摘要
化合物Ⅰ具有与呋喃唑酮相似的抗实验性大鼠溃疡活性,但小鼠口服急性毒性较后者小。化合物Ⅰ在剂量为40～100 mg/kg时对五种大鼠溃疡模型(消炎痛型、幽门结扎型、慢性醋酸型、和无水乙醇引起的大鼠溃疡模型)均有较好保护作用,但对水拘急性应激型溃疡无效。对胃酸分泌无明显影响,对胃蛋白酶分泌有轻度抑制作用;具有“细胞保护”样作用,对HCl和无水乙醇引起的大鼠溃疡显示出较好的保护作用;增加幽门结扎大鼠胃液中氨基己糖的含量,降低DNA含量。
Pyrrole aldehydephenyl semicarbazone was shown to be an effctive anti-ulcer agent in five experimental models in rats, namely, the indomethacin-induced, acetic acid-induced, pyloric ligation-induced and 0.6 mol HCl, absolute alcohol-induced ulcers, at doses of 40～100 mg/kg. Its anti-ulcer activity and characteristics are similar to those of furazolidone. Its oral acute toxicity in mouse is much lower than furazolidone. This compound exhibited mild inhibitory effects on gastric pepsin secretion, caused increases in hexosamine level and decreases of DNA content in gastric juice. It showed no influence on gastric acid secretion and was considered to tare 'cytoprotective action' on the gastric mucosa. However, this compound was found to be ineffective against the stress-restraint gastric ulcer model.
出处
《药学学报》
CAS
CSCD
北大核心
1989年第8期562-567,共6页
Acta Pharmaceutica Sinica
关键词
抗溃疡药
胃溃疡模型
化合物I
Pyrrole aldehydephenyl semicarbazone
Anti-ulcer ageat
Gastric ulcer models
Cimetidine
