Lima Rafael R, Guimaraes-Silva Joanilson, Oliveira Jorge L, Costa Ana Maria R, Souza-Rodrigues Renata D, Dos Santos Claudia D, Picanço-Diniz Cristovam W, Gomes-Leal Walace
Laboratory of Experimental Neuroprotection and Neuroregeneration, Department of Morphology, Biological Sciences Center, Federal University of Pará, Belém-Pará, Brazil.
Inflammation. 2008 Feb;31(1):24-35. doi: 10.1007/s10753-007-9046-y. Epub 2007 Sep 25.
White matter damage and inflammatory response are important secondary outcomes after acute neural disorders. Nevertheless, a few studies addressed the temporal outcomes of these pathological events using non-traumatic models of acute brain injury. In the present study, we describe acute inflammatory response and white matter neuropathology between 1 and 7 days after acute excitotoxic striatal damage. Twenty micrometer sections were stained by hematoxylin and eosin technique for gross histopathological analysis and immunolabed for neutrophils (anti-mbs-1), activated macrophages/microglia (anti-ed1), astrocytes (anti-gfap), damaged axons (anti-betaapp) and myelin basic protein (MBP). Recruitment peak of neutrophils and macrophages occurred at 1 and 7 days post-nmda injection, respectively. Diffuse damaged axons (beta-app + end-bulbs) were apparent at 7 days, concomitant with progressive myelin impairment and astrocytosis. Further studies using electron microscopy and blockers of inflammatory response and glutamatergic receptors should be performed to confirm and address the mechanisms of white matter damage following an excitotoxic lesion.
白质损伤和炎症反应是急性神经疾病后的重要继发性结果。然而,少数研究使用急性脑损伤的非创伤模型探讨了这些病理事件的时间性结果。在本研究中,我们描述了急性兴奋性毒性纹状体损伤后1至7天内的急性炎症反应和白质神经病理学变化。将20微米厚的切片用苏木精和伊红技术染色以进行大体组织病理学分析,并进行免疫标记以检测中性粒细胞(抗-mbs-1)、活化的巨噬细胞/小胶质细胞(抗-ed1)、星形胶质细胞(抗-gfap)、受损轴突(抗-betaapp)和髓鞘碱性蛋白(MBP)。中性粒细胞和巨噬细胞的募集高峰分别出现在注射NMDA后的第1天和第7天。弥漫性受损轴突(beta-app + 终球)在第7天明显可见,同时伴有进行性髓鞘损伤和星形胶质细胞增生。应进一步开展使用电子显微镜以及炎症反应和谷氨酸能受体阻滞剂的研究,以证实并探讨兴奋性毒性损伤后白质损伤的机制。