Literature DB >> 12453486

Identification of lingual motor control circuits using two strains of pseudorabies virus.

J B Travers1, L Rinaman.   

Abstract

First-order interneurons that project to hypoglossal motoneurons are distributed within reticular formation subdivisions in the pons and medulla in areas thought to control licking, swallowing, chewing, and respiration. Movement of the tongue in each of these functions is achieved by the coordinated action of both intrinsic and extrinsic lingual muscles. Interneuron populations that project to these different lingual motoneuronal pools appear to be largely overlapping in the reticular formation. Because of the functional coupling between intrinsic and extrinsic muscles during most tongue movements, one might predict that individual pre-hypoglossal interneurons project to multiple motoneuronal pools. To test this hypothesis, one strain of pseudorabies virus was injected into the styloglossus muscle (an extrinsic lingual muscle) and a second strain of pseudorabies virus was injected into the intrinsic lingual muscles of the anterior tongue in the same preparation. Rats were perfused with fixative 84-96 h later, and dual-labeling immunohistochemistry was performed to reveal populations of single- and double-labeled brainstem neurons. Motoneurons innervating the different lingual muscles were spatially segregated within the hypoglossal motor nucleus, and no double-labeled motoneurons were observed. In contrast, pre-hypoglossal neurons projecting to each lingual motoneuron pool were highly overlapping in the reticular formation, and many were double-labeled. These observations suggest that coactivation of lingual muscles can be achieved, at least in part, through divergent projections of first-order interneurons to anatomically and functionally distinct pools of lingual motoneurons in the hypoglossal nucleus.

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Year:  2002        PMID: 12453486     DOI: 10.1016/s0306-4522(02)00489-x

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  18 in total

1.  A computational model for motor pattern switching between taste-induced ingestion and rejection oromotor behaviors.

Authors:  Sharmila Venugopal; Joseph B Travers; David H Terman
Journal:  J Comput Neurosci       Date:  2007-04       Impact factor: 1.621

Review 2.  Recent findings on the organization of central nervous system structures involved in the innervation of endocrine glands and other organs; observations obtained by the transneuronal viral double-labeling technique.

Authors:  Ida Gerendai; Ida E Tóth; Zsolt Boldogkoi; Béla Halász
Journal:  Endocrine       Date:  2009-05-06       Impact factor: 3.633

3.  Differential activation of chemically identified neurons in the caudal nucleus of the solitary tract in non-entrained rats after intake of satiating vs. non-satiating meals.

Authors:  Alison D Kreisler; Elizabeth A Davis; Linda Rinaman
Journal:  Physiol Behav       Date:  2014-02-06

Review 4.  Interoceptive modulation of neuroendocrine, emotional, and hypophagic responses to stress.

Authors:  James W Maniscalco; Linda Rinaman
Journal:  Physiol Behav       Date:  2017-01-14

5.  Noradrenergic terminal density varies among different groups of hypoglossal premotor neurons.

Authors:  Caroline E Boyle; Anjum Parkar; Amanda Barror; Leszek Kubin
Journal:  J Chem Neuroanat       Date:  2019-05-22       Impact factor: 3.052

6.  Diverse physiological properties of hypoglossal motoneurons innervating intrinsic and extrinsic tongue muscles.

Authors:  J C Wealing; M Cholanian; E G Flanigan; R B Levine; R F Fregosi
Journal:  J Neurophysiol       Date:  2019-09-18       Impact factor: 2.714

7.  Serotonergic projections from the caudal raphe nuclei to the hypoglossal nucleus in male and female rats.

Authors:  Jessica R Barker; Cathy F Thomas; Mary Behan
Journal:  Respir Physiol Neurobiol       Date:  2008-11-27       Impact factor: 1.931

8.  Extensive reorganization of primary afferent projections into the gustatory brainstem induced by feeding a sodium-restricted diet during development: less is more.

Authors:  Jamie E Mangold; David L Hill
Journal:  J Neurosci       Date:  2007-04-25       Impact factor: 6.167

9.  Hindbrain glucagon-like peptide-1 neurons track intake volume and contribute to injection stress-induced hypophagia in meal-entrained rats.

Authors:  Alison D Kreisler; Linda Rinaman
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2016-03-02       Impact factor: 3.619

10.  Discharge of the hypoglossal nerve cannot distinguish eupnea from gasping, as defined by phrenic discharge, in the in situ mouse.

Authors:  Walter M St John; J C Leiter
Journal:  J Appl Physiol (1985)       Date:  2009-05-28
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