Literature DB >> 2118178

Discharge of vagal pulmonary receptors differentially alters neural activities during various stages of expiration in the cat.

W M St John1, D Zhou.   

Abstract

1. The purpose was to evaluate the hypothesis that neural expiration is composed of two phases: I, a post inspiratory period; and II, the period at which expiratory activities of spinal nerves reach peak values. We hypothesized that the discharge of pulmonary stretch receptors might differentially alter neural activities during these two phases. 2. Activities of the phrenic nerve, intercostal nerve and nerves innervating the thyroarytenoid muscle of the larynx and triangularis sterni muscle of the chest wall were recorded in decerebrate and paralysed cats. 3. The experimental animals were ventilated with a servo-respirator which produced changes in tracheal pressure, and lung volume, in parallel with alterations in integrated activity of the phrenic nerve. 4. In order to assess the influence of the discharge of slowly adapting pulmonary stretch receptors upon neural activities during expiration, lung volume was held at end-expiratory or end-inspiratory levels for individual respiratory cycles. 5. When pulmonary inflation was prevented, phrenic activity increased, as did activity of the thyroarytenoid nerve during early expiration. In contrast, activities of the triangularis sterni and intercostal nerves during mid- to late expiration declined. 6. Holding the lungs at end-inspiratory levels caused a reduction of thyroarytenoid activity and increases in peak triangularis sterni and intercostal activities. Neural expiration typically continued as long as the lungs were maintained at the end-inspiratory level. 7. Responses were qualitatively similar in hypocapnia, normocapnia and hypercapnia, but the magnitude of changes in neural activities was typically augmented with elevations in end-tidal fractional concentrations of CO2. 8. We conclude that the discharge of slowly adapting pulmonary stretch receptors inhibits neural activities during early expiration and augments activities during mid-to late expiration. Hence, our data support the concept that neural expiration is composed of two stages in which neural activities may be differentially controlled.

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Year:  1990        PMID: 2118178      PMCID: PMC1189797          DOI: 10.1113/jphysiol.1990.sp018051

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  12 in total

1.  Differing control of neural activities during various portions of expiration in the cat.

Authors:  W M St John; D Zhou
Journal:  J Physiol       Date:  1989-11       Impact factor: 5.182

2.  An inexpensive servo-respirator based upon regulation of a shunt resistance.

Authors:  J A Daubenspeck; D Pichon; K V Knuth; D Bartlett; W M St John
Journal:  Respir Physiol       Date:  1988-07

3.  The differential organization of medullary post-inspiratory activities.

Authors:  D W Richter; D Ballantyne; J E Remmers
Journal:  Pflugers Arch       Date:  1987-11       Impact factor: 3.657

4.  Reflex prolongation of stage I of expiration.

Authors:  J E Remmers; D W Richter; D Ballantyne; C R Bainton; J P Klein
Journal:  Pflugers Arch       Date:  1986-08       Impact factor: 3.657

5.  Post-synaptic inhibition of bulbar inspiratory neurones in the cat.

Authors:  D Ballantyne; D W Richter
Journal:  J Physiol       Date:  1984-03       Impact factor: 5.182

Review 6.  [Activity of the expiratory laryngeal motor neurons].

Authors:  J C Barillot; M Dussardier
Journal:  J Physiol (Paris)       Date:  1976-06

7.  Comparative influence of proprioceptors and chemoreceptors in the control of respiratory muscles.

Authors:  B Bishop; H Bachofen
Journal:  Acta Neurobiol Exp (Wars)       Date:  1973       Impact factor: 1.579

8.  Differential alteration by hypercapnia and hypoxia of the apneustic respiratory pattern in decerebrate cats.

Authors:  W M St John
Journal:  J Physiol       Date:  1979-02       Impact factor: 5.182

9.  Respiratory activities of intralaryngeal branches of the recurrent laryngeal nerve.

Authors:  D Zhou; Q Huang; W M St John; D Bartlett
Journal:  J Appl Physiol (1985)       Date:  1989-09

Review 10.  Generation and maintenance of the respiratory rhythm.

Authors:  D W Richter
Journal:  J Exp Biol       Date:  1982-10       Impact factor: 3.312

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  8 in total

1.  Vestibular and cerebellar modulation of expiratory motor activities in the cat.

Authors:  Q Huang; D Zhou; W M St John
Journal:  J Physiol       Date:  1991-05       Impact factor: 5.182

2.  Some reflex cardioinhibitory responses in the cat and their modulation by central inspiratory neuronal activity.

Authors:  M D Daly
Journal:  J Physiol       Date:  1991-08       Impact factor: 5.182

3.  Bifurcation of the respiratory response to lung inflation in anesthetized dogs.

Authors:  Jaroslaw R Romaniuk; Thomas E Dick; Eugene N Bruce; Anthony F DiMarco; Krzysztof E Kowalski
Journal:  Respir Physiol Neurobiol       Date:  2017-07-08       Impact factor: 1.931

4.  Interaction between central pattern generators for breathing and swallowing in the cat.

Authors:  T E Dick; Y Oku; J R Romaniuk; N S Cherniack
Journal:  J Physiol       Date:  1993-06       Impact factor: 5.182

5.  Phase-dependent dynamic responses of respiratory motor activities following perturbation of the cycle in the cat.

Authors:  Y Oku; T E Dick; N S Cherniack
Journal:  J Physiol       Date:  1993-02       Impact factor: 5.182

6.  Glycinergic inhibition is essential for co-ordinating cranial and spinal respiratory motor outputs in the neonatal rat.

Authors:  M Dutschmann; J F R Paton
Journal:  J Physiol       Date:  2002-09-01       Impact factor: 5.182

7.  The bulbar network of respiratory neurons during apneusis induced by a blockade of NMDA receptors.

Authors:  O Pierrefiche; A S Foutz; J Champagnat; M Denavit-Saubié
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

8.  The course of lung inflation alters the central pattern of tracheobronchial cough in cat-The evidence for volume feedback during cough.

Authors:  Ivan Poliacek; Michal Simera; Marcel Veternik; Zuzana Kotmanova; Teresa Pitts; Jan Hanacek; Jana Plevkova; Peter Machac; Nadezda Visnovcova; Jakub Misek; Jan Jakus
Journal:  Respir Physiol Neurobiol       Date:  2016-04-25       Impact factor: 1.931

  8 in total

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