Identifying functional populations among the interneurons in laminae I-III of the spinal dorsal horn

被引:143
作者
Todd, Andrew J. [1 ]
机构
[1] Univ Glasgow, Coll Med Vet & Life Sci, Inst Neurosci & Psychol, Glasgow G12 8QQ, Lanark, Scotland
来源
MOLECULAR PAIN | 2017年 / 13卷
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
Itch; neuropeptide; pain; spinal cord; SUBSTANTIA-GELATINOSA NEURONS; GASTRIN-RELEASING-PEPTIDE; NEUROKININ; RECEPTOR; GREEN FLUORESCENT PROTEIN; PRIMARY AFFERENT NEURONS; NITRIC-OXIDE SYNTHASE; ROOT GANGLION NEURONS; CALCIUM-BINDING PROTEINS; PRIMARY SENSORY NEURONS; LOCAL-CIRCUIT NEURONS;
D O I
10.1177/1744806917693003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The spinal dorsal horn receives input from primary afferent axons, which terminate in a modality-specific fashion in different laminae. The incoming somatosensory information is processed through complex synaptic circuits involving excitatory and inhibitory interneurons, before being transmitted to the brain via projection neurons for conscious perception. The dorsal horn is important, firstly because changes in this region contribute to chronic pain states, and secondly because it contains potential targets for the development of new treatments for pain. However, at present, we have only a limited understanding of the neuronal circuitry within this region, and this is largely because of the difficulty in defining functional populations among the excitatory and inhibitory interneurons. The recent discovery of specific neurochemically defined interneuron populations, together with the development of molecular genetic techniques for altering neuronal function in vivo, are resulting in a dramatic improvement in our understanding of somatosensory processing at the spinal level.
引用
收藏
页码:1 / 19
页数:19
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