Literature DB >> 2329188

Disposition of the slab-like modules formed by axon branches originating from single CA1 pyramidal neurons in the rat hippocampus.

N Tamamaki1, Y Nojyo.   

Abstract

The hippocampus is thought to be an area where the neuronal circuits for short-term memory or the cognitive map may reside. In order to advance theoretical studies and neuronal model simulations of such circuits, the projection of the CA1 pyramidal neurons in the rat dorsal hippocampus, especially in the subiculum, was studied by means of intracellular and extracellular HRP injection. The CA1 pyramidal neurons project principally to the subiculum where each forms a slab-like axonal field 2 mm long along the septotemporal axis, which may be regarded as a module for columnar organization, at a specific rostrocaudal level of the subiculum. The modules of the CA1a pyramidal neurons are disposed in the rostral part of the subiculum, those of the CA1c pyramidal neurons in the caudal part, and those of the CA1b pyramidal neurons in the middle part of the subiculum. The CA1 pyramidal neurons also participate in the construction of the lamellar organization in the hippocampus in that their axon branches run rostrocaudally following the stream of the alvear fibers. The CA1 pyramidal neurons in the dorsal rat hippocampus transfer the topographic map from field CA1 to the subiculum with reversed order in the lamellar direction. The topographical relationship is composed of partially shifted, overlapping slab-like modules. As a result, information conveyed through a lamella will diverge into the subiculum approximately 2 mm wide, and information through a group of lamellae 2 mm wide will converge upon single subicular neurons.

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Year:  1990        PMID: 2329188     DOI: 10.1002/cne.902910403

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  19 in total

1.  Selective inhibition of local excitatory synaptic transmission by serotonin through an unconventional receptor in the CA1 region of rat hippocampus.

Authors:  B Mlinar; A M Pugliese; R Corradetti
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2.  Spatiotemporal patterns of gamma frequency oscillations tetanically induced in the rat hippocampal slice.

Authors:  M A Whittington; I M Stanford; S B Colling; J G Jefferys; R D Traub
Journal:  J Physiol       Date:  1997-08-01       Impact factor: 5.182

3.  The mystery of structure and function of sensory processing areas of the neocortex: a resolution.

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Journal:  J Comput Neurosci       Date:  2002 Nov-Dec       Impact factor: 1.621

Review 4.  The role of synaptic reorganization in mesial temporal lobe epilepsy.

Authors:  Jose E Cavazos; Devin J Cross
Journal:  Epilepsy Behav       Date:  2006-02-24       Impact factor: 2.937

Review 5.  Spatial organization of direct hippocampal field CA1 axonal projections to the rest of the cerebral cortex.

Authors:  Lee A Cenquizca; Larry W Swanson
Journal:  Brain Res Rev       Date:  2007-05-10

6.  Distributed encoding and retrieval of spatial memory in the hippocampus.

Authors:  M B Moser; E I Moser
Journal:  J Neurosci       Date:  1998-09-15       Impact factor: 6.167

7.  Fine structure of neural spiking and synchronization in the presence of conduction delays.

Authors:  G B Ermentrout; N Kopell
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-03       Impact factor: 11.205

8.  Spatial learning with a minislab in the dorsal hippocampus.

Authors:  M B Moser; E I Moser; E Forrest; P Andersen; R G Morris
Journal:  Proc Natl Acad Sci U S A       Date:  1995-10-10       Impact factor: 11.205

9.  Zinc-positive afferents to the rat septum originate from distinct subpopulations of zinc-containing neurons in the hippocampal areas and layers. A combined fluoro-gold tracing and histochemical study.

Authors:  J C Sørensen; N Tønder; L Slomianka
Journal:  Anat Embryol (Berl)       Date:  1993-08

10.  Sprouting and synaptic reorganization in the subiculum and CA1 region of the hippocampus in acute and chronic models of partial-onset epilepsy.

Authors:  J E Cavazos; S M Jones; D J Cross
Journal:  Neuroscience       Date:  2004       Impact factor: 3.590

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