A benzodiazepine receptor inverse agonist inhibits stress-induced ulcer formation

Pharmacol Biochem Behav. 1987 May;27(1):35-9. doi: 10.1016/0091-3057(87)90473-4.

Abstract

The effects of a benzodiazepine receptor inverse agonist (FG 7142) on gastric ulcer formation were studied in restrained rats. FG 7142 (10-50 mg/kg) reduced in a dose-dependent fashion both the number and cumulative length of gastric ulcers elicited by restraint for 2 hr at 4 degrees C, but did not affect ulcer formation in unrestrained animals maintained in this environment. FG 7142 also reduced gastric ulcer formation in restrained rats maintained at 22 degrees C for 5 hr. The ability of FG 7142 to reduce restraint-stress induced gastric ulcer formation was blocked by the benzodiazepine receptor antagonist ZK 93426 and the beta-adrenoceptor antagonist propranolol. These findings suggest that FG 7142 produces a benzodiazepine-receptor mediated reduction in gastric ulcer formation, which may result from its ability to increase activity of the sympathetic nervous system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbolines / pharmacology*
  • Chlordiazepoxide / pharmacology
  • Male
  • Propranolol / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Receptors, GABA-A / drug effects*
  • Restraint, Physical
  • Stomach Ulcer / pathology
  • Stomach Ulcer / prevention & control*
  • Stress, Physiological / physiopathology*

Substances

  • Carbolines
  • Receptors, GABA-A
  • FG 7142
  • Chlordiazepoxide
  • ZK 93426
  • Propranolol