Kim S E, Hong Y S, Kim Y C, Lee J J
Natural Product Biosynthesis RU., Korea Research Institute of Bioscience and Biotechnology, Yusong, Taejon, Korea.
Planta Med. 1998 May;64(4):335-8. doi: 10.1055/s-2006-957446.
The mechanism of action of multidrug-resistance reversing activity of torilin was studied. In vitro experiments for the accumulation and efflux of vinblastine clearly indicated that MDR reversing effects of torilin would directly be associated with the increase of the intracellular accumulation of anticancer drugs by blocking the drug efflux. Furthermore, torilin increased the membrane ATPase activity from KB-V1 cells, suggesting that torilin might function by inhibiting drug transport mediated by P-glycoprotein.
研究了托瑞林多药耐药逆转活性的作用机制。长春碱蓄积和外排的体外实验清楚地表明,托瑞林的多药耐药逆转作用将直接与通过阻断药物外排增加抗癌药物的细胞内蓄积有关。此外,托瑞林增加了KB-V1细胞的膜ATP酶活性,提示托瑞林可能通过抑制P-糖蛋白介导的药物转运发挥作用。