Effect of Soy Extract Administration on Losartan Pharmacokinetics in Healthy Female Volunteers

Background Losartan is metabolized by CYP2C9 and CYP3A4 to an active metabolite, E-3174, which has greater antihypertensive activity than the parent compound. Soy extract has been shown to be an activator of CYP2C9 and CYP3A4 in vitro. Coadministration of soy extract and losartan may therefore after the pharmacokinetics of losartan and E-3174. Objective To determine whether, when losartan was used in combination with soy extract, a significant pharmacokinetic interaction would be observed in healthy female volunteers. Methods Eighteen healthy Chinese female volunteers were recruited. In an open-label, 2-phase study, losartan 50 mg was given to each subject, with and without soy extract. Plasma concentrations of losartan and E-3174 were determined by liquid chromatography–tandem mass spectrometry for 12 and 24 hours, respectively. On day 8 through day 21 of the study, following a 7-day washout period, each subject consumed two 1000-mg Genistein Soy Complex tablets orally after meals, twice daily, for 14 days. On day 22, all volunteers received losartan 50 mg and blood samples were collected again. Results All subjects completed the study, without adverse drug effects. Over the 14-day pretreatment period, soy extract did not significantly influence the pharmacokinetics of losartan or E-3174. The ratio of the area under the curve of the drug and metabolite after losartan administration, with and without soy extract ingestion, was 0.21 ± 0.05 and 0.23 ± 0.05 (mean ± SD), respectively. The difference was not statistically significant (p = 0.22). Conclusions Our data indicate that a significant interaction between soy extract and losartan is unlikely to occur in females.

[1]  R. Kato,et al.  The effect of bucolome, a CYP2C9 inhibitor, on the pharmacokinetics of losartan. , 2008, Drug metabolism and pharmacokinetics.

[2]  L. Bertilsson,et al.  Amodiaquine, its desethylated metabolite, or both, inhibit the metabolism of debrisoquine (CYP2D6) and losartan (CYP2C9) in vivo , 2006, European Journal of Clinical Pharmacology.

[3]  Y. Moon,et al.  Dietary flavonoids: effects on xenobiotic and carcinogen metabolism. , 2006, Toxicology in vitro : an international journal published in association with BIBRA.

[4]  D. Sica,et al.  Clinical Pharmacokinetics of Losartan , 2005, Clinical pharmacokinetics.

[5]  Alex Sparreboom,et al.  Herbal remedies in the United States: potential adverse interactions with anticancer agents. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[6]  T. Bradstreet,et al.  Effects of cimetidine on pharmacokinetics and pharmacodynamics of losartan, an AT1-selective non-peptide angiotensin II receptor antagonist , 2004, European Journal of Clinical Pharmacology.

[7]  K. Riffel,et al.  Simultaneous determination of losartan and EXP3174 in human plasma and urine utilizing liquid chromatography/tandem mass spectrometry. , 2003, Journal of pharmaceutical and biomedical analysis.

[8]  G. Anderson,et al.  Drug Interaction Potential of Soy Extract and Panax Ginseng , 2003, Journal of clinical pharmacology.

[9]  C. Funck-Brentano,et al.  Effect of grapefruit juice on digoxin pharmacokinetics in humans , 2001, Clinical pharmacology and therapeutics.

[10]  Shiew-Mei Huang,et al.  The effects of St John's wort (Hypericum perforatum) on human cytochrome P450 activity , 2001, Clinical pharmacology and therapeutics.

[11]  E. Scapa,et al.  Effect of Grapefruit Juice on the Pharmacokinetics of Losartan and Its Active Metabolite E3174 in Healthy Volunteers , 2001, Therapeutic drug monitoring.

[12]  R. Obach,et al.  Inhibition of human cytochrome P450 enzymes by constituents of St. John's Wort, an herbal preparation used in the treatment of depression. , 2000, The Journal of pharmacology and experimental therapeutics.

[13]  A. Burstein,et al.  St John's Wort: Effect on CYP3A4 activity , 2000 .

[14]  M. Lin,et al.  In vitro and in vivo effects of naringin on cytochrome P450-dependent monooxygenase in mouse liver. , 1999, Life sciences.

[15]  K. Williamson,et al.  The Effects of Fluvastatin, a CYP2C9 Inhibitor, on Losartan Pharmacokinetics in Healthy Volunteers , 1999, Journal of clinical pharmacology.

[16]  L Gillen,et al.  Phenotypic and genotypic investigations of a healthy volunteer deficient in the conversion of losartan to its active metabolite E‐3174 , 1999, Clinical pharmacology and therapeutics.

[17]  K. Adams,et al.  Effects of erythromycin or rifampin on losartan pharmacokinetics in healthy volunteers , 1998, Clinical pharmacology and therapeutics.

[18]  P. Neuvonen,et al.  Fluconazole but not itraconazole decreases the metabolism of losartan to E-3174 , 1998, European Journal of Clinical Pharmacology.

[19]  A. Huggett,et al.  Phyto-oestrogens in soy-based infant formula , 1997, The Lancet.

[20]  T. Bjornsson,et al.  Pharmacokinetics of losartan, an angiotensin II receptor antagonist, and its active metabolite EXP3174 in humans , 1995, Clinical pharmacology and therapeutics.

[21]  P. Chakravarty,et al.  Biotransformation of losartan to its active carboxylic acid metabolite in human liver microsomes. Role of cytochrome P4502C and 3A subfamily members. , 1995, Drug metabolism and disposition: the biological fate of chemicals.

[22]  P. Timmermans,et al.  Angiotensin II receptors and angiotensin II receptor antagonists. , 1993, Pharmacological reviews.

[23]  M. Nakashima,et al.  Pharmacokinetics and biochemical efficacy after single and multiple oral administration of losartan, an orally active nonpeptide angiotensin II receptor antagonist, in humans. , 1993, British journal of clinical pharmacology.

[24]  P. Timmermans,et al.  Nonpeptide angiotensin II receptor antagonists. XI. Pharmacology of EXP3174: an active metabolite of DuP 753, an orally active antihypertensive agent. , 1990, The Journal of pharmacology and experimental therapeutics.