Mechanical allodynia following contusion injury of the rat spinal cord is associated with loss of GABAergic inhibition in the dorsal horn

被引:131
作者
Drew, GM [1 ]
Siddall, PJ [1 ]
Duggan, AW [1 ]
机构
[1] Royal N Shore Hosp, Pain Management Res Inst, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
spinal cord injury; neuropathic pain; allodynia; GABA; inhibition; dorsal horn;
D O I
10.1016/j.pain.2004.02.007
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The present study investigated whether mechanical allodynia following contusive spinal cord injury (SCI) of the thoracic segments 12 and 13 of the rat was associated with a reduction in gamma-aminobutyric acid (GABA)ergic inhibition adjacent to the site of injury. Five to 7 days following SCI, extracellular recordings were obtained from dorsal horn neurones located 1-2 segments caudal to the injury, in non-allodynic and allodynic halothane anaesthetised rats and from comparable neurones in normal rats. To assess spinal GABAergic inhibition in the three groups of animals, spontaneous and evoked cell firing rates were recorded before, during and after microiontophoretic application of the GABA(A) receptor antagonist bicuculline. Administration of bicuculline to normal animals resulted in significant and reversible increases in the receptive field size, spontaneous firing rate, response to brushing and pinching the skin and afterdischarge activity of dorsal horn neurones, as well as decreasing paired-pulse depression of responses evoked by transcutaneous electrical stimulation. In non-allodynic SCI animals, bicuculline ejection led to significant changes in receptive field size, paired-pulse depression and responses to brush and pinch stimulation that were comparable to those observed in normal animals. By contrast, in allodynic SO animals, bicuculline ejection had little or no effect on dorsal horn neurone responses to mechanical skin stimuli and paired-pulse depression despite reliably blocking the inhibition of cell firing produced by similarly applied GABA. The demonstration of reduced GABAergic inhibition predominantly in the allodynic SO rats suggests that such a deficiency contributed to this pain-related behaviour acutely following SCI. (C) 2004 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:379 / 388
页数:10
相关论文
共 39 条
[1]   Excitatory actions of GABA during development: The nature of the nurture [J].
Ben-Ari, Y .
NATURE REVIEWS NEUROSCIENCE, 2002, 3 (09) :728-739
[2]   ACTIONS OF TRAINS AND PAIRS OF IMPULSES FROM SINGLE PRIMARY AFFERENT-FIBERS ON SINGLE SPINOCERVICAL TRACT CELLS IN CAT [J].
BROWN, AG ;
KOERBER, HR ;
NOBLE, R .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 382 :313-329
[3]   Mechanisms of touch-evoked pain (allodynia): A new model [J].
Cervero, F ;
Laird, JMA .
PAIN, 1996, 68 (01) :13-23
[4]   Effects of GABA receptor antagonist on trigeminal caudalis nociceptive neurons in normal and neonatally capsaicin-treated rats [J].
Chiang, CY ;
Kwan, CL ;
Ku, JW ;
Sessle, BJ .
JOURNAL OF NEUROPHYSIOLOGY, 1999, 82 (05) :2154-2162
[5]   Trans-synaptic shift in anion gradient in spinal lamina I neurons as a mechanism of neuropathic pain [J].
Coull, JAM ;
Boudreau, D ;
Bachand, K ;
Prescott, SA ;
Nault, F ;
Sik, A ;
De Koninck, P ;
De Koninck, Y .
NATURE, 2003, 424 (6951) :938-942
[6]   GABA, BICUCULLINE AND CENTRAL INHIBITION [J].
CURTIS, DR ;
DUGGAN, AW ;
FELIX, D ;
JOHNSTON, GA .
NATURE, 1970, 226 (5252) :1222-&
[7]  
DE KONINCK Y, 1994, J PHYSIOL-LONDON, V476, P89
[8]   Responses of spinal neurones to cutaneous and dorsal root stimuli in rats with mechanical allodynia after contusive spinal cord injury [J].
Drew, GM ;
Siddall, PJ ;
Duggan, AW .
BRAIN RESEARCH, 2001, 893 (1-2) :59-69
[9]   SUPRASPINAL INHIBITION OF THE EXCITATION OF DORSAL HORN NEURONS BY IMPULSES IN UNMYELINATED PRIMARY AFFERENTS - LACK OF EFFECT BY STRYCHNINE AND BICUCULLINE [J].
DUGGAN, AW ;
GRIERSMITH, BT ;
JOHNSON, SM .
BRAIN RESEARCH, 1981, 210 (1-2) :231-241
[10]  
GAME CJA, 1975, EXP BRAIN RES, V23, P75