Mode of action of cytokines on nociceptive neurons

被引:139
作者
Ueceyler, Nurcan [1 ]
Schaefers, Maria [2 ]
Sommer, Claudia [1 ]
机构
[1] Univ Wurzburg, Dept Neurol, D-97080 Wurzburg, Germany
[2] Univ Duisburg Essen, Dept Neurol, D-45122 Essen, Germany
关键词
Pro-inflammatory cytokines; Anti-inflammatory cytokines; Ion channels; MAP kinases; Prostaglandins; Neuropeptides; TUMOR-NECROSIS-FACTOR; DORSAL-ROOT GANGLION; REGIONAL-PAIN-SYNDROME; GENE-RELATED PEPTIDE; RAT SENSORY NEURONS; PROTEIN-KINASE-C; GLUTAMATE TRANSPORTER GLAST; LONG-TERM POTENTIATION; TNF-ALPHA EXPRESSION; MU-OPIOID RECEPTORS;
D O I
10.1007/s00221-009-1755-z
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Cytokines are pluripotent soluble proteins secreted by immune and glial cells and are key elements in the induction and maintenance of pain. They are categorized as pro-inflammatory cytokines, which are mostly algesic, and anti-inflammatory cytokines, which have analgesic properties. Progress has been made in understanding the mechanisms underlying the action of cytokines in pain. To date, several direct and indirect pathways are known that link cytokines with nociception or hyperalgesia. Cytokines may act via specific cytokine receptors inducing downstream signal transduction cascades, which then modulate the function of other receptors like the ionotropic glutamate receptor, the transient vanilloid receptors, or sodium channels. This receptor activation, either through amplification of the inflammatory reaction, or through direct modulation of ion channel currents, then results in pain sensation. Following up on results from animal experiments, cytokine profiles have recently been investigated in human pain states. An imbalance of pro- and anti-inflammatory cytokine expression may be of importance for individual pain susceptibility. Individual cytokine profiles may be of diagnostic importance in chronic pain states, and, in the future, might guide the choice of treatment.
引用
收藏
页码:67 / 78
页数:12
相关论文
共 156 条
[1]
Changes in cerebrospinal fluid levels of pro-inflammatory cytokines in CRPS [J].
Alexander, GM ;
van Rijn, MA ;
van Hilten, JJ ;
Perreault, MJ ;
Schwartzman, RJ .
PAIN, 2005, 116 (03) :213-219
[2]
Changes in immune and glial markers in the CSF of patients with Complex Regional Pain Syndrome [J].
Alexander, Guillermo M. ;
Perreault, Marielle J. ;
Reichenberger, Erin R. ;
Schwartzman, Robert J. .
BRAIN BEHAVIOR AND IMMUNITY, 2007, 21 (05) :668-676
[3]
Allen BJ, 1997, J NEUROSCI, V17, P5921
[4]
The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[5]
Control of synaptic strength by glial TNFα [J].
Beattie, EC ;
Stellwagen, D ;
Morishita, W ;
Bresnahan, JC ;
Ha, BK ;
Von Zastrow, M ;
Beattie, MS ;
Malenka, RC .
SCIENCE, 2002, 295 (5563) :2282-2285
[6]
Successful intravenous regional block with low-dose tumor necrosis factor-α antibody infliximab for treatment of complex regional pain syndrome 1 [J].
Bernateck, Michael ;
Rolke, Roman ;
Birklein, Frank ;
Treede, Rolf-Detlef ;
Fink, Matthias ;
Karst, Matthias .
ANESTHESIA AND ANALGESIA, 2007, 105 (04) :1148-1151
[7]
The important role of neuropeptides in complex regional pain syndrome [J].
Birklein, F ;
Schmelz, M ;
Schifter, S ;
Weber, M .
NEUROLOGY, 2001, 57 (12) :2179-2184
[8]
STAT6 transcription factor binding sites with mismatches within the canonical 5'-TTC...GAA-3' motif involved in regulation of δ- and μ-opioid receptors [J].
Börner, C ;
Wöltje, M ;
Höllt, V ;
Kraus, J .
JOURNAL OF NEUROCHEMISTRY, 2004, 91 (06) :1493-1500
[9]
Kinins in pain and inflammation [J].
Calixto, JB ;
Cabrini, DA ;
Ferreira, J ;
Campos, MM .
PAIN, 2000, 87 (01) :1-5
[10]
Primary afferent tachykinins are required to experience moderate to intense pain [J].
Cao, YQ ;
Mantyh, PW ;
Carlson, EJ ;
Gillespie, AM ;
Epstein, CJH ;
Basbaum, AI .
NATURE, 1998, 392 (6674) :390-394