Wada K, Kamisaki Y, Kitano M, Kishimoto Y, Nakamoto K, Itoh T
Department of Clinical Pharmacology, Faculty of Medicine, Tottori University, Yonago, Japan.
Life Sci. 1996;59(19):PL295-301. doi: 10.1016/0024-3205(96)00500-0.
A new model of gastric ulcer involving damage to the muscularis mucosae was developed by clamping the celiac artery in rat to induce ischemia-reperfusion (I-R) injury. Although erosions with falling off of the gastric mucosa were observed immediately, 24 and 36 hours after the I-R, gastric ulcers involving the injury of muscularis mucosae were observed in the area of gastric glands at 48 and 72 hours after initiation of injury. Administration of omeprazol, a proton pump inhibitor, or pentoxifylline, an anti-leukocyte drug, just after the initiation of injury significantly decreased the total area of ulcers at 72 hours. A combination of omeprazol and pentoxifylline was more effective than either drug alone. An anti-leukocyte adhesion molecule (anti-CD18 antibody) also showed significant inhibitory effect on the development of ulcers at 72 hours and the infiltration of leukocytes into both submucosa and mucosa. These results indicate that in our model, gastric acid together with leukocytes contribute to the development of ulcers following erosions. This model may be used to investigate the mechanisms of the development of gastric ulcer and evaluate antiulcer drugs in a preclinical setting.
通过夹闭大鼠腹腔动脉诱导缺血再灌注(I-R)损伤,建立了一种涉及黏膜肌层损伤的胃溃疡新模型。尽管在I-R后立即、24小时和36小时观察到胃黏膜有糜烂并脱落,但在损伤开始后48小时和72小时,在胃腺区域观察到涉及黏膜肌层损伤的胃溃疡。在损伤开始后立即给予质子泵抑制剂奥美拉唑或抗白细胞药物己酮可可碱,可显著降低72小时时溃疡的总面积。奥美拉唑和己酮可可碱联合使用比单独使用任何一种药物更有效。抗白细胞粘附分子(抗CD18抗体)在72小时时也对溃疡的形成以及白细胞浸润到黏膜下层和黏膜层均显示出显著的抑制作用。这些结果表明,在我们的模型中,胃酸与白细胞共同促成了糜烂后溃疡的形成。该模型可用于研究胃溃疡形成的机制,并在临床前环境中评估抗溃疡药物。