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槲皮素II相代谢对其抑制多药耐药相关蛋白1(MRP1)和多药耐药相关蛋白2(MRP2)潜力的影响。

The effect of quercetin phase II metabolism on its MRP1 and MRP2 inhibiting potential.

作者信息

van Zanden Jelmer J, van der Woude Hester, Vaessen Judith, Usta Mustafa, Wortelboer Heleen M, Cnubben Nicole H P, Rietjens Ivonne M C M

机构信息

Division of Toxicology, Wageningen University, PO Box 8000, 6700 EA, Wageningen, The Netherlands.

出版信息

Biochem Pharmacol. 2007 Jul 15;74(2):345-51. doi: 10.1016/j.bcp.2007.04.002. Epub 2007 Apr 6.

Abstract

The present study characterises the effect of phase II metabolism, especially methylation and glucuronidation, of the model flavonoid quercetin on its capacity to inhibit human MRP1 and MRP2 activity in Sf9 inside-out vesicles. The results obtained reveal that 3'-O-methylation does not affect the MRP inhibitory potential of quercetin. However, 4'-O-methylation appeared to reduce the potential to inhibit both MRP1 and MRP2. In contrast, glucuronidation in general, and especially glucuronidation at the 7-hydroxylmoiety, resulting in 7-O-glucuronosyl quercetin, significantly increased the potential of quercetin to inhibit MRP1 and MRP2 mediated calcein transport with inhibition of MRP1 being generally more effective than that of MRP2. Overall, the results of this study reveal that the major phase II metabolites of quercetin are equally potent or even better inhibitors of human MRP1 and MRP2 than quercetin itself. This finding indicates that phase II metabolism of quercetin could enhance the potential use of quercetin- or flavonoids in general-as an inhibitor to overcome MRP-mediated multidrug resistance.

摘要

本研究表征了模型类黄酮槲皮素的Ⅱ相代谢,尤其是甲基化和葡萄糖醛酸化,对其在Sf9外翻囊泡中抑制人MRP1和MRP2活性能力的影响。所得结果表明,3'-O-甲基化不影响槲皮素的MRP抑制潜力。然而,4'-O-甲基化似乎降低了抑制MRP1和MRP2的潜力。相比之下,一般的葡萄糖醛酸化,尤其是7-羟基部分的葡萄糖醛酸化,生成7-O-葡萄糖醛酸基槲皮素,显著增加了槲皮素抑制MRP1和MRP2介导的钙黄绿素转运的潜力,对MRP1的抑制通常比对MRP2更有效。总体而言,本研究结果表明,槲皮素的主要Ⅱ相代谢产物作为人MRP1和MRP2的抑制剂,与槲皮素本身具有同等效力甚至更好的抑制效果。这一发现表明,槲皮素的Ⅱ相代谢总体上可以增强槲皮素或类黄酮作为抑制剂克服MRP介导的多药耐药性的潜在用途。

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