NEUROPATHIC PAIN: FROM MECHANISMS TO TREATMENT

被引:611
|
作者
Finnerup, Nanna Brix [1 ,2 ,3 ]
Kuner, Rohini [1 ,2 ,3 ]
Jensen, Troels Staehelin [1 ,2 ,3 ]
机构
[1] Aarhus Univ, Danish Pain Res Ctr, Dept Clin Med, Aarhus, Denmark
[2] Aarhus Univ Hosp, Dept Neurol, Aarhus, Denmark
[3] Heidelberg Univ, Dept Pharmacol, Heidelberg, Germany
基金
欧盟地平线“2020”;
关键词
allodynia; ion channels; immune cells; neuropathic pain; pharmacology; primary neuron; spinal cord circuits; SPINAL-CORD-INJURY; GENE-RELATED PEPTIDE; BRACHIAL-PLEXUS AVULSION; PLACEBO-CONTROLLED TRIAL; PERIPHERAL-NERVE INJURY; SMALL FIBER NEUROPATHY; DORSAL-HORN NEURONS; CENTRAL POSTSTROKE PAIN; ROOT GANGLION NEURONS; OF-FUNCTION MUTATION;
D O I
10.1152/physrev.00045.2019
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Neuropathic pain caused by a lesion or disease of the somatosensory nervous system is a common chronic pain condition with major impact on quality of life. Examples include trigeminal neuralgia, painful polyneuropathy, postherpetic neuralgia, and central post-stroke pain. Most patients complain of an ongoing or intermittent spontaneous pain of, for example, burning, pricking, squeezing quality, which may be accompanied by evoked pain, particular to light touch and cold. Ectopic activity in, for example, nerve-end neuroma, compressed nerves or nerve roots, dorsal root ganglia, and the thalamus may in different conditions underlie the spontaneous pain. Evoked pain may spread to neighboring areas, and the underlying pathophysiology involves peripheral and central sensitization. Maladaptive structural changes and a number of cell-cell interactions and molecular signaling underlie the sensitization of nociceptive pathways. These include alteration in ion channels, activation of immune cells, glial-derived mediators, and epigenetic regulation. The major classes of therapeutics include drugs acting on alpha(2)delta subunits of calcium channels, sodium channels, and descending modulatory inhibitory pathways.
引用
收藏
页码:259 / 301
页数:43
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