Karpova M N, Pankov O Iu, Kryzhanovskiĭ G N, Glebov R N
Biull Eksp Biol Med. 1991 Sep;112(9):260-2.
In experiments on freely moving male Wistar rats it was shown that nifedipine in a dose 10 mg/kg (i.p.) suppressed the penicillin-induced focal epileptic activity in cerebral cortex. A similar suppressing effect of nifedipine was shown on acute generalized tonic-clonic pentylenetetrazol (PTZ) seizures (75 mg/kg, i.p.). Nifedipine in the same dose was not effective on chronic PTZ administration (PTZ-kindling, 30 mg/kg i.p. during 28 days): when injected 30 min before each PTZ administration it didn't delay the development of kindling induced seizure susceptibility and had no effect on the severity of seizures. The administration of nifedipine in a dose of 10 or 30 mg/kg to control kindled animals which had not been treated with nifedipine had no influence on the severity of seizures provoked by a testing dose of PTZ (30 mg/kg i.p.): its intensity was similar to that of caused by PTZ injection along.
在对自由活动的雄性Wistar大鼠进行的实验中发现,硝苯地平10毫克/千克(腹腔注射)的剂量可抑制青霉素诱导的大脑皮层局灶性癫痫活动。硝苯地平对急性全身性强直性阵挛性戊四氮(PTZ)惊厥(75毫克/千克,腹腔注射)也有类似的抑制作用。相同剂量的硝苯地平对慢性PTZ给药(PTZ点燃,28天内腹腔注射30毫克/千克)无效:在每次PTZ给药前30分钟注射时,它不会延迟点燃诱导的癫痫易感性的发展,对惊厥的严重程度也没有影响。对未用硝苯地平治疗的对照点燃动物给予10或30毫克/千克剂量的硝苯地平,对测试剂量的PTZ(30毫克/千克,腹腔注射)诱发的惊厥严重程度没有影响:其强度与单独注射PTZ引起的强度相似。