Iasnetsov V V, Prosvirova E P, Tsublova E G, Iasnetsov Vik V, Motin V G, Karsanova S K
Aviakosm Ekolog Med. 2012 Nov-Dec;46(6):41-5.
Experiments with mice showed that, unlike reamberin (100 mg/kg), mexidol (100 mg/kg) and cytoflavin (1 ml/kg) act as antihypoxants in pressure and hermetic chambers but not in case of acute hemic and histotoxic hypoxia. Amtisol succinate (100 mg/kg), a reference antihypoxant, excels the other tried succinate-containing drugs in all models of acute hypoxia except the hermetic chamber. In addition, the neuroprotective action of mexidol (100 mg/kg/d) and cytoflavin (100 ml/kg/d) in rats with induced ischemic stroke which was stronger than that of reamberin and amtisol succinate (100 mg/kg/d). Besides, mexidol (100 mg/kg) but not cytoflavin (1 ml/kg), reamberin or amtisol succinate (100 mg/kg) had a distinct analgesic effect in rabbits. On the neuronal level, mexidol interacts with the GABAA- benzodiazepine-receptor complex in nearly 60% cells and inhibits ion currents through the NMDA-receptor ion channels in nearly 80% neurons.
对小鼠的实验表明,与雷安匹林(100毫克/千克)不同,美西多福(100毫克/千克)和细胞色素C(1毫升/千克)在压力舱和密封舱中具有抗缺氧作用,但在急性血液性和组织中毒性缺氧情况下则不然。参考抗缺氧药物琥珀酸氨替索(100毫克/千克)在除密封舱外的所有急性缺氧模型中均优于其他受试含琥珀酸药物。此外,美西多福(100毫克/千克/天)和细胞色素C(100毫升/千克/天)对诱导性缺血性中风大鼠的神经保护作用强于雷安匹林和琥珀酸氨替索(100毫克/千克/天)。此外,美西多福(100毫克/千克)而非细胞色素C(1毫升/千克)、雷安匹林或琥珀酸氨替索(100毫克/千克)对兔子有明显的镇痛作用。在神经元水平上,美西多福在近60%的细胞中与GABAA-苯二氮䓬受体复合物相互作用,并在近80%的神经元中抑制通过NMDA受体离子通道的离子电流。