NMDA receptor involvement in neuroplastic changes induced by neonatal capsaicin treatment in trigeminal nociceptive neurons

被引:39
作者
Chiang, CY [1 ]
Hu, JW [1 ]
Sessle, BJ [1 ]
机构
[1] UNIV TORONTO, FAC DENT, TORONTO, ON M5G 1G6, CANADA
关键词
D O I
10.1152/jn.1997.78.5.2799
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study examines whether I) the neonatal loss of C-fiber afferents results in neuroplastic changes in the mechanoreceptive field (RF) properties and spontaneous activity of nociceptive neurons in trigeminal subnucleus caudalis (medullary dorsal horn) of adult rats, and that 2) N-methyl-D-aspartic acid (NMDA) receptor mechanisms are involved in these neuroplastic changes. Compared with vehicle-treated (i.e., control, CON) rats, capsaicin-treated (CAP) rats showed a marked increase in neuronal spontaneous activity and RF size per se, but these neuroplastic changes could be significantly reduced by MK-801 (1 mg/kg, iv), a noncompetitive NMDA receptor antagonist; RF size and spontaneous activity remained unchanged in CON rats after MK-801 administration and in CAP rats after vehicle (saline, iv). Administration of 7-chlorokynurenic acid intrathecally (5 mu g/10 mu l), an antagonist of strychnine-insensitive glycine binding sites on the NMDA receptor, also significantly reduced neuronal RF size and spontaneous activity in CAP rats, but not in CON rats. These data provide evidence that C-fiber afferents play a role in shaping the properties of nociceptive neurons and that the neuroplastic changes involve NMDA receptor mechanisms.
引用
收藏
页码:2799 / 2803
页数:5
相关论文
共 32 条
[1]  
BUCK SH, 1986, PHARMACOL REV, V38, P179
[2]   PROTEIN-KINASE-C REDUCES MG2+ BLOCK OF NMDA-RECEPTOR CHANNELS AS A MECHANISM OF MODULATION [J].
CHEN, L ;
HUANG, LYM .
NATURE, 1992, 356 (6369) :521-523
[3]  
Chiang C. Y., 1995, Society for Neuroscience Abstracts, V21, P647
[4]   PARABRACHIAL AREA AND NUCLEUS RAPHE MAGNUS-INDUCED MODULATION OF NOCICEPTIVE AND NONNOCICEPTIVE TRIGEMINAL SUBNUCLEUS CAUDALIS NEURONS ACTIVATED BY CUTANEOUS OR DEEP INPUTS [J].
CHIANG, CY ;
HU, JW ;
SESSLE, BJ .
JOURNAL OF NEUROPHYSIOLOGY, 1994, 71 (06) :2430-2445
[5]  
Dingledine R., 1990, EXCITATORY AMINO ACI, P17, DOI 10. 1007/978-1-4684-5769-8_3
[6]  
Dubner R, 1994, TXB PAIN, P225
[7]   CAPSAICIN AND SENSORY NEURONS - A REVIEW [J].
FITZGERALD, M .
PAIN, 1983, 15 (02) :109-130
[8]   DECREASE OF SUBSTANCE-P IN PRIMARY AFFERENT NEURONS AND IMPAIRMENT OF NEUROGENIC PLASMA EXTRAVASATION BY CAPSAICIN [J].
GAMSE, R ;
HOLZER, P ;
LEMBECK, F .
BRITISH JOURNAL OF PHARMACOLOGY, 1980, 68 (02) :207-213
[9]   DEVELOPMENTAL ALTERATIONS IN NOCICEPTIVE THRESHOLD, IMMUNOREACTIVE CALCITONIN GENE-RELATED PEPTIDE AND SUBSTANCE-P, AND FLUORIDE-RESISTANT ACID-PHOSPHATASE IN NEONATALLY CAPSAICIN-TREATED RATS [J].
HAMMOND, DL ;
RUDA, MA .
JOURNAL OF COMPARATIVE NEUROLOGY, 1991, 312 (03) :436-450
[10]  
HOLZER P, 1991, PHARMACOL REV, V43, P143