Labrid C, Dureng G, Boero C
C R Seances Soc Biol Fil. 1975;169(3):566-73.
The "gastric chamber" technique, performed in the anaesthetised rat, enables the study of gastric mucosal fragility induced by doses of phenylbutazone, which do not themselves cause ulceration or exulceration. The perfusion of buffered solution at pH 2-8 into the gastric chamber shows that prior oral administration of phenylbutazone 50 mg/kg increases the fragility of the mucosa. The optimal delay separating this administration from the time of experimentation is 6 hours. The effects seen are essentially vascular disorders.
在麻醉大鼠身上实施的“胃腔”技术,能够研究苯基丁氮酮剂量所诱发的胃黏膜脆性,而这些剂量本身并不会导致溃疡或溃疡形成。将pH值为2 - 8的缓冲溶液灌注到胃腔中显示,预先口服50毫克/千克的苯基丁氮酮会增加黏膜的脆性。从给药到实验的最佳间隔时间为6小时。所观察到的效应主要是血管紊乱。