Janać Branka, Selaković Vesna, Radenović Lidija
Department of Neurophysiology, Institute for Biological Research, Bulevar Despota Stefana 142, 11000 Belgrade, Serbia.
Behav Brain Res. 2008 Dec 1;194(1):72-8. doi: 10.1016/j.bbr.2008.06.031. Epub 2008 Jul 6.
The purpose of this study was to investigate the temporal pattern of NMDA receptors antagonist-MK-801 on motor behaviour parameters in gerbils submitted to different duration of global cerebral ischemia. The common carotid arteries of gerbils were occluded for 5, 10 or 15min. Gerbils were given MK-801 (3mg/kg i.p.) or saline immediately after the occlusion in normothermic conditions prior to testing. Motor activity was registered 1, 2, 4, 7, 14, 21 and 28 days after reperfusion during 60min by open field test. At the same time, the effect of NMDA receptor blockade was followed in vivo by monitoring the neurological status of whole animals or at the cellular level by standard light and confocal microscopy on brain slices. Post-ischemic gerbils quickly developed hypermotor response with the most intensity in animals submitted to 15min ischemia. MK-801 administrated immediately after ischemia significantly decreased this hyperactivity. In all ischemic-treated animals, behavioural suppression by MK-801 was observed already 1 day after occlusion and was lasting as far as observed ischemia-dependent hypermotor responses. Beneficial effect of MK-801 was also confirmed by morphological and neurological status data. These findings suggest that sustained ischemia-induced hyperactivity is related to abnormalities in NMDA glutamatergic function, as well as its manifestation could be completely abolished by NMDA receptor blockade immediately after ischemic insult.
本研究的目的是调查NMDA受体拮抗剂MK-801对经历不同时长全脑缺血的沙鼠运动行为参数的时间模式。沙鼠的双侧颈总动脉被阻断5、10或15分钟。在常温条件下阻断后立即给沙鼠腹腔注射MK-801(3mg/kg)或生理盐水,然后进行测试。在再灌注后的第1、2、4、7、14、21和28天,通过旷场试验在60分钟内记录运动活动。同时,通过监测全动物的神经状态在体内跟踪NMDA受体阻断的效果,或通过对脑切片进行标准光学显微镜和共聚焦显微镜观察在细胞水平上跟踪。缺血后的沙鼠迅速出现运动亢进反应,在经历15分钟缺血的动物中最为强烈。缺血后立即给予MK-801可显著降低这种多动。在所有缺血处理的动物中,在阻断后1天就观察到MK-801对行为的抑制作用,并且只要观察到缺血依赖性运动亢进反应,这种抑制作用就持续存在。MK-801的有益作用也得到了形态学和神经状态数据的证实。这些发现表明,持续性缺血诱导的多动与NMDA谷氨酸能功能异常有关,并且在缺血性损伤后立即阻断NMDA受体可完全消除其表现。