Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.
KMID : 0941820050150010055
Korean Journal of Clinical Pharmacy
2005 Volume.15 No. 1 p.55 ~ p.60
Effect of Naringin on Tamoxifen Pharmacokinetics in Rats
Kim Hyung-Seok

Choi Jun-Shik
Choe In
Abstract
The aim of this study is to investigate the effect of naringin on the pharmacokinetics of tamoxifen in rats. Tamoxifen (10 mg/kg) was administered orally 0.5 h and 3 days after oral administration of naringin (5 mg/kg). The plasma concentrations of tamoxifen were increased significantly tv naringin compared to control. Absorption rate constant (K_a) of tamoxifen with naringin was increased significantly compared to that of the control. The areas under the plasma concentration-time curve (AUC) and the peak concentrations (C_{max}) of tamoxifen with naringin were significantly higher than those of the control. Consequently, the relative bioavailability (R.B{%}) of tamoxifen with naringin was 2-3-fold higher than the control, and absolute bioavailability (A.B{%}) of tamoxifen were significantly higher (p<0.05 with coadministration, p<0.01 with pretreatment) than those of the control. The increased bioavailability of tamoxifen in rats with naringin might be associated with the inhibition by naringin of an efflux pump P-glycoprotein and the first-pass metabolizing enzyme CYP3A4.
KEYWORD
tamoxifen, naringin, pharmacokinetics, bioavailability, pretreatment
FullTexts / Linksout information
Listed journal information
ÇмúÁøÈïÀç´Ü(KCI)