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表观遗传基因沉默是神经性疼痛中 C 纤维功能障碍的基础。

Epigenetic gene silencing underlies C-fiber dysfunctions in neuropathic pain.

机构信息

Division of Molecular Pharmacology and Neuroscience, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8521, Japan.

出版信息

J Neurosci. 2010 Mar 31;30(13):4806-14. doi: 10.1523/JNEUROSCI.5541-09.2010.

Abstract

Peripheral nerve injury causes neuropathic pain, which is characterized by the paradoxical sensations of positive and negative symptoms. Clinically, negative signs are frequently observed; however, their underlying molecular mechanisms are largely unknown. Dysfunction of C-fibers is assumed to underlie negative symptoms and is accompanied by long-lasting downregulation of Na(v)1.8 sodium channel and mu-opioid receptor (MOP) in the dorsal root ganglion (DRG). In the present study, we found that nerve injury upregulates neuron-restrictive silencer factor (NRSF) expression in the DRG neurons mediated through epigenetic mechanisms. In addition, chromatin immunoprecipitation analysis revealed that nerve injury promotes NRSF binding to the neuron-restrictive silencer element within MOP and Na(v)1.8 genes, thereby causing epigenetic silencing. Furthermore, NRSF knockdown significantly blocked nerve injury-induced downregulations of MOP and Na(v)1.8 gene expressions, C-fiber hypoesthesia, and the losses of peripheral morphine analgesia and Na(v)1.8-selective blocker-induced hypoesthesia. Together, these data suggest that NRSF causes pathological and pharmacological dysfunction of C-fibers, which underlies the negative symptoms in neuropathic pain.

摘要

周围神经损伤引起病理性疼痛,其特征为阳性和阴性症状的矛盾感觉。临床上常观察到阴性体征;然而,其潜在的分子机制在很大程度上尚不清楚。假设 C 纤维功能障碍是阴性症状的基础,并伴有背根神经节(DRG)中钠离子通道 Na(v)1.8 和 μ 阿片受体(MOP)的持久下调。在本研究中,我们发现神经损伤通过表观遗传机制上调 DRG 神经元中的神经元限制沉默因子(NRSF)表达。此外,染色质免疫沉淀分析显示,神经损伤促进 NRSF 与 MOP 和 Na(v)1.8 基因内的神经元限制沉默元件结合,从而导致表观遗传沉默。此外,NRSF 敲低显著阻断了神经损伤诱导的 MOP 和 Na(v)1.8 基因表达、C 纤维感觉迟钝以及外周吗啡镇痛和 Na(v)1.8 选择性阻滞剂诱导的感觉迟钝的下调。总之,这些数据表明 NRSF 导致 C 纤维的病理性和药理学功能障碍,这是神经性疼痛中阴性症状的基础。

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