Literature DB >> 6664494

Neuronal configurations in lateral and basolateral amygdala.

O E Millhouse, J DeOlmos.   

Abstract

The lateral and basolateral nuclei of the rat amygdala have been studied with the rapid Golgi method. Both nuclei have similar cell types, which closely resemble cells in the cerebral cortex. Therefore, we suggest that what is known about cortical circuitry can be used as a guide for studying synaptic circuitry in the lateral and basolateral nuclei. The most abundant neurons that are impregnated in both nuclei are pyramidal cells. They have conical cell bodies and easily recognizable apical and basilar dendrites. The ones in the center of each nucleus have long axes that roughly parallel the long axis of the nucleus. Towards the periphery, pyramidal cells have apical dendrites that either stick directly across the nucleus or follow along a nuclear border. The peripheral dendrites tend to enclose the nuclei. There is considerable overlap among the dendritic trees and the dendrites of one nucleus extend into the territory of the other. Pyramidal cells have extensive axonal systems. The principal axon of basolateral cells usually projects rostrally but long collaterals leave the nucleus in other directions. The axons of lateral nucleus pyramidal cells are also widely distributed. The major thrust of their axons is caudal and lateral. Stellate cells are the most common variety of the non-pyramidal cells. They occur in both nuclei and have round cell bodies, 10-15 micron diameter, and spherical dendritic trees that are confined to a limited region of the nucleus. Their axons form dense terminal fields that remain within the vicinity of the parent cell's dendritic tree. Another type of non-pyramidal cell is the cone cell, whose non-spiny, varicose dendrites describe cones. These neurons are found mainly in the apex of the lateral nucleus. The most rare non-pyramidal cells are the extended neurons, which have long, straight dendrites that reach beyond the nucleus into surrounding neuropil. They are mostly in the rostral part of the basolateral nucleus but also occur in the lateral nucleus, near the ventricular border. The axons of cone cells and the extended neurons have been only partially impregnated. We also have examined stellate cells in the guinea-pig lateral and basolateral nuclei. They have many of the same features as those in the rat brain, except that their dendritic trees and axonal systems are more complicated. There are two large groups of afferents: one consists of longitudinally running axons and the other of transversely coursing fibers.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1983        PMID: 6664494     DOI: 10.1016/0306-4522(83)90112-4

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  28 in total

Review 1.  Architectural Representation of Valence in the Limbic System.

Authors:  Praneeth Namburi; Ream Al-Hasani; Gwendolyn G Calhoon; Michael R Bruchas; Kay M Tye
Journal:  Neuropsychopharmacology       Date:  2015-12-09       Impact factor: 7.853

2.  Demonstration of projections from the lateral nucleus to the basal nucleus of the amygdala: a PHA-L study in the monkey.

Authors:  A Pitkänen; D G Amaral
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

3.  Ultrastructure and synaptic associations of auditory thalamo-amygdala projections in the rat.

Authors:  J E LeDoux; C R Farb; T A Milner
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

4.  Pyramidal cells of the rat basolateral amygdala: synaptology and innervation by parvalbumin-immunoreactive interneurons.

Authors:  Jay F Muller; Franco Mascagni; Alexander J McDonald
Journal:  J Comp Neurol       Date:  2006-02-01       Impact factor: 3.215

5.  Cellular Classes in the Human Brain Revealed In Vivo by Heartbeat-Related Modulation of the Extracellular Action Potential Waveform.

Authors:  Clayton P Mosher; Yina Wei; Jan Kamiński; Anirban Nandi; Adam N Mamelak; Costas A Anastassiou; Ueli Rutishauser
Journal:  Cell Rep       Date:  2020-03-10       Impact factor: 9.423

6.  Diverse glutamatergic inputs target spines expressing M1 muscarinic receptors in the basolateral amygdala: An ultrastructural analysis.

Authors:  Alexander J McDonald; Grace C Jones; David D Mott
Journal:  Brain Res       Date:  2019-07-23       Impact factor: 3.252

7.  GABAergic somatostatin-immunoreactive neurons in the amygdala project to the entorhinal cortex.

Authors:  A J McDonald; V Zaric
Journal:  Neuroscience       Date:  2015-01-28       Impact factor: 3.590

Review 8.  Serotonergic innervation of the amygdala: targets, receptors, and implications for stress and anxiety.

Authors:  Esther Asan; Maria Steinke; Klaus-Peter Lesch
Journal:  Histochem Cell Biol       Date:  2013-03-15       Impact factor: 4.304

9.  Muscarinic responses of rat basolateral amygdaloid neurons recorded in vitro.

Authors:  M S Washburn; H C Moises
Journal:  J Physiol       Date:  1992-04       Impact factor: 5.182

10.  Parvalbumin-immunoreactive neurons and GABAergic neurons of the basal forebrain project to the rat basolateral amygdala.

Authors:  F Mascagni; A J McDonald
Journal:  Neuroscience       Date:  2009-03-11       Impact factor: 3.590

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