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首页> 外文期刊>Japanese Journal of Pharmacology >Effect of Elcatonin on Experimental Gastric and Duodenal Ulcers
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Effect of Elcatonin on Experimental Gastric and Duodenal Ulcers

机译:褪黑素对实验性胃和十二指肠溃疡的影响

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References(29) Cited-By(3) The antiulcer action of elcatonin, an analogue of natural eel calcitonin, was compared with that of cimetidine, secretin and solcoseryl. Elcatonin (3 to 10 u/kg, s.c.) inhibited the development of gastric ulcers induced by pylorus ligation, water-immersion stress, aspirin and reserpine and duodenal ulcers induced by cysteamine in rats. Moreover, once daily injections of elcatonin (1 to 10 u/kg/day, s.c.) promoted the healing of acetic acid-induced chronic gastric ulcers not only in rats but in dogs. The healing effect persisted after the cessation of administrations. Cimetidine (30 to 100 mg/kg, p.o.) inhibited the development of gastric ulcers induced by water-immersion stress, aspirin and reserpine and duodenal ulcers induced by cysteamine in rats. However, once daily administrations of cimetidine (30 to 100 mg/kg/day, p.o.) did not show significant effect on acetic acid-induced chronic gastric ulcers in rats. Secretin (30 to 100 u/kg, s.c.) inhibited the development of gastric ulcers induced by pylorus ligation, water-immersion stress, aspirin and reserpine in rats, but was not effective on cysteamine-induced duodenal ulcers and acetic acid-induced chronic gastric ulcers in rats. Solcoseryl (2 ml/kg, s.c.) inhibited only the development of water-immersion stress-induced gastric ulcers in rats. These results suggest that elcatonin is different from these reference drugs in its properties of action on experimental ulcers. Mechanisms of the antiulcer action of elcatonin which has a superior effect on experimental ulcers are discussed.
机译:参考文献(29)By-By(3)比较了天然鳗鱼降钙素类似物Elcatonin与西咪替丁,secretin和solcoseryl的抗溃疡作用。 Elcatonin(3至10 u / kg,s.c.)抑制幽门结扎,水浸应激,阿司匹林和利血平引起的胃溃疡的发展以及半胱胺诱发的十二指肠溃疡的发展。而且,每天一次注射降钙素(1至10u / kg /天,皮下注射)不仅促进了大鼠而且还促进了狗引起的乙酸诱导的慢性胃溃疡的愈合。停止给药后,愈合效果持续存在。西咪替丁(30至100 mg / kg,p.o.)抑制大鼠因水浸应激引起的胃溃疡,阿司匹林和利血平以及半胱胺引起的十二指肠溃疡的发展。但是,每天一次服用西咪替丁(30至100 mg / kg /天,口服)对乙酸诱导的大鼠慢性胃溃疡没有明显的作用。促胰液素(30至100 u / kg,sc)抑制大鼠幽门结扎,水浸应激,阿司匹林和利血平诱导的胃溃疡的发展,但对半胱胺诱导的十二指肠溃疡和乙酸诱导的慢性胃溃疡无效大鼠溃疡。 Solcoseryl(2 ml / kg,s.c.)仅抑制水浸应力诱发的大鼠胃溃疡的发展。这些结果表明,降钙素与这些参比药物在对实验性溃疡的作用特性上有所不同。讨论了降钙素的抗溃疡作用机理,该作用对实验性溃疡具有优越的作用。

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