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全球缺血持续时间对大鼠易损海马CA1亚区神经元、星形胶质细胞、少突胶质细胞和小胶质细胞反应的影响。

Effects of global ischemia duration on neuronal, astroglial, oligodendroglial, and microglial reactions in the vulnerable hippocampal CA1 subregion in rats.

作者信息

Sugawara Taku, Lewén Anders, Noshita Nobuo, Gasche Yvan, Chan Pak H

机构信息

Department of Neurosurgery, Stanford University School of Medicine, California, USA.

出版信息

J Neurotrauma. 2002 Jan;19(1):85-98. doi: 10.1089/089771502753460268.

Abstract

The hippocampal CA1 neurons are selectively vulnerable to global ischemia, and neuronal death occurs in a delayed manner. The threshold of global ischemia duration that induces neuronal death has been studied, but the relationship between ischemia duration and glial death in the hippocampal CA1 area has not been fully studied. We examined neuronal/glial viability and morphological changes in the CA1 subregion after different durations of global ischemia. Global ischemia was induced in Sprague-Dawley rats by 10, 5, and 3 min of bilateral common carotid artery occlusion and hypotension. At 1-56 days after ischemia, the morphological reactions of neurons, astrocytes, oligodendrocytes, and microglia were immunohistochemically evaluated. Most of the hippocampal CA1 pyramidal neurons underwent delayed death at 3 days after 10/5 min of ischemia, but not after 3 min of ischemia. The number of astrocytes gradually declined after 10/5 min of ischemia, and viable astrocytes showed characteristic staged morphological reactions. Oligodendrocytes also showed morphological changes in their processes after 10/5 min of ischemia. Microglia transformed into a reactive form at 5 days only after 10/5 min of ischemia. These data suggest that some morphological changes in glial cells were not dependent on neuronal cell death, but their own reactions to the different severity of ischemia.

摘要

海马体CA1神经元对全脑缺血具有选择性易损性,且神经元死亡呈延迟性发生。诱导神经元死亡的全脑缺血持续时间阈值已得到研究,但海马体CA1区缺血持续时间与胶质细胞死亡之间的关系尚未得到充分研究。我们检测了不同持续时间全脑缺血后CA1亚区的神经元/胶质细胞活力及形态变化。通过双侧颈总动脉闭塞和低血压分别持续10、5和3分钟,在Sprague-Dawley大鼠中诱导全脑缺血。在缺血后1至56天,通过免疫组织化学评估神经元、星形胶质细胞、少突胶质细胞和小胶质细胞的形态学反应。大多数海马体CA1锥体神经元在缺血10/5分钟后3天发生延迟死亡,但缺血3分钟后未发生。缺血10/5分钟后星形胶质细胞数量逐渐减少,存活的星形胶质细胞呈现特征性的阶段性形态学反应。缺血10/5分钟后少突胶质细胞的突起也出现形态变化。仅在缺血10/5分钟后5天,小胶质细胞转变为反应性形态。这些数据表明,胶质细胞的一些形态学变化并不依赖于神经元细胞死亡,而是它们自身对不同严重程度缺血的反应。

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