Literature DB >> 7019303

Ultrastructural demonstration of noradrenergic synapses in the rat central nervous system by dopamine-beta-hydroxylase immunocytochemistry.

J A Olschowka, M E Molliver, R Grzanna, F L Rice, J T Coyle.   

Abstract

Noradrenergic (NA) cell bodies and axonal processes were identified in the electron microscope by the immunocytochemical localization of the norepinephrine-synthesizing enzyme, dopamine-beta-hydroxylase (DBH). DBH immunoreactivity, visualized by the peroxidase-antiperoxidase method, was observed in the somata and proximal processes of locus coeruleus neurons and in the distal axons of several NA terminal fields. DBH immunoreactivity is distributed throughout the cytoplasm of the NA neuron, but demonstrates a selective association with endoplasmic reticulum, Golgi apparatus, mitochondrial outer membranes, large granular vesicles, and small, round synaptic vesicles. DBH-positive axonal profiles, typically interspersed between unlabeled dendrites, form two distinct populations: a) thin, unmyelinated intervaricose segments (ca. 0.28 micron) and b) spherical varicosities (ca. 1.00 micron). No DBH-positive varicosities were observed in contact with intracerebral capillaries. In order to determine whether or not NA axons typically form synaptic contacts, a quantitative analysis of selected areas of the diencephalon, cerebellum, and limbic cortex was carried out. More than half (58%) of all DBH-positive varicosities form axodendritic synapses characterized by specialized junctional appositions. The results suggest that NA neurons typically exert their influence on other neurons through highly restricted synaptic contacts.

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Year:  1981        PMID: 7019303     DOI: 10.1177/29.2.7019303

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  17 in total

Review 1.  Hindbrain noradrenergic A2 neurons: diverse roles in autonomic, endocrine, cognitive, and behavioral functions.

Authors:  Linda Rinaman
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-10-20       Impact factor: 3.619

2.  Evidence for functional separation of alpha-1 and alpha-2 noradrenaline receptors by pre-synaptic terminal re-uptake mechanisms.

Authors:  A J Clark; S P Butcher; P Winn
Journal:  Psychopharmacology (Berl)       Date:  1991       Impact factor: 4.530

3.  Electron-microscopic cytochemistry of the catecholaminergic innervation of TRH neurons in the rat hypothalamus.

Authors:  S Shioda; Y Nakai; A Sato; S Sunayama; Y Shimoda
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

4.  Evidence for widespread effects of noradrenaline on axon terminals in the rat frontal cortex.

Authors:  P Mobley; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

5.  Association of dopaminergic fibers with corticotropin releasing hormone (CRH)-synthesizing neurons in the paraventricular nucleus of the rat hypothalamus.

Authors:  Z Liposits; W K Paull
Journal:  Histochemistry       Date:  1989

6.  Locus coeruleus neuronal activity in awake monkeys: relationship to auditory P300-like potentials and spontaneous EEG.

Authors:  D Swick; J A Pineda; S Schacher; S L Foote
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

Review 7.  Locus coeruleus: From global projection system to adaptive regulation of behavior.

Authors:  G Aston-Jones; B Waterhouse
Journal:  Brain Res       Date:  2016-03-09       Impact factor: 3.252

8.  Catecholaminergic innervation of GRF-containing neurons in the rat hypothalamus revealed by electron-microscopic cytochemistry.

Authors:  A Sato; S Shioda; Y Nakai
Journal:  Cell Tissue Res       Date:  1989-10       Impact factor: 5.249

Review 9.  Visceral sensory inputs to the endocrine hypothalamus.

Authors:  Linda Rinaman
Journal:  Front Neuroendocrinol       Date:  2007-02-22       Impact factor: 8.606

10.  Characteristic distribution of noradrenergic terminals on the anterior horn motoneurons innervating the perineal striated muscles in the rat. An immuno-electromicroscopic study.

Authors:  M Kojima; T Matsuura; A Tanaka; T Amagai; J Imanishi; Y Sano
Journal:  Anat Embryol (Berl)       Date:  1985
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