Li Ming-Shan, Cen Juan, He Ling, Liu Lu, Ji Bian-Sheng
J Chemother. 2013 Dec;25(6):347-54. doi: 10.1179/1973947813Y.0000000094. Epub 2013 Dec 6.
Our previous study reported CJY, an isoflavone, can reverse P-glycoprotein (P-gp) efflux activity in rat brain microvessel endothelial cells (RBMECs). In the present report, by assessment of ATPase activity of RBMECs, we gained further insight into the nature of the CJY interactions with P-gp. The results revealed that the basal P-gp ATPase activity was increased by CJY. Kinetic studies on ATPase activity showed the effects of Tetrandrine (Tet) on CJY-stimulated, CsA on CJY-stimulated, and CsA on Tet-stimulated P-gp ATPase activity were all non-competitive inhibition, indicating that these substrates can simultaneously but independently bind to diverse sites on P-gp. Furthermore, the combined effects of CJY with Tet, and CJY with CsA were also evaluated isobolographically. The results showed synergistic interactions in both combinations, implying that combined treatment of CJY with other modulators may exert synergistic interactions for the drug's penetration into the brain and the treatment of neurological disorders.
我们之前的研究报道了异黄酮CJY可逆转大鼠脑微血管内皮细胞(RBMECs)中的P-糖蛋白(P-gp)外排活性。在本报告中,通过评估RBMECs的ATP酶活性,我们进一步深入了解了CJY与P-gp相互作用的本质。结果显示,CJY可提高基础P-gp ATP酶活性。对ATP酶活性的动力学研究表明,粉防己碱(Tet)对CJY刺激的P-gp ATP酶活性、环孢素A(CsA)对CJY刺激的P-gp ATP酶活性以及CsA对Tet刺激的P-gp ATP酶活性的影响均为非竞争性抑制,这表明这些底物可同时但独立地结合到P-gp的不同位点上。此外,还采用等效线图法评估了CJY与Tet以及CJY与CsA的联合作用。结果显示两种组合均存在协同相互作用,这意味着CJY与其他调节剂联合治疗可能对药物穿透血脑屏障及治疗神经疾病发挥协同作用。