Pan Lanying, Hu Haihong, Wang Xiangjun, Yu Lushan, Jiang Huidi, Chen Jianzhong, Lou Yan, Zeng Su
Laboratory of Pharmaceutical Analysis and Drug Metabolism, Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.
Laboratory of Natural Medicine, School of Forestry and Bio-technology, Zhejiang A&F University, Lin'an 311300, China.
Molecules. 2015 Feb 11;20(2):2931-48. doi: 10.3390/molecules20022931.
Stellera chamaejasme L. (Thymelaeaceae) is widely distributed in Mongolia, Tibet and the northern parts of China. Its roots are commonly used as "Langdu", which is embodied in the Pharmacopoeia of the P.R. China (2010) as a toxic Traditional Chinese Medicine. It is claimed to have antivirus, antitumor and antibacterial properties in China and other Asian countries. Studies were carried out to characterize the inhibition of neochamaejasmin B (NCB) on P-glycoprotein (P-gp, ABCB1, MDR1). Rhodamine-123 (R-123) transport and accumulation studies were performed in MDCK-hMDR1 cells. ABCB1 (MDR1) mRNA gene expression and P-gp protein expression were analyzed. Binding selectivity studies based on molecular docking were explored. R-123 transport and accumulation studies in MDCK-hMDR1 cells indicated that NCB inhibited the P-gp-mediated efflux in a concentration-dependent manner. RT-PCR and Western blot demonstrated that the P-gp expression was suppressed by NCB. To investigate the inhibition type of NCB on P-gp, Ki and Ki' values were determined by double-reciprocal plots in R-123 accumulation studies. Since Ki was greater than Ki', the inhibition of NCB on P-gp was likely a mixed type of competitive and non-competitive inhibition. The results were confirmed by molecular docking in our current work. The docking data indicated that NCB had higher affinity to P-gp than to Lig1 ((S)-5,7-dihydroxy-2-(4-hydroxyphenyl)chroman-4-one).
狼毒(瑞香科狼毒属植物)广泛分布于蒙古、西藏以及中国北方地区。其根通常被用作“狼毒”,在《中华人民共和国药典》(2010年版)中作为有毒的传统中药收录。在中国和其他亚洲国家,据称它具有抗病毒、抗肿瘤和抗菌特性。开展了相关研究以表征新狼毒素B(NCB)对P-糖蛋白(P-gp,ABCB1,MDR1)的抑制作用。在MDCK-hMDR1细胞中进行了罗丹明-123(R-123)转运和蓄积研究。分析了ABCB1(MDR1)mRNA基因表达和P-gp蛋白表达。探索了基于分子对接的结合选择性研究。MDCK-hMDR1细胞中的R-123转运和蓄积研究表明,NCB以浓度依赖性方式抑制P-gp介导的外排。逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法(Western blot)表明,NCB抑制P-gp表达。为研究NCB对P-gp的抑制类型,在R-123蓄积研究中通过双倒数作图法测定了抑制常数(Ki)和非竞争性抑制常数(Ki')。由于Ki大于Ki',NCB对P-gp的抑制可能是竞争性和非竞争性抑制的混合型。在我们当前的研究工作中,分子对接证实了该结果。对接数据表明,NCB对P-gp的亲和力高于对配体1((S)-5,7-二羟基-2-(4-羟基苯基)苯并二氢吡喃-4-酮)的亲和力。