Division of Chemical Biology and Medicinal Chemistry, UNC Eshelman School of Pharmacy and ⊥Department of Chemistry, University of North Carolina , Chapel Hill, North Carolina 27599, United States.
J Med Chem. 2013 Jul 25;56(14):5931-9. doi: 10.1021/jm4007092. Epub 2013 Jul 3.
We have reported that compounds containing a biaryl linked unit (Ar-X-Ar') modulated Na(+) currents by promoting slow inactivation and fast inactivation processes and by inducing frequency (use)-dependent inhibition of Na(+) currents. These electrophysiological properties have been associated with the mode of action of several antiepileptic drugs. In this study, we demonstrate that the readily accessible (biphenyl-4-yl)methylammonium chlorides (compound class B) exhibited a broad range of anticonvulsant activities in animal models, and in the maximal electroshock seizure test the activity of (3'-trifluoromethoxybiphenyl-4-yl)methylammonium chloride (8) exceeded that of phenobarbital and phenytoin upon oral administration to rats. Electrophysiological studies of 8 using mouse catecholamine A-differentiated cells and rat embryonic cortical neurons confirmed that 8 promoted slow and fast inactivation in both cell types but did not affect the frequency (use)-dependent block of Na(+) currents.
我们曾报道过,含有联芳基连接单元(Ar-X-Ar')的化合物通过促进缓慢失活和快速失活过程,以及诱导钠离子电流的频率(使用)依赖性抑制,来调节钠离子电流。这些电生理特性与几种抗癫痫药物的作用模式有关。在这项研究中,我们证明了易于获得的(联苯-4-基)甲基氯化铵(化合物 B 类)在动物模型中表现出广泛的抗惊厥活性,并且在最大电休克惊厥试验中,(3'-三氟甲氧基联苯-4-基)甲基氯化铵(8)在口服给予大鼠时的活性超过了苯巴比妥和苯妥英。使用小鼠儿茶酚胺 A 分化细胞和大鼠胚胎皮质神经元的 8 电生理研究证实,8 促进了这两种细胞类型中的缓慢和快速失活,但不影响钠离子电流的频率(使用)依赖性阻断。