发育大鼠脑缺氧缺血时神经元变化的时间演化:定量光镜研究。

J. Towfighi, D. Mauger
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引用次数: 26

摘要

对成年动物短暂性脑缺氧缺血(HI)和缺血模型的研究表明,纹状体等部分区域神经元死亡的形态学证据出现较早,而大脑皮层和海马CA1区等其他区域神经元死亡的形态学证据则延迟数天,称为延迟性神经元死亡(DND)。此外,在某些区域,如CA2/CA3,早期“反应性”神经元变化可能是可逆的。这项研究的目的是确定这种变化是否也可能发生在发育中的大脑中。为此,通过右颈总动脉结扎和低氧血症(呼吸8% O2)在出生后13,21和30天(p13, p21, p30)产生单侧脑HI,并在恢复后24小时,36小时,72小时和96小时检查其大脑。结果表明:(1)DND存在于发育中的大脑中,但其区域分布随动物年龄的不同而不同。在大脑皮层中,p30大鼠比年轻动物更明显。在海马中,比较不同年龄组相似严重程度的病变,p13大鼠CA2/CA3区域的DND比老年动物更明显,但CA1神经元的DND程度在不同年龄组之间没有显著差异。(2)“反应性”神经元变化的特征是尼氏染色减少和神经元核周嗜酸,在恢复24小时出现最小的核异常。这些变化在某些区域,如CA1和皮层,进展到神经元死亡,而在其他区域,如CA2/CA3,可能是可逆的。(iii) CA2/CA3区的反应性神经元的恢复与年龄有关,在老年组中有明显的恢复,但在p13大鼠中没有。反应性神经元变化的发病机制、导致DND或神经元恢复的一系列事件以及年龄在这些过程中的影响仍有待阐明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Temporal evolution of neuronal changes in cerebral hypoxia-ischemia in developing rats: a quantitative light microscopic study.
Studies in adult animal models of transient cerebral hypoxia-ischemia (HI) and ischemia suggest that morphologic evidence of neuronal death in some regions such as striatum appears early, while in other regions such as cerebral cortex and CA1 region of hippocampus it is delayed for few days and is referred to as delayed neuronal death (DND). Moreover, in some regions such as CA2/CA3 early 'reactive' neuronal changes occur that are potentially reversible. The aim of this study was to determine whether such changes may also occur in the developing brain. To that end, unilateral cerebral HI was produced in postnatal rats of 13, 21, and 30 days (p13, p21, p30) by right common carotid artery ligation and hypoxemia (breathing 8% O2), and their brains were examined at 24 h, 36 h, 72 h, and 96 h of recovery. The results suggest that: (i) DND is present in developing brain, but its regional distribution varies with animals' age. In cerebral cortex, it is more pronounced in p30 rats than in younger animals. In hippocampus, comparison of lesions of similar severity at different age groups shows a more pronounced DND in CA2/CA3 region of p13 rats than in older animals, but no significant differences exist in the degree of DND in CA1 neurons among different age groups. (ii) 'Reactive' neuronal changes characterized by reduction in Nissl staining and acidophilia of neuronal perikaryon with minimal nuclear abnormality are present at 24 h of recovery. These changes in some regions, such as in CA1 and cortex, progress to neuronal death, while in other regions such as in CA2/CA3 are potentially reversible. (iii) Recovery of reactive neurons in CA2/CA3 region is age dependent in that there is significant recovery in the older age groups, but not in p13 rats. The pathogenetic mechanisms of the reactive neuronal changes, the chain of events leading to DND or neuronal recovery, and the influence of age in these processes remain to be elucidated.
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