Goldberg M R, Lo M W, Bradstreet T E, Ritter M A, Höglund P
Merck Research Laboratories West Point, Pennsylvania 19486, USA.
Eur J Clin Pharmacol. 1995;49(1-2):115-9. doi: 10.1007/BF00192369.
This was a 2-period randomized, crossover study in 8 healthy males to determine the effects of cimetidine (400 mg q.i.d. for 6 days) on the pharmacokinetics and pharmacodynamic effects of the angiotensin II receptor antagonist, losartan (100 mg). Cimetidine increased the AUC for losartan 18% without affecting the AUC for E-3174, the active metabolite of losartan. The increase in plasma renin activity following losartan was not affected by cimetidine (maximum mean increases 12.6 and 12.1 ng Ang I.ml-1.h-1 without and with cimetidine, respectively). These results indicate that cimetidine does not appear to alter the pharmacokinetics or pharmacodynamics of losartan to a clinically significant extent.
这是一项在8名健康男性中进行的两阶段随机交叉研究,旨在确定西咪替丁(400毫克,每日4次,共6天)对血管紧张素II受体拮抗剂氯沙坦(100毫克)的药代动力学和药效学作用的影响。西咪替丁使氯沙坦的AUC增加了18%,而不影响氯沙坦的活性代谢物E-3174的AUC。氯沙坦给药后血浆肾素活性的增加不受西咪替丁的影响(分别在无西咪替丁和有西咪替丁的情况下,最大平均增加量为12.6和12.1纳克血管紧张素I·毫升-1·小时-1)。这些结果表明,西咪替丁似乎不会在临床上显著改变氯沙坦的药代动力学或药效学。