Acute electric field downregulates human plasma immunoreactive interleukin-6 and -1β levels: Molecular mechanisms underlying inflammation alleviation through electric field therapy

Yuzo Nakagawa-Yag, H. Hara, Chisato Kanai, Masashi Sato, A. Hara
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引用次数: 2

Abstract

Medical treatment using high-voltage electric potential (HELP) devices to generate an electric field (EF) is an alternative therapy commonly used in Japan. However, the mechanisms underlying potential health benefits of this therapy are still unclear. Therefore, we investigated the effect of HELP exposure (9 kV/electrode+9 kV/ electrode, 30 min) on several cytokines and hormones using enzyme-linked immunosorbent assays in plasma samples obtained from healthy human subjects before and after a single treatment session. Immunoreactive interleukin (IL)-1β and IL-6 levels were significantly downregulated following HELP exposure. Under these treatment conditions, HELP exposure did not exert on immunoreactive IL-10, IL-18, transforming growth factor-beta 1 (TGF-β1), tumor necrosis factor-alpha (TNF-α) adrenaline, serotonin, histamine, neuropeptide Y, somatostatin, insulin, or dehydroepiandrosterone sulfate (DHEAS) levels. The activation of transient receptor potential melastatin 8 (TRPM8) induces the suppression of the levels of inflammatory markers. Therefore, we further examined the in silico docking simulation of lysoPC-22:4, lysoPE-20:4, and lysoPE-22:6 with TRPM8 using a homology model. The binding energies were -10.8, -10.4, and -11.4 kcal/mol for lysoPC-22:4, lysoPE-20:4, and lysoPE-22:6, respectively. Our findings provide new insights into the molecular mechanisms underlying pain control and sleep quality alleviation following EF therapy. Abbreviations: CRP: C-reactive protein; DHEAS: dehydroepiandrosterone sulfate; EF: electric field; HELP: high-voltage electric potential; HODE: hydroxyoctadecadienoic acid; IL: interleukin; lysoPC: lysophosphatidylcholine; lysoPC-22:4: (2-{[(2R)-3-[(7Z,10Z,13Z,16Z)docosa-7,10,13,16-tetraenoyloxy]-2-hydropropyl phosphonato]oxy} ethyl)trimethylazanium; lysoPE: lysophosphatidylethanolamine; lysoPE-22:6: (2-aminoethoxy)[(2R)-2-[(4Z, 7Z, 10Z, 13Z, 16Z, 19Z)docosa-4,7,10,13,16-hexaenoyloxy]-3-hydroxypropoxy]phosphinic acid; lysoPE-20:4: (2-aminoethoxy) [(2R)-2-hydroxy-3-[(5Z, 8Z, 11Z, 14Z)-icosa-5,8,11,14-tetraenoyloxy] propoxy] phosphinic acid; OEA: Oleoylethanolamide; TGF-β: transforming growth factor beta; TNF-α: tumor necrosis factor alpha; TRPM8: transient receptor potential melastatin 8; TRPV1: transient receptor potential vanilloid 1.
急性电场下调人血浆免疫反应性白细胞介素-6和-1β水平:电场治疗炎症缓解的分子机制
使用高压电势(HELP)装置产生电场(EF)的医疗治疗是日本常用的替代疗法。然而,这种疗法潜在的健康益处机制尚不清楚。因此,我们研究了HELP暴露(9 kV/电极+9 kV/电极,30分钟)对几种细胞因子和激素的影响,使用酶联免疫吸附法测定了健康人在单次治疗前后的血浆样本。免疫反应性白细胞介素(IL)-1β和IL-6水平在HELP暴露后显著下调。在这些治疗条件下,HELP暴露对免疫反应性IL-10、IL-18、转化生长因子-β1 (TGF-β1)、肿瘤坏死因子-α (TNF-α)肾上腺素、血清素、组胺、神经肽Y、生长抑素、胰岛素或硫酸脱氢表雄酮(DHEAS)水平没有影响。瞬时受体电位美拉他汀8 (TRPM8)的激活诱导炎症标志物水平的抑制。因此,我们使用同源性模型进一步研究了lysoPC-22:4、lysoPE-20:4和lysoPE-22:6与TRPM8的硅对接模拟。lysoPC-22:4、lysoPE-20:4和lysoPE-22:6的结合能分别为-10.8、-10.4和-11.4 kcal/mol。我们的研究结果为EF治疗后疼痛控制和睡眠质量缓解的分子机制提供了新的见解。缩写:CRP: c反应蛋白;DHEAS:硫酸脱氢表雄酮;EF:电场;HELP:高压电势;羟基十八烯二烯酸;IL:白介素;lysoPC: lysophosphatidylcholine;lysoPC-22:4: (2-{[(2R)-3-[(7Z,10Z,13Z,16Z)docosa-7,10,13,16-四烯氧基]-2-羟丙基膦]氧}乙基)三甲基噻嗪;lysoPE: lysophosphatidylethanolamine;lysoPE-22:6:(2-氨基乙氧基)[(2R)-2-[(4Z, 7Z, 10Z, 13Z, 16Z, 19Z)docosa-4,7,10,13,16-六烯氧基]-3-羟基丙氧基]膦酸;lysoPE-20:4:(2-氨基乙氧基)[(2R)-2-羟基-3-[(5Z, 8Z, 11Z, 14Z)-二氧基-5,8,11,14-四烯氧基]丙氧基]膦酸;OEA: Oleoylethanolamide;TGF-β:转化生长因子;TNF-α:肿瘤坏死因子;TRPM8:瞬时受体电位美拉西汀8;TRPV1:瞬时受体电位香草素1。
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