The gap junction blocker carbenoxolone attenuates nociceptive behavior and medullary dorsal horn central sensitization induced by partial infraorbital nerve transection in rats

被引:35
作者
Wang, Hua [1 ]
Cao, Ye [1 ]
Chiang, Chen-Yu [1 ]
Dostrovsky, Jonathan O. [1 ,2 ]
Sessle, Barry J. [1 ,2 ]
机构
[1] Univ Toronto, Fac Dent, Dept Oral Physiol, Toronto, ON M5G 1G6, Canada
[2] Univ Toronto, Fac Med, Dept Physiol, Toronto, ON M5G 1G6, Canada
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
Carbenoxolone; Central sensitization; Gap junction; Infraorbital nerve; Medulla; Neuropathic pain; SPINAL SUBNUCLEUS CAUDALIS; INFERIOR ALVEOLAR NERVE; NEUROPATHIC PAIN; CALCIUM WAVES; PATHOLOGICAL PAIN; ASTROCYTE CALCIUM; GLIAL ACTIVATION; NEURONS; CORD; MECHANISMS;
D O I
10.1016/j.pain.2013.11.004
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Glial cells are being increasingly implicated in mechanisms underlying pathological pain, and recent studies suggest glial gap junctions involving astrocytes may contribute. The aim of this study was to examine the effect of a gap junction blocker, carbenoxolone (CBX), on medullary dorsal horn (MDH) nociceptive neuronal properties and facial mechanical nociceptive behavior in a rat trigeminal neuropathic pain model involving partial transection of the infraorbital nerve (p-IONX). p-IONX produced facial mechanical hypersensitivity reflected in significantly reduced head withdrawal thresholds that lasted for more than 3 weeks. p-IONX also produced central sensitization in MDH nociceptive neurons that was reflected in significantly increased receptive field size, reduction of mechanical activation threshold, and increases in noxious stimulation-evoked responses. Intrathecal CBX treatment significantly attenuated the p-IONX-induced mechanical hypersensitivity and the MDH central sensitization parameters, compared to intrathecal vehicle treatment. These results provide the first documentation that gap junctions may be critically involved in orofacial neuropathic pain mechanisms. (C) 2013 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:429 / 435
页数:7
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