Kito M, Maehara M, Watanabe K
Department of Pediatrics, Minami Seikyo Hospital, Nagoya, Japan.
Seizure. 1996 Jun;5(2):115-9. doi: 10.1016/s1059-1311(96)80104-x.
We investigated the effects of zonisamide, a new antiepileptic drug, on voltage-dependent T-type calcium current (ICa) in cultured neuroblastoma cells of human origin (NB-I). Zonisamide reduced T-type ICa in a concentration-dependent manner without evoking any change in its inactivation kinetics or voltage dependence of action. The mean percent reduction was 38.3 +/- 5.8% at 50 microM. Further, zonisamide shifted the inactivation curve approximately 20 mV negative compared to the control. These resting blocking actions suggest that zonisamide shifts the channel population toward the inactivation state, allowing fewer channels to open during membrane depolarization. The blockade of T-type calcium channels by zonisamide could suppress an important component of inward current that underlies epileptiform cellular bursting, thereby inhibiting the spread of seizure activity.
我们研究了新型抗癫痫药物唑尼沙胺对源自人神经母细胞瘤细胞(NB-I)中电压依赖性T型钙电流(ICa)的影响。唑尼沙胺以浓度依赖性方式降低T型ICa,而不引起其失活动力学或作用电压依赖性的任何变化。在50微摩尔时,平均降低百分比为38.3±5.8%。此外,与对照组相比,唑尼沙胺使失活曲线向负方向移动约20毫伏。这些静息阻断作用表明,唑尼沙胺使通道群体向失活状态转变,从而在膜去极化期间允许更少的通道开放。唑尼沙胺对T型钙通道的阻断可抑制构成癫痫样细胞爆发基础的内向电流的一个重要成分,从而抑制癫痫活动的传播。