Literature DB >> 1702107

Nuclei of origin of monoaminergic, peptidergic, and cholinergic afferents to the cat trigeminal motor nucleus: a double-labeling study with cholera-toxin as a retrograde tracer.

P Fort1, P H Luppi, K Sakai, D Salvert, M Jouvet.   

Abstract

The aim of the present study was to determine the brainstem afferents and the location of neurons giving rise to monoaminergic, cholinergic, and peptidergic inputs to the cat trigeminal motor nucleus (TMN). This was done in colchicine treated animals by using a very sensitive double immunostaining technique with unconjugated cholera-toxin B subunit (CT) as a retrograde tracer. After CT injections in the TMN, retrogradely labeled neurons were most frequently seen bilaterally in the nuclei reticularis parvicellularis and dorsalis of the medulla oblongata, the alaminar spinal trigeminal nucleus (magnocellular division), and the adjacent pontine juxtatrigeminal region and in the ipsilateral mesencephalic trigeminal nucleus. We further observed that inputs to the TMN arise from the medial medullary reticular formation (the nuclei retricularis magnocellularis and gigantocellularis), the principal bilateral sensory trigeminal nucleus, and the dorsolateral pontine tegmentum. In addition, the present study demonstrated that the TMN received 1) serotonergic afferents, mainly from the nuclei raphe obscurus, pallidus, and dorsalis; 2) catecholaminergic afferent projections originating exclusively in the dorsolateral pontine tegmentum, including the Kölliker-Fuse, parabrachialis lateralis, and locus subcoeruleus nuclei; further, that 3) methionin-enkephalin-like inputs were located principally in the medial medullary reticular formation (nuclei reticularis magnocellularis and gigantocellularis and nucleus paragigantocellularis lateralis), in the caudal raphe nuclei (Rpa and Rob) and the dorsolateral pontine tegmentum; 4) substance P-like immunoreactive neurons projecting to the TMN were present in the caudal raphe and Edinger-Westphal nuclei; and 5) cholinergic afferents originated in the whole extent of the nuclei reticularis parvicellularis and dorsalis including an area located ventral to the nucleus of the solitary tract at the level of the obex. In the light of these anatomical data, the present report discusses the possible physiological involvement of TMN inputs in the generation of the trigeminal jaw-closer muscular atonia occurring during the periods of paradoxical sleep in the cat.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 1702107     DOI: 10.1002/cne.903010209

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


  15 in total

1.  Nitrergic ventro-medial medullary neurons activated during cholinergically induced active (rapid eye movement) sleep in the cat.

Authors:  I Pose; S Sampogna; M H Chase; F R Morales
Journal:  Neuroscience       Date:  2010-10-31       Impact factor: 3.590

2.  Hypoglossal premotor neurons of the intermediate medullary reticular region express cholinergic markers.

Authors:  Denys V Volgin; Irma Rukhadze; Leszek Kubin
Journal:  J Appl Physiol (1985)       Date:  2008-09-04

3.  Differential respiratory control of the upper airway and diaphragm muscles induced by 5-HT1A receptor ligands.

Authors:  Stephane Besnard; Hanan Khemiri; Fabienne Masse; Pierre Denise; Marion Verdaguer; Christian Gestreau
Journal:  Sleep Breath       Date:  2011-01-09       Impact factor: 2.816

Review 4.  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

5.  c-fos expression in brainstem premotor interneurons during cholinergically induced active sleep in the cat.

Authors:  F R Morales; S Sampogna; J Yamuy; M H Chase
Journal:  J Neurosci       Date:  1999-11-01       Impact factor: 6.167

6.  Raphespinal and reticulospinal neurons project to the dorsal vagal complex in the rat.

Authors:  S Manaker; P F Fogarty
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

7.  Exercise-induced pain requires NMDA receptor activation in the medullary raphe nuclei.

Authors:  Kathleen A Sluka; Jessica Danielson; Lynn Rasmussen; Luis Felipe DaSilva
Journal:  Med Sci Sports Exerc       Date:  2012-03       Impact factor: 5.411

Review 8.  The anatomical, cellular and synaptic basis of motor atonia during rapid eye movement sleep.

Authors:  Elda Arrigoni; Michael C Chen; Patrick M Fuller
Journal:  J Physiol       Date:  2016-07-03       Impact factor: 5.182

9.  Behaviour of raphe cells projecting to the dorsomedial medulla during carbachol-induced atonia in the cat.

Authors:  G Woch; R O Davies; A I Pack; L Kubin
Journal:  J Physiol       Date:  1996-02-01       Impact factor: 5.182

10.  Activation properties of trigeminal motoneurons in participants with and without bruxism.

Authors:  Jessica M D'Amico; Ş Utku Yavuz; Ahmet Saraçoglu; Elif Sibel Atiş; Monica A Gorassini; Kemal S Türker
Journal:  J Neurophysiol       Date:  2013-09-25       Impact factor: 2.714

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.