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. 1988 Mar;29(3):319–324. doi: 10.1136/gut.29.3.319

Source of endogenous arachidonate and 5-lipoxygenase products in human neutrophils stimulated by bradykinin and A23187.

O H Nielsen 1, K Bukhave 1, I Ahnfelt-Rønne 1, J Rask-Madsen 1
PMCID: PMC1433608  PMID: 2833432

Abstract

The lipoxygenase products of arachidonic acid (AA) metabolism, 5-hydroxyeicosatetraenoic acid (5-HETE) and leucotriene B4 (LTB4), are considered to have an important pathophysiological role in inflammatory bowel disease by stimulating the inflammatory response and by contributing to the diarrhoea. The present studies were designed to investigate the effect of the physiological stimulants bradykinin (BK) and 5-hydroxytryptamine (5-HT), in addition to the influence of the calcium ionophore A23187, on the source of AA release and 5-lipoxygenation in human neutrophils (PMNs) in vitro. This was done to elucidate the specificity of the mechanism by which PMNs respond to physiological, extracellular Ca2+ dependent agonists. The results of the study indicate that stimulation of 1-14C-AA-prelabelled PMNs with BK liberates AA mainly from phosphatidylinositol, while A23187 causes release of AA from phosphatidylcholine, phosphatidylethanolamine, and possibly phosphatidylserine. Furthermore BK (10(-9)-10(-6)M) dose-dependently stimulated the formation of 5-HETE and LTB4, reaching a maximum at 10(-7)M, while 5-HT (10(-8)-10(-4)M) released only negligible amounts of eicosanoids, similar to those observed in control experiments. Stimulation with A23187 (10(-5)M) caused a high release of both 5-HETE and LTB4. These results offer evidence that BK, but not 5-HT, initiates formation of lipoxygenase products by binding to specific receptors on the external surface of PMNs, whereas A23187 accelerates 5-lipoxygenation through mechanisms which do not involve a cell surface receptor.

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Selected References

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

  1. Bareis D. L., Manganiello V. C., Hirata F., Vaughan M., Axelrod J. Bradykinin stimulates phospholipid methylation, calcium influx, prostaglandin formation, and cAMP accumulation in human fibroblasts. Proc Natl Acad Sci U S A. 1983 May;80(9):2514–2518. doi: 10.1073/pnas.80.9.2514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bell R. L., Baenziger N. L., Majerus P. W. Bradykinin-stimulated release of arachidonate from phosphatidyl inositol in mouse fibrosarcoma cells. Prostaglandins. 1980 Aug;20(2):269–274. doi: 10.1016/s0090-6980(80)80045-1. [DOI] [PubMed] [Google Scholar]
  3. Bell R. L., Kennerly D. A., Stanford N., Majerus P. W. Diglyceride lipase: a pathway for arachidonate release from human platelets. Proc Natl Acad Sci U S A. 1979 Jul;76(7):3238–3241. doi: 10.1073/pnas.76.7.3238. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Berridge M. J., Irvine R. F. Inositol trisphosphate, a novel second messenger in cellular signal transduction. Nature. 1984 Nov 22;312(5992):315–321. doi: 10.1038/312315a0. [DOI] [PubMed] [Google Scholar]
  5. Beubler E., Bukhave K., Rask-Madsen J. Significance of calcium for the prostaglandin E2-mediated secretory response to 5-hydroxytryptamine in the small intestine of the rat in vivo. Gastroenterology. 1986 Jun;90(6):1972–1977. doi: 10.1016/0016-5085(86)90269-6. [DOI] [PubMed] [Google Scholar]
  6. Brown D. J., Khan J. A., Copeland G., Jewell D. P. Alpha 2-macroglobulin in patients with inflammatory bowel disease. J Clin Lab Immunol. 1980 Jul;4(1):53–57. [PubMed] [Google Scholar]
  7. Böyum A. Isolation of leucocytes from human blood. A two-phase system for removal of red cells with methylcellulose as erythrocyte-aggregating agent. Scand J Clin Lab Invest Suppl. 1968;97:9–29. [PubMed] [Google Scholar]
  8. Cuschieri A., Onabanjo O. A. Kinin release after gastric surgery. Br Med J. 1971 Sep 4;3(5774):565–566. doi: 10.1136/bmj.3.5774.565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Donowitz M. Arachidonic acid metabolites and their role in inflammatory bowel disease. An update requiring addition of a pathway. Gastroenterology. 1985 Feb;88(2):580–587. doi: 10.1016/0016-5085(85)90525-6. [DOI] [PubMed] [Google Scholar]
  10. Donowitz M., Tai Y. H., Asarkof N. Effect of serotonin on active electrolyte transport in rabbit ileum, gallbladder, and colon. Am J Physiol. 1980 Dec;239(6):G463–G472. doi: 10.1152/ajpgi.1980.239.6.G463. [DOI] [PubMed] [Google Scholar]
  11. Goetzl E. J., Payan D. G., Goldman D. W. Immunopathogenetic roles of leukotrienes in human diseases. J Clin Immunol. 1984 Mar;4(2):79–84. doi: 10.1007/BF00915039. [DOI] [PubMed] [Google Scholar]
  12. Lauritsen K., Hansen J., Bytzer P., Bukhave K., Rask-Madsen J. Effects of sulphasalazine and disodium azodisalicylate on colonic PGE2 concentrations determined by equilibrium in vivo dialysis of faeces in patients with ulcerative colitis and healthy controls. Gut. 1984 Nov;25(11):1271–1278. doi: 10.1136/gut.25.11.1271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Lauritsen K., Laursen L. S., Bukhave K., Rask-Madsen J. Effects of topical 5-aminosalicylic acid and prednisolone on prostaglandin E2 and leukotriene B4 levels determined by equilibrium in vivo dialysis of rectum in relapsing ulcerative colitis. Gastroenterology. 1986 Oct;91(4):837–844. doi: 10.1016/0016-5085(86)90684-0. [DOI] [PubMed] [Google Scholar]
  14. Litosch I., Saito Y., Fain J. N. 5-HT-stimulated arachidonic acid release from labeled phosphatidylinositol in blowfly salivary glands. Am J Physiol. 1982 Nov;243(5):C222–C226. doi: 10.1152/ajpcell.1982.243.5.C222. [DOI] [PubMed] [Google Scholar]
  15. Majerus P. W., Connolly T. M., Deckmyn H., Ross T. S., Bross T. E., Ishii H., Bansal V. S., Wilson D. B. The metabolism of phosphoinositide-derived messenger molecules. Science. 1986 Dec 19;234(4783):1519–1526. doi: 10.1126/science.3024320. [DOI] [PubMed] [Google Scholar]
  16. McConn R., Wasserman F., Haberland G. The kallikrein-kinin system in the acutely-ill: (A) changes in plasma kininogen in acutely-ill patients. (B) the efficacy of pulmonary clearance of bradykinin. Adv Exp Med Biol. 1983;156(Pt B):1019–1035. [PubMed] [Google Scholar]
  17. McKean M. L., Smith J. B., Silver M. J. Formation of lysophosphatidylcholine by human platelets in response to thrombin. Support for the phospholipase A2 pathway for the liberation of arachidonic acid. J Biol Chem. 1981 Feb 25;256(4):1522–1524. [PubMed] [Google Scholar]
  18. Nielsen O. H., Bukhave K., Ahnfelt-Rønne I., Elmgreen J. Arachidonic acid metabolism in human neutrophils: lack of effect of cyclosporine A. Int J Immunopharmacol. 1986;8(4):419–426. doi: 10.1016/0192-0561(86)90126-8. [DOI] [PubMed] [Google Scholar]
  19. Nielsen O. H., Elmgreen J. Activation of neutrophil chemotaxis by leukotriene B4 and 5-hydroxyeicosatetraenoic acid in chronic inflammatory bowel disease. Scand J Clin Lab Invest. 1987 Oct;47(6):605–611. doi: 10.1080/00365518709168476. [DOI] [PubMed] [Google Scholar]
  20. Nishizuka Y. The role of protein kinase C in cell surface signal transduction and tumour promotion. Nature. 1984 Apr 19;308(5961):693–698. doi: 10.1038/308693a0. [DOI] [PubMed] [Google Scholar]
  21. OATES J. A., MELMON K., SJOERDSMA A., GILLESPIE L., MASON D. T. RELEASE OF A KININ PEPTIDE IN THE CARCINOID SYNDROME. Lancet. 1964 Mar 7;1(7332):514–517. doi: 10.1016/s0140-6736(64)92907-1. [DOI] [PubMed] [Google Scholar]
  22. Prescott S. M., Majerus P. W. Characterization of 1,2-diacylglycerol hydrolysis in human platelets. Demonstration of an arachidonoyl-monoacylglycerol intermediate. J Biol Chem. 1983 Jan 25;258(2):764–769. [PubMed] [Google Scholar]
  23. Rampton D. S., Sladen G. E., Youlten L. J. Rectal mucosal prostaglandin E2 release and its relation to disease activity, electrical potential difference, and treatment in ulcerative colitis. Gut. 1980 Jul;21(7):591–596. doi: 10.1136/gut.21.7.591. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Rask-Madsen J. Eicosanoids and their role in the pathogenesis of diarrhoeal diseases. Clin Gastroenterol. 1986 Jul;15(3):545–566. [PubMed] [Google Scholar]
  25. Raz A., Schwartzman M. Bradykinin-stimulated differential incorporation of arachidonic acid into lipids of kidney cortex and medulla. Biochem Pharmacol. 1983 Oct 1;32(19):2843–2846. doi: 10.1016/0006-2952(83)90386-6. [DOI] [PubMed] [Google Scholar]
  26. Roch-Arveiller M., Caranikas S., Regoli D., Giroud J. P. Effects of bradykinin and some of its fragments on smooth muscles and chemotaxis. Eur J Pharmacol. 1983 Mar 18;88(1):99–103. doi: 10.1016/0014-2999(83)90396-5. [DOI] [PubMed] [Google Scholar]
  27. Roscher A. A., Manganiello V. C., Jelsema C. L., Moss J. Autoregulation of bradykinin receptors and bradykinin-induced prostacyclin formation in human fibroblasts. J Clin Invest. 1984 Aug;74(2):552–558. doi: 10.1172/JCI111452. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Schremmer J. M., Blank M. L., Wykle R. L. Bradykinin-stimulated release of [3H]arachidonic acid from phospholipids of HSDM1C1 cells: comparison of diacyl phospholipids and plasmalogens as sources of prostaglandin precursors. Prostaglandins. 1979 Oct;18(4):491–505. doi: 10.1016/0090-6980(79)90018-2. [DOI] [PubMed] [Google Scholar]
  29. Sharon P., Stenson W. F. Enhanced synthesis of leukotriene B4 by colonic mucosa in inflammatory bowel disease. Gastroenterology. 1984 Mar;86(3):453–460. [PubMed] [Google Scholar]
  30. Sharon P., Stenson W. F. Metabolism of arachidonic acid in acetic acid colitis in rats. Similarity to human inflammatory bowel disease. Gastroenterology. 1985 Jan;88(1 Pt 1):55–63. doi: 10.1016/s0016-5085(85)80132-3. [DOI] [PubMed] [Google Scholar]
  31. Silverstein E., Fierst S. M., Simon M. R., Weinstock J. V., Friedland J. Angiotensin-converting enzyme in Crohn's disease and ulcerative colitis. Am J Clin Pathol. 1981 Feb;75(2):175–178. doi: 10.1093/ajcp/75.2.175. [DOI] [PubMed] [Google Scholar]
  32. Sundsmo J. S., Fair D. S. Relationships among the complement, kinin, coagulation and fibrinolytic systems in the inflammatory reaction. Clin Physiol Biochem. 1983;1(2-5):225–284. [PubMed] [Google Scholar]
  33. Wong P. Y., Talamo R. C., Babior B. M., Raymond G. G., Colman R. W. Kallikrein-kinin system in postgastrectomy dumping syndrome. Ann Intern Med. 1974 May;80(5):577–581. doi: 10.7326/0003-4819-80-5-577. [DOI] [PubMed] [Google Scholar]
  34. Zeitlin I. J., Smith A. N. 5-hydroxyindoles and kinins in the carcinoid and dumping syndromes. Lancet. 1966 Nov 5;2(7471):986–991. doi: 10.1016/s0140-6736(66)92924-2. [DOI] [PubMed] [Google Scholar]
  35. Zeitlin I. J., Smith A. N. Mobilization of tissue kallikrein in inflammatory disease of the colon. Gut. 1973 Feb;14(2):133–138. doi: 10.1136/gut.14.2.133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Zipser R. D., Patterson J. B., Kao H. W., Hauser C. J., Locke R. Hypersensitive prostaglandin and thromboxane response to hormones in rabbit colitis. Am J Physiol. 1985 Oct;249(4 Pt 1):G457–G463. doi: 10.1152/ajpgi.1985.249.4.G457. [DOI] [PubMed] [Google Scholar]

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