Literature DB >> 10540360

Trigeminal projections to hypoglossal and facial motor nuclei in the rat.

G Pinganaud1, I Bernat, P Buisseret, C Buisseret-Delmas.   

Abstract

This study was undertaken to identify the trigeminal nuclear regions connected to the hypoglossal (XII) and facial (VII) motor nuclei in rats. Anterogradely transported tracers (biotinylated dextran amine, biocytin) were injected into the various subdivisions of the sensory trigeminal complex, and labeled fibers and terminals were searched for in the XII and VII. In a second series of experiments, injections of retrogradely transported tracers (biotinylated dextran amine, gold-horseradish peroxidase complex, fluoro-red, fluoro-green) were made into the XII and the VII, and labeled cells were searched for in the principal sensory trigeminal nucleus, and in the pars oralis, interpolaris, and caudalis of the spinal trigeminal nucleus. Trigeminohypoglossal projections were distributed throughout the ventral and dorsal region of the XII. Neurons projecting to the XII were found in all subdivisions of the sensory trigeminal complex with the greatest concentration in the dorsal part of each spinal subnucleus and exclusively in the dorsal part of the principal nucleus. Trigeminofacial projections reached all subdivisions of the VII, with a gradual decreasing density from lateral to medial cell groups. They mainly originated from the ventral part of the principal nucleus. In the spinal nucleus, most of the neurons projecting to the VII were in the dorsal part of the nucleus, but some were also found in its central and ventral parts. By using retrograde double labeling after injections of different tracers in the XII and VII on the same side, we examined whether neurons in the trigeminal complex project to both motor nuclei. These experiments demonstrate that in the spinal trigeminal nucleus, neurons located in the pars caudalis and pars interpolaris project by axon collaterals to XII and VII. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10540360     DOI: 10.1002/(sici)1096-9861(19991206)415:1<91::aid-cne7>3.0.co;2-a

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


  13 in total

1.  Excitability of the human trigeminal motoneuronal pool and interactions with other brainstem reflex pathways.

Authors:  G Cruccu; A Truini; A Priori
Journal:  J Physiol       Date:  2001-03-01       Impact factor: 5.182

2.  Functional circuitry involved in the regulation of whisker movements.

Authors:  Alexis M Hattox; Catherine A Priest; Asaf Keller
Journal:  J Comp Neurol       Date:  2002-01-14       Impact factor: 3.215

3.  The Brainstem Oscillator for Whisking and the Case for Breathing as the Master Clock for Orofacial Motor Actions.

Authors:  David Kleinfeld; Jeffrey D Moore; Fan Wang; Martin Deschênes
Journal:  Cold Spring Harb Symp Quant Biol       Date:  2015-04-15

4.  Parallel Inhibitory and Excitatory Trigemino-Facial Feedback Circuitry for Reflexive Vibrissa Movement.

Authors:  Marie-Andrée Bellavance; Jun Takatoh; Jinghao Lu; Maxime Demers; David Kleinfeld; Fan Wang; Martin Deschênes
Journal:  Neuron       Date:  2017-07-20       Impact factor: 17.173

Review 5.  Generation of the central masticatory pattern and its modification by sensory feedback.

Authors:  James P Lund; Arlette Kolta
Journal:  Dysphagia       Date:  2006-07       Impact factor: 3.438

6.  Feedback in the brainstem: an excitatory disynaptic pathway for control of whisking.

Authors:  David W Matthews; Martin Deschênes; Takahiro Furuta; Jeffrey D Moore; Fan Wang; Harvey J Karten; David Kleinfeld
Journal:  J Comp Neurol       Date:  2015-01-30       Impact factor: 3.215

7.  Orofacial Movements Involve Parallel Corticobulbar Projections from Motor Cortex to Trigeminal Premotor Nuclei.

Authors:  Nicole Mercer Lindsay; Per M Knutsen; Adrian F Lozada; Daniel Gibbs; Harvey J Karten; David Kleinfeld
Journal:  Neuron       Date:  2019-10-03       Impact factor: 17.173

8.  Manual stimulation of the whisker pad after hypoglossal-facial anastomosis (HFA) using a Y-tube conduit does not improve recovery of whisking function.

Authors:  Umut Ozsoy; Bahadir Murat Demirel; Arzu Hizay; Ozlem Ozsoy; Janina Ankerne; Srebrina Angelova; Levent Sarikcioglu; Yasar Ucar; Murat Turhan; Sarah Dunlop; Doychin N Angelov
Journal:  Exp Brain Res       Date:  2014-03-13       Impact factor: 1.972

9.  Response properties of temporomandibular joint mechanosensitive neurons in the trigeminal sensory complex of the rabbit.

Authors:  Osuke Suzuki; Akito Tsuboi; Takayoshi Tabata; Yasuo Takafuji; Takeshi Sakurai; Makoto Watanabe
Journal:  Exp Brain Res       Date:  2012-08-02       Impact factor: 1.972

10.  Application and evaluation of automated methods to extract neuroanatomical connectivity statements from free text.

Authors:  Leon French; Suzanne Lane; Lydia Xu; Celia Siu; Cathy Kwok; Yiqi Chen; Claudia Krebs; Paul Pavlidis
Journal:  Bioinformatics       Date:  2012-09-06       Impact factor: 6.937

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