Department of Pharmacy, College of Pharmacy, Dankook University, Cheonan 31116, Korea.
Department of Food Science and Nutrition, Hallym University, Chuncheon 24252, Korea.
Int J Mol Sci. 2022 May 3;23(9):5096. doi: 10.3390/ijms23095096.
Neuronal loss (death) occurs selectively in vulnerable brain regions after ischemic insults. Astrogliosis is accompanied by neuronal death. It can change the molecular expression and morphology of astrocytes following ischemic insults. However, little is known about cerebral ischemia and reperfusion injury that can variously lead to damage of astrocytes according to the degree of ischemic injury, which is related to neuronal damage/death. Thus, the purpose of this study was to examine the relationship between damage to cortical neurons and astrocytes using gerbil models of mild and severe transient forebrain ischemia induced by blocking the blood supply to the forebrain for five or 15 min. Significant ischemia tFI-induced neuronal death occurred in the deep layers (layers V and VI) of the motor cortex: neuronal death occurred earlier and more severely in gerbils with severe ischemia than in gerbils with mild ischemia. Distinct astrogliosis was detected in layers V and VI. It gradually increased with time after both ischemiae. The astrogliosis was significantly higher in severe ischemia than in mild ischemia. The ischemia-induced increase of glial fibrillary acidic protein (GFAP; a maker of astrocyte) expression in severe ischemia was significantly higher than that in mild ischemia. However, GFAP-immunoreactive astrocytes were apparently damaged two days after both ischemiae. At five days after ischemiae, astrocyte endfeet around capillary endothelial cells were severely ruptured. They were more severely ruptured by severe ischemia than by mild ischemia. However, the number of astrocytes stained with S100 was significantly higher in severe ischemia than in mild ischemia. These results indicate that the degree of astrogliosis, including the disruption (loss) of astrocyte endfeet following ischemia and reperfusion in the forebrain, might depend on the severity of ischemia and that the degree of ischemia-induced neuronal damage may be associated with the degree of astrogliosis.
神经元丢失(死亡)选择性地发生在缺血性损伤后的易损脑区。星形胶质细胞增生伴随着神经元死亡。它可以改变星形胶质细胞在缺血性损伤后的分子表达和形态。然而,对于脑缺血和再灌注损伤,我们知之甚少,根据缺血损伤的程度,它可以导致星形胶质细胞的不同程度的损伤,这与神经元损伤/死亡有关。因此,本研究的目的是使用阻断大脑前部血液供应 5 或 15 分钟诱导的轻度和重度短暂性前脑缺血的沙鼠模型,研究皮质神经元和星形胶质细胞损伤之间的关系。在运动皮层的深层(V 和 VI 层)发生了显著的缺血性 tFI 诱导的神经元死亡:严重缺血的沙鼠比轻度缺血的沙鼠更早、更严重地发生神经元死亡。在 V 和 VI 层检测到明显的星形胶质细胞增生。它在两种缺血后随着时间的推移逐渐增加。严重缺血时的星形胶质细胞增生明显高于轻度缺血。缺血诱导的严重缺血时 GFAP(星形胶质细胞标志物)表达增加明显高于轻度缺血。然而,两种缺血后两天,GFAP 免疫反应性星形胶质细胞明显受损。在缺血后 5 天,毛细血管内皮细胞周围的星形胶质细胞终足严重破裂。严重缺血时的破裂比轻度缺血时更严重。然而,严重缺血时 S100 染色的星形细胞数量明显高于轻度缺血。这些结果表明,星形胶质细胞增生的程度,包括缺血和再灌注后前脑星形胶质细胞终足的破坏(丢失),可能取决于缺血的严重程度,而缺血诱导的神经元损伤的程度可能与星形胶质细胞增生的程度有关。