Montero Maria, Nielsen Marianne, Rønn Lars Christian B, Møller Arne, Noraberg Jens, Zimmer Jens
Anatomy and Neurobiology, Institute of Medical Biology, University of Southern Denmark, Winslowparken 21st, DK-5000 Odense C, Denmark.
Brain Res. 2007 Oct 26;1177:124-35. doi: 10.1016/j.brainres.2007.08.038. Epub 2007 Aug 24.
PNQX (9-methyl-amino-6-nitro-hexahydro-benzo(F)quinoxalinedione) is a selective AMPA antagonist with demonstrated neuroprotective effects in focal ischemia in rats. Here we report corresponding effects in mouse hippocampal slice cultures subjected to oxygen and glucose deprivation (OGD) and in transient global cerebral ischemia in gerbils. For in vitro studies, hippocampal slice cultures derived from 7-day-old mice and grown for 14 days, were submersed in oxygen-glucose deprived medium for 30 min and exposed to PNQX for 24 h, starting together with OGD, immediately after OGD, or 2 h after OGD. For comparison, other cultures were exposed to the NMDA antagonist MK-801 using the same protocol. Both PNQX and MK-801 displayed significant neuroprotective effects in all hippocampal subfields when present during and after OGD. When added just after OGD, only PNQX retained some neuroprotective effect. When added 2 h after OGD neither PNQX nor MK-801 had an effect. Transient global cerebral ischemia was induced in Mongolian gerbils by occlusion of both common carotid arteries for 4.5 min, with PNQX (10 mg/kg) being injected i.p. 30, 60 and 90 min after the insult. Subsequent analysis of brain sections stained for the neurodegeneration marker Fluoro-Jade B and immunostained for the astroglial marker glial fibrillary acidic protein revealed a significant PNQX-induced decrease in neuronal cell death and astroglial activation. We conclude that, PNQX provided neuroprotection against both global cerebral ischemia in gerbils in vivo and oxygen-glucose deprivation in mouse hippocampal slice cultures.
PNQX(9-甲基氨基-6-硝基六氢苯并(F)喹喔啉二酮)是一种选择性AMPA拮抗剂,已证实对大鼠局灶性缺血具有神经保护作用。在此,我们报告了其在氧糖剥夺(OGD)处理的小鼠海马切片培养物以及沙土鼠短暂全脑缺血模型中的相应作用。在体外研究中,将源自7日龄小鼠并培养14天的海马切片培养物浸没于氧糖剥夺培养基中30分钟,然后从OGD开始时、OGD结束后立即或OGD后2小时开始,使其暴露于PNQX中24小时。作为对照,其他培养物按照相同方案暴露于NMDA拮抗剂MK-801。在OGD期间及之后存在时,PNQX和MK-801在所有海马亚区均表现出显著的神经保护作用。仅在OGD结束后添加时,只有PNQX保留了一些神经保护作用。在OGD后2小时添加时,PNQX和MK-801均无作用。通过结扎双侧颈总动脉4.5分钟,在蒙古沙土鼠中诱导短暂全脑缺血,在缺血后30、60和90分钟腹腔注射PNQX(10毫克/千克)。随后对用神经退行性变标志物Fluoro-Jade B染色并对星形胶质细胞标志物胶质纤维酸性蛋白进行免疫染色的脑切片进行分析,结果显示PNQX显著减少了神经元细胞死亡和星形胶质细胞活化。我们得出结论,PNQX对沙土鼠体内的全脑缺血以及小鼠海马切片培养物中的氧糖剥夺均具有神经保护作用。