Pharmacokinetics and tissue distribution of pterostilbene in the rat

Methods and results: Upon intravenous (iv) administration (88 mu mol/kg), Pt was cleared from blood with a half-life of 1.8 +/- 0.3 h. Oral administration (same dose) resulted in moderate Pt bioavailability (similar to 35%) and in an increased abundance of Pt-S in blood (AUC(Pt)/AUC(Pt-S) similar to 0.75 and similar to 0.05 after iv or oral administration, respectively). Pt-S was the major species in all organs except the brain, where intact Pt was predominant (AUC(Pt)/AUC(Pt-S) similar to 5). Both Pt and Pt-S peaked in all tissues at approximately 2 h. The highest levels (similar to 200 nmoles/g for Pt-S and 40 nmoles/g for Pt) were measured in the liver, the lowest (<= 7 nmol/g) in skeletal muscles and testes.

Scope: Pterostilbene (Pt) is emerging as an important health-promoting natural compound. Pharmacokinetic studies so far have focused on plasma levels, while Pt distribution in tissues is most relevant for biological action. This study determined tissue distribution of Pt and its major metabolite, pterostilbene-4'-sulfate (Pt-S), in rats after oral administration.