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

机译:NF-κB相关性疼痛相关性神经肽在椎间盘退变疾病患者中的表达

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摘要

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. RELA, NFKB1, CGRP, TAC1, TRPV1, and MMP-3 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 TRPV1 and MMP-3 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.
机译:激活的B细胞核因子κ轻链增强子(NF-κB)的作用在炎症和神经性疼痛过程的潜在机制中得到了强调。本研究旨在调查在与退行性椎间盘疾病(DDD)相关的慢性背痛患者中NF-κB信号是否与疼痛相关的神经肽表达相关。从四十名接受椎间盘置换或融合手术的DDD患者和十八名死后(PM)对照受试者中收集椎间盘(IVD)组织。通过RT-qPCR分析RELA,NFKB1,CGRP,TAC1,TRPV1和MMP-3基因表达,而核提取物中的NF-κB亚基RelA和NF-κB1-DNA结合和降钙素基因相关肽(CGRP),P物质(SP)和组织的胞质提取物中的瞬时受体电位,亚家族V,成员1(TRPV1)蛋白水平通过酶联免疫吸附测定(ELISA)进行了评估。与PM对照相比,DDD患者观察到NF-κB1-DNA结合上调,CGRP和TRPV1蛋白水平更高。在DDD患者中,NF-κB1-DNA结合与核RelA水平呈正相关。此外,在DDD患者中,NF-κB1-DNA结合与TRPV1和MMP-3基因以及SP和TRPV1蛋白表达呈正相关。我们的结果表明,IVD组织中SP和TRPV1的表达与NF-κB激活有关。此外,NF-κB可能通过调节DDD患者的疼痛相关神经肽表达来参与周围疼痛机制的产生或维持。

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