Interactions between glutamate and capsaicin in inducing muscle pain and sensitization in humans

被引:29
作者
Arendt-Nielsen, L. [1 ]
Svensson, P. [1 ,2 ]
Sessle, B. J. [3 ]
Cairns, B. E. [4 ]
Wang, K. [1 ]
机构
[1] Univ Aalborg, Orofacial Pain Lab, Ctr Sensory Motor Interact, DK-9220 Aalborg, Denmark
[2] Univ Aarhus, Sch Dent, Dept Clin Oral Physiol, DK-8000 Aarhus C, Denmark
[3] Univ Toronto, Fac Dent, Toronto, ON M5G 1G6, Canada
[4] Univ British Columbia, Fac Pharmaceut Sci, Vancouver, BC V6T 1Z3, Canada
关键词
sensory physiology; trigeminal pain; allodynia; human experimental pain models;
D O I
10.1016/j.ejpain.2007.10.013
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The aim of the study was to investigate the interaction between glutamate and capsaicin in inducing muscle pain and sensitization in humans. Fifteen male volunteers participated. Glutamate or capsaicin or isotonic saline, in a paired-sequence order, was injected randomly into the right or left masseter muscle. Two injections were given in a double-blinded design 25 min apart in 1 session/week over 4 weeks: saline (A1) followed by glutamate (A2), capsaicin (B1) followed by glutamate (132), saline (C1) followed by capsaicin (C2), and glutamate (D1) followed by capsaicin (B2). The subjects drew the area of perceived pain and scored pain intensity on a 0-10 visual analogue scale (VAS). Pressure pain threshold (PPT) at the injection site, at a site 2-cm away, and on the contralateral side, as well as pressure pain tolerance (PPTol) at the injection site and contralateral site, were also measured before and after injection and subsequently at 5-min intervals. Paired t-test analyses showed that the pain drawing area was significantly smaller in the B2 compared to the A2 condition (P = 0.028), and significantly larger in the D2 compared to the C2 condition (P = 0.027). It also revealed significantly lower VAS peak pain intensity (P = 0.008) and smaller VAS area under the curve (P = 0.003) for the B2 compared to the A2 condition, and significantly higher VAS peak pain (P = 0.015) and larger VAS area under the curve (P = 0.037) for the D2 compared to the C2 condition. There was a significant PPT and PPTol decrease at the injection site after glutamate or capsaicin injection (ANOVA: P < 0.028). The percentage decrease in PPT or PPTol (at the injection site) was not significantly different for the B2 compared to the A2 condition (Paired t-test: P > 0.682) or for the D2 compared to the C2 condition (P > 0.133). Significant PPT changes were also observed at the site 2 cm away, but not on the contralateral side. In conclusion, these findings indicate that intramuscular administrations of glutamate and capsaicin interact and influence pain and sensitization of muscle nociceptors: glutamate causes a sensitization to subsequent administration of capsaicin, whereas capsaicin is associated with a desensitization to subsequent injection of glutamate. These findings support previous animal data. (C) 2007 European Federation of Chapters of the International Association for the Study of Pain. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:661 / 670
页数:10
相关论文
共 48 条
[1]   In vivo microdialysis and immunohistochemical analyses of tendon tissue demonstrated high amounts of free glutamate and glutamate NMDAR1 receptors, but no signs of inflammation, in Jumper's knee [J].
Alfredson, H ;
Forsgren, S ;
Thorsen, K ;
Lorentzon, R .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2001, 19 (05) :881-886
[2]  
Arima T, 2000, J OROFAC PAIN, V14, P213
[3]  
Balla Z, 2001, Acta Physiol Hung, V88, P173, DOI 10.1556/APhysiol.88.2001.3-4.1
[4]   NEUROGENIC HYPERALGESIA - THE SEARCH FOR THE PRIMARY CUTANEOUS AFFERENT-FIBERS THAT CONTRIBUTE TO CAPSAICIN-INDUCED PAIN AND HYPERALGESIA [J].
BAUMANN, TK ;
SIMONE, DA ;
SHAIN, CN ;
LAMOTTE, RH .
JOURNAL OF NEUROPHYSIOLOGY, 1991, 66 (01) :212-227
[5]   Influence of sex on reflex jaw muscle activity evoked from the rat temporomandibular joint [J].
Cairns, BE ;
Sim, Y ;
Bereiter, DA ;
Sessle, BJ ;
Hu, JW .
BRAIN RESEARCH, 2002, 957 (02) :338-344
[6]   Ketamine attenuates glutamate-induced mechanical sensitization of the masseter muscle in human males [J].
Cairns, BE ;
Svensson, P ;
Wang, KL ;
Castrillon, E ;
Hupfeld, S ;
Sessle, BJ ;
Arendt-Nielsen, L .
EXPERIMENTAL BRAIN RESEARCH, 2006, 169 (04) :467-472
[7]   Activation of peripheral NMDA receptors contributes to human pain and rat afferent discharges evoked by injection of glutamate into the masseter muscle [J].
Cairns, BE ;
Svensson, P ;
Wang, KL ;
Hupfeld, S ;
Graven-Nielsen, T ;
Sessle, BJ ;
Berde, CB ;
Arendt-Nielsen, L .
JOURNAL OF NEUROPHYSIOLOGY, 2003, 90 (04) :2098-2105
[8]  
Cairns BE, 2003, J OROFAC PAIN, V17, P317
[9]   Glutamate-induced sensitization of rat masseter muscle fibers [J].
Cairns, BE ;
Gambarota, G ;
Svensson, P ;
Arendt-Nielsen, L ;
Berde, CB .
NEUROSCIENCE, 2002, 109 (02) :389-399
[10]   Sex-related differences in human pain and rat afferent discharge evoked by injection of glutamate into the masseter muscle [J].
Cairns, BE ;
Hu, JW ;
Arendt-Nielsen, L ;
Sessle, BJ ;
Svensson, P .
JOURNAL OF NEUROPHYSIOLOGY, 2001, 86 (02) :782-791