Article (Scientific journals)
Blood-brain barrier permeability towards small and large tracers in a mouse model of osmotic demyelination syndrome.
Scalisi, Joshua; Balau, Benoît; Deneyer, Lynn et al.
2021In Neuroscience Letters, 746, p. 135665
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Keywords :
Blood-brain barrier; Endothelium; Mouse; Osmotic demyelination syndrome; Permeability; Tracer; Fluorescent Dyes; Animals; Biological Transport/drug effects; Biological Transport/physiology; Blood-Brain Barrier/drug effects; Blood-Brain Barrier/metabolism; Blood-Brain Barrier/pathology; Capillary Permeability/drug effects; Capillary Permeability/physiology; Demyelinating Diseases/metabolism; Demyelinating Diseases/pathology; Endothelial Cells/drug effects; Endothelial Cells/metabolism; Endothelial Cells/pathology; Fluorescent Dyes/administration & dosage; Fluorescent Dyes/metabolism; Male; Mice; Mice, Inbred C57BL; Osmosis/drug effects; Osmosis/physiology; Syndrome; Biological Transport; Capillary Permeability; Demyelinating Diseases; Endothelial Cells; Osmosis; Neuroscience (all); General Neuroscience
Abstract :
[en] During osmotic demyelination syndrome (ODS), myelin and oligodendrocyte are lost according to specific patterns in centro- or extra-pontine regions. In both experimental model of ODS and human cases, brain lesions are locally correlated with the disruption of the blood brain-barrier (BBB). The initiation, the degree and the duration of blood-brain barrier (BBB) opening as well as its contribution to brain damages are still a matter of debate. Using a panel of intravascular tracers from low- to high- molecular weight (from 0.45 kDa 150 kDa), we have assessed the BBB permeability at different timings of ODS induced experimentally in mice. ODS was mimicked according to a protocol of rapid correction of a chronic hyponatremia. We demonstrated that BBB leakage towards smallest tracers Lucifer Yellow (0.45 kDa) and Texas Red-dextran (3 kDa) was delayed by 36 h compared to the first clues of oligodendrocyte loss (occurring 12 h post-correction of hyponatremia). At 48 h post-correction and concomitantly to myelin loss, BBB was massively disrupted as attested by accumulation of Evans Blue (69 kDa) and IgG (150 kDa) in brain parenchyma. Analysis of BBB ultrastructure verified that brain endothelial cells had minimal alterations during chronic hyponatremia and at 12 h post-correction of hyponatremia. However, brain endothelium yielded worsened alterations at 48 h, such as enlarged vesicular to tubular-like cytoplasmic profiles of pinocytosis and/or transcytosis, local basal laminae abnormalities and sub-endothelial cavities. The protein expressions of occludin and claudin-1, involved in inter-endothelial tight junctions, were also downregulated at 48 h post-correction of hyponatremia. Our results revealed that functional BBB opening occured late in pre-established ODS lesions, and therefore was not a primary event initiating oligodendrocyte damages in the mouse model of ODS.
Disciplines :
Neurology
Author, co-author :
Scalisi, Joshua ;  Université de Liège - ULiège > GIGA ; URPhyM - NARILIS, Université de Namur, Namur, Belgium, HEPH-Condorcet, Catégorie Paramédicale Charleroi, Charleroi, Belgium. Electronic address: jo-scalisi@hotmail.com
Balau, Benoît;  URPhyM - NARILIS, Université de Namur, Namur, Belgium. Electronic address: benoit.balau@unamur.be
Deneyer, Lynn;  URPhyM - NARILIS, Université de Namur, Namur, Belgium, HEPH-Condorcet, Catégorie Paramédicale Charleroi, Charleroi, Belgium. Electronic address: ldeneyer4@gmail.com
Bouchat, Joanna;  URPhyM - NARILIS, Université de Namur, Namur, Belgium. Electronic address: joanna.bouchat@unamur.be
Gilloteaux, Jacques;  URPhyM - NARILIS, Université de Namur, Namur, Belgium, Department of Anatomical Sciences, St George's University School of Medicine, Newcastle upon Tyne, United Kingdom. Electronic address: jacques.gilloteaux@unamur.be
Nicaise, Charles;  URPhyM - NARILIS, Université de Namur, Namur, Belgium. Electronic address: charles.nicaise@unamur.be
Language :
English
Title :
Blood-brain barrier permeability towards small and large tracers in a mouse model of osmotic demyelination syndrome.
Publication date :
16 February 2021
Journal title :
Neuroscience Letters
ISSN :
0304-3940
eISSN :
1872-7972
Publisher :
Elsevier Ireland Ltd, Ireland
Volume :
746
Pages :
135665
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 27 February 2023

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