| Autor: |
Khodanovich MY; Laboratory of Neurobiology, Tomsk State University, Tomsk, Russian Federation., Gubskiy IL; Research Institute of Cerebrovascular Pathology and Stroke, Pirogov Russian Medical University, Moscow, Russian Federation., Kudabaeva MS; Laboratory of Neurobiology, Tomsk State University, Tomsk, Russian Federation., Namestnikova DD; Research Institute of Cerebrovascular Pathology and Stroke, Pirogov Russian Medical University, Moscow, Russian Federation., Kisel AA; Laboratory of Neurobiology, Tomsk State University, Tomsk, Russian Federation.; Department of Radiology, University of Washington, Seattle, USA., Anan'ina TV; Laboratory of Neurobiology, Tomsk State University, Tomsk, Russian Federation., Tumentceva YA; Laboratory of Neurobiology, Tomsk State University, Tomsk, Russian Federation., Mustafina LR; Department of histology, embriology, and cytology, Siberian State Medical University, Tomsk, Russian Federation., Yarnykh VL; Laboratory of Neurobiology, Tomsk State University, Tomsk, Russian Federation.; Department of Radiology, University of Washington, Seattle, USA. |
| Abstrakt: |
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. |
