White matter damage and glymphatic dysfunction in a model of vascular dementia in rats with no prior vascular pathologies
Recommended Citation
Venkat P, Chopp M, Zacharek A, Cui C, Zhang L, Li Q, Lu M, Zhang T, Liu A, and Chen J. White matter damage and glymphatic dysfunction in a model of vascular dementia in rats with no prior vascular pathologies. Neurobiol Aging 2017; 50:96-106.
Document Type
Article
Publication Date
2-1-2017
Publication Title
Neurobiology of aging
Abstract
We investigated cognitive function, axonal/white matter (WM) changes and glymphatic function of vascular dementia using a multiple microinfarction (MMI) model in retired breeder (RB) rats. The MMI model induces significant (p < 0.05) cognitive decline that worsens with age starting at 2 weeks, which persists until at least 6 weeks after MMI. RB rats subjected to MMI exhibit significant axonal/WM damage identified by decreased myelin thickness, oligodendrocyte progenitor cell numbers, axon density, synaptic protein expression in the cortex and striatum, cortical neuronal branching, and dendritic spine density in the cortex and hippocampus compared with age-matched controls. MMI evokes significant dilation of perivascular spaces as well as water channel dysfunction indicated by decreased Aquaporin-4 expression around blood vessels. MMI-induced glymphatic dysfunction with delayed cerebrospinal fluid penetration into the brain parenchyma via paravascular pathways as well as delayed waste clearance from the brain. The MMI model in RB rats decreases Aquaporin-4 and induces glymphatic dysfunction which may play an important role in MMI-induced axonal/WM damage and cognitive deficits.
Medical Subject Headings
Aging; Animals; Aquaporin 4; Axons; Brain; Cerebrospinal Fluid; Cognition; Dementia, Vascular; Disease Models, Animal; Lymphatic System; Male; Myelin Sheath; Neuroglia; Oligodendroglia; Rats, Wistar; White Matter
PubMed ID
27940353
Volume
50
First Page
96
Last Page
106