Kryzhanovskiĭ G N, Karpova M N, Pankov O Iu
Biull Eksp Biol Med. 1990 Oct;110(10):348-50.
In experiments on rats it was shown that i.p. administration of finoptin (verapamil), magnesium sulfate or ryodipine (an 1,4-dihydropyridine) 15 min before each daily injection of pentylenetetrazole (PTZ) in a subconvulsive dose (30 mg/kg i.p.) significantly (for 10-12 days delayed the development of pentylenetetrazole-induced kindling and attenuated kindled seizure reaction as compared with the controls. In animals sensitive to PTZ which were selected on the test of their reaction to previous single PTZ injection in a dose of 40 mg/kg finoptin, magnesium or finoptin + magnesium resulted in suppression of kindling development at late stages (after 2-week administration of drugs together with PTZ). After the withdrawal of the drugs there was a tendency to an increase of seizure reaction to the testing PTZ dose (30 mg/kg). The enhanced seizure susceptibility to test PTZ dose has being persisted during all observation period (8 months). Finoptin administered 15 min prior to PTZ had no effect on the severity of seizure reaction of fully kindled animals which had not received the drugs. The results obtained show that organic Ca-antagonists and magnesium delay the development of kindling induced seizure susceptibility, but cannot completely prevent it. The results also suggest that mechanisms of the chronic epileptogenesis (development of kindling induced seizure susceptibility) and those of the acute convulsive reaction to the epileptogen are not similar.
在大鼠实验中表明,在每天以亚惊厥剂量(腹腔注射30毫克/千克)注射戊四氮(PTZ)前15分钟腹腔注射非洛地平(维拉帕米)、硫酸镁或硝苯地平(一种1,4 - 二氢吡啶),与对照组相比,显著(持续10 - 12天)延迟了戊四氮诱导的点燃过程,并减弱了点燃性癫痫发作反应。在对PTZ敏感的动物中,通过对先前单次腹腔注射40毫克/千克PTZ的反应测试进行筛选,非洛地平、镁或非洛地平 + 镁在后期(与PTZ一起给药2周后)导致点燃发展受到抑制。停药后,对测试PTZ剂量(30毫克/千克)的癫痫发作反应有增加的趋势。在整个观察期(8个月)内,对测试PTZ剂量的癫痫易感性增强一直持续。在PTZ前15分钟给予非洛地平对未接受药物的完全点燃动物的癫痫发作反应严重程度没有影响。所获得的结果表明,有机钙拮抗剂和镁会延迟点燃诱导的癫痫易感性的发展,但不能完全预防它。结果还表明,慢性癫痫发生(点燃诱导的癫痫易感性发展)的机制与对癫痫原的急性惊厥反应的机制不相似。