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神经病理性疼痛:从机制到治疗。

Neuropathic Pain: From Mechanisms to Treatment.

机构信息

Danish Pain Research Center, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark; Department of Neurology, Aarhus University Hospital, Aarhus, Denmark; and Department of Pharmacology, Heidelberg University, Heidelberg, Germany.

出版信息

Physiol Rev. 2021 Jan 1;101(1):259-301. doi: 10.1152/physrev.00045.2019. Epub 2020 Jun 25.


DOI:10.1152/physrev.00045.2019
PMID:32584191
Abstract

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 poststroke 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 αδ subunits of calcium channels, sodium channels, and descending modulatory inhibitory pathways.

摘要

由躯体感觉神经系统的损伤或疾病引起的神经性疼痛是一种常见的慢性疼痛病症,对生活质量有重大影响。例如,三叉神经痛、痛性多发性神经病、带状疱疹后神经痛和中风后中枢性疼痛。大多数患者会抱怨持续或间歇性的自发性疼痛,例如烧灼感、刺痛感、挤压感,可能伴有诱发疼痛,特别是对轻触和冷感。神经末梢神经瘤、受压神经或神经根、背根神经节和丘脑的异位活动可能是自发性疼痛的基础。诱发疼痛可能会扩散到邻近区域,其潜在的病理生理学涉及外周和中枢敏化。伤害感受通路的敏化是由适应性结构改变和许多细胞-细胞相互作用和分子信号转导引起的。这些包括离子通道的改变、免疫细胞的激活、胶质衍生的介质和表观遗传调控。主要的治疗药物类别包括作用于钙通道的 αδ 亚单位、钠通道和下行调节抑制途径的药物。

相似文献

[1]
Neuropathic Pain: From Mechanisms to Treatment.

Physiol Rev. 2021-1-1

[2]
Elucidation of pathophysiology and treatment of neuropathic pain.

Cent Nerv Syst Agents Med Chem. 2012-12

[3]
Anticonvulsants in neuropathic pain: rationale and clinical evidence.

Eur J Pain. 2002

[4]
[Pathophysiology of neuropathic pain: review of experimental models and proposed mechanisms].

Presse Med. 2008-2

[5]
Spinal dorsal horn calcium channel alpha2delta-1 subunit upregulation contributes to peripheral nerve injury-induced tactile allodynia.

J Neurosci. 2004-9-29

[6]
Neuropathic pain: a clinical perspective.

Handb Exp Pharmacol. 2009

[7]
[Pathophysiology of neuropathic pain: molecular mechanisms underlying central sensitization in the dorsal horn in neuropathic pain].

Brain Nerve. 2012-11

[8]
Pathophysiologic mechanisms of neuropathic pain.

Curr Pain Headache Rep. 2001-4

[9]
Involvement of hyperpolarization-activated, cyclic nucleotide-gated cation channels in dorsal root ganglion in neuropathic pain.

Sheng Li Xue Bao. 2008-10-25

[10]
Fibroblast Growth Factors as Tools in the Management of Neuropathic Pain Disorders.

Curr Drug Targets. 2020

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CNS Neurosci Ther. 2025-9

[2]
The simultaneous activation of μ- and δ-opioid receptors by (-)-2-LP2 rescues allodynia with the contribution of TGF-β1 signaling in a rat chronic constriction injury model.

Curr Res Pharmacol Drug Discov. 2025-8-6

[3]
EEG neurofeedback for the treatment of neuropathic pain in the elderly-a mechanistic review.

Geroscience. 2025-8-30

[4]
Unlocking Relief: Investigating the Impact of a Fixed Combination of Acetyl-L-Carnitine and Palmitoylethanolamide on Traumatic Acute Low Back Pain.

Eur J Neurol. 2025-8

[5]
Epigenomic Interactions Between Chronic Pain and Recurrent Pressure Injuries After Spinal Cord Injury.

Epigenomes. 2025-7-23

[6]
Peak Alpha Frequency Is Not Significantly Altered by Five Days of Experimental Pain and Repetitive Transcranial Stimulation of the Left Dorsolateral Prefrontal Cortex.

Eur J Neurosci. 2025-8

[7]
A systematic review and meta-analysis of pharmacological methods to manipulate experimentally induced secondary hypersensitivity.

Pain. 2025-4-15

[8]
SLC45A4 is a pain gene encoding a neuronal polyamine transporter.

Nature. 2025-8-20

[9]
Knowledge, attitudes, and practices of healthcare professionals regarding neuropathic pain in spinal cord injury in Hunan, China.

Sci Rep. 2025-8-20

[10]
Roles of Ion Channels in Oligodendrocyte Precursor Cells: From Physiology to Pathology.

Int J Mol Sci. 2025-7-29

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