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Effect of Rebamipide a Novel Antiulcer Agent on Helicobacter pylori Adhesion to Gastric Epithelial Cells

机译:新型抗溃疡药瑞巴派特对幽门螺杆菌对胃上皮细胞粘附的影响

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摘要

Helicobacter pylori is a major etiological agent in gastroduodenal disorders. The adhesion of H. pylori to human gastric epithelial cells is the initial step of H. pylori infection. Inhibition of H. pylori adhesion is thus a therapeutic target in the prevention of H. pylori infection. Experiments were performed to evaluate the effect of rebamipide, a novel antiulcer agent, on H. pylori adhesion to gastric epithelial cells. MKN-28 and MKN-45 cells, derived from human gastric carcinomas, were used as target cells. Ten H. pylori strains isolated from patients with chronic gastritis and gastric ulcer were used in the study. We evaluated the effect of rebamipide on H. pylori adhesion to MKN-28 and MKN-45 cells quantitatively using our previously established enzyme-linked immunosorbent assay. The adhesion of H. pylori to MKN-28 and MKN-45 cells was significantly inhibited by pretreatment of these cells with 100 μg of rebamipide per ml. However, the adhesion was not affected by the pretreatment of H. pylori with rebamipide. On the other hand, the viabilities of H. pylori, MKN-28 cells, and MKN-45 cells were not affected by rebamipide. Our studies suggest that rebamipide inhibits the adhesion of H. pylori to gastric epithelial cells.
机译:幽门螺杆菌是胃十二指肠疾病的主要病因。幽门螺杆菌对人胃上皮细胞的粘附是幽门螺杆菌感染的第一步。因此,抑制幽门螺杆菌粘附是预防幽门螺杆菌感染的治疗靶标。进行实验以评估新型抗溃疡剂瑞巴派特对幽门螺杆菌粘附于胃上皮细胞的影响。来自人胃癌的MKN-28和MKN-45细胞用作靶细胞。该研究使用了从慢性胃炎和胃溃疡患者中分离出的10株幽门螺杆菌菌株。我们使用先前建立的酶联免疫吸附测定法定量评估了瑞巴派特对幽门螺杆菌对MKN-28和MKN-45细胞粘附的影响。幽门螺杆菌对MKN-28和MKN-45细胞的粘附通过用每毫升100μg瑞巴派特预处理这些细胞而得到显着抑制。但是,用瑞巴派特对幽门螺杆菌进行预处理不会影响粘附。另一方面,瑞巴派特不影响幽门螺杆菌,MKN-28细胞和MKN-45细胞的活力。我们的研究表明,瑞巴派特可抑制幽门螺杆菌对胃上皮细胞的粘附。

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