Metabolic interaction between biflavonoids in Ginkgo biloba leaves and tacrolimus.

The aim of this study was to investigate the effect of biflavonoids in Ginkgo biloba leaves on tacrolimus metabolism. Firstly, the inhibitory effects of 5 main biflavonoids (amentoflavone, sciadopitysin, ginkgetin, isoginkgetin, bilobetin) in Ginkgo biloba leaves on tacrolimus metabolism were investigated in vitro in human liver microsomes (HLM), and the concentration-dependent inhibition was further calculated. Then the time-dependent inhibition activities of 5 biflavonoids were studied and the drug interaction was studied in SD rats. Finally, the molecular mechanism of inhibition was explored by molecular docking. The results of in vitro incubation in HLM showed tacrolimus metabolism was strongly inhibited by amentoflavone, ginkgetin and bilobetin, which IC50 value was 5.57, 3.16 and 5.03 μM, respectively. The time-dependent inhibition of the 3 above biflavonoids at 50 μM was 33.47%∼50.89%. In the in vivo study in rats, the AUC0-t and Cmax of tacrolimus increased 3.8 folds and 2.5 folds after oral pre-administration with amentoflavone. Molecular docking results showed that the inhibitory effect may be related to the formation of hydrogen bonds. The results showed that long-term combination of Ginkgo biloba leaves and tacrolimus may cause drug-drug interactions. This study provided theoretical and experimental basis for rational drug use in clinical practice. This article is protected by copyright. All rights reserved.