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Biomed Res Int ; 2013: 789184, 2013.
Article in English | MEDLINE | ID: mdl-24369535

ABSTRACT

The purpose of this study was to determine the effect of apigenin on the pharmacokinetics of imatinib and N-desmethyl imatinib in rats. Healthy male SD rats were randomly divided into four groups: A group (the control group), B group (the long-term administration of 165 mg/kg apigenin for 15 days), C group (a single dose of 165 mg/kg apigenin), and D group (a single dose of 252 mg/kg apigenin). The serum concentrations of imatinib and N-desmethyl imatinib were measured by HPLC, and pharmacokinetic parameters were calculated using DAS 3.0 software. The parameters of AUC(0-t), AUC(0-∞), Tmax, V(z)/F, and CL(z)/F for imatinib in group B were different from those in group A (P < 0.05). Besides, MRT(0-t) and MRT(0-∞) in groups C and D differed distinctly from those in group A as well. The parameters of AUC(0-t) and Cmax for N-desmethyl imatinib in group C were significantly lower than those in group A (P < 0.05); however, compared with groups B and D, the magnitude of effect was modest. Those results indicated that apigenin in the short-term study inhibited the metabolism of imatinib and its metabolite N-desmethyl imatinib, while in the long-term study the metabolism could be accelerated.


Subject(s)
Apigenin/administration & dosage , Benzamides/metabolism , Benzamides/pharmacokinetics , Piperazines/metabolism , Piperazines/pharmacokinetics , Pyrimidines/metabolism , Pyrimidines/pharmacokinetics , Animals , Benzamides/antagonists & inhibitors , Benzamides/blood , Chromatography, High Pressure Liquid , Humans , Imatinib Mesylate , Piperazines/antagonists & inhibitors , Piperazines/blood , Pyrimidines/antagonists & inhibitors , Pyrimidines/blood , Rats
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