rTMS和TENS通过调节中枢神经系统TRPV1和神经炎症减轻CCI模型大鼠神经性疼痛。

IF 4.4 3区 医学 Q2 CELL BIOLOGY
Mediators of Inflammation Pub Date : 2024-11-21 eCollection Date: 2024-01-01 DOI:10.1155/mi/8500317
Zhangyu Xu, Quanzhen Zhong, Fei Xing, Yuanliang Zhu, Yue Hu, Maomao Huang, Mouwang Zhou, Jianxiong Wang
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引用次数: 0

摘要

背景:重复经颅磁刺激(rTMS)前额叶皮质(PFC)和经皮神经电刺激(TENS)都被证明能有效缓解神经性疼痛(NP)。然而,这两种神经调节技术的比较疗效及其作用的具体神经机制尚不清楚。目的:本研究旨在比较rTMS在PFC和TENS中减轻周围NP的疗效,并探讨rTMS对神经炎症的影响。方法:18只成年雄性Sprague-Dawley大鼠随机分为NP(慢性收缩损伤[CCI]组,n = 6)、rTMS组(n = 6)和TENS组(n = 6)。术后1周,rTMS应用于PFC, TENS应用于右后肢。该治疗方案每日1次,每周5天,连续4周。测量足爪退缩机械阈值(PWMT),评估rTMS和TENS的镇痛效果。我们进一步采用酶联免疫吸附试验(elisa)测量PFC和L4-L6脊髓中白细胞介素(IL)-1β、IL-6和肿瘤坏死因子α (TNF-α)的水平,以评估它们对神经炎症的影响。此外,我们利用western blotting和实时定量逆转录酶聚合酶链反应(qRT-PCR)检测了PFC和L4-L6脊髓中的瞬时受体电位香草样蛋白1 (TRPV1)表达,以探讨其潜在机制。进一步对坐骨神经进行苏木精、伊红(H&E)染色,观察病理变化。结果:与CCI组相比,rTMS组和TENS组的PWMT均显著增加,rTMS组的PWMT明显高于TENS组。此外,rTMS治疗引发PFC和脊髓中IL-1β、IL-6和TNF-α水平的显著降低,而TENS仅降低这些区域IL-1β的表达。两组脊髓TRPV1表达均明显降低,H&E染色显示坐骨神经病理表现改善。结论:rTMS和TENS均能有效改善cci诱导的NP,其中rTMS对PFC的效果更佳。这两种治疗方法都降低了TRPV1的表达,抑制了脊髓的神经炎症,表明这可能是它们发挥治疗作用的机制之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
rTMS and TENS Relieve Neuropathic Pain in CCI Model Rats by Modulating Central Nervous System TRPV1 and Neuroinflammation.

Background: Repetitive transcranial magnetic stimulation (rTMS) of the prefrontal cortex (PFC) and transcutaneous electrical nerve stimulation (TENS) have both been demonstrated as effective at alleviating neuropathic pain (NP). However, the comparative efficacy of these two neuromodulation techniques and the specific neural mechanisms underlying their effects remain unclear. Objective: This study aims to compare the efficacy of rTMS in the PFC and TENS in mitigating peripheral NP and to investigate the impact of rTMS on neuroinflammation. Methods: Eighteen adult male Sprague-Dawley rats were randomly divided into three groups: NP (chronic constriction injury [CCI] group, n = 6), rTMS (n = 6), and TENS (n = 6). rTMS was applied to the PFC, while TENS was applied to the right hind limb of the rats 1 week postoperatively. This treatment regimen was administered once daily, 5 days a week, for 4 consecutive weeks. The paw withdrawal mechanical threshold (PWMT) was measured to assess the pain-alleviating effects of rTMS and TENS. We further conducted enzyme-linked immunosorbent assays (ELISAs) to measure the levels of interleukin (IL)-1β, IL-6, and tumor necrosis factor alpha (TNF-α) in the PFC and L4-L6 spinal cord to evaluate their impact on neuroinflammation. Additionally, we examined transient receptor potential vanilloid type 1 (TRPV1) expression in the PFC and the L4‒L6 spinal cord using western blotting and real-time quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) to explore the potential mechanisms involved. Hematoxylin and eosin (H&E) staining of the sciatic nerve was further performed to observe pathological changes. Results: Compared to the CCI group, both the rTMS and TENS groups exhibited a significant increase in PWMT, with the rTMS group demonstrating a notably greater PWMT than the TENS group. Furthermore, rTMS treatment triggered a significant decrease in IL-1β, IL-6, and TNF-α levels in the PFC and spinal cord, while TENS only decreased IL-1β expression in these regions. In both treatment groups, TRPV1 expression was significantly lower in the spinal cord, while H&E staining indicated improved pathological manifestations in the sciatic nerve. Conclusion: Both rTMS and TENS effectively ameliorated CCI-induced NP, with rTMS of the PFC showing superior performance. Both treatments reduced TRPV1 expression and suppressed neuroinflammation in the spinal cord, indicating that this may be one of the mechanisms through which they exert their therapeutic effects.

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来源期刊
Mediators of Inflammation
Mediators of Inflammation 医学-免疫学
CiteScore
8.70
自引率
0.00%
发文量
202
审稿时长
4 months
期刊介绍: Mediators of Inflammation is a peer-reviewed, Open Access journal that publishes original research and review articles on all types of inflammatory mediators, including cytokines, histamine, bradykinin, prostaglandins, leukotrienes, PAF, biological response modifiers and the family of cell adhesion-promoting molecules.
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