White matter injury in young and aged rats after intracerebral hemorrhage

• Published in: Experimental neurology 2008-12, Vol.214 (2), p.266-275
• Main Authors: Wasserman, Jason K., Schlichter, Lyanne C.
• Format: Article
• Language: English
• Subjects: Age Factors; Aging; Amyloid beta-Protein Precursor - metabolism; Amyloid precursor protein; Animals; Axonal injury; Biological and medical sciences; Brain Injuries - pathology; Cerebral Hemorrhage - pathology; Demyelinating Diseases - pathology; Demyelination; Disease Models, Animal; Injuries of the nervous system and the skull. Diseases due to physical agents; Male; Medical sciences; Microglia - pathology; Microglial activation; Myelin Basic Protein - metabolism; Nerve Fibers, Myelinated - metabolism; Nerve Fibers, Myelinated - pathology; Neuritis - pathology; Neurology; Rats; Rats, Sprague-Dawley; Stroke; Stroke - pathology; Traumas. Diseases due to physical agents; Traumatic brain injury
• ISSN: 0014-4886; 1090-2430
• DOI: 10.1016/j.expneurol.2008.08.010

Experimental studies of intracerebral hemorrhage (ICH) have focused on neuron death, with little or no information on axonal and myelin damage outside the hematoma. Because development of effective therapies will require an understanding of white matter injury, we examined white matter injury and its spatial and temporal relationship with microglial/macrophage activation in a collagenase model of rat striatal ICH. The hematoma and parenchyma surrounding the hematoma were assessed in young and aged animals at 6 h, 1, 3 and 28 days after ICH onset. Demyelination occurred inside and at the edge of the hematoma; regions where we have shown substantial neuron death. In contrast, there was axonal damage without demyelination at the edge of the hematoma, and by 3 days this damage had spread to the surrounding parenchyma, a region where we have shown there is no neuron death. Because the axonal damage preceded infiltration of activated microglia into the white matter tracts (seen at 3 days), our results support the hypothesis that these cells respond to, rather than perpetrate the damage. Importantly, axonal damage was worse in aged animals, which provides a plausible explanation for the poorer functional recovery of older animals after ICH, despite a similar loss of grey matter. Our findings support strategies that target white matter injury to reduce neurological impairment after ICH.