Lippert K, Welsch M, Krieglstein J
Institut für Pharmacokologie und Toxikologie, Fachbereich Pharmazie und Lebensmittelchemie, Philipps-Universität, Marburg, Germany.
Eur J Pharmacol. 1994 Mar 3;253(3):207-13. doi: 10.1016/0014-2999(94)90193-7.
Several reports have indicated that the two glutamate receptor antagonists, dizocilpine (that binds to the phencyclidine recognition site of the NMDA (N-methyl-D-aspartate) receptor) and NBQX (2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo(F)quinoxaline, that binds to the AMPA (alpha-amino-3-hydroxy-5-methyl-isoxazole) receptor), protect neurons against damage caused by hypoxia, ischemia or excitotoxicity. We, therefore, used a combination of these drugs to achieve enhanced neuroprotection. Primary cultures of rat hippocampal neurons were challenged by glutamate intoxication. Both dizocilpine and NBQX produced dose-dependent increases in the percentage of viable neurons. Combined treatment with both glutamate receptor antagonists had an over-additive neuroprotective effect. Simultaneous administration of dizocilpine and NBQX also had a pronounced neuroprotective effect in vivo in mice subjected to focal cerebral ischemia and rats with global forebrain ischemia. This suggest that such a combination may have therapeutic relevance.
几份报告指出,两种谷氨酸受体拮抗剂,地佐环平(与NMDA(N-甲基-D-天冬氨酸)受体的苯环利定识别位点结合)和NBQX(2,3-二羟基-6-硝基-7-氨磺酰基-苯并(F)喹喔啉,与AMPA(α-氨基-3-羟基-5-甲基异恶唑)受体结合),可保护神经元免受缺氧、缺血或兴奋性毒性所致的损伤。因此,我们使用这两种药物的组合以实现增强的神经保护作用。大鼠海马神经元原代培养物用谷氨酸中毒进行刺激。地佐环平和NBQX均可使存活神经元的百分比呈剂量依赖性增加。两种谷氨酸受体拮抗剂联合治疗具有超相加的神经保护作用。同时给予地佐环平和NBQX在局灶性脑缺血的小鼠和全脑缺血的大鼠体内也具有显著的神经保护作用。这表明这种组合可能具有治疗意义。