医学
多发性硬化
白质
髓鞘少突胶质细胞糖蛋白
脊髓
少突胶质细胞
中枢神经系统
灰质
髓鞘
神经科学
炎症
病理
脑脊髓炎
实验性自身免疫性脑脊髓炎
免疫学
磁共振成像
生物
内科学
放射科
精神科
作者
Muammer Üçal,Michaela Tanja Haindl,Milena Z. Adzemovic,Manuel Zeitelhofer,Ute Schaefer,Franz Fazekas,Sonja Hochmeister
摘要
Multiple sclerosis (MS) is the most common immune-mediated disease of the central nervous system (CNS) and progressively leads to physical disability and death, caused by white matter lesions in the spinal cord and cerebellum, as well as by demyelination in grey matter. Whilst conventional models of experimental allergic encephalomyelitis are suitable for the investigation of the cell-mediated inflammation in the spinal and cerebellar white matter, they fail to address grey matter pathologies. Here, we present the experimental protocol for a novel rat model of cortical demyelination allowing the investigation of the pathological and molecular mechanisms leading to cortical lesions. The demyelination is induced by an immunization with low-dose myelin oligodendrocyte glycoprotein (MOG) in an incomplete Freund's adjuvant followed by a catheter-mediated intracerebral delivery of pro-inflammatory cytokines. The catheter, moreover, enables multiple rounds of demyelination without causing injection-induced trauma, as well as the intracerebral delivery of potential therapeutic drugs undergoing a preclinical investigation. The method is also ethically favorable as animal pain and distress or disability are controlled and relatively minimal. The expected timeframe for the implementation of the entire protocol is around 8 - 10 weeks.
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