Hyperalgesia and allodynia: peripheral mechanisms

被引:120
作者
Coutaux, A
Adam, F
Willer, JC
Le Bars, D
机构
[1] Pitie Salpetriere Sch Med, INSERM E 0349, Res Unit, F-75013 Paris, France
[2] Pitie Salpetriere Sch Med, Neurophysiol Lab, F-75013 Paris, France
[3] Teaching Hosp, F-75013 Paris, France
[4] Pitie Salpetriere Teaching Hosp, Dept Rheumatol, F-75013 Paris, France
[5] Pitie Salpetriere Sch Med, INSERM E 0331, Res Unit, F-75013 Paris, France
[6] Ambroise Pare Teaching Hosp, Anaesthesia & Intens Care Unit, F-92100 Boulogne, France
关键词
nociceptors; pain; hyperalgesia; allodynia; inflammation;
D O I
10.1016/j.jbspin.2004.01.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nociceptive signals are generated by peripheral sensory organs called nociceptors, which are endings of small-diameter nerve fibers responsive to the tissue environment. The myriad chemical mediators capable of activating, sensitizing, or arousing nociceptors include kinins, proinflammatory and anti-inflammatory cytokines, prostanoids, lipooxygenases, the "central immune response mediator" NF-kappa B, neurotrophins and other growth factors, neuropeptides, nitric oxide, histamine, serotonin, proteases, excitatory amino acids, adrenergic amines, and opioids. These mediators may act in combination or at a given time in the inflammatory process, producing subtle changes that result in hyperalgesia or allodynia. We will review the most extensively studied molecular and cellular mechanisms underlying these two clinical abnormalities. The role of the peripheral nervous system in progression of inflammatory joint disease to chronicity is discussed. (c) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:359 / 371
页数:13
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