Involvement of spinal N-methyl-D-aspartate receptors in capsaicin-induced in vivo release of substance P in the rat dorsal horn

被引:38
作者
Afrah, AW [1 ]
Stiller, CO
Olgart, L
Brodin, E
Gustafsson, H
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, Div Pharmacol Pain Res, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Karolinska Hosp, Dept Med, Div Clin Pharmacol, S-10401 Stockholm, Sweden
关键词
substance P; capsaicin; glutamate; spinal cord; microdialysis; pain; radioimmunoassay;
D O I
10.1016/S0304-3940(01)02380-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The aim of the present in vivo microdialysis study was to determine the possible contribution of N-methyl-D-aspartate (NMDA) or alpha -amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA)/kainate (KA) receptors to capsaicin-induced release of substance P-like immunoreactivity (SP-LI) in the dorsal horn of the rat. Perfusion of a microdialysis probe with capsaicin (50 or 100 muM) induced a significant eight-fold increase of the extracellular SP-LI level. The capsaicin (50 LM)evoked release of SP-LI was blocked by spinal administration of the NMDA antagonist 2-amino-5-phosphonopentanoic acid (D-APV; 5 mM), but not by the AMPA/KA antagonist 6-vitro-7-sulphamoylbenzo[f]quinoxaline-2,3-dione disodium (NBQX; 0.5 mM). In contrast, the SP-LI release induced by 100 muM capsaicin could not be prevented by D-APV (10 mM) or NBQX (0.5 mM). The data suggest that the spinal SP-LI release induced by a moderate concentration of capsaicin is in part dependent on the release of glutamate acting on NMDA receptors. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:83 / 86
页数:4
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