University of Goettingen, Department of Neurology/Department of Medical Psychology and Medical Sociology, Robert-Koch-Str. 40, D-37099 Goettingen, Germany.
Neurosci Lett. 2010 May 14;475(2):104-7. doi: 10.1016/j.neulet.2010.03.059. Epub 2010 Mar 27.
The rabbit model provides an important experimental setting for the evaluation of antibiotic agents against pneumococcal meningitis. One of the primary targets of this model is the study of neuronal and glial cell damage in bacterial meningitis. The aim of this investigation was to evaluate whether a significant increase of S100B in the cerebrospinal fluid (CSF) as an indicator of white matter damage could be observed in this meningitis model. Seven rabbits were infected intracisternally with S. pneumoniae, and CSF S100B concentrations were examined serially before infection, at 12h, 14h, 17h, 20h, and at 24h after infection. The course of CSF S100B increase and its relation to other parameters of brain tissue destruction and CSF inflammation were measured. Axonal damage was visualized by amyloid precursor protein (APP) immunostaining and demyelination by Luxol Fast Blue/Periodic Acid Schiff (LFB-PAS) stain. In each animal, we observed a distinct rise in S100B concentration in the CSF due to pneumococcal meningitis. We conclude that the CSF concentration of the glial S100B protein can be used as an additional parameter for future interventional studies focusing on glial cell damage in the rabbit model of bacterial meningitis.
兔模型为评估抗肺炎球菌性脑膜炎的抗生素提供了重要的实验环境。该模型的主要目标之一是研究细菌性脑膜炎中神经元和神经胶质细胞的损伤。本研究旨在评估在这种脑膜炎模型中是否可以观察到脑脊液(CSF)中 S100B 显著增加作为白质损伤的指标。7 只兔子通过脑室内感染肺炎链球菌,并在感染前、感染后 12h、14h、17h、20h 和 24h 时连续检测 CSF S100B 浓度。测量 CSF S100B 增加的过程及其与脑组织破坏和 CSF 炎症的其他参数的关系。通过淀粉样前体蛋白(APP)免疫染色观察轴突损伤,通过卢索快速蓝/过碘酸希夫(LFB-PAS)染色观察脱髓鞘。在每只动物中,我们观察到由于肺炎球菌性脑膜炎导致 CSF 中 S100B 浓度明显升高。我们得出结论,CSF 中神经胶质 S100B 蛋白的浓度可以作为未来干预性研究的附加参数,重点关注细菌性脑膜炎兔模型中的神经胶质细胞损伤。