Forskning ved Københavns Universitet - Københavns Universitet


Artemisinin induces omeprazole metabolism in human beings

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Ulrika S.H. Svensson
  • Michael Ashton
  • Trinh Ngoc Hai
  • Leif Bertilsson
  • Dinh Xuan Huong
  • Nguyen Van Huong
  • Nguyen Thi Niêu
  • Nguyen Duy Sy
  • Lykkesfeldt, Jens
  • Le Dinh Công

Objective: This study investigated whether time-dependent artemisinin pharmacokinetics correlated to CYP3A4 or CYP2C19 activity in vivo. Methods: Artemisinin (two oral doses per day of 250 mg) was given to nine healthy Vietnamese subjects for 7 days (day 1 to day 7). Single 20 mg doses of omeprazole were given orally on day-7, day 1, and day 7. Single doses of artemisinin and omeprazole were given in combination on day 14 after a 6-day washout period. The pharmacokinetics of artemisinin, omeprazole, hydroxyomeprazole, and omeprazole sulfone were evaluated on days -7, 1, 7, and 14. On the same days urine was collected for the determination of 6β- hydroxycortisol and cortisol excretion. Results: Areas under plasma concentration-time curves (AUC) for artemisinin and omeprazole decreased on day 7 to 20% (95% confidence intervals, 13%, 28%) and 35% (25%, 46%), respectively, compared with values on day 1. AUC ratios for hydroxyomeprazole/omeprazole increased 2.2-fold (1.7, 2.7) on day 7 compared with values on day 1. All values were normalized at day 14. There were no significant changes in the omeprazole sulfone/omeprazole ratio or in the 6β- hydroxycortisol/cortisol ratio between the study days. In one subject found to have poor CYP2C19 metabolization, the elimination of omeprazole increased after artemisinin exposure, with no change in the hydroxyomeprazole/omeprazole AUC ratio. Conclusion: Artemisinin did not alter CYP3A4 activity, whereas an increase in CYP2C19 activity was observed. The increased elimination of omeprazole in both poor and extensive CYP2C19 metabolizers suggests artemisinin induces both CYP2C19 and another enzyme.

TidsskriftClinical Pharmacology and Therapeutics
Udgave nummer2
Sider (fra-til)160-167
Antal sider8
StatusUdgivet - 1 aug. 1998

ID: 204500174