Inflammation-mediated hyperexcitability of sensory neurons

被引:37
作者
Gold, MS
Flake, NM
机构
[1] Univ Maryland, Sch Dent, Dept Biomed Sci, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Program Neurosci, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Anat & Neurobiol, Baltimore, MD 21201 USA
关键词
second messenger pathway; neuroplasticity; target of innervation;
D O I
10.1159/000087653
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
One of the most prominent signs of tissue injury and inflammation is pain and pain continues to be the primary reason people seek medical attention. Inflammatory pain reflects, at least in part, an increase in the excitability, or sensitization, of subpopulations of primary afferent neurons. While the sensitization of high threshold afferents was observed almost 40 years ago, the basis for this phenomenon continues to be an active and fertile area of research today. This review will summarize recent advances in our mechanistic understanding of sensitization, focusing on four general areas where research has been most active or productive. These include: (1) the characterization of second messenger pathways underlying inflammation-induced changes in afferent excitability; (2) the impact of previous injury on the afferent response to subsequent inflammation; (3) the impact of target of innervation on the specific afferent response to inflammation, and (4) the impact of sex hormones on the sensitization of high threshold afferents. Work in these areas highlights how much has been learned about this process as well as how much there is yet to learn. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:147 / 157
页数:11
相关论文
共 116 条
[1]  
Aley KO, 1998, J NEUROSCI, V18, P7008
[2]   Chronic hypersensitivity for inflammatory nociceptor sensitization mediated by the ε isozyme of protein kinase C [J].
Aley, KO ;
Messing, RO ;
Mochly-Rosen, D ;
Levine, JD .
JOURNAL OF NEUROSCIENCE, 2000, 20 (12) :4680-4685
[3]   Nociceptor sensitization by extracellular signal-regulated kinases [J].
Aley, KO ;
Martin, A ;
McMahon, T ;
Mok, J ;
Levine, JD ;
Messing, RO .
JOURNAL OF NEUROSCIENCE, 2001, 21 (17) :6933-6939
[4]   Long-term behavioral effects of repetitive pain in neonatal rat pups [J].
Anand, KJS ;
Coskun, V ;
Thrivikraman, KV ;
Nemeroff, CB ;
Plotksy, PM .
PHYSIOLOGY & BEHAVIOR, 1999, 66 (04) :627-637
[5]   Mechanical and heat sensitization of cutaneous nociceptors after peripheral inflammation in the rat [J].
Andrew, D ;
Greenspan, JD .
JOURNAL OF NEUROPHYSIOLOGY, 1999, 82 (05) :2649-2656
[6]   Nerve growth factor evokes hyperalgesia in mice lacking the low-affinity neurotrophin receptor p75 [J].
Bergmann, I ;
Reiter, R ;
Toyka, KV ;
Koltzenburg, M .
NEUROSCIENCE LETTERS, 1998, 255 (02) :87-90
[7]   FUNCTIONAL DIFFERENCES BETWEEN AFFERENT-FIBERS IN THE HYPOGASTRIC AND PELVIC NERVES INNERVATING FEMALE REPRODUCTIVE-ORGANS IN THE RAT [J].
BERKLEY, KJ ;
ROBBINS, A ;
SATO, Y .
JOURNAL OF NEUROPHYSIOLOGY, 1993, 69 (02) :533-544
[8]   Sex differences in pain [J].
Berkley, KJ .
BEHAVIORAL AND BRAIN SCIENCES, 1997, 20 (03) :371-+
[9]  
Bevan S., 1999, TXB PAIN, P85
[10]   cAMP-dependent protein kinase regulates desensitization of the capsaicin receptor (VR1) by direct phosphorylation [J].
Bhave, G ;
Zhu, WG ;
Wang, HB ;
Brasier, DJ ;
Oxford, GS ;
Gereau, RW .
NEURON, 2002, 35 (04) :721-731