Smith M L, Auer R N, Siesjö B K
Acta Neuropathol. 1984;64(4):319-32. doi: 10.1007/BF00690397.
The density and distribution of brain damage after 2-10 min of cerebral ischemia was studied in the rat. Ischemia was produced by a combination of carotid clamping and hypotension, followed by 1 week recovery. The brains were perfusion-fixed with formaldehyde, embedded in paraffin, subserially sectioned, and stained with acid fuchsin/cresyl violet. The number of necrotic neurons in the cerebral cortex, hippocampus, and caudate nucleus was assessed by direct visual counting. Somewhat unexpectedly, mild brain damage was observed in some animals already after 2 min, and more consistently after 4 min of ischemia. This damage affected CA4 and CA1 pyramids in the hippocampus, and neurons in the subiculum. Necrosis of neocortical cells began to appear after 4 min and CA3 hippocampal damage after 6 min of ischemia, while neurons in the caudoputamen were affected first after 8-10 min. Selective neuronal necrosis of the cerebral cortex worsened into infarction after higher doses of insult. Damage was worst over the superolateral convexity of the hemisphere, in the middle laminae of the cerebral cortex. The caudate nucleus showed geographically demarcated zones of selective neuronal necrosis, damage to neurons in the dorsolateral portion showing an all-or-none pattern. Other structures involved included the amygdaloid, the thalamic reticular nucleus, the septal nuclei, the pars reticularis of the substantia nigra, and the cerebellar vermis.
研究了大鼠脑缺血2 - 10分钟后脑损伤的密度和分布情况。通过夹闭颈动脉和降低血压相结合的方式造成缺血,随后恢复1周。将大脑用甲醛灌注固定,石蜡包埋,连续切片,并用酸性品红/甲酚紫染色。通过直接视觉计数评估大脑皮质、海马体和尾状核中坏死神经元的数量。有些出乎意料的是,在一些动物中,缺血2分钟后就观察到了轻度脑损伤,4分钟后则更一致地出现。这种损伤影响海马体中的CA4和CA1锥体以及下托中的神经元。新皮质细胞坏死在缺血4分钟后开始出现,海马体CA3损伤在缺血6分钟后出现,而尾壳核中的神经元在8 - 10分钟后首先受到影响。更高剂量损伤后,大脑皮质的选择性神经元坏死恶化为梗死。损伤在半球的上外侧凸面、大脑皮质的中层最为严重。尾状核显示出有地理界限的选择性神经元坏死区域,背外侧部分的神经元损伤呈现全或无模式。其他受累结构包括杏仁核、丘脑网状核、隔核、黑质网状部和小脑蚓部。