Literature DB >> 8450947

Localization of GABA-like immunoreactivity in the monkey amygdala.

A J McDonald1, J R Augustine.   

Abstract

Neurons exhibiting GABA-like immunoreactivity were identified in the monkey amygdala using an avidin-biotin immunohistochemical technique. The pattern of GABA immunoreactivity was very similar in the basolateral and superficial amygdaloid nuclei. In these regions GABA-positive cells were nonpyramidal neurons that were often arranged in clusters or curvilinear rows. These GABA-positive nonpyramidal neurons constituted about 25% of the total neuronal population of the basolateral and superficial amygdaloid nuclei. Numerous GABA-positive puncta resembling axon terminals were observed both in the neuropil and encapsulating the perikarya of GABA-negative pyramidal cells. The pattern of GABA-like immunoreactivity was different in the central and medial amygdaloid nuclei. These regions contained a very dense array of GABA-positive puncta. There were numerous GABA-positive neurons in the lateral subdivision of the central nucleus and fewer cells in the medial nucleus and medial subdivision of the central nucleus. Many immunoreactive puncta were observed contacting the perikarya and dendrites of GABA-positive cells in these regions. The intercalated nuclei consisted of numerous, small, GABA-positive neurons and a few, larger, GABA-negative cells. Both cell types were contacted by GABA-positive puncta. This study indicates that neuronal subpopulations in each of the amygdaloid nuclei of the monkey are GABAergic. The pattern of immunoreactivity varies in different amygdaloid regions and is very similar to that described in the rat. Certain aspects of the functional organization of this rich GABAergic circuitry can be elucidated by correlating the findings of the present investigation with previous anatomical, physiological, and pharmacological studies of the amygdala.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8450947     DOI: 10.1016/0306-4522(93)90156-a

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


  71 in total

1.  An inhibitory interface gates impulse traffic between the input and output stations of the amygdala.

Authors:  S Royer; M Martina; D Paré
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  Bistable behavior of inhibitory neurons controlling impulse traffic through the amygdala: role of a slowly deinactivating K+ current.

Authors:  S Royer; M Martina; D Pare
Journal:  J Neurosci       Date:  2000-12-15       Impact factor: 6.167

3.  Differential fear conditioning induces reciprocal changes in the sensory responses of lateral amygdala neurons to the CS(+) and CS(-).

Authors:  D R Collins; D Paré
Journal:  Learn Mem       Date:  2000 Mar-Apr       Impact factor: 2.460

Review 4.  Plastic synaptic networks of the amygdala for the acquisition, expression, and extinction of conditioned fear.

Authors:  Hans-Christian Pape; Denis Pare
Journal:  Physiol Rev       Date:  2010-04       Impact factor: 37.312

Review 5.  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

Review 6.  The Physiology of Fear: Reconceptualizing the Role of the Central Amygdala in Fear Learning.

Authors:  Orion P Keifer; Robert C Hurt; Kerry J Ressler; Paul J Marvar
Journal:  Physiology (Bethesda)       Date:  2015-09

7.  Projections from the subfornical region of the lateral hypothalamic area.

Authors:  Marina Goto; Newton S Canteras; Gully Burns; Larry W Swanson
Journal:  J Comp Neurol       Date:  2005-12-19       Impact factor: 3.215

8.  Synaptic heterogeneity between mouse paracapsular intercalated neurons of the amygdala.

Authors:  Raffaella Geracitano; Walter A Kaufmann; Gabor Szabo; Francesco Ferraguti; Marco Capogna
Journal:  J Physiol       Date:  2007-10-04       Impact factor: 5.182

9.  Immunohistochemical characterization of parvalbumin-containing interneurons in the monkey basolateral amygdala.

Authors:  F Mascagni; E C Muly; D G Rainnie; A J McDonald
Journal:  Neuroscience       Date:  2008-11-17       Impact factor: 3.590

10.  Cortical inputs innervate calbindin-immunoreactive interneurons of the rat basolateral amygdaloid complex.

Authors:  Gunes Unal; Jean-Francois Paré; Yoland Smith; Denis Paré
Journal:  J Comp Neurol       Date:  2014-06-01       Impact factor: 3.215

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.