Patel S S, Wilde M I
Adis International Limited, Auckland, New Zealand.
Drugs. 1996 Jun;51(6):974-80; discussion 981. doi: 10.2165/00003495-199651060-00006.
Ebrotidine is the first of a new generation of H2 receptor antagonists with gastroprotective activity It stimulates epithelial cell proliferative activity and produces beneficial physicochemical changes in the gastric mucus that contribute to its gastro-protective action against ethanol-, aspirin- or stress-induced gastric mucosal damage The antisecretory properties of ebrotidine are similar to those of ranitidine and approximately 10-fold greater than those of cimetidine This drug exhibits anti-Helicobacter pylori activity that is synergistic with a number of antibacterial agents; it inhibits the urease enzyme and the proteolytic and mucolytic activities of H. pylori, and counteracts the inhibitory effects of H. pylori lipo-polysaccharide Ebrotidine is as effective as ranitidine for the treatment of patients with gastric or duodenal ulcers or erosive reflux oesophagitis Ebrotidine therapy results in significantly better ulcer healing rates than ranitidine treatment in patients who smoke.
依布替丁是新一代具有胃保护活性的H2受体拮抗剂中的首个药物。它刺激上皮细胞增殖活性,并在胃黏液中产生有益的物理化学变化,这有助于其对乙醇、阿司匹林或应激诱导的胃黏膜损伤发挥胃保护作用。依布替丁的抗分泌特性与雷尼替丁相似,比西咪替丁大约强10倍。该药物具有抗幽门螺杆菌活性,与多种抗菌剂具有协同作用;它抑制脲酶以及幽门螺杆菌的蛋白水解和黏液溶解活性,并抵消幽门螺杆菌脂多糖的抑制作用。依布替丁在治疗胃溃疡、十二指肠溃疡或糜烂性反流性食管炎患者方面与雷尼替丁同样有效。在吸烟患者中,依布替丁治疗导致的溃疡愈合率明显优于雷尼替丁治疗。