对多发性硬化症患者促炎细胞因子干扰素- γ、肿瘤坏死因子- α和一氧化氮的降温作用

ISRN Neurology Pub Date : 2013-05-16 Print Date: 2013-01-01 DOI:10.1155/2013/964572
Turan Poyraz, Egemen Idiman, Sezer Uysal, Leyla Iyilikci, Serkan Ozakbaş, Esra Coskuner Poyraz, Fethi Idiman
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引用次数: 6

摘要

多发性硬化症(MS)是年轻人中最常见的中枢神经系统(CNS)炎症性脱髓鞘疾病。已知炎症细胞产生的促炎细胞因子如干扰素γ (IFN-γ)、肿瘤坏死因子α (TNF-α)和一氧化氮(NO)在ms的发病机制中起关键作用,一些代谢变化可能影响轴突传递,白细胞NO和其他炎症介质如细胞因子可能受到冷却过程的影响。在这项研究中,我们评估了身体冷却过程对促炎细胞因子如TNF-α、IFN-γ和NO水平的影响。对20例多发性硬化症患者进行评估。女性13例,男性7例(平均年龄:33.6±7.5岁)。使用“麦迪文北极太阳温度管理系统”设备,体温大约在1小时内平均降低1°C。在我们的研究中,冷却后TNF-α、IFN-γ水平的下降无统计学意义,而冷却后no水平的平均下降为4.63±7.4 μmol/L,具有统计学意义(P = 0.002)。这些结果表明,一氧化氮水平的降低改善了多发性硬化冷却后脱髓鞘轴突段的传导阻滞。
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The cooling effect on proinflammatory cytokines interferon-gamma, tumor necrosis factor-alpha, and nitric oxide in patients with multiple sclerosis.

Multiple sclerosis (MS) is the most common inflammatory demyelinating disease of the central nervous system (CNS) in young adults. The proinflammatory cytokines such as interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), and nitric oxide (NO) which are known to be produced by inflammatory cells play a key role in the pathogenesis of MS. Some metabolic changes may have an effect on axonal transmission, and white blood cells NO and other inflammatory mediators such as cytokines may be affected from cooling process. In this study, we evaluated the effects of body cooling procedure on proinflammatory cytokines such as TNF-α, IFN-γ, and NO levels. Twenty patients with MS were evaluated. Thirteen of the patients were women, 7 were men (mean age: 33.6 ± 7.5 yrs.). Body temperature was reduced by an average of 1°C approximately in 1 hour with using the "Medivance Arctic Sun Temperature Management System" device. In our study, the decrease in TNF-α, IFN-γ levels after the cooling procedure has no statistical significance, whereas the decrease in the mean level of NO level after the cooling procedure is 4.63 ± 7.4 μmol/L which has statistical significance (P = 0.002). These results suggested that the decrease in NO level improves conduction block in demyelinated axonal segments after cooling procedure in multiple sclerosis.

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