Increased WDR spontaneous activity and receptive field size in rats following a neuropathic or inflammatory injury: implications for mechanical sensitivity

被引:36
作者
Chu, KL [1 ]
Faltynek, CR [1 ]
Jarvis, MF [1 ]
McGaraughty, S [1 ]
机构
[1] Abbott Labs, Global Pharmaceut Res & Dev, Neurosci Res, Abbott Pk, IL 60064 USA
关键词
allodynia; wide dynamic range; neuropathic; inflammation; spontaneous activity; receptive field; dorsal horn neuron;
D O I
10.1016/j.neulet.2004.09.025
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Spontaneous activity and receptive field size for spinal wide dynamic range (WDR) neurons were measured and related to the mechanical allodynia in both neuropathic (L5-L6 ligation, 14 days post-injury) and complete Freund's adjuvant-inflamed rats (CFA, 2 days post-injury). The size of the WDR receptive field located on the hindpaw expanded significantly (p < 0.01) following both modes of injury, with no difference between CFA and neuropathic animals. Likewise, the spontaneous firing of WDR neurons was significantly elevated following both the CFA (4.4 +/- 0.6 spikes/s, p < 0.01) and neuropathic (3.2 +/- 0.3 spikes/s, p < 0.05) injuries compared to naive (2.1 +/- 0.2 spikes/s) and sham-neuropathic (1.9 +/- 0.3 spikes/s) rats. Furthermore, the spontaneous WDR activity recorded from CFA rats was also significantly greater (p < 0.05) than neuropathic rats. Mechanical allodynia, as measured by application of a von Frey hair stimulus, was observed from both CFA and neuropathic rats, however, the degree of sensitivity was significantly greater (p < 0.01) for the CFA animals. These data suggest that the differences in mechanical sensitivity between CFA and neuropathic rats may be related to their respective changes in WDR spontaneous activity, but not to the changes in receptive field size, and is further demonstration of the importance of spontaneous WDR activity in determining mechanical sensitivity following injury. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:123 / 126
页数:4
相关论文
共 28 条
[1]   PARTIAL SCIATIC-NERVE LIGATION RESULTS IN AN ENLARGEMENT OF THE RECEPTIVE-FIELD AND ENHANCEMENT OF THE RESPONSE OF DORSAL HORN NEURONS TO NOXIOUS-STIMULATION BY AN ADENOSINE AGONIST [J].
BEHBEHANI, MM ;
DOLLBERGSTOLIK, O .
PAIN, 1994, 58 (03) :421-428
[2]   Anti-allodynic action of the tormentic acid, a triterpene isolated from plant, against neuropathic and inflammatory persistent pain in mice [J].
Bortalanza, LB ;
Ferreira, J ;
Hess, SC ;
Delle Monache, F ;
Yunes, RA ;
Calixto, JB .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2002, 453 (2-3) :203-208
[3]   Electrophysiological characterization of spinal neuronal response properties in anaesthetized rats after ligation of spinal nerves L5-L6 [J].
Chapman, V ;
Suzuki, R ;
Dickenson, AH .
JOURNAL OF PHYSIOLOGY-LONDON, 1998, 507 (03) :881-894
[4]  
DUBNER R, 1991, P 6 WORLD C PAIN, P264
[5]   PAINFUL NEUROPATHY - ALTERED CENTRAL PROCESSING MAINTAINED DYNAMICALLY BY PERIPHERAL INPUT [J].
GRACELY, RH ;
LYNCH, SA ;
BENNETT, GJ .
PAIN, 1992, 51 (02) :175-194
[6]  
Hoheisel U, 1997, Eur J Pain, V1, P243, DOI 10.1016/S1090-3801(97)90034-3
[7]   EXPANSION OF RECEPTIVE-FIELDS OF SPINAL LAMINA-I PROJECTION NEURONS IN RATS WITH UNILATERAL ADJUVANT-INDUCED INFLAMMATION - THE CONTRIBUTION OF DORSAL HORN MECHANISMS [J].
HYLDEN, JLK ;
NAHIN, RL ;
TRAUB, RJ ;
DUBNER, R .
PAIN, 1989, 37 (02) :229-243
[8]   Molecular mechanisms of nociception [J].
Julius, D ;
Basbaum, AI .
NATURE, 2001, 413 (6852) :203-210
[9]  
KIM SH, 1992, PAIN, V50, P355, DOI 10.1016/0304-3959(92)90041-9
[10]   AN ELECTROPHYSIOLOGICAL STUDY OF DORSAL HORN NEURONS IN THE SPINAL-CORD OF RATS WITH AN EXPERIMENTAL PERIPHERAL NEUROPATHY [J].
LAIRD, JMA ;
BENNETT, GJ .
JOURNAL OF NEUROPHYSIOLOGY, 1993, 69 (06) :2072-2085