The transition from acute to chronic pain: understanding how different biological systems interact

被引:0
作者
Mifflin, Katherine A. [1 ]
Kerr, Bradley J. [1 ,2 ,3 ]
机构
[1] Univ Alberta, Ctr Neurosci, Edmonton, AB, Canada
[2] Univ Alberta, Dept Anesthesiol & Pain Med, Edmonton, AB T6G 2G3, Canada
[3] Univ Alberta, Dept Pharmacol, Edmonton, AB, Canada
来源
CANADIAN JOURNAL OF ANESTHESIA-JOURNAL CANADIEN D ANESTHESIE | 2014年 / 61卷 / 02期
关键词
MONOCYTE CHEMOATTRACTANT PROTEIN-1; PERIPHERAL-NERVE INJURY; PRIMARY SENSORY NEURONS; LONG-LASTING ALLODYNIA; DORSAL-ROOT GANGLIA; SPINAL-CORD-INJURY; NMDA-RECEPTOR; NEUROPATHIC PAIN; SEX-DIFFERENCES; NITRIC-OXIDE;
D O I
暂无
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Although pain is an adaptive sensory experience necessary to prevent further bodily harm, the transition from acute to chronic pain is not adaptive and results in the development of a chronic clinical condition. How this transition occurs has been the focus of intense study for some time. The focus of the current review is on changes in neuronal plasticity as well as the role of immune cells and glia in the development of chronic pain from acute tissue injury and pain. Our understanding of the complex pathways that mediate the transition from acute to chronic pain continues to increase. Work in this area has already revealed the complex interactions between the nervous and immune system that result in both peripheral and central sensitization, essential components to the development of chronic pain. Taken together, a thorough characterization of the cellular mechanisms that generate chronic pain states is essential for the development of new therapies and treatments. Basic research leading to the development of new therapeutic targets is promising with the development of chloride extrusion enhancers. It is hoped that one day they will provide relief to patients with chronic pain. A better understanding of how chronic pain develops at a mechanistic level can aid clinicians in treating their patients by showing how the underlying biology of chronic pain contributes to the clinical manifestations of pain. A thorough understanding of how chronic pain develops may also help identify new targets for future analgesic drugs.
引用
收藏
页码:112 / 122
页数:11
相关论文
共 97 条
[81]   Fractakine (CX3CL1) and fractakine receptor (CX3CR1) distribution in spinal cord and dorsal root ganglia under basal and neuropathic pain conditions [J].
Verge, GM ;
Milligan, ED ;
Maier, SF ;
Watkins, LR ;
Naevel, GS ;
Foster, AC .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2004, 20 (05) :1150-1160
[82]   Estrous cycle modulation of nociceptive behaviors elicited by electrical stimulation and formalin [J].
Vincler, M ;
Maixner, W ;
Vierck, CJ ;
Light, AR .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2001, 69 (3-4) :315-324
[83]  
Viviani B, 2003, J NEUROSCI, V23, P8692
[84]   TRPV1 is important for mechanical and heat sensitivity in uninjured animals and development of heat hypersensitivity after muscle inflammation [J].
Walder, Roxanne Y. ;
Radhakrishnan, Rajan ;
Loo, Lipin ;
Rasmussen, Lynn A. ;
Mohapatra, Durga P. ;
Wilson, Steven P. ;
Sluka, Kathleen A. .
PAIN, 2012, 153 (08) :1664-1672
[85]   Excitatory monocyte chemoattractant protein-1 signaling is up-regulated in sensory neurons after chronic compression of the dorsal root ganglion [J].
White, FA ;
Sun, JH ;
Waters, SM ;
Ma, C ;
Ren, DJ ;
Ripsch, M ;
Steflik, J ;
Cortright, DN ;
LaMotte, RH ;
Miller, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) :14092-14097
[86]  
White R J, 2009, J Wound Care, V18, P245
[87]  
Willis WD, 2001, ANN NY ACAD SCI, V933, P142
[88]  
WOOLF CJ, 1986, J NEUROSCI, V6, P1433
[89]  
WOOLF CJ, 1990, J NEUROSCI, V10, P2717
[90]   EVIDENCE FOR A CENTRAL COMPONENT OF POST-INJURY PAIN HYPERSENSITIVITY [J].
WOOLF, CJ .
NATURE, 1983, 306 (5944) :686-688