4.6 Article

Long-term monitoring of chronic demyelination and remyelination in a rat ischemic stroke model using macromolecular proton fraction mapping

Journal

JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM
Volume 41, Issue 11, Pages 2856-2869

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/0271678X211020860

Keywords

Macromolecular proton fraction; middle cerebral artery occlusion; myelin; magnetic resonance imaging; histology

Funding

  1. Russian Science Foundation [14-45-00040, 18-15-00229, 19-75-20142]
  2. NIH [R24NS104098, R21NS109727]
  3. Russian Foundation for Basic Research [19-315-90119]
  4. Russian Science Foundation [14-45-00040, 19-75-20142] Funding Source: Russian Science Foundation

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This study investigated the feasibility of monitoring demyelination and remyelination in experimental stroke using MPF. Results showed distinct sub-regions within the infarct with different patterns of myelin damage and repair, with remyelination zones demonstrating active axonal regrowth and neuronal proliferation while demyelination zones showed extensive astrogliosis. Overall, MPF mapping was validated as a novel approach for assessing myelin damage and repair in ischemic stroke.
Remyelination is a key process enabling post-stroke brain tissue recovery and plasticity. This study aimed to explore the feasibility of demyelination and remyelination monitoring in experimental stroke from the acute to chronic stage using an emerging myelin imaging biomarker, macromolecular proton fraction (MPF). After stroke induction by transient middle cerebral artery occlusion, rats underwent repeated MRI examinations during 85 days after surgery with histological endpoints for the animal subgroups on the 7th, 21st, 56th, and 85th days. MPF maps revealed two sub-regions within the infarct characterized by distinct temporal profiles exhibiting either a persistent decrease by 30%-40% or a transient decrease followed by return to nearly normal values after one month of observation. Myelin histology confirmed that these sub-regions had nearly similar extent of demyelination in the sub-acute phase and then demonstrated either chronic demyelination or remyelination. The remyelination zones also exhibited active axonal regrowth, reconstitution of compact fiber bundles, and proliferation of neuronal and oligodendroglial precursors. The demyelination zones showed more extensive astrogliosis from the 21st day endpoint. Both sub-regions had substantially depleted neuronal population over all endpoints. These results histologically validate MPF mapping as a novel approach for quantitative assessment of myelin damage and repair in ischemic stroke.

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