Schneiderman J H, Schwartzkroin P A
Neurology. 1982 Jul;32(7):730-8. doi: 10.1212/wnl.32.7.730.
We used both intracellular and field potential recordings to study the effects of phenytoin (20 to 40 micrograms milliliter) on CA3 and CA1 neurons of guinea pig hippocampal slices, with or without exposure to the convulsant sodium penicillin G. Phenytoin did not change resting membrane potential, input resistance, action potential amplitude or duration, or the threshold intensity for activating action potentials or bursts with intracellular current pulses. Suppression of penicillin-induced bursting was associated with an increased threshold for orthodromically activating neurons. The intrinsic bursting mechanisms of the cells remained intact. Phenytoin seemed to suppress penicillin-induced epileptiform activity by decreasing synaptic transmission.
我们使用细胞内记录和场电位记录来研究苯妥英(20至40微克/毫升)对豚鼠海马切片CA3和CA1神经元的影响,无论是否暴露于惊厥剂青霉素G。苯妥英不会改变静息膜电位、输入电阻、动作电位幅度或持续时间,也不会改变用细胞内电流脉冲激活动作电位或爆发的阈值强度。青霉素诱导的爆发抑制与正向激活神经元的阈值增加有关。细胞的内在爆发机制保持完整。苯妥英似乎通过减少突触传递来抑制青霉素诱导的癫痫样活动。