Skip to main content
Gut logoLink to Gut
. 1995 Apr;36(4):553–557. doi: 10.1136/gut.36.4.553

Role of 5-hydroxytryptamine in intestinal water and electrolyte movement during gut anaphylaxis.

F H Mourad 1, L J O'Donnell 1, E Ogutu 1, J A Dias 1, M J Farthing 1
PMCID: PMC1382496  PMID: 7737563

Abstract

Exposure of sensitised intestine to specific allergen is known to produce appreciable reduction in water and electrolyte absorption. The mediators participating in this process have not been fully characterised. The effects of the 5-hydroxytryptamine2 (5-HT2) and 5-HT3 receptor antagonists, ketanserin and granisetron, respectively, on water movement during intestinal anaphylaxis were studied. Hooded Lister rats (120-150 g) were sensitised to ovalbumen and 14 days later, intestinal water and electrolyte movement was assessed at 10 minute intervals by in situ jejunal perfusion with a plasma electrolyte solution (PES) or PES containing 20 mg/l ovalbumen. Within 20 minutes of exposure to PES+ovalbumen, net water secretion that could be completely prevented by the mast cell stabilising agent doxantrazole occurred compared with absorption with PES alone (median -20 microliters/min/g (interquartile range -43 to -5), n = 11), v (107 (86 to 113), n = 10; p < 0.01). Pre-treatment with subcutaneous ketanserin 200 micrograms/kg (n = 7) or granisetron 300 micrograms/kg (n = 8) partially inhibited the secretory response to PES+ovalbumen (18 (11 to 48) and 13 (6 to 32) respectively; both p < 0.01 compared with PES+ovalbumen control). After 40 minutes perfusion with PES+ovalbumen, the changes in water movement were less pronounced 24 (-3 to 43) and neither ketanserin or granisetron had any effect (ketanserin: 48 (28 to 87), granisetron: 41 (32 to 83); NS). In all experiments, sodium and chloride movement paralleled that of water. Thus, the profound water secretion that occurs in the early stages of intestinal anaphylaxis is partly 5-HT dependent because it can be reversed by 5-HT2 and 5-HT3 receptor antagonists. Other mediators must also be involved, especially in the late phase of anaphylaxis.

Full text

PDF
553

Selected References

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

  1. Baird A. W., Cuthbert A. W. Neuronal involvement in type 1 hypersensitivity reactions in gut epithelia. Br J Pharmacol. 1987 Nov;92(3):647–655. doi: 10.1111/j.1476-5381.1987.tb11368.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Beubler E., Horina G. 5-HT2 and 5-HT3 receptor subtypes mediate cholera toxin-induced intestinal fluid secretion in the rat. Gastroenterology. 1990 Jul;99(1):83–89. doi: 10.1016/0016-5085(90)91233-v. [DOI] [PubMed] [Google Scholar]
  3. Beubler E., Schirgi-Degen A., Gamse R. Inhibition of 5-hydroxytryptamine- and enterotoxin-induced fluid secretion by 5-HT receptor antagonists in the rat jejunum. Eur J Pharmacol. 1993 Aug 2;248(2):157–162. doi: 10.1016/0926-6917(93)90038-r. [DOI] [PubMed] [Google Scholar]
  4. Castro G. A., Harari Y., Russell D. Mediators of anaphylaxis-induced ion transport changes in small intestine. Am J Physiol. 1987 Oct;253(4 Pt 1):G540–G548. doi: 10.1152/ajpgi.1987.253.4.G540. [DOI] [PubMed] [Google Scholar]
  5. Crowe S. E., Sestini P., Perdue M. H. Allergic reactions of rat jejunal mucosa. Ion transport responses to luminal antigen and inflammatory mediators. Gastroenterology. 1990 Jul;99(1):74–82. doi: 10.1016/0016-5085(90)91232-u. [DOI] [PubMed] [Google Scholar]
  6. Hanglow A. C., Bienenstock J., Perdue M. H. Effects of platelet-activating factor on ion transport in isolated rat jejunum. Am J Physiol. 1989 Nov;257(5 Pt 1):G845–G850. doi: 10.1152/ajpgi.1989.257.5.G845. [DOI] [PubMed] [Google Scholar]
  7. Jaffe B. M., Ferrara A., Sherlock D. J. Comparative effects of ketanserin, atropine and methysergide on the gastrointestinal effects of hyperserotoninemia in the awake dog. J Pharmacol Exp Ther. 1986 Aug;238(2):536–541. [PubMed] [Google Scholar]
  8. Kajosaari M. Food allergy in Finnish children aged 1 to 6 years. Acta Paediatr Scand. 1982 Sep;71(5):815–819. doi: 10.1111/j.1651-2227.1982.tb09525.x. [DOI] [PubMed] [Google Scholar]
  9. Lessof M. H., Wraith D. G., Merrett T. G., Merrett J., Buisseret P. D. Food allergy and intolerance in 100 patients---local and systemic effects. Q J Med. 1980;49(195):259–271. [PubMed] [Google Scholar]
  10. Miller H. R., Woodbury R. G., Huntley J. F., Newlands G. Systemic release of mucosal mast-cell protease in primed rats challenged with Nippostrongylus brasiliensis. Immunology. 1983 Jul;49(3):471–479. [PMC free article] [PubMed] [Google Scholar]
  11. Patrick M. K., Dunn I. J., Buret A., Miller H. R., Huntley J. F., Gibson S., Gall D. G. Mast cell protease release and mucosal ultrastructure during intestinal anaphylaxis in the rat. Gastroenterology. 1988 Jan;94(1):1–9. doi: 10.1016/0016-5085(88)90603-8. [DOI] [PubMed] [Google Scholar]
  12. Perdue M. H., Chung M., Gall D. G. Effect of intestinal anaphylaxis on gut function in the rat. Gastroenterology. 1984 Mar;86(3):391–397. [PubMed] [Google Scholar]
  13. Perdue M. H., Gall D. G. Intestinal anaphylaxis in the rat: jejunal response to in vitro antigen exposure. Am J Physiol. 1986 Apr;250(4 Pt 1):G427–G431. doi: 10.1152/ajpgi.1986.250.4.G427. [DOI] [PubMed] [Google Scholar]
  14. Perdue M. H., Gall D. G. Rat jejunal mucosal response to histamine and anti-histamines in vitro. Comparison with antigen-induced changes during intestinal anaphylaxis. Agents Actions. 1986 Oct;19(1-2):5–9. doi: 10.1007/BF01977249. [DOI] [PubMed] [Google Scholar]
  15. Serafin W. E., Austen K. F. Mediators of immediate hypersensitivity reactions. N Engl J Med. 1987 Jul 2;317(1):30–34. doi: 10.1056/NEJM198707023170106. [DOI] [PubMed] [Google Scholar]

Articles from Gut are provided here courtesy of BMJ Publishing Group

RESOURCES