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Prostaglandin E2 and reactive oxygen metabolite damage in the cecum in a pony model of acute colitis.

Abstract: The objective of this project was to determine early tissue biochemical events associated with increased colonic secretion during the acute stage of castor-oil-induced colitis by measuring cecal mucosal and submucosal malondialdehyde (MDA) and prostaglandin E2 (PGE2), levels in ponies. Intestinal tissue (inflamed or healthy) samples were obtained from 4 age- and sex-matched Shetland ponies. Biochemical methods were used to determine MDA and PGE2 levels in intestinal tissue samples from inflamed and healthy equine intestine. Inflamed tissue MDA and PGE2 levels increased with time after castor oil challenge and correlated with granulocyte infiltration, as determined by myeloperoxidase levels in a companion study. Elevated intestinal tissue MDA levels suggest that lipid peroxidation could be attributed to reactive oxygen metabolites (ROM) released from stimulated, recruited, and resident granulocytes. Tissue levels of MDA and PGE2 suggest a role for granulocyte-derived mediators of intestinal inflammation in the massive secretory response in cases of acute equine colitis. Tissue MDA and PGE2 levels may be useful laboratory tools to quantify and characterize intestinal secretory inflammatory responses in acute inflammatory conditions in the equine colon.
Publication Date: 2002-02-23 PubMed ID: 11858649PubMed Central: PMC226982
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research aims to understand the associations between increased colon secretion during acute colitis in ponies by observing the levels of cecal mucosal and submucosal malondialdehyde (MDA) and prostaglandin E2 (PGE2). A discovery of lipid peroxidation, attributed to reactive oxygen metabolites (ROM), and evidence of granulocyte-driven inflammation are indicated.

Objective and Methodology

  • The study aimed to explore early tissue chemical reactions associated with increased colonic secretion during the acute stage of colitis induced by castor oil.
  • The research targeted these biochemical events by measuring levels of cecal mucosal and submucosal malondialdehyde (MDA) and prostaglandin E2 (PGE2).
  • These measurements were made using intestinal tissue samples, both inflamed and healthy, from four Shetland ponies matched for age and sex.
  • Biochemical methods were used to determine MDA and PGE2 levels in these tissue samples.

Results and Findings

  • Levels of MDA and PGE2 in inflamed tissue samples were found to rise over time following a castor oil challenge.
  • These increases were correlated with granulocyte infiltration – as determined through measuring myeloperoxidase levels in a parallel study.
  • Elevated levels of MDA in intestinal tissues suggest that lipid peroxidation might be due to ROM (reactive oxygen metabolites) released from both resident and recruited granulocytes that have been stimulated.
  • The findings provide evidence for a role for granulocyte-derived mediators in the intestinal inflammation seen in acute equine colitis.

Implications of the Study

  • Levels of tissue MDA and PGE2 could offer a means to quantify and characterize intestinal secretory inflammatory responses in acute inflammatory conditions of the equine colon.
  • This study provides valuable insights in understanding the biochemical reactions that are associated with the inflammation in cases of equine colitis and could guide in the formulation of more effective treatments for this condition.

Cite This Article

APA
McConnico RS, Argenzio RA, Roberts MC. (2002). Prostaglandin E2 and reactive oxygen metabolite damage in the cecum in a pony model of acute colitis. Can J Vet Res, 66(1), 50-54.

Publication

ISSN: 0830-9000
NlmUniqueID: 8607793
Country: Canada
Language: English
Volume: 66
Issue: 1
Pages: 50-54

Researcher Affiliations

McConnico, Rebecca S
  • Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge 70803, USA. mcconnico@vetmed.lsu.edu
Argenzio, Robert A
    Roberts, Malcolm C

      MeSH Terms

      • Acute Disease
      • Animals
      • Castor Oil / adverse effects
      • Cecum / metabolism
      • Cecum / pathology
      • Colitis / chemically induced
      • Colitis / metabolism
      • Colitis / pathology
      • Colitis / veterinary
      • Dinoprostone / analysis
      • Dinoprostone / metabolism
      • Disease Models, Animal
      • Female
      • Granulocytes / immunology
      • Horse Diseases / chemically induced
      • Horse Diseases / metabolism
      • Horse Diseases / pathology
      • Horses
      • Inflammation / veterinary
      • Intestinal Mucosa / chemistry
      • Intestinal Mucosa / immunology
      • Intestinal Mucosa / pathology
      • Lipid Peroxidation
      • Male
      • Malondialdehyde / analysis
      • Malondialdehyde / metabolism
      • Peroxidase / metabolism
      • Reactive Oxygen Species

      References

      This article includes 31 references
      1. Weiss SJ. Tissue destruction by neutrophils.. N Engl J Med 1989;320:6,365–376.
        pubmed: 2536474
      2. Verspaget HW, Mulder TPJ, Van Der Sluys Veer A, Pean AS, Lamers CBHW. Reactive oxygen metabolites and colitis: A disturbed balance between damage and protection.. Scand J Gastroenterol 1991;26:44–51.
        pubmed: 1663660
      3. Granger RN, Rutili G. Neutrophil-mediated mucosal injury. Role of reactive oxygen metabolites.. Dig Dis Sci 1988;33:6S–15S.
        pubmed: 2831016
      4. Wardle TD, Hall L, Turnberg LA. Inter-relationships between inflammatory mediators released from colonic mucosa in ulcerative colitis and their effects on colonic secretion.. Gut 1993;34: 503–508.
        pmc: PMC1374311pubmed: 8491398
      5. Rooney JR, Bryans JT, Prickett ME, Zent WW. Exhaustion shock in the horse.. Cornell Vet 1966;56:220–235.
        pubmed: 6006347
      6. Johnson CM, Cullen JM, Roberts MC. Morphologic characterization of castor oil-induced colitis in ponies.. Vet Path 1993;30: 248–255.
        pubmed: 8333106
      7. Cordes DO, Perry BD, Rikihisa Y, Chickering WR. Enterocolitis caused by Ehrlichia sp. in the horse (Potomac Horse Fever).. Vet Pathol 1986;23:471–477.
        pubmed: 3750739
      8. Meschter CL, Tyler DE, White NA, Moore J. Histologic findings in the gastrointestinal tract of horses with colic.. Am J Vet Res 1986;47:598–606.
        pubmed: 3963560
      9. Labo G, Facchini A, Stefanine GF. Immunology of Inflammatory Bowel Diseases.. Proc Int Symp Gastroenterol, Bologna, Italy 1983:167–181.
      10. Teather S, Cuthbert AW. Induction of bradykinin B1 receptors in rat colonic epithelium.. Br J Pharmacol 1997;121(5): 1005–1011.
        pmc: PMC1564778pubmed: 9222560
      11. Perdue MH, McKay DM. Integrative immunophysiology in the intestinal mucosa.. Am J Physiol 1994;30:G151–G165.
        pubmed: 8074215
      12. Powell DW. Immunophysiology of intestinal electrolyte transport.. Handbook of Physiology: The Gastrointestinal System Rockville: Am Physiol Soc, 1991:591–641.
      13. Racusen LC, Binder HJ. Effect of prostaglandins on ion transport across isolated colonic mucosa.. Dig Dis Sci 1980;25:900–904.
        pubmed: 6256142
      14. Berschneider HM, Powell DW. Fibroblasts modulate intestinal secretory responses to inflammatory mediators.. J Clin Invest 1992;89:484–489.
        pmc: PMC442877pubmed: 1737838
      15. Roberts MC, Clarke LL, Johnson CM. Castor oil-induced diarrhoea in ponies: a model for acute colitis.. Eq Vet J 1989; (Suppl 7):60–67.
        pubmed: 9118109
      16. Krawisz JE, Sharon P, Stenson WF. Quantitative assay for acute intestinal inflammation based on myeloperoxidase activity.. Gastroenterology 1984;87:1344–1350.
        pubmed: 6092199
      17. Grisham MB, Benoit JN, Granger DN. Assessment of leukocyte involvement during ischemia and reperfusion of intestine.. Methods Enzymol 1990;186:729–742.
        pubmed: 2172726
      18. McConnico RS, Weinstock D, Poston ME, Roberts MC. Myeloperoxidase activity of the large colon in an equine model of acute colitis.. Am J Vet Res 1999;60:807–814.
        pubmed: 10407471
      19. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction.. Anal Biochem 1979;95:351–358.
        pubmed: 36810
      20. Luck H. Methods of Enzymatic Analysis.. Academic Press New York: Academic Press, 1963:885–894.
      21. Barrett KE. Effect of the diglyceride lipase inhibitor, RG80267, on epithelial chloride secretion induced by various agents.. Cell Signal 1995;7(3):225–33.
        pubmed: 7662511
      22. Barrett KE, Dharmsathaphorn K. Secretion and absorption: small intestine and colon.. Textbook of Gastroenterology Philadelphia: Lippincott, 1991:265–294.
      23. Frieling T, Rupprecht C, Dobreva G, Schemann M. Differential effects of inflammatory mediators on ion secretion in the guinea-pig colon.. Comp Biochem Physiol 1997;118(2):341–343.
        pubmed: 9366066
      24. Weymer A, Huott P, Liu W, McRoberts JA, Dharmsathaphorn K. Chloride secretory mechanism induced by prostaglandin E1 in a colonic epithelial cell line.. J Clin Invest 1985;76:1828–1836.
        pmc: PMC424218pubmed: 2997290
      25. Argenzio RA, Lecce J, Powell DW. Prostanoids inhibit intestinal NaCl absorption in experimental porcine cryptosporidiosis.. Gastroenterology 1993;104:440–447.
        pubmed: 8425686
      26. Gaginella TS, Bass P. Laxatives: An update on mechanism of action.. Life Sci 1978;23:1001–1010.
        pubmed: 713678
      27. Phillips SF, Gaginella TS. Intestinal secretion as a mechanism in diarrheal disease.. Progr Gastroenterol New York: Grune & Stratton,1977:481–504.
      28. Capasso F, Mascolo N, Autore G, Romano V. Laxatives and the production of autocoids by rat colon.. J Pharm Pharmacol 1986; 38:627–629.
        pubmed: 2876085
      29. Pinto A, Autore G, Mascolo N. Time course of Paf formation by gastrointestinal tissue in rats after castor oil challenge.. J Pharm 1992;44(3):224–226.
        pubmed: 1354728
      30. Mascolo N, Izzo AA, Autore G, Barbato F, Capasso F. Nitric oxide and castor oil induced diarrhea.. J Pharm Exper Ther 1994;268:291–295.
        pubmed: 8301570
      31. Izzo AA, Mascolo N, Capasso F. Nitric oxide as a modulator of intestinal water and electrolyte transport. Dig Dis Sci 1998; 43(8):1605–1620.
        pubmed: 9724140