PubMed · 11859464
Marked decrease of cyclosporin absorption caused by phellamurin in rats.
Abstract
Phellamurin is a flavonoid glycoside that is abundant in the leaves of Phellodendron wilsonii Hayata et Kanehira (Rutaceae). In vitro everted rat intestine study indicated that phellamurin inhibited intestinal P-glycoprotein in a dose-dependent manner. In order to investigate the effect of phellamurin on cyclosporin absorption and disposition, rats were given cyclosporin (5 mg/kg) with or without phellamurin in a parallel design. Fluorescence polarization immunoassay was used to determine the blood concentration of cyclosporin. Unanticipatedly, our results indicated that the coadministration of phellamurin significantly decreased the Cmax of cyclosporin by 77 % and reduced the AUC(0-infinity) of cyclosporin by 56 %. This indicated that a serious interaction occurred between phellamurin with cyclosporin. To ensure the efficacy of cyclosporin, we suggest that the coadministration of phellamurin or Phellodendron wilsonii with cyclosporin should be avoided.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Hung-Yi Chen, Tian-Shung Wu, Sheng-Fang Su, Sheng-Chu Kuo, Pei-Dawn Lee Chao. 2002. Marked decrease of cyclosporin absorption caused by phellamurin in rats.. https://doi.org/10.1055/s-2002-20244
Cite the original work for its findings. Save a collection to share your selection of sources.