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Cyclo‐oxygenase isozymes in mucosal ulcerogenic and functional responses following barrier disruption in rat stomachs
Author(s) -
Hirata Takuya,
Ukawa Hideki,
Yamakuni Hisashi,
Kato Shinichi,
Takeuchi Koji
Publication year - 1997
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0701399
Subject(s) - nimesulide , gastric mucosa , prostaglandin , in vivo , chemistry , stomach , taurocholic acid , prostaglandin e , isozyme , medicine , prostaglandin e2 , endocrinology , intestinal mucosa , pharmacology , enzyme , biology , biochemistry , bile acid , microbiology and biotechnology
1 We examined the effects of selective and nonselective cyclo‐oxygenase (COX) inhibitors on various functional changes in the rat stomach induced by topical application of taurocholate (TC) and investigated the preferential role of COX isozymes in these responses. 2 Rat stomachs mounted in ex vivo chambers were perfused with 50 m M HCl and transmucosal potential difference (p.d.), mucosal blood flow (GMBF), luminal acid loss and luminal levels of prostaglandin E 2 (PGE 2 ) were measured before, during and after exposure to 20 m M TC. 3 Mucosal application of TC in control rats caused a reduction in p.d., followed by an increase of luminal acid loss and GMBF, and produced only minimal damage in the mucosa 2 h later. Pretreatment with indomethacin (10 mg kg −1 , s.c.), a nonselective COX‐1 and COX‐2 inhibitor, attenuated the gastric hyperaemic response caused by TC without affecting p.d. and acid loss, resulting in haemorrhagic lesions in the mucosa. In contrast, selective COX‐2 inhibitors, such as NS‐398 and nimesulide (10 mg kg −1 , s.c.), had no effect on any of the responses induced by TC and did not cause gross damage in the mucosa. 4 Luminal PGE 2 levels were markedly increased during and after exposure to TC and this response was significantly inhibited by indomethacin but not by either NS‐398 or nimesulide. The expression of COX‐1‐mRNA was consistently detected in the gastric mucosa before and after TC treatment, while a faint expression of COX‐2‐mRNA was detected only 2 h after TC treatment. 5 Both NS‐398 and nimesulide significantly suppressed carrageenan‐induced rat paw oedema, similar to indomethacin. 6 These results confirmed a mediator role for prostaglandins in the gastric hyperaemic response following TC‐induced barrier disruption, and suggest that COX‐1 but not COX‐2 is a key enzyme in maintaining ‘housekeeping’ functions in the gastric mucosa under both normal and adverse conditions.British Journal of Pharmacology (1997) 122 , 447–454; doi: 10.1038/sj.bjp.0701399