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发育中大鼠脑缺氧缺血时神经元变化的时间演变:一项定量光学显微镜研究。

Temporal evolution of neuronal changes in cerebral hypoxia-ischemia in developing rats: a quantitative light microscopic study.

作者信息

Towfighi J, Mauger D

机构信息

Department of Pathology (Anatomic Pathology), The Milton S. Hershey Medical Center, The Pennsylvania State University College of Medicine, P.O. Box 850, Hershey, PA 17033-0850, USA.

出版信息

Brain Res Dev Brain Res. 1998 Aug 8;109(2):169-77. doi: 10.1016/s0165-3806(98)00077-7.

Abstract

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.

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,纹状体等一些区域的神经元死亡形态学证据出现较早,而大脑皮层和海马体CA1区等其他区域则会延迟数天出现,这被称为延迟性神经元死亡(DND)。此外,在CA2/CA3等一些区域会出现早期的“反应性”神经元变化,这些变化可能是可逆的。本研究的目的是确定这些变化是否也会在发育中的大脑中发生。为此,通过结扎右侧颈总动脉并使其低氧(呼吸8%氧气),在出生后13天、21天和30天(p13、p21、p30)的新生大鼠中产生单侧脑HI,并在恢复24小时、36小时、72小时和96小时后检查它们的大脑。结果表明:(i)DND存在于发育中的大脑中,但其区域分布随动物年龄而变化。在大脑皮层中,p30大鼠比年幼动物更明显。在海马体中,比较不同年龄组相似严重程度的损伤发现,p13大鼠CA2/CA3区的DND比年长动物更明显,但不同年龄组CA1神经元的DND程度没有显著差异。(ii)恢复24小时时出现以尼氏染色减少和神经元胞体嗜酸性增加且核异常最小为特征的“反应性”神经元变化。这些变化在一些区域,如CA1和皮层,会发展为神经元死亡,而在其他区域,如CA2/CA3,则可能是可逆的。(iii)CA2/CA3区反应性神经元的恢复与年龄有关,即年长年龄组有显著恢复,而p13大鼠则没有。反应性神经元变化的发病机制、导致DND或神经元恢复的事件链以及年龄在这些过程中的影响仍有待阐明。

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