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Article ; Online: Acute intermittent hypoxia alters disease course and promotes CNS repair including resolution of inflammation and remyelination in the experimental autoimmune encephalomyelitis model of MS.

Tokarska, Nataliya / Naniong, Justin M A / Johnston, Jayne M / Salapa, Hannah E / Muir, Gillian D / Levin, Michael C / Popescu, Bogdan F / Verge, Valerie M K

Glia

2023  Volume 71, Issue 8, Page(s) 2045–2066

Abstract: Remyelination and neurodegeneration prevention mitigate disability in Multiple Sclerosis (MS). We have shown acute intermittent hypoxia (AIH) is a novel, non-invasive and effective therapy for peripheral nerve repair, including remyelination. Thus, we ... ...

Abstract Remyelination and neurodegeneration prevention mitigate disability in Multiple Sclerosis (MS). We have shown acute intermittent hypoxia (AIH) is a novel, non-invasive and effective therapy for peripheral nerve repair, including remyelination. Thus, we posited AIH would improve repair following CNS demyelination and address the paucity of MS repair treatments. AIH's capacity to enhance intrinsic repair, functional recovery and alter disease course in the experimental autoimmune encephalomyelitis (EAE) model of MS was assessed. EAE was induced by MOG
MeSH term(s) Encephalomyelitis, Autoimmune, Experimental/pathology ; Encephalomyelitis, Autoimmune, Experimental/therapy ; Multiple Sclerosis/pathology ; Multiple Sclerosis/therapy ; Remyelination ; Animals ; Mice ; Mice, Inbred C57BL ; Anaerobiosis ; Oxygen ; Female
Chemical Substances Oxygen (S88TT14065)
Language English
Publishing date 2023-05-03
Publishing country United States
Document type Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 639414-0
ISSN 1098-1136 ; 0894-1491
ISSN (online) 1098-1136
ISSN 0894-1491
DOI 10.1002/glia.24381
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