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Selective vulnerability of inhibitory networks in multiple sclerosis.
Zoupi, Lida; Booker, Sam A; Eigel, Dimitri; Werner, Carsten; Kind, Peter C; Spires-Jones, Tara L; Newland, Ben; Williams, Anna C.
Affiliation
  • Zoupi L; Centre for Regenerative Medicine, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh, EH16 4UU, UK.
  • Booker SA; Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH8 9XD, UK.
  • Eigel D; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh, EH8 9XD, UK.
  • Werner C; Patrick Wild Centre for Autism Research, University of Edinburgh, Edinburgh, EH8 9XD, UK.
  • Kind PC; Leibniz-Institut Für Polymerforschung Dresden E.V, Max Bergmann Center of Biomaterials Dresden, Hohe Straße 6, 01069, Dresden, Germany.
  • Spires-Jones TL; Leibniz-Institut Für Polymerforschung Dresden E.V, Max Bergmann Center of Biomaterials Dresden, Hohe Straße 6, 01069, Dresden, Germany.
  • Newland B; Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH8 9XD, UK.
  • Williams AC; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh, EH8 9XD, UK.
Acta Neuropathol ; 141(3): 415-429, 2021 03.
Article in En | MEDLINE | ID: mdl-33449171
In multiple sclerosis (MS), a chronic demyelinating disease of the central nervous system, neurodegeneration is detected early in the disease course and is associated with the long-term disability of patients. Neurodegeneration is linked to both inflammation and demyelination, but its exact cause remains unknown. This gap in knowledge contributes to the current lack of treatments for the neurodegenerative phase of MS. Here we ask if neurodegeneration in MS affects specific neuronal components and if it is the result of demyelination. Neuropathological examination of secondary progressive MS motor cortices revealed a selective vulnerability of inhibitory interneurons in MS. The generation of a rodent model of focal subpial cortical demyelination reproduces this selective neurodegeneration providing a new preclinical model for the study of neuroprotective treatments.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain / Demyelinating Diseases / Multiple Sclerosis, Chronic Progressive / Nerve Degeneration / Neurons Limits: Aged / Animals / Female / Humans / Male / Middle aged Language: En Journal: Acta Neuropathol Year: 2021 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain / Demyelinating Diseases / Multiple Sclerosis, Chronic Progressive / Nerve Degeneration / Neurons Limits: Aged / Animals / Female / Humans / Male / Middle aged Language: En Journal: Acta Neuropathol Year: 2021 Document type: Article Country of publication: