Meyer F B, Tally P W, Anderson R E, Sundt T M, Yaksh T L, Sharbrough F W
Brain Res. 1986 Oct 1;384(1):180-3. doi: 10.1016/0006-8993(86)91236-9.
Nimodipine, a calcium channel blocker with high affinity for central dihydropyridine Ca2+ channels, produced a dose-dependent suppression of electrically induced seizures in the rabbit. Verapamil, a diphenylalkylamine which acts at peripheral Ca2+ channels, was ineffective. Phenytoin was less effective than nimodipine. These results suggest that calcium flux into neurons may be a biochemical precipitant for seizure genesis. Centrally acting calcium channel blockers may prove to be a new class of anticonvulsants.
尼莫地平是一种对中枢二氢吡啶Ca2+通道具有高亲和力的钙通道阻滞剂,它能对家兔电诱导的癫痫发作产生剂量依赖性抑制作用。维拉帕米是一种作用于外周Ca2+通道的二苯烷基胺,无此效果。苯妥英钠的效果不如尼莫地平。这些结果表明,钙离子流入神经元可能是癫痫发作的生化促发因素。作用于中枢的钙通道阻滞剂可能会被证明是一类新型抗惊厥药物。