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Lung reflexes and receptor activity in a rabbit model of pulmonary fibrosis

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Abstract

Our objective was to see if activity of individual slowly and rapidly adapting pulmonary receptors was changed by pulmonary fibrosis.

Diffuse interstitial lung fibrosis of several weeks’ standing was induced in 8 rabbits. They displayed changes in lung mechanics and patterns of breathing, when compared to control rabbits, similar to those seen in patients who develop pulmonary fibrosis. Lung reflexes in the fibrotic rabbits were more profoundly changed than eupneic breathing in a way that could be interpreted as slowly adapting receptor activity, which was increased, being overpowered by a prepotent input from pulmonary rapidly adapting receptors. An increase in number of active rapidly adapting receptors was found in the fibrotic rabbits during direct vagal recording. We have demonstrated that pulmonary receptor activity is changed by lung fibrosis. It may be that these changes in receptor activity produce conflicting respiratory drives that could result in the sensation of dyspnea.

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References

  1. Armstrong DJ, Miller SA (1980) Lung irritant and C-fibre responses to embolism in thrombocytopenic rabbits. J Physiol 303:41–42

    Google Scholar 

  2. Bartlett D Jr, Sant’ Ambrogio G, Wise JCM (1976) Transduction properties of tracheal stretch receptors. J Physiol 258:421–432

    PubMed  Google Scholar 

  3. Bradley GW, Scheumier N (1977) The transduction properties of tracheal stretch receptors in vitro. Respir Physiol 31:356–375

    Article  Google Scholar 

  4. Carrington CG (1968) Organizing interstitial pneumonia: definition of the lesion and attempts to devise an experimental model. Yale J Biol Med 40:352–363

    PubMed  CAS  Google Scholar 

  5. Coleridge HM, Coleridge JCG (1986) Reflexes evoked from the respiratory tract. In: Fishman AP (ed) Handbook of physiology: respiration. Washington, DC: Am Physiol Soc p 395–429

    Google Scholar 

  6. Clark FJ, Euler C von (1972) On the regulation of depth and rate of breathing. J Physiol 222:267–295

    PubMed  CAS  Google Scholar 

  7. Davies A, Roumy M (1982) The effect of transient stimulation of lung irritant receptors on the pattern of breathing in rabbits. J Physiol (London) 324:389–401

    CAS  Google Scholar 

  8. Derks CM, Jacobovitz-Derks DJ (1977) Embolic pneumopathy induced by oleic acid; a systematic morphologic study. Am J Pathol 87:143–151

    PubMed  CAS  Google Scholar 

  9. Euler C von (1970) Fusimotor activity in spindle control of natural movements with special reference to respiration. In: Andersen D, Jansen J (eds) Excitatory synaptic mechanisms. London: Plenum Press, pp 341–347

    Google Scholar 

  10. Frankstein SI, Sergeeva ZN (1966) Tonic activity of lung receptors in normal and pathological states. Nature 210:1054–1055

    Article  PubMed  CAS  Google Scholar 

  11. Guz A, Noble MIM, Widdicombe JG, Trenchard D, Mushin WW (1966) The role of the vagal and glossopharyngeal afferent nerves in respiratory sensation, control of breathing and arterial pressure regulation in conscious man. Clin Sci 30:161–170

    PubMed  CAS  Google Scholar 

  12. Homberger AC (1968) Beitrag zum Nachweis von Kollapsafferenzen im Lungenvagus des Kaninchens. Helv Physiol Pharmacol Acta 6:97–118

    Google Scholar 

  13. Knowlton GC, Larraby MG (1970) A unitary analysis of pulmonary volume receptors. Am J Physiol 151:547–553

    Google Scholar 

  14. Knox CK (1973) Characteristics of inflation and deflation reflexes during expiration in the cat. J Neurophysiol 36:284–295

    PubMed  CAS  Google Scholar 

  15. Kohl J, Koller EA (1980) Stretch receptor activity during irritant induced tachypnoea in the rabbit. Pfluegers Arch 386:231–237

    Article  CAS  Google Scholar 

  16. Lourenco RV, Turino GM, Davidson LAG, Fishman AP (1965) The regulation of ventilation in diffuse pulmonary fibrosis. Am J Med 38:199–216

    Article  PubMed  CAS  Google Scholar 

  17. Marshall R, Karlish AJ (1971) Lung function in sarcoidosis. Thorax 26:402–405

    Article  PubMed  CAS  Google Scholar 

  18. Mead J, Whittenberger JL (1953) Physical properties of human lungs measured during spontaneous respiration. J Appl Physiol 5:779–796

    Google Scholar 

  19. Mills J, Sellick H, Widdicombe JG (1973) The role of lung irritant receptors in respiratory responses to multiple pulmonary embolism, anaphylaxis and histamine-induced bronchoconstriction. J Physiol 235:775–782

    Google Scholar 

  20. Nadel JA, Widdicombe JG (1962) Effects of changes in blood gas tensions and carotid sinus pressure on tracheal volume and total lung resistance to air flow. J Physiol (Lond) 63:13–33

    Google Scholar 

  21. Paintal AS (1973) Vagal sensory receptors and their reflex effects. Physiol Rev 53:159–227

    PubMed  CAS  Google Scholar 

  22. Peltier LF (1956) Fat embolism III. The toxic properties of neutral fat and free fatty acids. Surgery 40:665–670

    PubMed  CAS  Google Scholar 

  23. Phillipson EA, Murphy E, Kozar LF, Schultze RK (1975) Role of vagal stimuli in exercise ventilation in dogs with experimental pneumonitis. J Appl Physiol 39:76–85

    PubMed  CAS  Google Scholar 

  24. Renzi G, Milic-Emili J, Grassino AE (1982) The pattern of breathing in diffuse lung fibrosis. Clin Respir Physiol 18:461–472

    CAS  Google Scholar 

  25. Sant’Ambrogio, G (1982) Information arising from the tracheobronchial tree of mammals. Physiol Rev 62:531–569

    PubMed  CAS  Google Scholar 

  26. Sellick H, Widdicombe JG (1969) The activity of lung irritant receptors during pneumothorax, hyperpnoea and pulmonary vascular congestion. J Physiol (London) 203:359–382

    CAS  Google Scholar 

  27. Snider GL, Lucey EC, Stone PJ (1986) Animal models of emphysema. Am Rev Respir Dis 133:49–169

    Google Scholar 

  28. Vizek M, Frydrychova M, Houstek S, Palecek F (1983) Effect of vagal cooling on lung functional residual capacity in rats with pneumonia. Bull Eur Physiopathol Respir 19:23–26

    PubMed  CAS  Google Scholar 

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Davies, A., Pack, R.J. Lung reflexes and receptor activity in a rabbit model of pulmonary fibrosis. Lung 169, 263–273 (1991). https://doi.org/10.1007/BF02714162

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