Deng Feng, Sjöstedt Noora, Kidron Heidi
Centre for Drug Research, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, Helsinki, Finland.
PLoS One. 2016 Oct 5;11(10):e0163886. doi: 10.1371/journal.pone.0163886. eCollection 2016.
The ABC transporters multidrug resistance associated protein 2 (MRP2) and breast cancer resistance protein (BCRP) are of interest in drug development, since they affect the pharmacokinetics of several drugs. Membrane vesicle transport assays are widely used to study interactions with these proteins. Since albumin has been found to affect the kinetics of metabolic enzymes in similar membrane preparations, we investigated whether albumin affects the kinetic parameters of efflux transport. We found that albumin increased the Vmax of 5(6)-carboxy-2',7'-dichlorofluorescein (CDCF) and estradiol-17-β-D-glucuronide uptake into MRP2 vesicles in the presence of 0.1% bovine serum albumin (BSA) by 2 and 1.5-fold, respectively, while BSA increased Lucifer yellow uptake by 30% in BCRP vesicles. Km values increased slightly, but the change was not statistically significant. The effect of BSA on substrate uptake was dependent on the vesicle amount, while increasing BSA concentration did not significantly improve substrate uptake. These results indicate a minor effect of albumin on MRP2 and BCRP, but it should be considered if albumin is added to transporter assays for example as a solubilizer, since the effect may be substrate or transporter specific.
ABC转运蛋白多药耐药相关蛋白2(MRP2)和乳腺癌耐药蛋白(BCRP)在药物研发中备受关注,因为它们会影响多种药物的药代动力学。膜囊泡转运试验被广泛用于研究与这些蛋白的相互作用。由于已发现白蛋白会影响类似膜制剂中代谢酶的动力学,我们研究了白蛋白是否会影响外排转运的动力学参数。我们发现,在存在0.1%牛血清白蛋白(BSA)的情况下,白蛋白使MRP2囊泡对5(6)-羧基-2',7'-二氯荧光素(CDCF)和雌二醇-17-β-D-葡萄糖醛酸苷的摄取Vmax分别增加了2倍和1.5倍,而BSA使BCRP囊泡对路西法黄的摄取增加了30%。Km值略有增加,但变化无统计学意义。BSA对底物摄取的影响取决于囊泡量,而增加BSA浓度并不能显著提高底物摄取。这些结果表明白蛋白对MRP2和BCRP有轻微影响,但如果在转运体试验中添加白蛋白作为增溶剂等,应予以考虑,因为这种影响可能具有底物或转运体特异性。