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 reflet 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 Balo disease, 10 Guillain-Barre 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±5.59μg / ml: p<0.05)were increased rather than in inactive phase (5.05±2.44μg / ml) and control (5.41±1.40μg / ml), the levels of myeloperoxidase in HAM (95.5±89.1ng / ml: p<0.05) were increased rather than in controls (21.5±4.1ng / 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 Balo disease (myeloperoxidase 487,762ng / ml; not signigicant, lactoferrin 2.58, 2.77ng / ml; not significant) than in control (myeloperoxidase 21.5±4.1ng / ml, lactoferrin 0.69±0.32ng / ml). In conclusion, we have here first demonstrated that the levels of these enzyme were not paralleled in MS and Balo 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 Balo, and may reflect the activity of the defense of MS.
View full abstract