clonazepam;
ethanol;
gastric damage;
in vitro;
rat;
ro;
15-4513;
flumazenil;
D O I:
10.1046/j.1472-8206.2001.00017.x
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The protective effects of drugs acting at the benzodiazepine receptors against ethanol-induced gastric damage were investigated using a newly developed in vitro model of the ethanol-induced gastric damage. The rat stomachs were isolated from the whole animal and kept in Kreb's solution at 37 degreesC. Gastric damage was induced by administration of 1 mL of 50% V/V ethanol into the isolated rat stomach. Administration of the benzodiazepine agonist, clonazepam (25, 50, 100 mug), or the partial benzodiazepine inverse agonist Ro15-4513 (50 or 100 mug), significantly protected against ethanol-induced gastric damage when these agents were administered 15 min before ethanol. The protective effects of these drugs were blocked by the benzodiazepine receptor antagonist flumazenil (200-400 mug). Flumazenil alone was found to aggravate ethanol-induced gastric damage (200-400 mug). The results of this study give evidence for the involvement of central-type benzodiazepine receptors located in the stomach in the protective action of benzodiazepines against ethanol-induced gastric damage.