Skip to main content
Log in

Ipratropium bromide protects against bronchoconstriction during bronchoscopy

  • Published:
Lung Aims and scope Submit manuscript

Abstract

Pulmonary function is reportedly impaired by fiberoptic bronchoscopy. We investigated the effect of two anticholinergic agents, intramuscular atropine and inhaled ipratropium bromide, on bronchoconstriction in 29 patients who were undergoing diagnostic bronchoscopy. The patients were divided into three groups; the first received 0.5 mg of atropine intramuscularly; the second took four puffs of 0.02 mg ipratropium bromide aerosolized by a metered-dose inhaler, and the third inhaled four puffs of a placebo. Fifteen minutes later a standardized topical anesthetic, lidocaine, was administered, and a bronchoscopic examination was performed. Pulmonary function was measured before and 15 minutes after each step. Pulmonary function was not affected by the treatment with anticholinergics or the placebo. In the placebo and the atropine groups, the topical anesthesia produced significant reductions in forced expiratory volume in 1 second (FEV,) and peak expiratory flow rate (PEFR); further reductions in these values were observed after bronchoscopy. In the group treated with ipratropium bromide there were no significant changes in FEV, and PEFR after topical anesthesia. Bronchoscopy induced significant reductions in FEV1 and PEFR, but the changes were significantly smaller than those seen in the placebo and atropine groups. The results suggest that the deleterious effect of bronchoscopy on pulmonary function is due to topical lidocaine anesthesia and to the bronchoscopic examination itself. Inhaled ipratropium bromide protects against these deleterious effects, whereas intramuscular atropine does not.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Aizawa H, Chung KF, Leikauf GD, Ueki I, Bethel RA, O'Byrne PM, Hirose T, Nadal JA (1985) Significance of thromboxane generation in ozone-induced airway hyperresponsiveness in dogs. J Appl Physiol 59:1918–1923

    Google Scholar 

  2. Anggard E, Samuelsson B (1965) Biosynthesis of prostaglandins from arachidonic acid in guinea pig lung. J Biol Chem 240:3518–3521

    Google Scholar 

  3. Beasley RCW, Featherstone RL, Church MK, Rafferty P, Varley JG, Harris A, Robinson C, Hollgate ST (1989) Effects of a thrombovane receptor antagonist on PGD2- and allergen-induced bronchoconstriction. J Appl Physiol 66:1685–1693

    Google Scholar 

  4. Chung KF, Aizawa H, Becker AB, Frick O, Gold WN, Nadal JA (1986) Inhibition of antigen-induced airway hyperresponsiveness by a thromboxane synthetase inhibitor (OKY-046) in allergic dogs. Am Rev Respir Dis 134:258–261

    Google Scholar 

  5. Chung KF, Aizawa H, Leikauf GD, Ueki I, Evans TW, Nadal JA (1986) Airway hyperresponsiveness induced by platelet-activating factor: role of thromboxane generation. J Pharmacol Exp Ther 236:580–584

    Google Scholar 

  6. Coleridge HM, Coleridge JCG (1986) Reflexes evoked from the tracheobranchial tree and lungs. In: Cherniack NS, Widdicombe JG (eds) Handbook of Physiology, Section 3. The respiratory system, vol. 11, part 2: Control of respiration. American Physiological Society, Washington, D.C., pp 395–429

    Google Scholar 

  7. Graybar GB, Harrington JK, Cowen KH, Spannhake EW, Hyman AL, McNamara DB, Kadowitz PJ (1986) Cyclooxygenase mediated airway response to leukotriene D4 in the cat. Prostaglandins 31:167–177

    Google Scholar 

  8. Greenberg R, Antonaccio MJ, Steinbacher T (1982) Thromboxane A2 mediated bronchoconstriction in anesthetized guinea pig. Eur J Pharmacol 80:19–27

    Google Scholar 

  9. Hamberg M, Samuelsson B (1973) Detection and isolation of an endoperooxidase intermediate in prostaglandin biosynthesis. Proc Natl Acad Sci USA 70:899–903

    Google Scholar 

  10. Hamberg M, Samuelsson B (1974) Prostaglandin endoperoxidases. VII. Novel transformation of arachidonic acid in guinea pig lung. Biochem Biophys Res Commun 61:942–949

    Google Scholar 

  11. Hamberg M, Sevensson J, Samuelsson B (1975) Thromboxanes: a new group of biologically active compounds derived from prostaglandin endoperoxidases. Proc Natl Acad Sci USA 72:2994–2998

    Google Scholar 

  12. Hanasaki K, Arita H (1988) Characterization of a new compound, S-145, as a specific TXA2 receptor antagonist in platelets. Thromb Res 50:365–376

    Google Scholar 

  13. Hanasaki K, Nagasaki T, Arita H (1989) Characterization of platelet thromboxane A2/prostaglandin H2 receptor by a novel tromboane receptor antagonist, [3H]S-145. Biochem Pharmacol 38:2007–2017

    Google Scholar 

  14. Laurindo FRM, Goldstein RE, Davenport NJ, Ezra D, Feuerstein GZ (1989) Mechanisms of hypotension produced by platelet-activating factor. J Appl Physiol 66:2681–2690

    Google Scholar 

  15. Liu F, Carrithers JA, Shirer HW, Orr JA (1992) Thromboxane A2 mimetic, U46619, and slowly adapting stretch receptor activity in the rabbit. Respir Physiol 88:77–86

    Google Scholar 

  16. Mais DE, Saussy DL, Chaikhouni A, Kochel PJ, Knapp DR, Hamanaka N, Halushka PV (1985) Pharmacological characterization of human and canine thromboxane A2/prostaglandin H2 receptors in platelets and blood vessels: evidence for different receptors. J Pharmacol Exp Ther 233:418–424

    Google Scholar 

  17. Munoz NM, Shioya T, Murphy TM, Primack S, Dame C, Sands MF, Leff AR (1986) Potentiation of vagal contractile response by the thromboxane mimetic U-46619. J Appl Physiol 61:1173–1179

    Google Scholar 

  18. Narisada M, Ohtani M, Watanabe F, Uchida K, Arita H, Doteuchi M, Hanasaki K, Kakushi H, Otani K, Hara S (1988) Synthesis and in vitro activity of various derivations of a novel thromboxane receptor antagonist, (+)-5(Z)-7-(3-endo-phenyl-sulfonylamine-[2,2,1]bicyclohept-2-exo-yl) heptenomic acid. J Med Chem 31: 1847–1854

    Google Scholar 

  19. Nugteren DH, Hazelhop E (1973) Isolation and properties of intermediates in prostaglandin biosynthesis. Biochem Biophys Acta 326:448–461

    Google Scholar 

  20. O'Byrne PM, Leikauf GD, Aizawa H, Bethel RA, Ueki I, Holtzman MJ, Nadel JA (1985) Leukotriene B4 induces airway hyperresponsiveness in dogs. J Appl Physiol 59:1941–1946

    Google Scholar 

  21. Spannhake EW, Lemen RJ, Wegmann MJ, Hyman AL, Kadowitz PJ (1978) Analysis of airway effects of PGH2 analogue in the anesthetized dog. J Appl Physiol 44:406–415

    Google Scholar 

  22. Svensson J, Standberg K, Tuvemo T, Hamberg M (1977) Thromboxane A2: effects on airway and vascular smooth muscle. Prostaglandins 14:425–436

    Google Scholar 

  23. Takano S, Ishimoto H, Nakahata N, Nakanishi H (1992) Thromboxane A2 receptor characterization in human astrocytoma cells and rabbit platelets by a new thromboxane antagonist, [3H]ONO NT-126. Res Commun Chem Path Pharmacol 76:155–170

    Google Scholar 

  24. Toda N, Nakajima M, Okamura T, Miyazaki M (1986) Interactions of thromboxane A2 analogs and prostaglandins in isolated dog arteries. J Cardiovasc Pharmacol 8:818–825

    Google Scholar 

  25. Tymkewycz PM, Jones RL, Wilson NH, Marr CG (1991) Heterogeneity of thromboxane A2 (TP-) receptors: evidence from antagonist but not agonist potency measurements. Br J Pharmacol 102:607–614

    Google Scholar 

  26. Underwood DC, Kriseman T, MacNamara DB, Hyman AL, Kadowitz PJ (1987) Blockade of thromboxane responses in the airway of the cat by SQ29548. J Appl Physiol 62:2193–2200

    Google Scholar 

  27. Vargaftig BB, Lefort J, Chingnard M, Benveniste J (1980) Platelet-activating factor induces a platelet-dependent bronchoconstriction unrelated to the formation of prostaglandin derivatives. Eur J Pharmacol 65:185–192

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Offprint request to: H. Aizawa

Rights and permissions

Reprints and permissions

About this article

Cite this article

Inoue, H., Aizawa, H., Takata, S. et al. Ipratropium bromide protects against bronchoconstriction during bronchoscopy. Lung 172, 293–298 (1994). https://doi.org/10.1007/BF00164311

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00164311

Key words

Navigation