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. 1986 Apr;66:61–71. doi: 10.1289/ehp.866661

Pulmonary function analysis in the rabbit following bronchochallenge to causative agents and mediators of the acute byssinotic response.

M P Bishop, P A Pilia, W J Moorman, S K Ainsworth
PMCID: PMC1474379  PMID: 3519204

Abstract

New Zealand White rabbits were acutely bronchochallenged for 5 min to ascertain airway responsiveness with six potential byssinogenic agents and mediators: 0.1 g/mL cotton dust extract (CDE), 0.1 g/mL cotton bract extract (CBE), 1 mg/mL endotoxin, 1 mg/mL n-formyl methionyl peptide (n-fMet), 10 mg/mL 5-hydroxytryptamine (5-HT), and 1 mg/mL prostaglandin F2 alpha (PGF2 alpha). Methacholine (MC), 10 mg/mL, was used as a control bronchoconstrictor. Clinically objective criteria were established using increases in resistance values compared to those obtained with saline controls. Animals were classified as: mild responders (Mi) = 125-149%; moderate responders (Mo) = 150-199%; or severe responders (S) = greater than 200%. Three of five (2Mo, 1S) rabbits showed increased pulmonary resistance to CDE bronchochallenge, 3/5 (1Mi, 1Mo, 1S) to CBE, 1/5 (Mo) to purified endotoxin, 4/5 (1Mo, 3S) to n-fMet, 3/5 (1Mi, 1Mo, 1S) to 5-HT, and 2/5 (1Mo, 1S) to PGF2 alpha. All five rabbits (1Mo, 4S) responded to MC bronchochallenge. Rabbits responded minimally to saline, the common solvent of all test agents; however, when challenged with methacholine, a known bronchoconstrictor, rabbits showed significant overt symptoms of acute respiratory distress with immediate and substantial increases in resistance over saline controls. CDE, CBE, and n-fMet inhalation challenge resulted in a majority or all animals showing increased resistance. 5-HT contained in CDE and CBE, exhibited similar resistance increases; however, endotoxin, also found in cotton dust, showed little airway reactivity. The rabbit is useful for characterizing changes in pulmonary function parameters seen in the acute byssinotic reaction. This study has demonstrated that bronchochallenge in the rabbit with potential byssinogenic agents (CDE, CBE, endotoxin, and n-fMet) and mediators (5-HT and PGF2 alpha) result in measurable changes in airway function, particularly increased resistance. Since bronchoconstriction is the major clinical manifestation of the acute byssinotic reaction in man and animals, it is likely that bronchoconstriction observed in cotton mill workers may be in part or totally the result of inherent dust constrictor substances or secondarily released mediators.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ainsworth S. K., Neuman R. E. Chemotaxins in cotton mill dust: possible etiologic agent(s) in byssinosis. Am Rev Respir Dis. 1981 Sep;124(3):280–284. doi: 10.1164/arrd.1981.124.3.280. [DOI] [PubMed] [Google Scholar]
  2. Ainsworth S. K., Neuman R. E. Chemotaxins in cotton mill dust: possible etiologic agent(s) in byssinosis. Am Rev Respir Dis. 1981 Sep;124(3):280–284. doi: 10.1164/arrd.1981.124.3.280. [DOI] [PubMed] [Google Scholar]
  3. Ainsworth S. K., Neuman R. E., Harley R. A. Histamine release from platelets for assay of byssinogenic substances in cotton mill dust and related materials. Br J Ind Med. 1979 Feb;36(1):35–42. doi: 10.1136/oem.36.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BULL J. W., MARSHALL J., SHAW D. A. Cerebral angiography in the diagnosis of the acute stroke. Lancet. 1960 Mar 12;1(7124):562–565. doi: 10.1016/s0140-6736(60)92774-4. [DOI] [PubMed] [Google Scholar]
  5. Bomski H., Otawski J., Bomska H. Hämatologische und serologische Untersuchungen bei Byssinose-gefährdeten Arbeitern. Int Arch Arbeitsmed. 1971;27(4):309–323. [PubMed] [Google Scholar]
  6. Bouhuys A. Byssinosis: scheduled asthma in the textile industry. Lung. 1976 Dec 29;154(1):3–16. doi: 10.1007/BF02713514. [DOI] [PubMed] [Google Scholar]
  7. Boushey H. A., Holtzman M. J., Sheller J. R., Nadel J. A. Bronchial hyperreactivity. Am Rev Respir Dis. 1980 Feb;121(2):389–413. doi: 10.1164/arrd.1980.121.2.389. [DOI] [PubMed] [Google Scholar]
  8. Cartier A., Malo J. L., Bégin P., Sestier M., Martin R. R. Time course of the bronchoconstriction induced by inhaled histamine and methacholine. J Appl Physiol Respir Environ Exerc Physiol. 1983 Mar;54(3):821–826. doi: 10.1152/jappl.1983.54.3.821. [DOI] [PubMed] [Google Scholar]
  9. Cavagna G., Foà V., Vigliani E. C. Effects in man and rabbits of inhalation of cotton dust or extracts and purified endotoxins. Br J Ind Med. 1969 Oct;26(4):314–321. doi: 10.1136/oem.26.4.314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Cinkotai F. F., Lockwood M. G., Rylander R. Airborne micro-organisms and prevalence of byssinotic symptoms in cotton mills. Am Ind Hyg Assoc J. 1977 Oct;38(10):554–559. doi: 10.1080/0002889778507669. [DOI] [PubMed] [Google Scholar]
  11. Eiser N. M., Mills J., McRae K. D., Snashall P. D., Guz A. Histamine receptors in normal human bronchi. Clin Sci (Lond) 1980 Jun;58(6):537–544. doi: 10.1042/cs0580537. [DOI] [PubMed] [Google Scholar]
  12. Elissalde M. H., Jr, Greenblatt G. A., Ziprin R. L. The role of prostaglandin F2 alpha in byssinosis. Am Ind Hyg Assoc J. 1980 May;41(5):382–384. doi: 10.1080/15298668091424924. [DOI] [PubMed] [Google Scholar]
  13. Fowler S. R., Ziprin R. L., Elissalde M. H., Jr, Greenblatt G. A. The etiology of byssinosis--possible role of prostaglandin F2alpha synthesis by alveolar macrophages. Am Ind Hyg Assoc J. 1981 Jun;42(6):445–448. doi: 10.1080/15298668191420035. [DOI] [PubMed] [Google Scholar]
  14. Harris T. R., Merchant J. A., Kilburn K. H., Hamilton J. D. Byssinosis and respiratory diseases of cotton mill workers. J Occup Med. 1972 Mar;14(3):199–206. doi: 10.1097/00043764-197203000-00001. [DOI] [PubMed] [Google Scholar]
  15. Hitchcock M., Piscitelli D. M., Bouhuys A. Histamine release from human lung by a component of cotton bracts. Arch Environ Health. 1973 Apr;26(4):177–182. doi: 10.1080/00039896.1973.10666252. [DOI] [PubMed] [Google Scholar]
  16. Holt P. G., Holt B. J., Beijer L., Rylander R. Platelet serotonin release by human polymorphonuclear leucocytes stimulated by cotton dust bacteria. Clin Exp Immunol. 1983 Jan;51(1):185–190. [PMC free article] [PubMed] [Google Scholar]
  17. Hook W. A., Schiffmann E., Aswanikumar S., Siraganian R. P. Histamine release by chemotactic, formyl methionine-containing peptides. J Immunol. 1976 Aug;117(2):594–596. [PubMed] [Google Scholar]
  18. Lopez-Vidriero M. T., Das I., Smith A. P., Picot R., Reid L. Bronchial secretion from normal human airways after inhalation of prostaglandin F2alpha, acetylcholine, histamine, and citric acid. Thorax. 1977 Dec;32(6):734–739. doi: 10.1136/thx.32.6.734. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Mathé A. A., Hedqvist P., Strandberg K., Leslie C. A. Aspects of prostaglandin function in the lung (first of two parts). N Engl J Med. 1977 Apr 14;296(15):850–855. doi: 10.1056/NEJM197704142961505. [DOI] [PubMed] [Google Scholar]
  20. Merchant J. A., Halprin G. M., Hudson A. R., Kilburn K. H., McKenzie W. N., Hurst D. J., Bermazohn P. Responses to cotton dust. Arch Environ Health. 1975 May;30(5):222–229. doi: 10.1080/00039896.1975.10666685. [DOI] [PubMed] [Google Scholar]
  21. Merchant J. A., Lumsden J. C., Kilburn K. H., O'Fallon W. M., Ujda J. R., Germino V. H., Jr, Hamilton J. D. Dose response studies in cotton textile workers. J Occup Med. 1973 Mar;15(3):222–230. [PubMed] [Google Scholar]
  22. Morey P. R. Botanically what is raw cotton dust? Am Ind Hyg Assoc J. 1979 Aug;40(8):702–707. doi: 10.1080/15298667991430181. [DOI] [PubMed] [Google Scholar]
  23. Mundie T. G., Boackle R. J., Ainsworth S. K. In vitro alternative and classical activation of complement by extracts of cotton mill dust: a possible mechanism in the pathogenesis of byssinosis. Environ Res. 1983 Oct;32(1):47–56. doi: 10.1016/0013-9351(83)90190-1. [DOI] [PubMed] [Google Scholar]
  24. Mundie T. G., Cordova-Salinas M., Bray V. J., Ainsworth S. K. Bioassays of smooth muscle contracting agents in cotton mill dust and bract extracts: arachidonic acid metabolites as possible mediators of the acute byssinotic reaction. Environ Res. 1983 Oct;32(1):62–71. doi: 10.1016/0013-9351(83)90192-5. [DOI] [PubMed] [Google Scholar]
  25. Nogrady S. G., Bevan C. Inhaled antihistamines--bronchodilatation and effects on histamine- and methacholine-induced bronchoconstriction. Thorax. 1978 Dec;33(6):700–704. doi: 10.1136/thx.33.6.700. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Orehek J., Gayrard P. Les tests de provocation bronchique non-spécifiques dans l'asthme. Bull Eur Physiopathol Respir. 1976 Jul-Aug;12(4):565–598. [PubMed] [Google Scholar]
  27. PERNIS B., VIGLIANI E. C., CAVAGNA C., FINULLI M. The role of bacterial endotoxins in occupational diseases caused by inhaling vegetable dusts. Br J Ind Med. 1961 Apr;18:120–129. doi: 10.1136/oem.18.2.120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Russell J. A., Gilberstadt M. L., Rohrbach M. S. Constrictor effect of cotton bract extract on isolated canine airways. Am Rev Respir Dis. 1982 Jun;125(6):727–733. doi: 10.1164/arrd.1982.125.6.727. [DOI] [PubMed] [Google Scholar]
  29. Rylander R., Snella M. C. Acute inhalation toxicity of cotton plant dusts. Br J Ind Med. 1976 Aug;33(3):175–180. doi: 10.1136/oem.33.3.175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Schiffmann E., Corcoran B. A., Wahl S. M. N-formylmethionyl peptides as chemoattractants for leucocytes. Proc Natl Acad Sci U S A. 1975 Mar;72(3):1059–1062. doi: 10.1073/pnas.72.3.1059. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Smith A. P., Cuthbert M. F. Prostaglandins and resistance to beta adrenoceptor stimulants. Br Med J. 1972 Apr 15;2(5806):166–166. doi: 10.1136/bmj.2.5806.166-b. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Snyderman R., Gewurz H., Mergenhagen S. E. Interactions of the complement system with endotoxic lipopolysaccharide. Generation of a factor chemotactic for polymorphonuclear leukocytes. J Exp Med. 1968 Aug 1;128(2):259–275. doi: 10.1084/jem.128.2.259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Snyderman R., Pike M. C. N-Formylmethionyl peptide receptors on equine leukocytes initiate secretion but not chemotaxis. Science. 1980 Jul 25;209(4455):493–495. doi: 10.1126/science.6248959. [DOI] [PubMed] [Google Scholar]
  34. Svenssen J., Strandberg K., Tuvemo T., Hamberg M. Thromboxane A2: effects on airway and vascular smooth muscle. Prostaglandins. 1977 Sep;14(3):425–436. doi: 10.1016/0090-6980(77)90258-1. [DOI] [PubMed] [Google Scholar]
  35. Van der Zwan J. C., Orie N. G., Kauffman H. F., Wiers P. W., de Vries K. Bronchial obstructive reactions after inhalation with endotoxin and precipitinogens of Haemophilus influenzae in patients with chronic non-specific lung disease. Clin Allergy. 1982 Nov;12(6):547–559. doi: 10.1111/j.1365-2222.1982.tb02553.x. [DOI] [PubMed] [Google Scholar]
  36. Williams L. T., Snyderman R., Pike M. C., Lefkowitz R. J. Specific receptor sites for chemotactic peptides on human polymorphonuclear leukocytes. Proc Natl Acad Sci U S A. 1977 Mar;74(3):1204–1208. doi: 10.1073/pnas.74.3.1204. [DOI] [PMC free article] [PubMed] [Google Scholar]

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