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J Cereb Blood Flow Metab ; 25(1): 98-107, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15678116

ABSTRACT

The inhibitory activity of myelin-associated glycoprotein (MAG) on neurons is thought to contribute to the lack of regenerative capacity of the CNS after injury. The interaction of MAG and its neuronal receptors mediates bidirectional signaling between neurons and oligodendrocytes. The novel finding that an anti-MAG monoclonal antibody not only possesses the ability to neutralise the inhibitory effect of MAG on neurons but also directly protects oligodendrocytes from glutamate-mediated oxidative stress-induced cell death is reported here. Furthermore, administration of anti-MAG antibody (centrally and systemically) starting 1 hour after middle cerebral artery occlusion in the rat significantly reduced lesion volume at 7 days. This neuroprotection was associated with a robust improvement in motor function compared with animals receiving control IgG1. Together, these data highlight the potential for the use of anti-MAG antibodies as therapeutic agents for the treatment of stroke.


Subject(s)
Antibodies, Monoclonal/administration & dosage , Brain/physiology , Infarction, Middle Cerebral Artery/drug therapy , Myelin-Associated Glycoprotein , Neuroprotective Agents/administration & dosage , Regeneration/drug effects , Stroke/drug therapy , Animals , Brain/pathology , Cell Death/drug effects , Dose-Response Relationship, Drug , Glutamic Acid/metabolism , Immunoglobulin G/administration & dosage , Infarction, Middle Cerebral Artery/metabolism , Infarction, Middle Cerebral Artery/pathology , Male , Mice , Myelin Sheath/metabolism , Myelin Sheath/pathology , Myelin-Associated Glycoprotein/metabolism , Oxidative Stress/drug effects , Rats , Rats, Sprague-Dawley , Regeneration/physiology , Stroke/metabolism , Stroke/pathology
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