Huber Vincent J, Tsujita Mika, Kwee Ingrid L, Nakada Tsutomu
Center for Integrated Human Brain Science, Brain Research Institute, University of Niigata, 1 Asahimachi, Niigata 951-8585, Japan.
Bioorg Med Chem. 2009 Jan 1;17(1):418-24. doi: 10.1016/j.bmc.2007.12.038. Epub 2008 Jan 4.
The potential of antiepileptic drugs (AEDs) to inhibit the water transport properties of aquaporin 4 (AQP4) was investigated using a combination of in silico and in vitro screening methods. Virtual docking studies on 14 AEDs indicated a range of docking energies that spanned approximately 40 kcal/mol, where the most stabilized energies were consistent with that of the previously identified AQP4 inhibitor acetazolamide. Nine AEDs and one bio-active metabolite were further investigated in a functional assay using AQP4 expressing Xenopus oocytes. Seven of the assayed compounds were found to inhibit AQP4 function, while three did not. A linear correlation was indicated between the in silico docking energies and the in vitro AQP4 inhibitory activity at 20 microM.
采用计算机模拟和体外筛选相结合的方法,研究了抗癫痫药物(AEDs)抑制水通道蛋白4(AQP4)水转运特性的潜力。对14种AEDs进行的虚拟对接研究表明,对接能量范围约为40 kcal/mol,其中最稳定的能量与先前鉴定的AQP4抑制剂乙酰唑胺的能量一致。使用表达AQP4的非洲爪蟾卵母细胞,通过功能测定对9种AEDs和1种生物活性代谢物进行了进一步研究。发现7种被测化合物可抑制AQP4功能,而3种则无此作用。在20 microM时,计算机模拟对接能量与体外AQP4抑制活性之间呈线性相关。