Effects of cimetidine on pharmacokinetics and pharmacodynamics of losartan, an AT1-selective non-peptide angiotensin II receptor antagonist

Eur J Clin Pharmacol. 1995;49(1-2):115-9. doi: 10.1007/BF00192369.

Abstract

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.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Angiotensin Receptor Antagonists*
  • Antihypertensive Agents / therapeutic use
  • Biphenyl Compounds / antagonists & inhibitors
  • Biphenyl Compounds / pharmacokinetics*
  • Cimetidine / pharmacology*
  • Cross-Over Studies
  • Histamine H2 Antagonists / pharmacology*
  • Humans
  • Hypertension / drug therapy
  • Imidazoles / antagonists & inhibitors
  • Imidazoles / pharmacokinetics*
  • Imidazoles / therapeutic use
  • Losartan
  • Male
  • Tetrazoles / antagonists & inhibitors
  • Tetrazoles / pharmacokinetics*
  • Tetrazoles / therapeutic use

Substances

  • Angiotensin Receptor Antagonists
  • Antihypertensive Agents
  • Biphenyl Compounds
  • Histamine H2 Antagonists
  • Imidazoles
  • Tetrazoles
  • Cimetidine
  • losartan carboxylic acid
  • Losartan