Dimethyl-prostaglandin E2 prevents stress ulceration with minimal complications

K. S. Ephgrave, J. Horton, D. Burns

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Gastric mucosal damage produced by topical application of necrotizing agents is diminished by topical or systemic pretreatment with a variety of E and F prostaglandins. The rat restraint model of gastric mucosal injury is more analogous to clinical stress ulceration than are models using intragastric application of toxic solutions; however, previous use of prostaglandin E1 in the restraint model resulted in a prohibitive incidence of GI morbidity. The current study used the restraint model of stress ulceration to compare the effects of a more potent prostaglandin analogue, 16,16-dimethyl prostaglandin E2, with hyperosmolar glucose and antacids. All three agents afforded significant protection from grossly apparent mucosal lesions, alone and in combination. Although other physiologic effects of each agent differed, the only effect which correlated with prevention of mucosal lesions was suppression of gastric acidity. Since effective doses of cytoprotective prostaglandins did not produce notable morbidity in comparison with other agents, they may prove to be a useful adjunct to stress ulcer prophylaxis in clinical settings.

Original languageEnglish (US)
Pages (from-to)53-57
Number of pages5
JournalCritical care medicine
Volume17
Issue number1
DOIs
StatePublished - Jan 1 1989

ASJC Scopus subject areas

  • Critical Care and Intensive Care Medicine

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