Effect of CGS 9896 on stress-induced gastric ulcer in rat

Clin Exp Pharmacol Physiol. 1990 Feb;17(2):157-161. doi: 10.1111/j.1440-1681.1990.tb01298.x.

Abstract

1. The effects of CGS 9896, a partial benzodiazepine agonist, and chlordiazepoxide, a full benzodiazepine agonist, on stress-induced gastric ulcers as well as blood glucose were compared. 2. Ulceration in the glandular stomach was induced by 2 h restraint at 4 degrees C. 3. CGS 9896 reduced significantly the ulcer parameters but did not affect blood glucose. The effect of CGS 9896 was dose-dependently blocked by the benzodiazepine antagonist flumazepil. 4. Chlordiazepoxide reduced the ulcer parameters but increased blood glucose. 5. Since CGS 9896 lacks sedative effects but reduced ulcer parameters, the anti-ulcer and sedative effects of drugs acting at benzodiazepine receptors are disassociated. 6. Benzodiazepine-induced hyperglycaemia does not play a major role in the anti-ulcer effects.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Benzodiazepines / pharmacology
  • Chlordiazepoxide / pharmacology
  • Cold Temperature
  • Drug Therapy, Combination
  • Flumazenil / pharmacology
  • Hyperglycemia / chemically induced
  • Male
  • Pyrazoles / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Stomach Ulcer / drug therapy*
  • Stress, Physiological*

Substances

  • Pyrazoles
  • Benzodiazepines
  • Flumazenil
  • Chlordiazepoxide
  • 2-(4-chlorophenyl)-2,5-dihydropyrazolo(4,3-c)quinoline-3(3H)-one