Huang Chin-Wei, Ueno Shinya, Okada Motohiro, Kaneko Sunao
Department of Neurology, Institute of Clinical Medicine, National Cheng-Kung University Medical Center, No. 1, University Road, Tainan, Taiwan.
Epilepsy Res. 2005 Oct-Nov;67(1-2):51-60. doi: 10.1016/j.eplepsyres.2005.08.006. Epub 2005 Sep 26.
We investigated the effect of Zonisamide (ZNS), a newer anti-epileptic drug, on field potentials and neuropropagation in rat frontal cortex, with the aid of the 64-channel multi-electrode dish (MED64) system. The amplitude and propagation of field potentials were expressed dimensionally in the MED64 system. ZNS (3-100 microM) inhibited the amplitude and propagation of field excitatory postsynaptic potentials (fEPSP) in a concentration dependent manner. In contrast, ZNS could not suppress the amplitude and propagation of the presynaptic fiber volley (PrV) at clinically relevant concentrations (10-30 microM). Stimulating dependency with reduction fEPSP was seen in the presence of ZNS at clinically relevant concentrations, but not with PrV. The reduction of fEPSP amplitude was not accompanied by a change in paired-pulse facilitation. These data suggest that at clinically relevant concentrations of ZNS, the suppression of neuronal propagation is at least partially due to the postsynaptic mechanism, probably through alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors.
我们借助64通道多电极培养皿(MED64)系统,研究了新型抗癫痫药物唑尼沙胺(ZNS)对大鼠额叶皮质场电位和神经传导的影响。在MED64系统中,场电位的幅度和传导以维度形式表示。ZNS(3 - 100微摩尔)以浓度依赖性方式抑制场兴奋性突触后电位(fEPSP)的幅度和传导。相比之下,在临床相关浓度(10 - 30微摩尔)下,ZNS不能抑制突触前纤维峰电位(PrV)的幅度和传导。在临床相关浓度的ZNS存在下,观察到fEPSP降低存在刺激依赖性,但PrV不存在。fEPSP幅度的降低并未伴随双脉冲易化的改变。这些数据表明,在ZNS的临床相关浓度下,神经元传导的抑制至少部分归因于突触后机制,可能是通过α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体。