Neuropathic Pain: A Maladaptive Response of the Nervous System to Damage

被引:1448
作者
Costigan, Michael [1 ]
Scholz, Joachim
Woolf, Clifford J.
机构
[1] Massachusetts Gen Hosp, Neural Plast Res Grp, Dept Anesthesia & Crit Care, Boston, MA 02129 USA
关键词
neural plasticity; synaptic facilitation; disinhibition; neuroimmune interaction; pain phenotype; SPINAL DORSAL-HORN; CHRONIC CONSTRICTION INJURY; PRIMARY SENSORY NEURONS; GATED SODIUM-CHANNELS; ROOT GANGLION NEURONS; SUBSTANTIA-GELATINOSA NEURONS; PERIPHERAL-NERVE; CENTRAL SENSITIZATION; SCIATIC-NERVE; UP-REGULATION;
D O I
10.1146/annurev.neuro.051508.135531
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Neuropathic pain is triggered by lesions to the somatosensory, nervous system that alter its structure and function so that pain occurs spontaneously and responses to noxious and innocuous stimuli are pathologically amplified. The pain is an expression of maladaptive plasticity within the nociceptive system, a series of changes that constitute a neural disease state. Multiple alterations distributed widely across the nervous system contribute to complex pain phenotypes. These alterations include ectopic generation of action potentials, facilitation and disinhibition of synaptic transmission, loss of synaptic connectivity and formation of new synaptic circuits, and neuroimmune interactions. Although neural lesions are necessary, they are not sufficient to generate neuropathic pain; genetic polymorphisms, gender, and age all influence the risk of developing persistent pain. Treatment needs to move from merely Suppressing symptoms to a disease-modifying strategy aimed at both preventing maladaptive plasticity and reducing intrinsic risk.
引用
收藏
页码:1 / 32
页数:32
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