Sambol N C, Upton R A, Chremos A N, Lin E T, Williams R L
Department of Pharmacy, School of Pharmacy, University of California, San Francisco.
Br J Clin Pharmacol. 1989 Jan;27(1):83-7. doi: 10.1111/j.1365-2125.1989.tb05338.x.
The H2-receptor antagonist cimetidine has been reported to decrease the hepatic clearance of numerous drugs by inhibiting cytochrome P-450 metabolism, decreasing liver blood flow or both. In this open-label, randomized crossover study we determined whether therapeutic doses of famotidine, a newer H2-receptor antagonist, has similar effects. Ten healthy subjects received single doses of both phenytoin 100 mg orally and indocyanine green intravenously without other treatment, and then again during treatment with famotidine or cimetidine. After a drug-free period, this sequence was repeated with the alternate H2-receptor antagonist. Cimetidine decreased the plasma clearance of phenytoin by 16% +/- 14% (mean +/- s.d.), but was not found to have a significant influence on phenytoin volume of distribution or terminal elimination rate constant nor on blood clearance of indocyanine green. Famotidine was not found to alter either phenytoin or indocyanine green kinetics.
据报道,H2受体拮抗剂西咪替丁可通过抑制细胞色素P - 450代谢、降低肝血流量或两者兼而有之,来降低多种药物的肝清除率。在这项开放标签、随机交叉研究中,我们确定了新型H2受体拮抗剂法莫替丁的治疗剂量是否具有类似作用。10名健康受试者在未接受其他治疗的情况下,口服100 mg苯妥英钠并静脉注射吲哚菁绿,然后在法莫替丁或西咪替丁治疗期间再次进行上述操作。在一段无药期后,用另一种H2受体拮抗剂重复此序列。西咪替丁使苯妥英钠的血浆清除率降低了16%±14%(均值±标准差),但未发现其对苯妥英钠的分布容积或终末消除速率常数以及吲哚菁绿的血液清除率有显著影响。未发现法莫替丁改变苯妥英钠或吲哚菁绿的动力学。