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[神经免疫性疾病患者血清中自由基防御与氧化应激的研究]

[A study of free radical defense and oxidative stress in the sera of patients with neuroimmunological disorders].

作者信息

Sakai T, Inoue A, Koh C S, Ikeda S

机构信息

Department of Medicine (Neurology), Shinshu University School of Medicine.

出版信息

Arerugi. 2000 Jan;49(1):12-8.

Abstract

Free radicals are molecules that contain at least one unpaired electron and by nature are highly reactive and potentially destructive. Free radical damage can play an important role of demyelination. Glutathione peroxidase, which plays a role in free radical defenses, and myeloperoxidase and lactoferrin, which are considered to reflect the strength of oxidative stress, were examined by monoclonal antibody-based enzyme immunoassay on serum samples taken from patients with neuroimmunological disorders, namely, 35 multiple sclerosis(MS), and 2 Baló disease, 10 Guillain-Barré syndrome(GBS), and 25 human T-lymphotropic virus type-1 associated myelopathy (HAM). The levels of glutathione peroxidase in active phase of MS (8.37 +/- 5.59 micrograms/ml: p < 0.05) were increased rather than in inactive phase (5.05 +/- 2.44 micrograms/ml) and control (5.41 +/- 1.40 micrograms/ml), the levels of myeloperoxidase in HAM (95.5 +/- 89.1 ng/ml: p < 0.05) were increased rather than in controls (21.5 +/- 4.1 ng/ml), and the levels of lactoferrin were not significantly increased than in other disease and control. Moreover the levels of myeloperoxidase and lactoferrin are increased in Baló disease (myeloperoxidase 487, 762 ng/ml; not significant, lactoferrin 2.58, 2.77 ng/ml; not significant) than in control (myeloperoxidase 21.5 +/- 4.1 ng/ml, lactoferrin 0.69 +/- 0.32 ng/ml). In conclusion, we have here first demonstrated that the levels of these enzyme were not paralleled in MS and Baló diseases. In GBS the levels of all these enzyme were not increased. Thus, these findings suggest that these enzyme may play an important role of the disease activity of Baló, and may reflect the activity of the defense of MS.

摘要

自由基是含有至少一个未配对电子的分子,其本质上具有高反应性且可能具有破坏性。自由基损伤在脱髓鞘过程中可能起重要作用。通过基于单克隆抗体的酶免疫测定法,对取自神经免疫疾病患者的血清样本中的谷胱甘肽过氧化物酶(在自由基防御中起作用)、髓过氧化物酶和乳铁蛋白(被认为可反映氧化应激强度)进行了检测。这些神经免疫疾病患者包括35例多发性硬化症(MS)患者、2例巴洛病患者、10例吉兰 - 巴雷综合征(GBS)患者以及25例1型人类嗜T淋巴细胞病毒相关脊髓病(HAM)患者。MS活动期谷胱甘肽过氧化物酶水平(8.37±5.59微克/毫升:p<0.05)高于非活动期(5.05±2.44微克/毫升)和对照组(5.41±1.40微克/毫升);HAM患者髓过氧化物酶水平(95.5±89.1纳克/毫升:p<0.05)高于对照组(21.5±4.1纳克/毫升);乳铁蛋白水平与其他疾病及对照组相比无显著升高。此外,巴洛病患者髓过氧化物酶和乳铁蛋白水平(髓过氧化物酶487、762纳克/毫升;无显著差异,乳铁蛋白2.58、2.77纳克/毫升;无显著差异)高于对照组(髓过氧化物酶21.5±4.1纳克/毫升,乳铁蛋白0.69±0.32纳克/毫升)。总之,我们首次证明这些酶的水平在MS和巴洛病中并不平行。在GBS中,所有这些酶的水平均未升高。因此,这些发现表明这些酶可能在巴洛病的疾病活动中起重要作用,并且可能反映MS的防御活性。

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