期刊
NEUROBIOLOGY OF AGING
卷 33, 期 1, 页码 162-175出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2010.02.002
关键词
Astrocytes; Hippocampus; Inflammation; Microglia; TNF-alpha
资金
- GlaxoSmithKline
- Industrial Development Agency Ireland
- Health Research Board (Ireland) [HRB RP/2006/2012-Lynch]
Neuroinflammation is a significant and consistent feature of many neurodegenerative disorders, including Alzheimer's disease (AD) and Parkinson's disease (PD). The greatest risk factor for neurodegenerative disorders is age and a proinflammatory phenotype in the aged brain is believed to contribute to these neurodegenerative conditions. In animal models, neuroinflammatory changes, characterized by increased microglial activation, have been associated with a loss of synaptic plasticity and here we show that treatment of aged rats with the PPAR gamma agonist, rosiglitazone, modulates the inflammatory changes and restores synaptic function. The evidence presented highlights an important role for astrocytes in inducing inflammatory changes and suggests that the age-related astrogliosis and astrocytosis is responsible for the increase in the proinflammatory cytokine, tumor necrosis factor alpha (TNF-alpha). Magnetic resonance (MR) imaging revealed an age-related increase in T1 relaxation time and, importantly, treatment of aged rats with rosiglitazone reversed the age-related increases in astrogliosis and astrocytosis, TNF-alpha concentration and T1 relaxation time. The evidence indicates that the site of action for rosiglitazone is endothelial cells, and suggests that its effect on astrocytes is secondary to its effect on endothelial cells. (C) 2012 Elsevier Inc. All rights reserved.
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