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Effect of sulfur dioxide on mucociliary activity and ciliary beat frequency in guinea pig trachea

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Summary

The effects of 30 min exposure to sulfur dioxide on mucociliary activity (MCA) and ciliary beat frequency (CBF) were studied in 31 guinea pig tracheas. MCA was measured by recording the light reflected from ciliated mucous membranes using an infrared bar code reader. CBF of single ciliated cells obtained by brushing was measured with phase-contrast microscopy. Each tracheal sample was exposed to SO2 at concentrations ranging from 2.5 to 12.5 ppm, or to air for control purposes. MCA and CBF were measured before and immediately after gas exposure. A reduction in mean MCA of 63% (P = 0.0007) and statistically insignificant changes in CBF (P > 0.05) were recorded at concentrations of 2.5 PPM SO2. Higher SO2 concentrations caused a further impairment of MCA as well as a dose-dependent decrease in CBF (P = 0.002). A concentration of 12.5 PPM SO2 induced a decrease from baseline values of approximately 80% in mean MCA and of roughly 70% in mean CBE This study demonstrates a dose-dependent SO2-induced decrease in MCA of guinea pig tracheas. The decrease in MCA was associated with an impairment of CBF only at SO2 concentrations higher than 5.0 ppm.

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References

  1. Abraham WM, Sielczak MW, Delehunt JC, Marchette B, Wanner A (1986) Impairment of tracheal mucociliary clearance but not ciliary beat frequency by a combination of low level ozone and sulfur dioxide in sheep. Eur J Respir Dis 68:114–120

    PubMed  Google Scholar 

  2. Andersen I, Lundqvist GR, Jensen PL, Proctor DF (1974) Human response to controlled levels of sulfur dioxide. Arch Environ Health 28:31–39

    PubMed  Google Scholar 

  3. Asmundsson T, Kilburn KH, McKenzie WN (1973) Injury and metaplasia of airway cells due to SO2. Lab Invest 29:41–53

    PubMed  Google Scholar 

  4. Bethel RA, Epstein J, Sheppard D, Nadel JA, Boushey HA (1983) Sulfur dioxide-induced bronchoconstriction in freely breathing, exercising, asthmatic subjects. Am Rev Resp Dis 128:987–990

    PubMed  Google Scholar 

  5. Buechley RW, Riggan WB, Hasselblad V, Van Bruggen JB (1973) SO2 levels and perturbations in mortality. Arch Environ Health 27:134–137

    PubMed  Google Scholar 

  6. Cralley LV (1942) The effect of irritant gases upon the rate of ciliary activity. J Ind Hyg Toxic 24:193–198

    Google Scholar 

  7. Dalham T (1961) Studies on the effect of sulfur dioxide on ciliary activity in rabbit trachea in vivo and in vitro and on the resorptional capacity of the nasal cavity. Am Rev Resp Dis 83:566–567

    PubMed  Google Scholar 

  8. Frank NR, Yoder RE, Brain JD, Yokoyama E (1969) SO2 (35S labeled) absorption by the nose and mouth under conditions of varying concentration and flow. Arch Environ Health 18:315–322

    PubMed  Google Scholar 

  9. French JG, Lowrimore G, Nelson WC, Finklea JF, English T, Hertz M (1973) The effect of sulfur dioxide and suspended sulfates on respiratory disease. Arch Environ Health 27:129–133

    PubMed  Google Scholar 

  10. Giddens WE, Fairchild GA (1972) Effects of sulfur dioxide on the nasal mucosa of mice. Arch Environ Health 25:166–173

    PubMed  Google Scholar 

  11. Glasser M, Grienberg L, Field F (1967) Mortality and morbidity during a period of high levels of air pollution: New York, November 23–25, 1965. Arch Environ Health 15:684–694

    PubMed  Google Scholar 

  12. Hirsch JA, Swenson EW, Wanner A (1975) Tracheal mucous transport in beagles after long-term exposure to 1 ppm sulfur dioxide. Arch Environ Health 30:249–253

    PubMed  Google Scholar 

  13. Holma BO (1985) Influence of buffer capacity and pH-dependent rheological properties of respiratory mucus on health effects due to acidic pollution. Sci Tot Environ 41:101–123

    Google Scholar 

  14. Holma BO (1989) Effects of inhaled acids on airway mucus and its consequences for health. Environ Health Perspect 79:109–113

    PubMed  Google Scholar 

  15. Holma BO, Lindegren M, Andersen JM (1977) pH effects on ciliomotility and morphology of respiratory mucosa. Arch Environ Health 32:216–226

    PubMed  Google Scholar 

  16. Hyde D, Orthoefer J, Dungworth D, Tyler W, Carter R, Lum H (1978) Morphometric and morphologic evaluation of pulmonary lesions in beagle dogs chronically exposed to high ambient levels of air pollutants. Lab Invest 38:455–469

    PubMed  Google Scholar 

  17. Iravani J (1968) Das Flimmerepithel. Beitr Klin Tuberk 138:313–324

    Google Scholar 

  18. Kirkpatrick MB, Sheppard D, Nadel JA, Boushey HA (1982) Effect of the oronasal breathing route on sulfur dioxide-induced bronchoconstriction in exercising asthmatic subjects. Am Rev Resp Dis 125:627–631

    PubMed  Google Scholar 

  19. Lopez-Vidriero MT (1981) Airway mucus: production and composition. Chest 80:799–804

    PubMed  Google Scholar 

  20. Lopez-Vidriero MT, Charman J, Keal E, Silva DJ, Reid LM (1973) Sputum viscocity: correlation with chemical and clinical features in chronic bronchitis. Thorax 28:401–408

    PubMed  Google Scholar 

  21. Majima Y, Swift DL, Bang BS, Bang FB (1985) Mechanism of slowing of mucociliary transport induced by SO2 exposure. Ann Biomed Eng 13(6):515–530

    PubMed  Google Scholar 

  22. Seltzer J, Scanlon, Drazen JM, Ingram RH, Reid L (1984) Morphologic correlation of physiologic changes caused by SO2-induced bronchitis is dogs. Am Rev Resp Dis 129:790–797

    PubMed  Google Scholar 

  23. Sheppard D, Wong WS, Uehara CF, Nadel JA, Boushey HA (1980) Lower threshold and greater bronchomotor responsiveness of asthmatic subjects to sulfur dioxide. Am Rev Resp Dis 122:873–878

    PubMed  Google Scholar 

  24. Sheppard D, Saisho A, Nadel JA, Boushey HA (1981) Exercise increases sulfur dioxide-induced bronchoconstriction in asthmatic subjects. Am Rev Resp Dis 123:486–491

    PubMed  Google Scholar 

  25. Shih CK, Litt M, Khan MA, Wolf DP (1977) Effect of nondialyzable solids concentration and viscoelasticity on ciliary transport of tracheal mucus. Am Rev Resp Dis 115:989–995

    PubMed  Google Scholar 

  26. Spiegelman JR, Hanson GD, Lazarus A, Bennett RJ, Lippmann M, Albert RE (1978) Effect of acute sulfur dioxide exposure on bronchial clearance in the donkey. Arch Environ Health 17:321–326

    Google Scholar 

  27. Ukai K, Bang BG, Bang FB (1984) Effect of infection and SO2 exposure on nasal and paranasal mucociliary clearance in intact chickens. Arch Otorhinolaryngol 239:1–6

    PubMed  Google Scholar 

  28. Vai F, Fournier MF, Lafuma JC, Touaty E, Pariente R (1980) SO2-induced bronchopathy in the rat: abnormal permeability of the bronchial epithelium in vivo and in vitro after anatomic recovery. Am Rev Resp Dis 121:851–858

    PubMed  Google Scholar 

  29. Voisin C, Aerts C, Houdret JL (1974) Methode d'etude des effects du NO2 sur les macrophages alvéolaires de cobaye en survie in vitro. Rev Fr Mal Resp 2:93–97

    Google Scholar 

  30. Wakabayashi M, Bang BG, Bang FB (1977) Mucocililary transport in chickens infected with Newcastle disease virus an exposed to sulfur dioxide. Arch Environ Health 32(33):101–108

    PubMed  Google Scholar 

  31. Wollf RK, Dolovich M, Rossman CM, Newhouse MT (1975) Sulfur dioxide and tracheobronchial clearance in man. Arch Environ Health 30:521–527

    PubMed  Google Scholar 

  32. Wong LB, Yeates DB (1990) Stimulation of tracheal ciliary beat frequency by localized tissue incision. J Appl Physiol 68(1):411–416

    PubMed  Google Scholar 

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Knorst, M.M., Kienast, K., Riechelmann, H. et al. Effect of sulfur dioxide on mucociliary activity and ciliary beat frequency in guinea pig trachea. Int. Arch Occup Environ Heath 65, 325–328 (1994). https://doi.org/10.1007/BF00405697

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  • DOI: https://doi.org/10.1007/BF00405697

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