Nikolov R, Nikolova M, Dikova M, Mirzoyan R S, Ganshina T S, Volobueva T I
Chemical Pharmaceutical Research Institute, Sofia, Bulgaria.
Methods Find Exp Clin Pharmacol. 1990 Jul-Aug;12(6):411-8.
The cerebroprotective effect of flunarizine was studied using the following methods: hypobaric hypoxia in mice, complete ischemia by decapitation in mice, anoxic hypoxia in mice, hemic hypoxia in rats, incomplete ischemia by bilateral carotid ligation in rats and asphyxic hypoxia in cats. Piracetam, meclofenoxate, nicergoline, naftidrofuryl, cinnarizine and nifedipine were studied as reference drugs. Flunarizine increased the survival time in all survival models. Its effect was most pronounced in complete ischemia model, and considerably higher than that of reference drugs. In asphyxic hypoxia flunarizine increased cortical resistance and shortened cortical recovery. The EEG frequency-amplitude analysis during asphyxic hypoxia showed a significant decrease of the slow-waves amplitudes of delta and theta range, and an increase of the fast-waves amplitudes of beta-2 range, changes indicating protective action.
小鼠低压缺氧、小鼠断头全脑缺血、小鼠乏氧性缺氧、大鼠低张性缺氧、大鼠双侧颈总动脉结扎不完全缺血以及猫窒息性缺氧。以吡拉西坦、氯酯醒、尼麦角林、萘呋胺酯、桂利嗪和硝苯地平作为对照药物进行研究。氟桂利嗪在所有存活模型中均能延长存活时间。其作用在全脑缺血模型中最为显著,且明显高于对照药物。在窒息性缺氧时,氟桂利嗪可增加皮层抵抗力并缩短皮层恢复时间。窒息性缺氧期间的脑电图频率 - 振幅分析显示,δ波和θ波范围的慢波振幅显著降低,β - 2波范围的快波振幅增加,这些变化表明具有保护作用。