Literature DB >> 2454246

A comparison of the efferents of the amygdala and the hippocampal formation in the rhesus monkey: I. Convergence in the entorhinal, prorhinal, and perirhinal cortices.

R C Saunders1, D L Rosene.   

Abstract

This is the first in a series of papers investigating the neuroanatomical basis for the interaction of the amygdala and the hippocampal formation in the rhesus monkey. The present report focuses on the complementary and convergent projections of the amygdala and hippocampal formation to the entorhinal and perirhinal cortices. These results were obtained from complementary experiments using injections of radioactively labeled amino acids to identify the anterograde projection patterns and injections of horseradish peroxidase and fluorescent retrograde tracers to confirm the cytoarchitectonic location of the neurons of origin for each projection. The results of this investigation demonstrate that both the hippocampal formation and the amygdala project to the entorhinal and perirhinal cortices where, with a few exceptions, the major projections of each structure generally are found in different layers of the same cytoarchitecture subdivisions of the entorhinal cortex but overlap in the same layers of the perirhinal cortex. Thus, the lateral and accessory basal nuclei of the amygdala project to layer 3 of areas Pr1, 28I, 28L, and 28S, and the accessory basal nucleus projects strongly to layer 1 of these same areas. In contrast, the subiculum, prosubiculum, and subfield CA1 of the of the hippocampal formation all have a projection to layer 5 of these same areas. In area 28M, the accessory basal nucleus of the amygdala projects to layer 1, while the subiculum, prosubiculum, and subfield CA1 of the hippocampal formation all project to layer 5, and the presubiculum projects to layer 3. In addition to these complementary laminar projections, there are a few areas of laminar overlap. Thus in area 28S, both the presubiculum and the CA1 subfield project to layer 3, where the lateral and accessory basal amygdaloid nuclei also project. Similarly, in 28I there is a major projection from the presubiculum and a lighter projection from the subiculum and CA1 to layer 3, where the lateral and accessory basal nuclei also project. There is also extensive laminar overlap in the perirhinal cortex. From the amygdala, the accessory basal nucleus projects to layers 1 and 3 and the lateral basal nucleus to layers 3, 5, and 6, while from the hippocampal formation, the prosubiculum projects to layers 3, 5, and 6, and the CA1 subfield projects to layer 5. This pattern of hippocampal and amygdaloid projections to the entorhinal and perirhinal cortices indicates that these cortices constitute a region of potentially extensive interaction between the amygdala and the hippocampus.

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Year:  1988        PMID: 2454246     DOI: 10.1002/cne.902710202

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


  30 in total

1.  Projections from the entorhinal cortex, perirhinal cortex, presubiculum, and parasubiculum to the medial thalamus in macaque monkeys: identifying different pathways using disconnection techniques.

Authors:  Richard C Saunders; Mortimer Mishkin; John P Aggleton
Journal:  Exp Brain Res       Date:  2005-10-29       Impact factor: 1.972

2.  Cue and reward signals carried by monkey entorhinal cortex neurons during reward schedules.

Authors:  Yasuko Sugase-Miyamoto; Barry J Richmond
Journal:  Exp Brain Res       Date:  2007-03-30       Impact factor: 1.972

3.  Object recognition and location memory in monkeys with excitotoxic lesions of the amygdala and hippocampus.

Authors:  E A Murray; M Mishkin
Journal:  J Neurosci       Date:  1998-08-15       Impact factor: 6.167

4.  Occurrence of diffuse amyloid deposits in the presubicular parvopyramidal layer in Alzheimer's disease.

Authors:  H Akiyama; H Tago; S Itagaki; P L McGeer
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

5.  A description of the amygdalo-hippocampal interconnections in the macaque monkey.

Authors:  J P Aggleton
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

Review 6.  The role of the entorhinal cortex in paraphrenia.

Authors:  Manuel F Casanova
Journal:  Curr Psychiatry Rep       Date:  2010-06       Impact factor: 5.285

7.  Direct Visualization and Mapping of the Spatial Course of Fiber Tracts at Microscopic Resolution in the Human Hippocampus.

Authors:  Michael M Zeineh; Nicola Palomero-Gallagher; Markus Axer; David Gräßel; Maged Goubran; Andreas Wree; Roger Woods; Katrin Amunts; Karl Zilles
Journal:  Cereb Cortex       Date:  2017-03-01       Impact factor: 5.357

8.  Autoradiographic characterization of neurotensin receptors in the entorhinal cortex of schizophrenic patients and control subjects.

Authors:  S S Wolf; T M Hyde; R C Saunders; M M Herman; D R Weinberger; J E Kleinman
Journal:  J Neural Transm Gen Sect       Date:  1995

Review 9.  Topographical and laminar distribution of cortical input to the monkey entorhinal cortex.

Authors:  A Mohedano-Moriano; P Pro-Sistiaga; M M Arroyo-Jimenez; E Artacho-Pérula; A M Insausti; P Marcos; S Cebada-Sánchez; J Martínez-Ruiz; M Muñoz; X Blaizot; A Martinez-Marcos; D G Amaral; R Insausti
Journal:  J Anat       Date:  2007-06-15       Impact factor: 2.610

10.  Direct visualization of the perforant pathway in the human brain with ex vivo diffusion tensor imaging.

Authors:  Jean C Augustinack; Karl Helmer; Kristen E Huber; Sita Kakunoori; Lilla Zöllei; Bruce Fischl
Journal:  Front Hum Neurosci       Date:  2010-05-28       Impact factor: 3.169

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