High in situ rat intestinal permeability of artemisinin unaffected by multiple dosing and with no evidence of P-glycoprotein involvement

The objective of this study was to investigate whether the decrease in arte misinin bioavailability after repeated oral dosing in humans can be a resul t of increased efflux of artemisinin by P-glycoprotein or decreased membran e transport at the intestinal barrier, The effective jejunal permeability ( P-eff) of artemisinin was investigated using an in situ rat perfusion model . Fifty-four rats were randomized to one of three treatment arms: no pretre atment, pretreatment with artemisinin emulsion for 5 days (60 mg/kg/day, p. o.), or pretreatment with emulsion vehicle for 5 days, The rats within each treatment arm were randomized further to be jejunally perfused with either low (500 ng/ml) or high (5000 ng/ml) artemisinin concentration or low arte misinin concentration plus the P-glycoprotein inhibitor R,S-verapamil (400 mu g/ml). Perfusate samples were assayed for content of artemisinin, R,S-ve rapamil, and perfusion viability markers. Artemisinin P-eff was 1,44 +/- 0. 38, 1.17 +/- 0.32, and 1.71 +/- 0.29 (.10(-4), cm/s) in rats receiving no p retreatment and perfused with low, high, or low artemisinin concentration p lus verapamil, respectively. Multiple oral dosing of artemisinin did not af fect the jejunal permeability of artemisinin, R,S-verapamil P-eff was simil ar in artemisinin-pretreated rats (1.09 +/- 0.54.10(-4), cm/s) and rats pre treated with only vehicle (1.07 +/- 0.37.10(-4), cm/s), The decrease in art emisinin bioavailability after multiple oral dosing in human is probably no t a result of changes in P-glycoprotein expression or general intestinal tr ansport. It seems more likely attributed to increased hepatocellular activi ty. Furthermore, artemisinin exhibits high jejunal permeability and is neit her a substrate nor inducer of P-glycoprotein.