Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1983 Sep;80(1):47–53. doi: 10.1111/j.1476-5381.1983.tb11048.x

The effect of indomethacin on the contractile response of the guinea-pig lung parenchymal strip to leukotrienes B4, C4, D4 and E4.

K F Austen, E J Corey, J M Drazen, A G Leitch
PMCID: PMC2044975  PMID: 6652374

Abstract

Indomethacin (1 microgram ml-1) almost totally inhibited the dose-dependent contractile response of isolated lung parenchymal strips of the guinea-pig (GPLS) to leukotriene B4 (LTB4) over the concentration range 0.18-18 nM. LTC4 (0.63 pM-63 nM)-induced contractions of GPLS were not significantly inhibited by indomethacin (1.0 and 10.0 micrograms ml-1) except when the highest LTC4 concentration (63 nM) was tested in the presence of indomethacin (10 micrograms ml-1). LTD4 (1.3 fM-13 nM)-induced contractions of GPLS were not significantly inhibited by indomethacin (0.1-10 micrograms ml-1) except for contractions induced by concentrations of LTD4 greater than 0.13 nM and 13 nM. Indomethacin 1 microgram ml-1 and 10 micrograms ml-1 inhibited the contractile response to 13 nM LTD4 by 37 and 16% respectively. LTE4 (2.3 fM-23 nM)-induced contractions of GPLS were not significantly inhibited by indomethacin (0.1-10 micrograms ml-1). Contraction due to LTE4 23 pM was significantly potentiated by indomethacin (1 microgram ml-1). Clotrimazole (10 microM) significantly inhibited LTD4-induced contractions of GPLS at concentrations greater than 13 pM but had no significant effect on LTC4-induced contractions. Cyclo-oxygenase products, probably principally thromboxane A2, are important secondary mediators of LTB4-induced contractions of GPLS but make little or no contribution to contractions of GPLS induced by LTC4, LTD4, and LTE4, except at higher concentrations of LTD4 and possibly LTC4. Certain concentrations of LTE4 may generate bronchodilator PGE2 in GPLS.

Full text

PDF
47

Selected References

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

  1. Adcock J. J., Garland L. G. A possible role for lipoxygenase products as regulators of airway smooth muscle reactivity. Br J Pharmacol. 1980 Jun;69(2):167–169. doi: 10.1111/j.1476-5381.1980.tb07886.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BROCKLEHURST W. E. The release of histamine and formation of a slow-reacting substance (SRS-A) during anaphylactic shock. J Physiol. 1960 Jun;151:416–435. doi: 10.1113/jphysiol.1960.sp006449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Brink C., Duncan P. G., Douglas J. S. Histamine, endogenous prostaglandins and cyclic nucleotides in the regulation of airway muscle responses in the guinea pig. Prostaglandins. 1981 Nov;22(5):729–738. doi: 10.1016/0090-6980(81)90212-4. [DOI] [PubMed] [Google Scholar]
  4. Drazen J. M., Austen K. F., Lewis R. A., Clark D. A., Goto G., Marfat A., Corey E. J. Comparative airway and vascular activities of leukotrienes C-1 and D in vivo and in vitro. Proc Natl Acad Sci U S A. 1980 Jul;77(7):4354–4358. doi: 10.1073/pnas.77.7.4354. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Drazen J. M., Schneider M. W. Comparative responses of tracheal spirals and parenchymal strips to histamine and carbachol in vitro. J Clin Invest. 1978 Jun;61(6):1441–1447. doi: 10.1172/JCI109063. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Engineer D. M., Morris H. R., Piper P. J., Sirois P. The release of prostaglandins and thromboxanes from guinea-pig lung by slow reacting substance of anaphylaxis, and its inhibition. Br J Pharmacol. 1978 Oct;64(2):211–218. doi: 10.1111/j.1476-5381.1978.tb17291.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gordon D., Nouri A. M., Thomas R. U. Selective inhibition of thromboxane biosynthesis in human blood mononuclear cells and the effects of mitogen-stimulated lymphocyte proliferation. Br J Pharmacol. 1981 Oct;74(2):469–475. doi: 10.1111/j.1476-5381.1981.tb09992.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hamel R., Masson P., Ford-Hutchinson A. W., Jones T. R., Brunet G., Piechuta H. Differing mechanisms for leukotriene d4-induced bronchoconstriction in guinea pigs following intravenous and aerosol administration. Prostaglandins. 1982 Sep;24(3):419–432. doi: 10.1016/0090-6980(82)90168-x. [DOI] [PubMed] [Google Scholar]
  9. Krell R. D., Osborn R., Vickery L., Falcone K., O'Donnell M., Gleason J., Kinzig C., Bryan D. Contraction of isolated airway smooth muscle by synthetic leukotrienes C4 and D4. Prostaglandins. 1981 Sep;22(3):387–409. doi: 10.1016/0090-6980(81)90101-5. [DOI] [PubMed] [Google Scholar]
  10. Lewis R. A., Austen K. F., Drazen J. M., Clark D. A., Marfat A., Corey E. J. Slow reacting substances of anaphylaxis: identification of leukotrienes C-1 and D from human and rat sources. Proc Natl Acad Sci U S A. 1980 Jun;77(6):3710–3714. doi: 10.1073/pnas.77.6.3710. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Lewis R. A., Drazen J. M., Austen K. F., Clark D. A., Corey E. J. Identification of the C(6)-S-conjugate of leukotriene A with cysteine as a naturally occurring slow reacting substance of anaphylaxis (SRS-A). Importance of the 11-cis-geometry for biological activity. Biochem Biophys Res Commun. 1980 Sep 16;96(1):271–277. doi: 10.1016/0006-291x(80)91210-3. [DOI] [PubMed] [Google Scholar]
  12. Mathé A. A., Strandberg K., Yen S. S. Prostaglandin release by slow reacting substance from guinea pig and human lung tissue. Prostaglandins. 1977;14(6):1105–1115. doi: 10.1016/0090-6980(77)90288-x. [DOI] [PubMed] [Google Scholar]
  13. Morris H. R., Taylor G. W., Jones C. M., Piper P. J., Samhoun M. N., Tippins J. R. Slow reacting substances (leukotrienes): enzymes involved in their biosynthesis. Proc Natl Acad Sci U S A. 1982 Aug;79(16):4838–4842. doi: 10.1073/pnas.79.16.4838. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Morris H. R., Taylor G. W., Piper P. J., Tippins J. R. Structure of slow-reacting substance of anaphylaxis from guinea-pig lung. Nature. 1980 May 8;285(5760):104–106. doi: 10.1038/285104a0. [DOI] [PubMed] [Google Scholar]
  15. Murphy R. C., Hammarström S., Samuelsson B. Leukotriene C: a slow-reacting substance from murine mastocytoma cells. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4275–4279. doi: 10.1073/pnas.76.9.4275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Omini C., Folco G. C., Viganò T., Rossoni G., Brunelli G., Berti F. Leukotriene-C4 induces generation of PGI2 and TXA2 in guinea-pig in vivo. Pharmacol Res Commun. 1981 Jul;13(7):633–640. doi: 10.1016/s0031-6989(81)80051-3. [DOI] [PubMed] [Google Scholar]
  17. Orehek J., Douglas J. S., Lewis A. J., Bouhuys A. Prostaglandin regulation of airway smooth muscle tone. Nat New Biol. 1973 Sep 19;245(142):84–85. doi: 10.1038/newbio245084a0. [DOI] [PubMed] [Google Scholar]
  18. Piper P. J., Samhoun M. N. The mechanism of action of leukotrienes C4 and D4 in guinea-pig isolated perfused lung and parenchymal strips of guinea pig, rabbit and rat. Prostaglandins. 1981 May;21(5):793–803. doi: 10.1016/0090-6980(81)90236-7. [DOI] [PubMed] [Google Scholar]
  19. Schneider M. W., Drazen J. M. Comparative in vitro effects of arachidonic acid metabolites on tracheal spirals and parenchymal strips. Am Rev Respir Dis. 1980 May;121(5):835–842. doi: 10.1164/arrd.1980.121.5.835. [DOI] [PubMed] [Google Scholar]
  20. Sirois P., Borgeat P., Jeanson A., Roy S., Girard G. The action of leukotriene B4 (LTB4) on the lung. Prostaglandins Med. 1980 Dec;5(6):429–444. doi: 10.1016/0161-4630(80)90067-1. [DOI] [PubMed] [Google Scholar]
  21. Vargaftig B. B., Lefort J., Murphy R. C. Inhibition by aspirin of bronchoconstriction due to leukotrienes C4 and D4 in the guinea pig. Eur J Pharmacol. 1981 Jul 10;72(4):417–418. doi: 10.1016/0014-2999(81)90589-6. [DOI] [PubMed] [Google Scholar]
  22. Weichman B. M., Muccitelli R. M., Osborn R. R., Holden D. A., Gleason J. G., Wasserman M. A. In vitro and in vivo mechanisms of leukotriene-mediated bronchoconstriction in the guinea pig. J Pharmacol Exp Ther. 1982 Jul;222(1):202–208. [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES