Collins J D
Clinical Pharmacology Dept., Hoechst UK Limited, Walton, Buckinghamshire, England.
Scand J Gastroenterol Suppl. 1988;146:89-99. doi: 10.3109/00365528809099135.
Possible mechanisms of drug interactions with H2-antagonists are outlined. The mode of action of roxatidine acetate on hepatic microsomal enzymes is contrasted with those of cimetidine and ranitidine, and their differing structure-activity relationships are discussed. In the light of the mechanisms of drug interactions with H2-antagonists, clinical studies with roxatidine acetate are contrasted with published interaction data of cimetidine and ranitidine. The therapeutic consequences of these data are considered.
概述了与H2拮抗剂发生药物相互作用的可能机制。将醋酸罗沙替丁对肝微粒体酶的作用方式与西咪替丁和雷尼替丁的作用方式进行了对比,并讨论了它们不同的构效关系。根据与H2拮抗剂发生药物相互作用的机制,将醋酸罗沙替丁的临床研究与已发表的西咪替丁和雷尼替丁的相互作用数据进行了对比。考虑了这些数据的治疗意义。