Bingmann D, Speckmann E J
Poliklinik für zahnärztliche Chirurgie, Universität Mainz, Federal Republic of Germany.
Exp Brain Res. 1989;74(2):239-48. doi: 10.1007/BF00248856.
Antiepileptic actions of the organic calcium antagonists flunarizine (cinnarizine derivate) and verapamil (papaverin derivat) on pentylenetetrazol-induced epileptic bioelectric activity were tested in CA3 neurones of hippocampal slices. In all experiments both calcium antagonists reduced the amplitudes and/or durations of paroxysmal depolarizations as well as their rate of occurrence, when the bath concentrations of flunarizine or verapamil exceeded 20 mumol/l. When they were added to the bath solution before pentylenetetrazol application, recordings of the resting membrane potential, of the membrane resistance, of action potentials and of spontaneous as well as of evoked excitatory and inhibitory postsynaptic potentials gave no indication that the antiepileptic effects of these drugs are due to unspecific depressive actions on neuronal excitability or spread of excitation.
在海马切片的CA3神经元中测试了有机钙拮抗剂氟桂利嗪(桂利嗪衍生物)和维拉帕米(罂粟碱衍生物)对戊四氮诱导的癫痫生物电活动的抗癫痫作用。在所有实验中,当浴液中氟桂利嗪或维拉帕米的浓度超过20μmol/L时,两种钙拮抗剂均降低了阵发性去极化的幅度和/或持续时间及其发生率。当在应用戊四氮之前将它们添加到浴液中时,对静息膜电位、膜电阻、动作电位以及自发的和诱发的兴奋性和抑制性突触后电位的记录均未表明这些药物的抗癫痫作用是由于对神经元兴奋性或兴奋传播的非特异性抑制作用。