Role of interleukin-1β during pain and inflammation

被引:664
作者
Ren, Ke [2 ,3 ]
Torres, Richard [1 ]
机构
[1] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
[2] Univ Maryland, Dept Neural & Pain Sci, Sch Dent, Baltimore, MD 21201 USA
[3] Univ Maryland, Program Neurosci, Baltimore, MD 21201 USA
关键词
NERVE GROWTH-FACTOR; NECROSIS-FACTOR-ALPHA; COLD AUTOINFLAMMATORY SYNDROME; SPINAL GLIAL ACTIVATION; RECEPTOR NR1 SUBUNIT; PROTEIN-KINASE-A; NMDA-RECEPTOR; NEUROPATHIC PAIN; CYTOKINE EXPRESSION; INTRACEREBROVENTRICULAR INJECTION;
D O I
10.1016/j.brainresrev.2008.12.020
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The cytokine cascade in pain and inflammatory processes is a tremendously complex system, involving glial, immune, and neuronal cell interactions. IL-1 beta is a pro-inflammatory cytokine that has been implicated in pain, inflammation and autoimmune conditions. This review will focus on studies that shed light on the critical role of IL-1 beta in various pain states, including the role of the intracellular complex, the inflammasome, which regulates IL-1 beta production. Evidence will be presented demonstrating the importance of IL-1 beta in both the induction of pain and in the maintenance of pain in chronic states, such as after nerve injury. Additionally, the involvement of IL-1 beta, as a key mediator in the interaction between glia and neurons in pain states will be discussed. Taken together, the evidence presented in the current review showing the importance of IL-1 beta, in animal and human pain states, suggests that blockade of IL-1 beta be considered as a therapeutic opportunity. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 64
页数:8
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