Critchfield J W, Welsh C J, Phang J M, Yeh G C
Laboratory of Nutritional and Molecular Regulation, National Cancer Institute, NIH, Frederick, MD 21702.
Biochem Pharmacol. 1994 Oct 7;48(7):1437-45. doi: 10.1016/0006-2952(94)90568-1.
Since P-glycoprotein (P-gp) in normal tissues may serve as a cellular defense mechanism against naturally occurring xenobiotics, we considered whether physiologically active components of commonly ingested plant foods could influence P-gp function. To examine this possibility, a series of flavonoids commonly found in plant foods was tested for their ability to modulate [14C]Adriamycin ([14C]ADR) accumulation and efflux in P-gp-expressing HCT-15 colon cells. Many flavonoids, in the micromolar range, inhibited the accumulation of [14C]ADR. Detailed experiments utilizing flavonoids with the greatest activity in reducing [14C]ADR accumulation, i.e. galangin, kaempferol, and quercetin, revealed that the efflux of [14C]ADR is increased markedly in the presence of these compounds. Flavonoid-induced stimulation of efflux was rapid and was blocked by the multidrug-resistant (MDR) reversal agents verapamil, vinblastine, and quinidine. The magnitude of flavonoid-stimulated efflux in sodium butyrate-treated cells with a 4-fold induction of P-gp protein was similar to that in uninduced cells. [3H]Azidopine photoaffinity labeling of P-gp in crude membrane preparations revealed mild to no competition for binding by flavonoids possessing either activity or inactivity in reducing ADR accumulation. Although flavonoid hydrophobicity was found to be unrelated to flavonoid activity in altering [14C]ADR accumulation, certain structural features were associated with enhancement or diminution of activity. Finally, the significance of flavonoid-related reduction of [14C]ADR accumulation was underscored in cell growth studies, showing partial protection by quercetin against ADR-induced growth inhibition. It is concluded that certain naturally occurring plant flavonoids may acutely upregulate the apparent activity of P-gp.
由于正常组织中的P-糖蛋白(P-gp)可能作为一种细胞防御机制抵御天然存在的外源性物质,我们考虑常见摄入植物性食物的生理活性成分是否会影响P-gp功能。为检验这种可能性,对一系列常见于植物性食物中的黄酮类化合物调节[14C]阿霉素([14C]ADR)在表达P-gp的HCT-15结肠细胞中的积累和外排能力进行了测试。许多微摩尔浓度范围内的黄酮类化合物抑制了[14C]ADR的积累。利用在降低[14C]ADR积累方面活性最强的黄酮类化合物(即高良姜素、山奈酚和槲皮素)进行的详细实验表明,在这些化合物存在的情况下,[14C]ADR的外排显著增加。黄酮类化合物诱导的外排刺激迅速,且被多药耐药(MDR)逆转剂维拉帕米、长春碱和奎尼丁阻断。在P-gp蛋白诱导4倍增加的丁酸钠处理细胞中,黄酮类化合物刺激的外排幅度与未诱导细胞中的相似。粗膜制剂中P-gp的[3H]叠氮平光亲和标记显示,对于在降低ADR积累方面有活性或无活性的黄酮类化合物,其结合竞争轻微或不存在。尽管发现黄酮类化合物的疏水性与改变[14C]ADR积累的黄酮类化合物活性无关,但某些结构特征与活性的增强或减弱相关。最后,细胞生长研究强调了黄酮类化合物相关的降低[14C]ADR积累的重要性,显示槲皮素对ADR诱导的生长抑制有部分保护作用。结论是某些天然存在的植物黄酮类化合物可能急性上调P-gp的表观活性。