INDUCTION OF CYCLOOXYGENASE-2 IN GASTRIC-MUCOSAL LESIONS AND ITS INHIBITION BY THE SPECIFIC ANTAGONIST DELAYS HEALING IN MICE

Citation
H. Mizuno et al., INDUCTION OF CYCLOOXYGENASE-2 IN GASTRIC-MUCOSAL LESIONS AND ITS INHIBITION BY THE SPECIFIC ANTAGONIST DELAYS HEALING IN MICE, Gastroenterology, 112(2), 1997, pp. 387-397
Citations number
55
Categorie Soggetti
Gastroenterology & Hepatology
Journal title
ISSN journal
00165085
Volume
112
Issue
2
Year of publication
1997
Pages
387 - 397
Database
ISI
SICI code
0016-5085(1997)112:2<387:IOCIGL>2.0.ZU;2-3
Abstract
Background & Aims: The role of two forms of cyclooxygenase (COX-1 and COX-2) in gastric mucosal lesions is not well understood, The regulati on of both forms of COX and the effect of COX-2 on the repair process of gastric mucosal lesions in mice were investigated, Methods: Gastric mucosal erosions and ulcers were induced experimentally in mice. The level of COX messenger RNA (mRNA) was determined by reverse-transcript ion polymerase chain reaction, COX proteins were detected by Western b lot analysis, and COX activity was determined in the presence or absen ce of NS-398, a specific COX-2 antagonist. The effects of long-term ad ministration of NS-398 on gastric ulcers were examined, Results: COX-2 mRNA levels were not detected in control conditions but were high dur ing the acute stages of gastric erosions and ulcers, COX-2 protein was detected 5 days after ulcer induction but not in control mice, Gastri c ulceration was not associated with a change in COX-1 mRNA and protei n levels, Administration of NS-398 to mice with ulcers at acute stages impaired the healing of ulcers, Conclusions: High levels of COX-2 mRN A and protein during the acute stages of gastric mucosal lesions may b e involved in the repair process of these lesions in mice.