大鼠缺血性脑卒中后反应性星形胶质细胞的时间分布

Justin Stadler, Harrison Schurr, D. Doyle, Lucas Garmo, B. Srinageshwar, Marc R. Spencer, Robert B Petersen, G. Dunbar, J. Rossignol
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引用次数: 1

摘要

缺血性中风是一种使人衰弱的神经系统疾病,最常见的原因是脑血管阻塞。缺血/再灌注损伤通常是中风的结果,其特征是氧化应激、神经炎症和血液供应恢复后周围胶质细胞的激活。星形胶质细胞被认为是大脑中最重要的胶质细胞,在病理条件下,除其他病理外,显示激活(GFAP)与反应性程度成正比。该研究的主要目的是确定缺血性脑卒中后星形胶质细胞反应性的时间分布。34只Sprague-Dawley大鼠被分配到90分钟的大脑中动脉闭塞(MCAo)或假手术。按术后安乐死天数对动物进行分组;2天(n = 10), 4天(n = 11), 7天(n = 13)。荧光显微镜和密度测定定量GFAP免疫反应性,显示缺血/再灌注后GFAP免疫反应性呈非线性关系。结果显示,MCAo组的GFAP水平明显高于假手术组,在第4天安乐死的大鼠的大脑中显示出峰值的GFAP反应性。这些发现适用于未来的研究,特别是针对缺血性损伤后反应性星形胶质细胞的干预措施的研究。
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Temporal Profile of Reactive Astrocytes after Ischemic Stroke in Rats
Ischemic stroke is a debilitating neurological disease most commonly resulting from an occlusion within the cerebral vasculature. Ischemia/reperfusion injury is oftentimes a consequence of stroke, characterized by oxidative stress, neuroinflammation, and the activation of surrounding glial cells following restoration of blood supply. Astrocytes are regarded as the most prominent glial cell in the brain and, under pathologic conditions, display, among other pathologies, activated (GFAP) relatively proportional to the degree of reactivity. The primary objective of the study was to determine the temporal profile of astrocyte reactivity following ischemic stroke. Thirty-four Sprague-Dawley rats were assigned to surgery consisting of either 90-min middle cerebral artery occlusion (MCAo) or sham surgery. Animals were sub-grouped by postoperative euthanization day; 2 days (n = 10), 4 days (n = 11), and 7 days (n = 13). Fluorescence microscopy and densitometry were utilized to quantify GFAP immunoreactivity, which indicated a non-linear relationship following ischemia/reperfusion. Results demonstrated substantially higher GFAP levels in MCAo groups than in sham, with peak GFAP reactivity being shown in the brains of rats euthanized on day 4. These findings are applicable to future research, especially in the investigation of interventions that target reactive astrocytes following ischemic injury.
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