Bagshaw P F, Munster D J, Wilson J G
Gut. 1987 Mar;28(3):287-93. doi: 10.1136/gut.28.3.287.
Mucus was sampled from the gastric mucosal surface of anaesthetised rats. Three weeks later these rats were orally dosed each day with aspirin (375 mg/kg) for six months. Then the number and size of the aspirin induced chronic gastric ulcers were assessed. Gel filtration chromatography of the mucus samples showed that mucus glycoprotein was present in both high and low molecular weight forms. There was a natural variation between individual rats in the percentage of glycoprotein in the high molecular weight form (mean = 58.9%; SD = 9.6%; n = 23). This variation correlated strongly with the degree of subsequent aspirin induced chronic gastric ulceration (r = -0.85, p less than 0.001). This is the first time that a pre-existent variability in a mucosal defence factor has been shown to predict susceptibility of the stomach to chronic ulceration.
从麻醉大鼠的胃黏膜表面采集黏液样本。三周后,这些大鼠每天口服阿司匹林(375毫克/千克),持续六个月。然后评估阿司匹林诱导的慢性胃溃疡的数量和大小。对黏液样本进行凝胶过滤色谱分析表明,黏液糖蛋白以高分子量和低分子量两种形式存在。高分子量形式的糖蛋白在个体大鼠之间存在自然变异(平均值 = 58.9%;标准差 = 9.6%;n = 23)。这种变异与随后阿司匹林诱导的慢性胃溃疡程度密切相关(r = -0.85,p < 0.001)。这是首次表明黏膜防御因子预先存在的变异性可预测胃对慢性溃疡形成的易感性。