Alarm or curse? The pain of neuroinflammation

被引:38
作者
Saab, Carl Y. [1 ,2 ]
Waxman, Stephen G. [3 ,4 ,5 ]
Hains, Bryan C. [3 ,4 ,5 ]
机构
[1] Brown Univ, Rhode Isl Hosp, Brown Med Sch, Dept Surg, Providence, RI 02903 USA
[2] Brown Univ, Dept Neurosci, Providence, RI 02903 USA
[3] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06510 USA
[4] Yale Univ, Sch Med, Ctr Neurosci & Regenerat Res, New Haven, CT 06510 USA
[5] VA Connecticut Healthcare Syst, Rehabil Res Ctr, West Haven, CT 06516 USA
关键词
neurotrauma; pain; neutrophil; microglia; neuroimmune;
D O I
10.1016/j.brainresrev.2008.04.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The nociceptive nervous system and the immune system serve to defend and alarm the host of imminent or actual damage. However, persistent or recurring exposure of neurons to activated immune cells is associated with an increase in painful behavior following experimental neuropathic injuries. our understanding of the functional consequences of immune cell-neuron interaction is still incomplete. The purpose of this review is to focus on a seriously detrimental consequence of chronic activation of these two systems, by discussing the contributions of microglia and polymorphonuclear neutrophils to neuropathic pain following experimental spinal cord injury or peripheral nerve injury. Identification of molecules mediating pro-nociceptive signaling between immune cells and neurons, as well as the distinction between neuroprotective versus neuroexcitatory effects of activated immune cells, may be useful in the development of pharmacotherapy for the management of chronic pain and restoration of the beneficial alarm function of pain. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:226 / 235
页数:10
相关论文
共 136 条
[1]  
[Anonymous], 1990, MANAGEMENT PAIN
[2]   CLINICAL MANAGEMENT OF CHRONIC PAIN IN SPINAL-CORD INJURY [J].
BALAZY, TE .
CLINICAL JOURNAL OF PAIN, 1992, 8 (02) :102-110
[3]  
Bandtlow CE, 2000, GLIA, V29, P175, DOI 10.1002/(SICI)1098-1136(20000115)29:2<175::AID-GLIA11>3.0.CO
[4]  
2-F
[5]   Nerve growth factor induced hyperalgesia in the rat hind paw is dependent on circulating neutrophils [J].
Bennett, G ;
al-Rashed, S ;
Hoult, JRS ;
Brain, SD .
PAIN, 1998, 77 (03) :315-322
[6]   Does a neuroimmune interaction contribute to the genesis of painful peripheral neuropathies? [J].
Bennett, GJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (14) :7737-7738
[7]   Targeting the host inflammatory response in traumatic spinal cord injury [J].
Bethea, JR ;
Dietrich, WD .
CURRENT OPINION IN NEUROLOGY, 2002, 15 (03) :355-360
[8]   Control of inflammatory pain by chemokine-mediated recruitment of opioid-containing polymorphonuclear cells [J].
Brack, A ;
Rittner, HL ;
Machelska, H ;
Leder, K ;
Mousa, SA ;
Schäfer, M ;
Stein, C .
PAIN, 2004, 112 (03) :229-238
[9]   CNS-infiltrating CD4+ T lymphocytes contribute to murine spinal nerve transection-induced neuropathic pain [J].
Cao, Ling ;
DeLeo, Joyce A. .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2008, 38 (02) :448-458
[10]   Infiltrative microgliosis: activation and long-distance migration of subependymal microglia following periventricular insults [J].
Carbonell, W. Shawn ;
Murase, Shin-Ichi ;
Horwitz, Alan F. ;
Mandell, James W. .
JOURNAL OF NEUROINFLAMMATION, 2005, 2 (1)