SYSTEMIC INFECTION AND INFLAMMATION IN ACUTE CNS INJURY AND CHRONIC NEURODEGENERATION: UNDERLYING MECHANISMS

被引:207
作者
Teeling, J. L. [1 ]
Perry, V. H. [1 ]
机构
[1] Univ Southampton, Sch Biol Sci, CNS Inflammat Grp, Southampton SO16 7PX, Hants, England
基金
英国惠康基金;
关键词
sickness behavior; cytokines; prostaglandins; interferons; neurodegenerative disease; microglia; CENTRAL-NERVOUS-SYSTEM; INDUCED SICKNESS BEHAVIOR; NECROSIS-FACTOR-ALPHA; TOLL-LIKE RECEPTORS; POLY I-C; PROSTAGLANDIN-E SYNTHASE-1; MURINE PRION DISEASE; SPINAL-CORD-INJURY; NF-KAPPA-B; MULTIPLE-SCLEROSIS;
D O I
10.1016/j.neuroscience.2008.07.031
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have all at some time experienced the nonspecific symptoms that arise from being ill following a systemic infection. These symptoms, such as fever, malaise, lethargy and loss of appetite are often referred to as.,sickness behavior" and are a consequence of systemically produced pro-inflammatory mediators. These inflammatory mediators signal to the brain, leading to activation of microglial cells, which in turn, signal to neurons to induce adaptive metabolic and behavioral changes. In normal healthy persons this response is a normal part of our defense, to protect us from infection, to maintain homeostasis and causes no damage to neurons. However, in animals and patients with chronic neurodegenerative disease, multiple sclerosis, stroke and even during normal aging, systemic inflammation leads to inflammatory responses in the brain, an exaggeration of clinical symptoms and increased neuronal death. These observations imply that, as the population ages and the number of individuals with CNS disorders increases, relatively common systemic infections and inflammation will become significant risk factors for disease onset or progression. In this review we discuss the underlying mechanisms responsible for sickness behavior induced by systemic inflammation in the healthy brain and how they might be different in individuals with CNS pathology. (C) 2009 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1062 / 1073
页数:12
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