Advances in understanding nociception and neuropathic pain

被引:221
作者
Smith, Ewan St. John [1 ]
机构
[1] Univ Cambridge, Dept Pharmacol, Tennis Court Rd, Cambridge CB2 1PD, England
关键词
Chemogenetics; Neurocircuitry; Neuropathic pain; Nociceptor; Optogenetics; Voltage gated sodium channel (NaV); PERIPHERAL-NERVE INJURY; SODIUM-CHANNEL NA(V)1.9; ION CHANNELS; SENSORY PROFILES; TOUCH SENSATION; SCN9A MUTATIONS; ANION GRADIENT; ANIMAL-MODELS; UNITED-STATES; NEURON TYPES;
D O I
10.1007/s00415-017-8641-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Pain results from the activation of a subset of sensory neurones termed nociceptors and has evolved as a "detect and protect" mechanism. However, lesion or disease in the sensory system can result in neuropathic pain, which serves no protective function. Understanding how the sensory nervous system works and what changes occur in neuropathic pain are vital in identifying new therapeutic targets and developing novel analgesics. In recent years, technologies such as optogenetics and RNA-sequencing have been developed, which alongside the more traditional use of animal neuropathic pain models and insights from genetic variations in humans have enabled significant advances to be made in the mechanistic understanding of neuropathic pain.
引用
收藏
页码:231 / 238
页数:8
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