Literature DB >> 2466422

The rat inferior olive as seen with immunostaining for glutamate decarboxylase.

B J Nelson1, E Mugnaini.   

Abstract

Boutons presumed to use gamma-aminobutyric acid as neurotransmitter (GABAergic boutons) were detected by glutamate decarboxylase (GAD) immunocytochemistry in all regions of the rat inferior olive. The remarkably high concentration of these boutons allowed a clear visualization of olivary subnuclei boundaries. Regional variations in GAD immunostaining intensity were observed within the nuclear complex and were graded both visually and photometrically. The regional staining variations, for the most part, followed subnuclei boundaries and olivary zonal compartments that have been delineated by the topography of climbing fibre projections. Some subnuclei were grouped by similar staining intensities. The beta nucleus and a medial region in the ventral fold of the dorsal accessory olive were most intensely immunostained, followed by the subnucleus c of the medial accessory olive. Lower staining intensities were observed in the dorsomedial cell column, the dorsal fold of the dorsal accessory olive and the dorsal cap. The lowest intensities were observed in the subnuclei a and b of the medial accessory olive, the ventrolateral outgrowth, the rostral lamella of the medial accessory olive, the principal olive, and the lateral part of the ventral fold of the dorsal accessory olive. The factors contributing to the variations in immunostaining intensity (bouton size and frequency of occurrence) were investigated. The largest boutons were observed in the beta nucleus. Intermediate sized boutons were observed in the dorsomedial cell column, dorsal cap and the dorsal fold of the dorsal accessory olive. The smallest boutons were present in the remaining regions of the inferior olive, including the principal olive, the rostral lamella of the medial accessory olive, and the ventral fold of the dorsal accessory olive. The medial region of the dorsal accessory olive ventral fold contained a higher density of GABAergic boutons than other regions. GABAergic bouton size and innervation density therefore largely accounted for the variations in GAD immunostaining intensity. This study provides a map of the rat inferior olive based on the distribution of GABAergic nerve terminals, and may serve as a basis for characterizing different GABAergic afferent systems in the inferior olive.

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Year:  1988        PMID: 2466422     DOI: 10.1007/bf00304693

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  43 in total

1.  Descending connections to the inferior olive; an experimental study in the cat.

Authors:  F WALBERG
Journal:  J Comp Neurol       Date:  1956-02       Impact factor: 3.215

2.  Areal distribution of axonal and dendritic patterns in inferior olive.

Authors:  A BRODAL; A SCHEIBEL; M SCHEIBEL; F WALBERG
Journal:  J Comp Neurol       Date:  1956-11       Impact factor: 3.215

3.  Calcium binding protein-like immunoreactivity labels the terminal field of nucleus laminaris of the barn owl.

Authors:  T T Takahashi; C E Carr; N Brecha; M Konishi
Journal:  J Neurosci       Date:  1987-06       Impact factor: 6.167

4.  A study of afferent input to the inferior olivary complex in the rat by retrograde axonal transport of horseradish peroxidase.

Authors:  J T Brown; V Chan-Palay; S L Palay
Journal:  J Comp Neurol       Date:  1977-11-01       Impact factor: 3.215

5.  Innervation and reinnervation of rat inferior olive by neurons containing serotonin and substance P: an immunohistochemical study after 5,6-dihydroxytryptamine lesioning.

Authors:  M Paré; L Descarries; L Wiklund
Journal:  J Neurocytol       Date:  1987-04

6.  Synaptic control of electrotonic coupling between neurons.

Authors:  M E Spira; M V Bennett
Journal:  Brain Res       Date:  1972-02-25       Impact factor: 3.252

7.  The olivocerebellar projection in the monkey. Experimental studies with the method of retrograde tracing of horseradish peroxidase.

Authors:  P Brodal; A Brodal
Journal:  J Comp Neurol       Date:  1981-09-20       Impact factor: 3.215

8.  The inferior olivary connections to the cerebellum in the rat studied by retrograde axonal transport of horseradish peroxidase.

Authors:  P A Brown
Journal:  Brain Res Bull       Date:  1980 May-Jun       Impact factor: 4.077

9.  The olivocerebellar projection in the cat studied with the method of retrograde axonal transport of horseradish peroxidase. III. The projection to the vermal visual area.

Authors:  G H Hoddevik; A Brodal; F Walberg
Journal:  J Comp Neurol       Date:  1976-09-15       Impact factor: 3.215

10.  A new combination of WGA-HRP anterograde tracing and GABA immunocytochemistry applied to afferents of the cat inferior olive at the ultrastructural level.

Authors:  C I de Zeeuw; J C Holstege; F Calkoen; T J Ruigrok; J Voogd
Journal:  Brain Res       Date:  1988-05-03       Impact factor: 3.252

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  5 in total

1.  Morphological correlates of bilateral synchrony in the rat cerebellar cortex.

Authors:  C I De Zeeuw; E J Lang; I Sugihara; T J Ruigrok; L M Eisenman; E Mugnaini; R Llinás
Journal:  J Neurosci       Date:  1996-05-15       Impact factor: 6.167

2.  The GABAergic cerebello-olivary projection in the rat.

Authors:  B J Fredette; E Mugnaini
Journal:  Anat Embryol (Berl)       Date:  1991

3.  Inhibitory regulation of electrically coupled neurons in the inferior olive is mediated by asynchronous release of GABA.

Authors:  Aaron R Best; Wade G Regehr
Journal:  Neuron       Date:  2009-05-28       Impact factor: 17.173

4.  Corollary discharge in precerebellar nuclei of sleeping infant rats.

Authors:  Didhiti Mukherjee; Greta Sokoloff; Mark S Blumberg
Journal:  Elife       Date:  2018-12-05       Impact factor: 8.140

5.  Quasiperiodic rhythms of the inferior olive.

Authors:  Mario Negrello; Pascal Warnaar; Vincenzo Romano; Cullen B Owens; Sander Lindeman; Elisabetta Iavarone; Jochen K Spanke; Laurens W J Bosman; Chris I De Zeeuw
Journal:  PLoS Comput Biol       Date:  2019-05-06       Impact factor: 4.475

  5 in total

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