Planta Med 2010; 76 - P285
DOI: 10.1055/s-0030-1264583

Enhanced cellular uptake of paclitaxel in the presence of macelignan, a phytoestrogen and its implication in cancer chemotherapy

F Qiang 1, H Han 1
  • 1BK21 Project Team, College of Pharmacy, Chosun University, College of Pharmacy, 375 Seosuk-dong, Dong-gu, 501–759 Gwangju, Korea, Republic Of

This study investigated the effect of macelignan, a phytoestrogen isolated from Myristica fragrans, on the P-glycoprotein-mediated drug efflux as well as CYP3A4-medated drug metabolism and subsequently its in vivo implication on the bioavailability of paclitaxel. The inhibition effect of macelignan was negligible over the concentration range of 0.01–100µM in rat liver microsome while its estimated IC50 value was 93.63µM in human liver microsome, implying that the interaction of macelignan with CYP3A4 might be insignificant at the physiologically achievable concentrations. In contrast, macelignan (20µM) increased the cellular accumulation of paclitaxel by approximately 1.7 fold in NCI/ADR-RES cells overexpressing P-gp, while it did not alter the cellular accumulation of paclitaxel in OVCAR-8 cells lacking P-gp. The effect of macelignan on the systemic exposure of paclitaxel was also examined in rats after the intravenous and oral administration of paclitaxel in the presence and the absence of macelignan. The concurrent use of macelignan significantly (p<0.05) enhanced the oral exposure of paclitaxel in rats while it did not affect the intravenous pharmacokinetics of paclitaxel, implying that macelignan might be more effective to improve the intestinal absorption rather than reducing hepatic elimination. In conclusion, macelignan appeared to be effective to improve the cellular accumulation as well as oral exposure of paclitaxel mainly via the inhibition of P-gp-mediated cellular efflux, suggesting that the concomitant use of macelignan may provide a therapeutic benefit in improving the anticancer efficacy of paclitaxel.

Acknowledgements: This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (No. 2009–0083757).