Surface epithelial cell damage induced by restraint and water-immersion stress in rats. Effects of 16,16-dimethyl prostaglandin E2 on stress-induced gastric lesions.
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The time-course of gastric mucosal surface epithelial cell damage and macroscopically visible lesions in response to restraint and water-immersion stress (22°C) in rats was examined, and the effects on it of 16, 16-dimethyl prostaglandin E<SUB>2</SUB> (dmPGE<SUB>2</SUB>) were compared with those of papaverine, timoprazole and atropine. The stress produced surface epithelial cell damage prior to visible lesion, the former increasing in severity with time and reaching a plateau 60 min later, by which time exfoliation of surface epithelial cells was observable along the mucosal folds. In contrast, macroscopically visible lesions appeared 2 hr after stress, and severity continued to increase with time. Pretreatment injections (s.c.) of dmPGE<SUB>2</SUB> (3, 30 μg/kg), papaverine (100 mg/kg) and atropine (1 mg/kg) protected the surface cells against stress (1 hr)-induced damage, and inhibited visible lesion formation after 4 hr stress. Timoprazole (30 mg/kg, s.c.) did not protect the surface cells, but did markedly inhibit visible lesion formation. dmPGE<SUB>2</SUB>, papaverine and atropine, but not timoprazole, inhibited stress-induced increases in gastric contractions. dmPGE<SUB>2</SUB>, timoprazole and atropine, but not papaverine, inhibited acid secretion in stress-conditions. These results indicated that stress induced damage to the gastric mucosa within 1 hr due to increased gastric contractions, and the surface epithelial cell damage developed into macroscopically visible lesions in the presence of acid, and that dmPGE<SUB>2</SUB> protected the surface epithelium against stress-induced damage probably by inhibiting gastric contractions.
- 公益社団法人 日本薬理学会の論文
公益社団法人 日本薬理学会 | 論文
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