Neuroinflammation and Synaptic Loss

被引:226
作者
Rao, Jagadeesh S. [1 ]
Kellom, Matthew [1 ]
Kim, Hyung-Wook [1 ]
Rapoport, Stanley I. [1 ]
Reese, Edmund A. [1 ]
机构
[1] NIA, Brain Physiol & Metab Sect, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Arachidonic acid; Cytokines; Drebrin; Synaptophysin; Excitotoxicity; TUMOR-NECROSIS-FACTOR; NITRIC-OXIDE SYNTHASE; CYTOSOLIC PHOSPHOLIPASE A(2); NF-KAPPA-B; ARACHIDONIC-ACID METABOLISM; DENDRITIC SPINE PATHOLOGY; MESSENGER-RNA EXPRESSION; ALZHEIMERS-DISEASE; DREBRIN-A; GENE-EXPRESSION;
D O I
10.1007/s11064-012-0708-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Neuroinflammation plays a critical role in the progression of many neurodegenerative, neuropsychiatric and viral diseases. In neuroinflammation, activated microglia and astrocytes release cytokines and chemokines as well as nitric oxide, which in turn activate many signal transduction pathways. The cytokines, interleukin-1 beta and tumor necrosis factor alpha, regulate transcription of a number of genes within the brain, which can lead to the formation of pro-inflammatory products of the arachidonic acid cascade. Formation of pro-inflammatory agents and associated cytotoxic products during neuroinflammation can be detrimental to neurons by altering synaptic proteins. Neuroinflammation as well as excitotoxic insults reduce synaptic markers such as synaptophysin and drebrin. Neurodegenerative, neuropsychiatric illnesses and viral infections are accompanied by loss of both pre- and post-synaptic proteins. These synaptic changes may contribute to the progressive cognitive decline and behavioral changes associated with these illnesses.
引用
收藏
页码:903 / 910
页数:8
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