Literature DB >> 28250153

Microinjection of kynurenic acid in the rostral nucleus of the tractus solitarius disrupts spatiotemporal aspects of mechanically induced tracheobronchial cough.

Ivan Poliacek1,2, Teresa Pitts1,3, Melanie J Rose1, Paul W Davenport1, Michal Simera2, Marcel Veternik2, Zuzana Kotmanova2, Donald C Bolser4.   

Abstract

The importance of neurons in the nucleus of the solitary tract (NTS) in the production of coughing was tested by microinjections of the nonspecific glutamate receptor antagonist kynurenic acid (kyn; 100 mM in artificial cerebrospinal fluid) in 15 adult spontaneously breathing anesthetized cats. Repetitive coughing was elicited by mechanical stimulation of the intrathoracic airway. Electromyograms (EMG) were recorded from inspiratory parasternal and expiratory transversus abdominis (ABD) muscles. Bilateral microinjections of kyn into the NTS rostral to obex [55 ± 4 nl total in 2 locations (n = 6) or 110 ± 4 nl total in 4 locations (n = 5)], primarily the ventrolateral subnucleus, reduced cough number and expiratory cough efforts (amplitudes of ABD EMG and maxima of esophageal pressure) compared with control. These microinjections also markedly prolonged the inspiratory phase, all cough-related EMG activation, and the total cough cycle duration as well as some other cough-related time intervals. In response to microinjections of kyn into the NTS rostral to the obex respiratory rate decreased, and there were increases in the durations of the inspiratory and postinspiratory phases and mean blood pressure. However, bilateral microinjections of kyn into the NTS caudal to obex as well as control vehicle microinjections in the NTS location rostral to obex had no effect on coughing or cardiorespiratory variables. These results are consistent with the existence of a critical component of the cough rhythmogenic circuit located in the rostral ventral and lateral NTS. Neuronal structures of the rostral NTS are significantly involved specifically in the regulation of cough magnitude and phase timing.NEW & NOTEWORTHY The nucleus of the solitary tract contains significant neuronal structures responsible for control of 1) cough excitability, 2) motor drive during cough, 3) cough phase timing, and 4) cough rhythmicity. Significant elimination of neurons in the solitary tract nucleus results in cough apraxia (incomplete and/or disordered cough pattern). The mechanism of the cough impairment is different from that for the concomitant changes in breathing.
Copyright © 2017 the American Physiological Society.

Entities:  

Keywords:  abdominal muscle activity; cough; cough phase timing; kynurenate; nucleus of solitary tract

Mesh:

Substances:

Year:  2017        PMID: 28250153      PMCID: PMC5454471          DOI: 10.1152/jn.00935.2016

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  67 in total

Review 1.  Functional organization of the central cough generation mechanism.

Authors:  Donald C Bolser; Paul W Davenport
Journal:  Pulm Pharmacol Ther       Date:  2002       Impact factor: 3.410

2.  Identification of neurons receiving input from pulmonary rapidly adapting receptors in the cat.

Authors:  J Lipski; K Ezure; R B Wong She
Journal:  J Physiol       Date:  1991-11       Impact factor: 5.182

3.  Effects of focal cooling of medulla oblongata structures on quiet breathing in cats.

Authors:  J Jakus; A Stránsky; B Nagyová; A Oravec; L Bosel'ová; H Baráni
Journal:  Physiol Bohemoslov       Date:  1990

4.  The functional subdivisions of the nucleus tractus solitarii of the cat in relation to the carotid sinus nerve reflex.

Authors:  M Miura; K Takayama
Journal:  J Auton Nerv Syst       Date:  1986-01

5.  Presynaptic depolarization in myelinated vagal afferent fibres terminating in the nucleus of the tractus solitarius in the cat.

Authors:  D W Richter; D Jordan; D Ballantyne; M Meesmann; K M Spyer
Journal:  Pflugers Arch       Date:  1986-01       Impact factor: 3.657

6.  Kainic acid lesions to the lateral tegmental field of medulla: effects on cough, expiration and aspiration reflexes in anesthetized cats.

Authors:  J Jakus; A Stránsky; I Poliacek; H Baráni; L Bosel'ová
Journal:  Physiol Res       Date:  2000       Impact factor: 1.881

7.  Influence of central antitussive drugs on the cough motor pattern.

Authors:  D C Bolser; J A Hey; R W Chapman
Journal:  J Appl Physiol (1985)       Date:  1999-03

8.  Glutamate, gamma-aminobutyric acid and tachykinin-immunoreactive synapses in the cat nucleus tractus solitarii.

Authors:  S Saha; T F Batten; P N Mcwilliam
Journal:  J Neurocytol       Date:  1995-01

9.  Modulation of the cough reflex by antitussive agents within the caudal aspect of the nucleus tractus solitarii in the rabbit.

Authors:  Donatella Mutolo; Fulvia Bongianni; Elenia Cinelli; Giovanni A Fontana; Tito Pantaleo
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2008-05-14       Impact factor: 3.619

10.  The cough reflex is upregulated by lisinopril microinjected into the caudal nucleus tractus solitarii of the rabbit.

Authors:  Elenia Cinelli; Fulvia Bongianni; Tito Pantaleo; Donatella Mutolo
Journal:  Respir Physiol Neurobiol       Date:  2015-07-30       Impact factor: 1.931

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  3 in total

1.  Role of the dorsomedial medulla in suppression of cough by codeine in cats.

Authors:  Ivan Poliacek; Michal Simera; Marcel Veternik; Zuzana Kotmanova; Donald C Bolser; Peter Machac; Jan Jakus
Journal:  Respir Physiol Neurobiol       Date:  2017-08-01       Impact factor: 1.931

2.  GABA-ergic neurotransmission in the nucleus of the solitary tract modulates cough in the cat.

Authors:  Z Kotmanova; M Simera; M Veternik; L Martvon; J Misek; J Jakus; T Y Shen; M N Musselwhite; T Pitts; D C Bolser; I Poliacek
Journal:  Respir Physiol Neurobiol       Date:  2018-02-21       Impact factor: 1.931

3.  The role of neuronal excitation and inhibition in the pre-Bötzinger complex on the cough reflex in the cat.

Authors:  Tabitha Y Shen; Ivan Poliacek; Melanie J Rose; M Nicholas Musselwhite; Zuzana Kotmanova; Lukas Martvon; Teresa Pitts; Paul W Davenport; Donald C Bolser
Journal:  J Neurophysiol       Date:  2021-12-08       Impact factor: 2.714

  3 in total

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