Ionotropic glutamate receptors contribute to pain transmission and chronic pain

被引:100
作者
Zhuo, Min [1 ,2 ,3 ]
机构
[1] Univ Toronto, Dept Physiol, Fac Med, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Ctr Study Pain, Toronto, ON M5S 1A8, Canada
[3] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Ctr Neuron & Dis, Xian 710049, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
ANTERIOR CINGULATE CORTEX; LONG-TERM-POTENTIATION; MAMMALIAN SPINAL-CORD; SENSORY SYNAPTIC-TRANSMISSION; PRESYNAPTIC NMDA RECEPTORS; DORSAL HORN NEURONS; NEUROPATHIC PAIN; KAINATE RECEPTORS; INSULAR CORTEX; AMPA RECEPTOR;
D O I
10.1016/j.neuropharm.2016.08.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Investigation of the synaptic mechanisms for sensory transmission and modulation provide us with critical information about the transmission of painful sensation as well as the basic mechanisms of chronic pain. Recent studies consistently demonstrate that glutamatergic synapses not only play an important role in sensory transmission, including pain and itch transmission, but also contribute to nociceptive sensitization at different levels of the brain. Different subtypes of glutamate receptors play selective roles in synaptic transmission and long-term potentiation (LTP), as well as synaptic modulation. Understanding the contribution of each subtype of glutamate receptors, and related downstream signaling pathways may provide a new opportunity to design better medicine for the treatment of different forms of chronic pain. This article is part of the Special Issue entitled 'Ionotropic glutamate receptors'. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:228 / 234
页数:7
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