neurol., 236, 504, 10.1002/cne.902360407 · DOI
  19. Kohler, 1986, Intrinsic connections of the retrohippocampal region in the rat brain. II. The medial entorhinal cortex, J. comp. Neurol., 246, 149, 10.1002/cne.902460202 · DOI
  20. Kohler, 1988, Intrinsic connections of the retrohippocampal region in the rat brain. III. The lateral entorhinal area, J. comp. Neurol., 271, 208, 10.1002/cne.902710204 · DOI
  21. Kohler, 1978, Some retrohippocampal afferents to the entorhinal cortex. Cells of origin as studied by the HRP method in the rat and mouse, Neurosci. Lett., 10, 115, 10.1016/0304-3940(78)90021-6 · DOI
  22. Laurberg, 1979, Commissural and intrinsic connections of the rat hippocampus, J. comp. Neurol., 184, 685, 10.1002/cne.901840405 · DOI
  23. Laurberg, 1981, Associational and commissural collaterals of neurons in the hippocampal formation (hilus fasciae dentatae and subfield CA3), Brain Res., 212, 287, 10.1016/0006-8993(81)90463-7 · DOI
  24. Lomo, 1971, Patterns of activation in a monosynaptic cortical pathway: the perforant path input to the dentate area of the hippocampal formation, Expl Brain Res., 12, 18, 10.1007/BF00234414 · DOI
  25. Lorente de No, 1933, Studies on the structure of the cerebral cortex. I. The area entorhinalis, J. Psychol. Neurol., 45, 381
  26. Lorente de No, 1934, Studies on the structure of the cerebral cortex. II. Continuation of the study of the ammonic system, J. Psychol. Neurol., 46, 113
  27. Nafstad, 1967, An electron microscope study on the termination of the perforant path fibres in the hippocampus and the fascia dentata, Z. Zellforsch. mikrosk. Anat., 76, 532, 10.1007/BF00339754 · DOI
  28. Raisman, 1965, The extrinsic afferent, commissural and association fibres of the hippocampus, Brain, 88, 963, 10.1093/brain/88.5.963 · DOI
  29. Ramón y Cajal, 1893, Estructura del asta de Ammon y fascia dentata, Ann. Soc. Esp. Hist. Nat., 22
  30. Rawlins, 1977, Lamellar organisation in the rat hippocampus, Expl Brain Res., 28, 335, 10.1007/BF00235715 · DOI
  31. Renshaw, 1940, Activity of isocortex and hippocampus: electrical studies with micro-electrodes, J. Neurophysiol., 3, 74, 10.1152/jn.1940.3.1.74 · DOI
  32. Ribak, 1985, The development, ultrastructure and synaptic connections of the mossy cells of the dentate gyrus, J. Neurocytol., 14, 835, 10.1007/BF01170832 · DOI
  33. Ruth, 1982, Topography between the entorhinal cortex and the dentate septotemporal axis in rats. I. Medial and intermediate entorhinal projecting cells, J. comp. Neurol., 209, 69, 10.1002/cne.902090107 · DOI
  34. Ruth, 1988, Topographical relationship between the entorhinal cortex and the septotemporal axis of the dentate gyrus in rats: II. Cells projecting from lateral entorhinal subdivisions, J. comp. Neurol., 270, 506, 10.1002/cne.902700404 · DOI
  35. Shipley, 1975, The topographical and laminar organization of the presubiculum's projection to the ipsi- and contralateral entorhinal cortex in the guinea pig, J. comp. Neurol., 160, 127, 10.1002/cne.901600108 · DOI
  36. Sorensen, 1979, Projections from the subiculum to the deep layers of the ipsilateral presubicular and entorhinal cortices in the guinea pig, J. comp. Neurol., 188, 313, 10.1002/cne.901880208 · DOI
  37. Steward, 1976, Topographic organization of the projections from the entorhinal area to the hippocampal formation of the rat, J. comp. Neurol., 167, 285, 10.1002/cne.901670303 · DOI
  38. Steward, 1976, Cells of origin of entorhinal cortical afferents to the hippocampus and fascia dentata of the rat, J. comp. Neurol., 169, 347, 10.1002/cne.901690306 · DOI
  39. Struble, 1978, Anatomical evidence for interlamellar inhibition in the fascia dentata, Brain Res., 152, 580, 10.1016/0006-8993(78)91113-7 · DOI
  40. Swanson, 1980, Evidence that the commissural, associational and septal projections of the regio inferior of the hippocampus arise from the same neurons, Brain Res., 197, 207, 10.1016/0006-8993(80)90446-1 · DOI
  41. Swanson, 1981, Evidence for collateral projections by neurons in Ammon's horn, the dentate gyrus, and the subiculum: a multiple retrograde labeling study in the rat, J. Neurosci., 1, 548, 10.1523/JNEUROSCI.01-05-00548.1981 · DOI
  42. Swanson, 1978, An autoradiographic study of the organization of intrahippocampal association pathways in the rat, J. comp. Neurol., 181, 681, 10.1002/cne.901810402 · DOI
  43. Tamamaki, 1987, Columnar organization in the subiculum formed by axon branches originating from single CA1 pyramidal neurons in the rat hippocampus, Brain Res., 412, 156, 10.1016/0006-8993(87)91452-1 · DOI
  44. Van Groen, 1985, Septotemporal distribution of entorhinal projections to the hippocampus in the cat. Electrophysiological evidence, J. comp. Neurol., 238, 1, 10.1002/cne.902380102 · DOI
  45. Witter, 1984, Laminar origin and septotemporal distribution of entorhinal and perirhinal projections to the hippocampus in the cat, J. comp. Neurol., 224, 371, 10.1002/cne.902240305 · DOI
  46. Witter, 1988, Entorhinal projections to the hippocampal CA1 region in the rat: an underestimated pathway, Neurosci. Lett., 85, 193, 10.1016/0304-3940(88)90350-3 · DOI · Paper page
  47. Witter, 1986, Connections of the parahippocampal cortex in the cat. V. Intrinsic connections; comments on input/output connections with the hippocampus, J. comp. Neurol., 252, 78, 10.1002/cne.902520105 · DOI
  48. Witter, 1989, Topographical organization of the entorhinal projection to the dentate gyrus of the monkey, J. Neurosci., 9, 216, 10.1523/JNEUROSCI.09-01-00216.1989 · DOI
  49. Wyss, 1981, An autoradiographic study of the efferent connections of the entorhinal cortex in the rat, J. comp. Neurol., 199, 495, 10.1002/cne.901990405 · DOI
  50. Zimmer, 1971, Ipsilateral afferents to the commissural zone of the fascia dentata, demonstrated in decommissurated rats by silver impregnation, J. comp. Neurol., 142, 393, 10.1002/cne.901420402 · DOI

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Metadata

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

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