Kato H, Liu Y, Araki T, Kogure K
Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.
Brain Res. 1991 Jul 12;553(2):238-42. doi: 10.1016/0006-8993(91)90831-f.
We examined the response of the gerbil brain to secondary ischemic insult following pretreatment with brief ischemia at intervals of 5 min, 1 and 6 h, 1, 2, 4, 7 and 14 days. Two minutes of bilateral carotid artery occlusion produced no histopathological brain damage, whereas 3 min of occlusion caused a moderate to severe reduction in the number of hippocampal CA1 pyramidal cells. Two-minute occlusion followed by 3-min occlusion at 5-min, 1- and 6-h intervals resulted in almost complete destruction of CA1 neurons. Additional neuronal damage was observed in the striatum at a 1-h interval and in the thalamus and the neocortex at 1- and 6-h intervals. The neuronal damage was most severe at a 1-h interval. Two-minute ischemia followed by 3-min ischemia at intervals of 1, 2, 4 and 7 days, however, caused a marked protective effect, and the hippocampal CA1 neurons were preserved. The protective effect was not observed at a 14-day interval and following pretreatment with 1-min ischemia. Thus, pretreatment with brief ischemia leads to complex responses of the brain to secondary ischemic insult; cumulative damage at intervals of 1-6 h and protective effects at intervals of 1-7 days.
我们研究了沙土鼠大脑在分别间隔5分钟、1小时和6小时、1天、2天、4天、7天及14天进行短暂缺血预处理后对继发性缺血损伤的反应。双侧颈动脉闭塞2分钟未造成组织病理学上的脑损伤,而闭塞3分钟则导致海马CA1锥体细胞数量中度至重度减少。在间隔5分钟、1小时和6小时时,先进行2分钟闭塞,随后再进行3分钟闭塞,几乎导致CA1神经元完全破坏。在间隔1小时时纹状体出现额外的神经元损伤,在间隔1小时和6小时时丘脑和新皮层出现额外的神经元损伤。神经元损伤在间隔1小时时最为严重。然而,在间隔1天、2天、4天和7天时,先进行2分钟缺血,随后再进行3分钟缺血,产生了显著的保护作用,海马CA1神经元得以保留。在间隔14天时以及在进行1分钟缺血预处理后未观察到保护作用。因此,短暂缺血预处理会导致大脑对继发性缺血损伤产生复杂反应;在间隔1 - 6小时时出现累积损伤,在间隔1 - 7天时出现保护作用。