Literature DB >> 10992249

Distribution of parvalbumin, calretinin, and calbindin-D(28k) immunoreactivity in the rat amygdaloid complex and colocalization with gamma-aminobutyric acid.

S Kemppainen1, A Pitkänen.   

Abstract

To understand the organization of inhibitory circuitries in the rat amygdala, the distribution of parvalbumin, calretinin, and calbindin immunoreactivity was investigated in the rat amygdaloid complex. Colocalization of various calcium-binding proteins with the inhibitory transmitter gamma-aminobutyric acid (GABA) was studied by using the mirror technique. Parvalbumin-immunoreactive (-ir) elements were located mostly in the deep amygdaloid nuclei, whereas the calretinin-ir and calbindin-ir staining were most intense in the cortical nuclei as well as in the central nucleus and the amygdalohippocampal area. Second, the distribution of immunopositive neurons largely parallelled the distribution of terminal and neuropil labeling. Third, immunostained neurons could be divided into four major morphologic types (types 1-4) based on the characteristics of the somata and the dendritic trees. The fourth lightly stained neuronal type that had a pyramidal GABA-negative soma was observed only in calretinin and calbindin preparations. Fourth, parvalbumin-ir terminals formed basket-like plexus and cartridges, which suggests that parvalbumin labels GABAergic inhibitory basket cells and axo-axonic chandelier cells, respectively. Colocalization studies indicated that 521 of 553 (94%) of parvalbumin-ir, 419 of 557 (75%) of calbindin-ir, and 158 of 657 (24%) of calretinin-ir neurons were GABA-positive in the deep amygdaloid nuclei. A high density of large GABA-negative calbindin-ir neurons was observed caudally in the medial division of the lateral nucleus and GABA-negative calretinin-ir neurons were observed in the magnocellular division of the accessory basal nucleus as well as in the intermediate and parvicellular divisions of the basal nucleus. These data suggest that in various amygdaloid areas, neuronal excitability is controlled by GABAergic neurons that contain different calcium-binding proteins. The appearance of basket-like plexus and cartridges in the parvalbumin preparations, but not in calretinin preparations, suggests that like in the hippocampus, the distribution of inhibitory terminals in the dendritic and perisomatic regions of postsynaptic neurons in the rat amygdala is organized in a topographic manner. Copyright 2000 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10992249     DOI: 10.1002/1096-9861(20001023)426:3<441::aid-cne8>3.0.co;2-7

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


  67 in total

1.  In vitro ictogenesis and parahippocampal networks in a rodent model of temporal lobe epilepsy.

Authors:  G Panuccio; M D'Antuono; P de Guzman; L De Lannoy; G Biagini; M Avoli
Journal:  Neurobiol Dis       Date:  2010-05-07       Impact factor: 5.996

Review 2.  Of mice and rats: key species variations in the sexual differentiation of brain and behavior.

Authors:  P J Bonthuis; K H Cox; B T Searcy; P Kumar; S Tobet; E F Rissman
Journal:  Front Neuroendocrinol       Date:  2010-05-10       Impact factor: 8.606

Review 3.  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

4.  Detection of conspecific pheromones elicits fos expression in GABA and calcium-binding cells of the rat vomeronasal system-medial extended amygdala.

Authors:  German Leandro Pereno; Verónica Balaszczuk; Carlos A Beltramino
Journal:  J Physiol Biochem       Date:  2010-10-12       Impact factor: 4.158

5.  Neuronal localization of m1 muscarinic receptor immunoreactivity in the rat basolateral amygdala.

Authors:  Alexander Joseph McDonald; Franco Mascagni
Journal:  Brain Struct Funct       Date:  2010-05-26       Impact factor: 3.270

6.  α2-containing GABA(A) receptors: a requirement for midazolam-escalated aggression and social approach in mice.

Authors:  Emily L Newman; Kiersten S Smith; Aki Takahashi; Adam Chu; Lara S Hwa; Yang Chen; Joseph F DeBold; Uwe Rudolph; Klaus A Miczek
Journal:  Psychopharmacology (Berl)       Date:  2015-09-17       Impact factor: 4.530

Review 7.  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 8.  Functional neuroanatomy of amygdalohippocampal interconnections and their role in learning and memory.

Authors:  Alexander J McDonald; David D Mott
Journal:  J Neurosci Res       Date:  2016-02-14       Impact factor: 4.164

9.  Dexamethasone induces apoptosis in the developing rat amygdala in an age-, region-, and sex-specific manner.

Authors:  D G Zuloaga; D L Carbone; R Hiroi; D L Chong; R J Handa
Journal:  Neuroscience       Date:  2011-10-01       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.