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NF-κB 相关痛觉相关神经肽在退行性椎间盘疾病患者中的表达。

NF-κB-Associated Pain-Related Neuropeptide Expression in Patients with Degenerative Disc Disease.

机构信息

Department of Clinical Neuroscience, Karolinska Institutet, 171 77 Stockholm, Sweden.

Stockhom Spine Center, Löwenströmska Hospital, 194 89 Upplands Väsby, Sweden.

出版信息

Int J Mol Sci. 2019 Feb 3;20(3):658. doi: 10.3390/ijms20030658.

Abstract

The role of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) has been highlighted in mechanisms underlying inflammatory and neuropathic pain processes. The present study was designed to investigate whether NF-κB signaling is associated with pain-related neuropeptide expression in patients with chronic back pain related to degenerative disc disease (DDD). Intervertebral disc (IVD) tissues were collected from forty DDD patients undergoing disc replacement or fusion surgery, and from eighteen postmortem (PM) control subjects. , , , , , and gene expression were analyzed by RT-qPCR, while NF-κB subunit RelA and NF-κB1⁻DNA binding in nuclear extracts and calcitonin gene related peptide (CGRP), substance P (SP), and transient receptor potential, subfamily V, member 1 (TRPV1) protein levels in cytosolic extracts of tissues were assessed by enzyme-linked immunosorbent assay (ELISA). An upregulated NF-κB1⁻DNA binding, and higher CGRP and TRPV1 protein levels were observed in DDD patients compared to PM controls. In DDD patients, NF-κB1⁻DNA binding was positively correlated with nuclear RelA levels. Moreover, NF-κB1⁻DNA binding was positively associated with and gene and SP and TRPV1 protein expression in DDD patients. Our results indicate that the expression of SP and TRPV1 in IVD tissues was associated with NF-κB activation. Moreover, NF-κB may be involved in the generation or maintenance of peripheral pain mechanisms by the regulation of pain-related neuropeptide expression in DDD patients.

摘要

核因子 kappa 轻链增强子的活化 B 细胞 (NF-κB) 的作用在炎症和神经病理性疼痛过程的机制中得到了强调。本研究旨在探讨 NF-κB 信号是否与退行性椎间盘疾病 (DDD) 相关慢性背痛患者的疼痛相关神经肽表达有关。从接受椎间盘置换或融合手术的 40 例 DDD 患者和 18 例尸检 (PM) 对照中收集椎间盘 (IVD) 组织。通过 RT-qPCR 分析 、 、 、 、 和 基因表达,通过酶联免疫吸附测定 (ELISA) 评估核提取物中 NF-κB 亚基 RelA 和 NF-κB1-DNA 结合以及组织细胞质提取物中降钙素基因相关肽 (CGRP)、P 物质 (SP) 和瞬时受体电位,亚家族 V,成员 1 (TRPV1) 蛋白水平。与 PM 对照组相比,DDD 患者的 NF-κB1-DNA 结合上调,CGRP 和 TRPV1 蛋白水平升高。在 DDD 患者中,NF-κB1-DNA 结合与核 RelA 水平呈正相关。此外,NF-κB1-DNA 结合与 DDD 患者的 基因和 SP 及 TRPV1 蛋白表达呈正相关。我们的结果表明,SP 和 TRPV1 在 IVD 组织中的表达与 NF-κB 激活有关。此外,NF-κB 可能通过调节 DDD 患者疼痛相关神经肽的表达,参与外周疼痛机制的产生或维持。

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