DIFFERENT EFFECTS OF CYTOPROTECTIVE DRUGS ON ETHANOL-INDUCED AND ASPIRIN-INDUCED GASTRIC-MUCOSAL INJURY IN PYLORUS-LIGATED RATS

被引:9
作者
TAKEUCHI, K
NISHIWAKI, H
NIIDA, H
OKABE, S
机构
[1] Department of Applied Pharmacology, Kyoto Pharmaceutical University, Kyoto, 607, Misasagi, Yamashina
关键词
aspirin; cytoprotection; ethanol; gastric lesion; mucosal folds; pylorus-ligated rat;
D O I
10.1007/BF01536760
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In anesthetized rats oral administration (2 ml) of both ethanol (50% in 150 mM HCl) and aspirin (80 mM in 150 mM HCl) produced bandlike lesions in the stomach, while more generalized lesions occurred in the pylorus-ligated stomach when the irritant was given intragastrically through the fistula prepared in the rumen and the mucosal folds were removed by stomach distension. The bandlike lesions induced in the intact stomach by both irritants were significantly and dose-dependently prevented by 16,16-dimethyl PGE2 (dmPGE2: 3 and 10 μg/kg, subcutaneously), cysteamine (30 and 100 mg/kg, subcutaneously) or timoprazole (10 and 30 mg/kg, per os) at the doses which significantly inhibited gastric motility. In the pylorus-ligated stomach, however, neither of these agents showed any protection against the generalized lesions induced by ethanol, but such lesions caused by aspirin were significantly prevented only by dmPGE2. These agents also showed similar effects against the reduction of transmucosal PD in the pylorus-ligated stomach exposed to ethanol and aspirin. These results suggest that (1) the formation of bandlike lesions caused by ethanol and aspirin depends on the presence of mucosal folds and may be prevented by the agents that inhibit gastric motility, (2) the pathogenesis of the lesions induced by aspirin and ethanol may be different in the pylorus-ligated stomach, and (3) dmPGE2 has a unique protective ability that is not shared by usual cytoprotective agents. © 1990 Plenum Publishing Corporation.
引用
收藏
页码:178 / 185
页数:8
相关论文
共 25 条
[1]  
DAVENPORT HW, 1964, GASTROENTEROLOGY, V47, P142
[2]  
DAVENPORT HW, 1970, PROGR GASTROENTEROLO, P48
[4]   GASTRODUODENAL HCO3- TRANSPORT - CHARACTERISTICS AND PROPOSED ROLE IN ACIDITY REGULATION AND MUCOSAL PROTECTION [J].
FLEMSTROM, G ;
GARNER, A .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 242 (03) :G183-G193
[5]   EFFECT OF PGI2, PGE2 AND 6-KETO PGF1-ALPHA ON CANINE GASTRIC BLOOD-FLOW AND ACID SECRETION [J].
GERKENS, JF ;
GERBER, JG ;
SHAND, DG ;
BRANCH, RA .
PROSTAGLANDINS, 1978, 16 (05) :815-823
[6]  
HAWKEY CJ, 1988, GASTROENTEROLOGY, V94, P22
[7]  
KAWABE Y, 1989, AM J GASTROENTEROL, V84, P138
[8]   GASTRIC-MUCOSAL PROTECTION BY AGENTS ALTERING GASTRIC-MUCOSAL SULFHYDRYLS - ROLE OF ENDOGENOUS PROSTAGLANDINS [J].
KONTUREK, SJ ;
BRZOZOWSKI, T ;
PIASTUCKI, I ;
RADECKI, T ;
DUPUY, D ;
SZABO, S .
DIGESTION, 1987, 37 (02) :65-71
[9]   ROLE OF LOCALLY GENERATED PROSTAGLANDINS IN ADAPTIVE GASTRIC CYTOPROTECTION [J].
KONTUREK, SJ ;
BRZOZOWSKI, T ;
PIASTUCKI, I ;
RADECKI, T ;
DEMBINSKI, A ;
DEMBINSKAKIEC, A .
DIGESTIVE DISEASES AND SCIENCES, 1982, 27 (11) :967-971
[10]  
MAIN IMH, 1974, BRIT J PHARMACOL, V49, P428