CIRCUITRY AND PLASTICITY OF THE DORSAL HORN - TOWARD A BETTER UNDERSTANDING OF NEUROPATHIC PAIN

被引:79
作者
West, S. J. [1 ]
Bannister, K. [2 ]
Dickenson, A. H. [2 ]
Bennett, D. L. [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Neural Injury Grp, Oxford OX3 9DU, England
[2] UCL, Dept Neurosci Pharmacol & Physiol, London WC1E 6BT, England
基金
英国惠康基金;
关键词
neuropathic pain; plasticity; dorsal horn; descending control; primary afferent; RAT SPINAL-CORD; ROSTRAL VENTROMEDIAL MEDULLA; PERIPHERAL-NERVE INJURY; LONG-TERM POTENTIATION; CHRONIC CONSTRICTION INJURY; QUALITY-OF-LIFE; LAMINAE-I-III; VASOACTIVE INTESTINAL POLYPEPTIDE; SUBSTANCE-P RECEPTOR; METHYL-D-ASPARTATE;
D O I
10.1016/j.neuroscience.2015.05.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Maladaptive plasticity within the dorsal horn (DH) of the spinal cord is a key substrate for development of neuropathic pain following peripheral nerve injury. Advances in genetic engineering, tracing techniques and opto-genetics are leading to a much better understanding of the complex circuitry of the spinal DH and the radical changes evoked in such circuitry by nerve injury. These changes can be viewed at multiple levels including: synaptic remodeling including enhanced excitatory and reduced inhibitory drive, morphological and electrophysiological changes which are observed both to primary afferent inputs as well as DH neurons, and ultimately circuit-level rewiring which leads to altered connectivity and aberrant processing of sensory inputs in the DH. The DH should not be seen in isolation but is subject to important descending modulation from the brainstem, which is further dysregulated by nerve injury. Understanding which changes relate to specific disease-states is essential, and recent work has aimed to stratify patient populations in a mechanistic fashion. In this review we will discuss how such pathophysiological mechanisms may lead to the distressing sensory phenomena experienced by patients suffering neuropathic pain, and the relationship of such mechanisms to current and potential future treatment modalities. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:254 / 275
页数:22
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