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首页> 外文期刊>BMC Complementary and Alternative Medicine >NK cells mediate the cumulative analgesic effect of electroacupuncture in a rat model of neuropathic pain
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NK cells mediate the cumulative analgesic effect of electroacupuncture in a rat model of neuropathic pain

机译:NK细胞介导电针在神经性疼痛大鼠模型中的累积镇痛作用

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Background Cumulating evidence has revealed the effectiveness of acupuncture therapy in relieving pain via immunoregulation. However, its underlying mechanism remains unknown. The present study was designed to determine the changes of immunogenic responses at different time-points of electroacupuncture (EA) interventions in neuropathic pain rats. Methods The neuropathic pain model was established by ligature of the left sciatic nerve to induce chronic constriction injury (CCI). EA was applied at Zusanli (ST36) and Yanglingquan (GB34) for the EA groups. The thermal pain threshold was detected with an algesia-detector. The subgroups of plasma and splenic lymphocytes were determined via fluorescence-activated cell sorting. Specific inflammatory cytokines were assayed using an ELISA-based bead multiplex assay. The activities of splenic natural killer (NK) cells and cytotoxic T lymphocytes were detected by methyl thiazolyl tetrazolium colorimetric method. For confirming the involvement of NK cell in EA-analgesia, anti-asialo-ganglio-N-tetraosylceramide (anti-asialo-GM1) antibody was given to CCI rats before EA. Results Following CCI, the thermal pain threshold of the affected hind footpad was significantly decreased, and increased from the 3rd day to the 12th day after EA interventions, presenting a time-dependent tendency from the 5th day on. From day 3 to 5 of EA interventions, the percentages and activity of splenic NK cells, concentrations of splenic interleukin-2 (IL-2) and beta-endorphin (β-EP) were significantly increased. Meanwhile, the concentrations of plasma IL-2, IL-1β and gamma-interferon (IFN-γ) were significantly decreased and returned to the normal level on day 12 following EA. Plasma transforming growth factor-β (TGF-β) levels were considerably upregulated on day 5 and 12 following EA. The CD4+/CD8+ T cell ratio was markedly downregulated compared with the control and CCI groups on day 5 and returned to the normal level on day 12 following EA. After depleting NK cells by anti-asialo-GM1 antibody, the increased thermal pain threshold following EA intervention was obviously reduced. Conclusions Repeated EA interventions have a time-dependent cumulative analgesic effect in neuropathic pain rats, which is closely associated with its regulatory effects on NK cells, splenic IL-2, β-EP, and plasma IL-2, IL-1β, IFN-γ and TGF-β levels.
机译:背景技术越来越多的证据表明,针灸疗法可通过免疫调节缓解疼痛。但是,其潜在机制仍然未知。本研究旨在确定神经性疼痛大鼠在不同时间电针(EA)干预的免疫原性反应的变化。方法通过结扎左坐骨神经诱发慢性压迫性损伤(CCI),建立神经性疼痛模型。 EA组在祖三里(ST36)和杨凌泉(GB34)应用了EA。用痛觉检测器检测热痛阈值。通过荧光激活细胞分选确定血浆和脾淋巴细胞的亚组。使用基于ELISA的微珠多重测定法测定特异性炎性细胞因子。甲基噻唑基四唑比色法检测脾脏自然杀伤(NK)细胞和细胞毒性T淋巴细胞的活性。为了证实NK细胞参与EA镇痛,在EA之前向CCI大鼠给予抗-神经节神经节-N-四糖基神经酰胺(抗-神经节-GM1)抗体。结果CCI后,受影响的后足垫的热痛阈值从EA干预后的第3天增加到第12天,显着降低,并持续了一段时间。从第5天开始的依赖趋势。从EA干预的第3天到第5天,脾NK细胞的百分比和活性,脾白介素2(IL-2)和β-内啡肽(β-EP)的浓度均显着增加。同时,EA后第12天血浆IL-2,IL-1β和γ-干扰素(IFN-γ)的浓度显着降低并恢复到正常水平。 EA后第5天和第12天血浆转化生长因子-β(TGF-β)水平显着上调。与第5天的对照组和CCI组相比,CD4 + / CD8 + T细胞比率显着下调,并在EA后第12天恢复正常水平。在用抗亚洲人GM1抗体耗尽NK细胞后,EA干预后增加的热痛阈值明显降低。结论重复EA干预对神经性疼痛大鼠具有时间依赖性的累积镇痛作用,这与其对NK细胞,脾脏IL-2,β-EP和血浆IL-2,IL-1β,IFN-γ的调节作用密切相关。 γ和TGF-β水平。

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