Literature DB >> 25194193

Discharge properties of upper airway motor units during wakefulness and sleep.

John Trinder1, Amy S Jordan2, Christian L Nicholas2.   

Abstract

Upper airway muscle motoneurons, as assessed at the level of the motor unit, have a range of different discharge patterns, varying as to whether their activity is modulated in phase with the respiratory cycle, are predominantly inspiratory or expiratory, or are phasic as opposed to tonic. Two fundamental questions raised by this observation are: how are synaptic inputs from premotor neurons distributed over motoneurons to achieve these different discharge patterns; and how do different discharge patterns contribute to muscle function? We and others have studied the behavior of genioglossus (GG) and tensor palatini (TP) single motor units at transitions from wakefulness to sleep (sleep onset), from sleep to wakefulness (arousal from sleep), and during hypercapnia. Results indicate that decreases or increases in GG and TP muscle activity occur as a consequence of derecruitment or recruitment, respectively, of phasic and tonic inspiratory-modulated motoneurons, with only minor changes in rate coding. Further, sleep-wake state and chemical inputs to this "inspiratory system" appear to be mediated through the respiratory pattern generator. In contrast, phasic and tonic expiratory units and units with a purely tonic pattern, the "tonic system," are largely unaffected by sleep-wake state, and are only weakly influenced by chemical stimuli and the respiratory cycle. We speculate that the "inspiratory system" produces gross changes in upper airway muscle activity in response to changes in respiratory drive, while the "tonic system" fine tunes airway configuration with activity in this system being determined by local mechanical conditions.
© 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  genioglossus; motoneuron; motor unit; sleep; tensor palatini; upper airway muscles

Mesh:

Year:  2014        PMID: 25194193     DOI: 10.1016/B978-0-444-63488-7.00004-5

Source DB:  PubMed          Journal:  Prog Brain Res        ISSN: 0079-6123            Impact factor:   2.453


  6 in total

1.  Common drive to the upper airway muscle genioglossus during inspiratory loading.

Authors:  Michael J Woods; Christian L Nicholas; John G Semmler; Julia K M Chan; Amy S Jordan; John Trinder
Journal:  J Neurophysiol       Date:  2015-09-16       Impact factor: 2.714

2.  Catecholaminergic A1/C1 neurons contribute to the maintenance of upper airway muscle tone but may not participate in NREM sleep-related depression of these muscles.

Authors:  Irma Rukhadze; Nancy J Carballo; Sathyajit S Bandaru; Atul Malhotra; Patrick M Fuller; Victor B Fenik
Journal:  Respir Physiol Neurobiol       Date:  2017-07-12       Impact factor: 1.931

3.  Computational model of brain-stem circuit for state-dependent control of hypoglossal motoneurons.

Authors:  Mohsen Naji; Maxim Komarov; Giri P Krishnan; Atul Malhotra; Frank L Powell; Irma Rukhadze; Victor B Fenik; Maxim Bazhenov
Journal:  J Neurophysiol       Date:  2018-04-04       Impact factor: 2.714

Review 4.  Neural Control of the Upper Airway: Respiratory and State-Dependent Mechanisms.

Authors:  Leszek Kubin
Journal:  Compr Physiol       Date:  2016-09-15       Impact factor: 9.090

5.  Arousal Intensity is a Distinct Pathophysiological Trait in Obstructive Sleep Apnea.

Authors:  Jason Amatoury; Ali Azarbarzin; Magdy Younes; Amy S Jordan; Andrew Wellman; Danny J Eckert
Journal:  Sleep       Date:  2016-12-01       Impact factor: 5.849

Review 6.  Sleeping tongue: current perspectives of genioglossus control in healthy individuals and patients with obstructive sleep apnea.

Authors:  Jennifer M Cori; Fergal J O'Donoghue; Amy S Jordan
Journal:  Nat Sci Sleep       Date:  2018-06-15
  6 in total

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