Romano M, Lesch C A, Meise K S, Veljaca M, Sanchez B, Kraus E R, Boland C R, Guglietta A, Coffey R J
Department of Medicine (Gastroenterology), Vanderbilt University, Nashville, Tennessee, USA.
Gastroenterology. 1996 May;110(5):1448-55. doi: 10.1053/gast.1996.v110.pm8613050.
BACKGROUND & AIMS: The mechanism by which gastric mucosa becomes more resistant to damage by repeated aspirin administration is not known. Transforming growth factor alpha (TGF-alpha) and epidermal growth factor (EGF) prevent drug-induced gastric injury. The aim of this study was to determine whether gastroduodenal tissue levels of TGF-alpha and EGF protein were altered during adaptation to aspirin-induced injury in monkeys and rats in vivo.
Animals were given aspirin daily for up to 28 days. Gross mucosal injury was assessed by computerized image analysis in rats and by endoscopy in monkeys. Mucosal concentrations of TGF-alpha and EGF were quantitated by radioimmunoassays from endoscopic biopsy samples in monkeys and from scraped mucosa in rats.
Long-term administration of aspirin caused a significant increase in gastric and duodenal tissue levels of TGF-alpha in monkeys and rats; the increased levels of TGF-alpha significantly correlated with the decrease in aspirin-induced injury. No change in the gastroduodenal tissue levels of EGF was observed. Adaptation was not associated with any significant change in basal gastric acid secretion in monkeys and occurred despite a significant decrease in gastric mucin in rats.
Adaptation of the gastric mucosa to the damaging effect of aspirin is associated with a significant and specific increase in TGF-alpha protein in the gastroduodenum.
胃黏膜如何通过反复服用阿司匹林而变得更具抗损伤能力的机制尚不清楚。转化生长因子α(TGF-α)和表皮生长因子(EGF)可预防药物诱导的胃损伤。本研究的目的是确定在体内猴子和大鼠适应阿司匹林诱导的损伤过程中,胃十二指肠组织中TGF-α和EGF蛋白水平是否发生改变。
动物连续28天每日给予阿司匹林。通过计算机图像分析评估大鼠的大体黏膜损伤,通过内镜检查评估猴子的损伤。通过放射免疫分析法对猴子内镜活检样本和大鼠刮取的黏膜中的TGF-α和EGF的黏膜浓度进行定量。
长期给予阿司匹林导致猴子和大鼠胃和十二指肠组织中TGF-α水平显著升高;TGF-α水平的升高与阿司匹林诱导的损伤的减轻显著相关。未观察到胃十二指肠组织中EGF水平的变化。适应过程与猴子基础胃酸分泌的任何显著变化无关,并且在大鼠胃黏液显著减少的情况下仍会发生。
胃黏膜对阿司匹林损伤作用的适应与胃十二指肠中TGF-α蛋白的显著且特异性增加有关。