Literature DB >> 1975547

Catecholamine-containing axon terminals in the hypoglossal nucleus of the rat: an immuno-electronmicroscopic study.

L D Aldes1, B Shaw, R B Chronister, J W Haycock.   

Abstract

A correlative light and electron microscopic investigation was undertaken to determine the morphology and distribution of catecholamine (CA)-containing axon terminals in the hypoglossal nucleus (XII) of the rat. This was accomplished immunocytochemically with antibody to tyrosine hydroxylase (TH). The major findings in this study were the following: 1) Immunoreactive profiles were found throughout XII and included unmyelinated axons, varicosities, axon terminals and dendrites; 2) Nonsynaptic immunoreactive profiles (preterminal axons, varicosities) were more frequently observed (55.2%) than synaptic profiles (43.5%); 3) CA-containing axon terminals ending on dendrites were more numerous (71.8%) than those synapsing on somata (25.4%) or non-labeled axon terminals (2.7%); 4) The morphology of labeled axon terminals was variable. Axodendritic terminals typically contained numerous small, round agranular vesicles, a few large dense-core vesicles and were associated with either a symmetric or no synaptic specialization, axosomatic terminals were often associated with a presynaptic membrane thickening or a symmetric synaptic specialization and contained small, round and a few elliptical-shaped vesicles, while axoaxonic synapses formed asymmetric postsynaptic specializations; and 5) CA-positive dendritic processes were identified in XII. These findings confirm the CA innervation of XII, and suggest a complex, multifunctional role for CA in controlling oro-lingual motor behavior.

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Year:  1990        PMID: 1975547     DOI: 10.1007/bf00230113

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  48 in total

1.  Differential distribution of biogenic amines in the hypoglossal nucleus of the rat.

Authors:  L D Aldes; R C Chronister; L A Marco; J W Haycock; J Thibault
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

2.  Organization of spinal motoneuron dendrites in bundles.

Authors:  M E Scheibel; A B Scheibel
Journal:  Exp Neurol       Date:  1970-07       Impact factor: 5.330

3.  The ultrastructural localisation of amine storage sites in the central nervous system with the aid of a specific marker, 5-hydroxydopamine.

Authors:  J G Richards; J P Tranzer
Journal:  Brain Res       Date:  1970-02-03       Impact factor: 3.252

4.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures.

Authors:  S M Hsu; L Raine; H Fanger
Journal:  J Histochem Cytochem       Date:  1981-04       Impact factor: 2.479

5.  Control of genioglossus muscle inspiratory activity.

Authors:  R T Brouillette; B T Thach
Journal:  J Appl Physiol Respir Environ Exerc Physiol       Date:  1980-11

6.  Visual input to the hypoglossal nucleus.

Authors:  O Mameli; E Tolu
Journal:  Exp Neurol       Date:  1985-11       Impact factor: 5.330

7.  Facilitation of the lumbar monosynaptic reflexes by locus coeruleus stimulation.

Authors:  J C Strahlendorf; H K Strahlendorf; R E Kingsley; J Gintautas; C D Barnes
Journal:  Neuropharmacology       Date:  1980-02       Impact factor: 5.250

8.  Facilitation of spinal motoneurone excitability by 5-hydroxytryptamine and noradrenaline.

Authors:  S R White; R S Neuman
Journal:  Brain Res       Date:  1980-04-21       Impact factor: 3.252

9.  Pharmacological antagonism of facilitatory but not inhibitory effects of serotonin and norepinephrine on excitability of spinal motoneurons.

Authors:  S R White; R S Neuman
Journal:  Neuropharmacology       Date:  1983-04       Impact factor: 5.250

10.  Rat medulla oblongata. II. Dopaminergic, noradrenergic (A1 and A2) and adrenergic neurons, nerve fibers, and presumptive terminal processes.

Authors:  M Kalia; K Fuxe; M Goldstein
Journal:  J Comp Neurol       Date:  1985-03-15       Impact factor: 3.215

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  6 in total

1.  REM sleep-like atonia of hypoglossal (XII) motoneurons is caused by loss of noradrenergic and serotonergic inputs.

Authors:  Victor B Fenik; Richard O Davies; Leszek Kubin
Journal:  Am J Respir Crit Care Med       Date:  2005-08-11       Impact factor: 21.405

2.  Chronic intermittent hypoxia alters density of aminergic terminals and receptors in the hypoglossal motor nucleus.

Authors:  Irma Rukhadze; Victor B Fenik; Kate E Benincasa; Andrea Price; Leszek Kubin
Journal:  Am J Respir Crit Care Med       Date:  2010-07-09       Impact factor: 21.405

Review 3.  Synaptic control of motoneuronal excitability.

Authors:  J C Rekling; G D Funk; D A Bayliss; X W Dong; J L Feldman
Journal:  Physiol Rev       Date:  2000-04       Impact factor: 37.312

4.  Synaptic interactions of retrogradely labeled hypoglossal motoneurons with substance P-like immunoreactive nerve terminals in the cat: a dual-labeling electron microscopic study.

Authors:  P J Gatti; W C Coleman; M Shirahata; T A Johnson; V J Massari
Journal:  Exp Brain Res       Date:  1996-07       Impact factor: 1.972

5.  Inhibition of pontine noradrenergic A7 cells reduces hypoglossal nerve activity in rats.

Authors:  V B Fenik; I Rukhadze; L Kubin
Journal:  Neuroscience       Date:  2008-09-11       Impact factor: 3.590

6.  Genioglossal hypoglossal motoneurons contact substance P-like immunoreactive nerve terminals in the cat: a dual labeling electron microscopic study.

Authors:  Kimberlei A Richardson; Philip J Gatti
Journal:  Exp Brain Res       Date:  2003-11-13       Impact factor: 1.972

  6 in total

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