Fisher M, Levine P H, Doyle E M, Arpano M M, Bergeron D A, Cohen R A, Hoogasian J J
Department of Neurology, Medical Center of Central Massachusetts-Memorial, Worcester 01605.
Neurology. 1991 Feb;41(2 ( Pt 1)):297-9. doi: 10.1212/wnl.41.2_part_1.297.
Monocytes are recruited to active sites of multiple sclerosis (MS) demyelination and may promote local tissue injury by generating an inflammatory response, mediated in part by the production of toxic oxygen metabolites. Corticosteroids are frequently and effectively used to ameliorate MS exacerbations, despite inadequate knowledge about the mechanism. We assessed the effects of a 21-aminosteroid, U74500A, a new class of steroid derivatives without glucocorticoid or mineralocorticoid effects, on the production of hydrogen peroxide (H2O2) and chemiluminescence by stimulated monocytes harvested from 8 stable MS patients and age- and sex-matched controls. H2O2 measurements and chemiluminescence were significantly reduced in both groups by U74500A. These results demonstrate that 21-aminosteroids reduce production of toxic oxygen metabolites by monocytes and thus their inflammatory potential, suggesting that these agents may be potentially effective and safe treatment for MS exacerbations.
单核细胞被募集到多发性硬化症(MS)脱髓鞘的活跃部位,并可能通过产生炎症反应促进局部组织损伤,部分炎症反应由有毒氧代谢产物的产生介导。尽管对其机制了解不足,但皮质类固醇经常被有效地用于改善MS病情的加重。我们评估了一种21-氨基类固醇U74500A(一种无糖皮质激素或盐皮质激素作用的新型类固醇衍生物)对从8名病情稳定的MS患者以及年龄和性别匹配的对照者采集的受刺激单核细胞产生过氧化氢(H2O2)和化学发光的影响。U74500A使两组的H2O2测量值和化学发光均显著降低。这些结果表明,21-氨基类固醇可减少单核细胞有毒氧代谢产物的产生,从而降低其炎症潜能,提示这些药物可能是治疗MS病情加重的潜在有效且安全的药物。