Kato H, Kogure K, Araki T, Itoyama Y
Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.
Brain Res. 1994 Nov 21;664(1-2):69-76. doi: 10.1016/0006-8993(94)91955-0.
Preconditioning of the brain with sublethal ischemia protects against neuronal damage following subsequent longer periods of ischemia (ischemic tolerance). In this study, we investigated astroglial and microglial reactions in the hippocampus following ischemia in a gerbil model of ischemic tolerance. Two minutes of forebrain ischemia (preconditioning ischemia) or sham operation was followed by 3 min of ischemia (second ischemia) 3 days later. The brains were perfusion-fixed after 4 h, 1 day, 2 days, and 7 days. Paraffin sections were used for the visualization of astrocytes by immunostaining against glial fibrillary acidic protein (GFAP) and for the visualization of microglia by histochemical staining with isolectin-B4 from Griffonia simplicifolia. The preconditioning ischemia induced a moderate increase in astroglial and microglial staining. Two days after the second ischemia, GFAP staining further increased in astrocytes in the hippocampus with ischemic tolerance. In the CA1 region of the hippocampus without ischemic tolerance, in contrast, microglial activation with increased staining and morphological changes was pronounced. After 7 days, neuronal destruction resulted in the CA1 region without tolerance, where hypertrophic reactive astroglia and reactive microglia with phagocytic transformation accumulated intensely. However, the ischemic preconditioning prevented the CA1 neuronal damage and the activation of microglia was subsiding after 7 days. Thus, activation of glial cells occurred in a graded fashion in response to different degrees of neuronal injury. Astroglial but not microglial activation may have implications in neuronal survival in ischemic tolerance.(ABSTRACT TRUNCATED AT 250 WORDS)
用亚致死性缺血对大脑进行预处理可保护其免受随后较长时间缺血所致的神经元损伤(缺血耐受)。在本研究中,我们在沙鼠缺血耐受模型中研究了缺血后海马体中的星形胶质细胞和小胶质细胞反应。先进行两分钟的前脑缺血(预处理缺血)或假手术,3天后再进行3分钟的缺血(第二次缺血)。在4小时、1天、2天和7天后对大脑进行灌注固定。石蜡切片用于通过针对胶质纤维酸性蛋白(GFAP)的免疫染色来观察星形胶质细胞,以及通过用来自西非豆科植物的异凝集素B4进行组织化学染色来观察小胶质细胞。预处理缺血导致星形胶质细胞和小胶质细胞染色适度增加。在具有缺血耐受的海马体中,第二次缺血两天后,星形胶质细胞中的GFAP染色进一步增加。相比之下,在没有缺血耐受的海马体CA1区,小胶质细胞激活伴随着染色增加和形态变化明显。7天后,在没有耐受性的CA1区出现神经元破坏,肥大的反应性星形胶质细胞和具有吞噬转化的反应性小胶质细胞大量积聚。然而,缺血预处理可防止CA1神经元损伤,且7天后小胶质细胞的激活逐渐减弱。因此,胶质细胞的激活根据神经元损伤的不同程度呈分级发生。星形胶质细胞而非小胶质细胞的激活可能对缺血耐受中的神经元存活有影响。(摘要截短至250字)