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Rat Model of Widespread Cerebral Cortical Demyelination Induced by an Intracerebral Injection of Pro-Inflammatory Cytokines.
Üçal, Muammer; Haindl, Michaela Tanja; Adzemovic, Milena Z; Zeitelhofer, Manuel; Schaefer, Ute; Fazekas, Franz; Hochmeister, Sonja.
Affiliation
  • Üçal M; Research Unit of Experimental Neurotraumatology, Department of Neurosurgery, Medical University Graz.
  • Haindl MT; Department of Neurology, Medical University Graz.
  • Adzemovic MZ; Centre for Molecular Medicine, Department of Clinical Neuroscience, Karolinska Institutet.
  • Zeitelhofer M; Division of Vascular Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet.
  • Schaefer U; Research Unit of Experimental Neurotraumatology, Department of Neurosurgery, Medical University Graz.
  • Fazekas F; Department of Neurology, Medical University Graz.
  • Hochmeister S; Department of Neurology, Medical University Graz; sonja.hochmeister@medunigraz.at.
J Vis Exp ; (175)2021 09 21.
Article in En | MEDLINE | ID: mdl-34633360
ABSTRACT
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Encephalomyelitis, Autoimmune, Experimental / Multiple Sclerosis Type of study: Guideline Aspects: Ethics Limits: Animals Language: En Journal: J Vis Exp Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Encephalomyelitis, Autoimmune, Experimental / Multiple Sclerosis Type of study: Guideline Aspects: Ethics Limits: Animals Language: En Journal: J Vis Exp Year: 2021 Document type: Article