Derelanko M J, Long J F
Dig Dis Sci. 1982 Feb;27(2):149-54. doi: 10.1007/BF01311709.
The purpose of the present study was to investigate the effect of prednisolone on gastric injury induced by ethanol in the rat. Gastric damage was produced by oral administration of 1 ml of absolute ethanol to rats previously fasted for 24 hr and deprived of water for 19 hr. The severity of the ethanol-induced gastric damage varied considerably within the vehicle-treated group of rats which served as controls. Prednisolone, administered orally as a single dose 15 min before alcohol challenge, significantly decreased the number of rats which developed severe lesions. Prednisolone was effective in increasing the resistance of the gastric mucosa to ethanol when given from 1 to 60 min before alcohol. The steroid proved ineffective when 90 min elapsed between prednisolone and ethanol administration, or when the steroid was given at the same time (0 min) as alcohol. The dose-response curve for prednisolone plateaued at high doses. Our results suggest that a prostaglandin-mediated endogenous cytoprotective potential exists in the rat gastric mucosa. Prednisolone may enhance the degree of mucosal protection afforded by this mechanism.
本研究的目的是探讨泼尼松龙对乙醇诱导的大鼠胃损伤的影响。通过给先前禁食24小时并禁水19小时的大鼠口服1毫升无水乙醇来造成胃损伤。在作为对照的赋形剂处理组大鼠中,乙醇诱导的胃损伤严重程度差异很大。在酒精激发前15分钟口服单剂量泼尼松龙,可显著减少出现严重损伤的大鼠数量。在酒精前1至60分钟给予泼尼松龙,可有效提高胃黏膜对乙醇的抵抗力。当泼尼松龙与乙醇给药间隔90分钟,或当类固醇与酒精同时(0分钟)给药时,该类固醇无效。泼尼松龙的剂量反应曲线在高剂量时趋于平稳。我们的结果表明,大鼠胃黏膜中存在前列腺素介导的内源性细胞保护潜能。泼尼松龙可能会增强这种机制所提供的黏膜保护程度。