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在全身性红斑狼中异常的硫氧化
C Gordon1, H Bradley, R H Waring
1Department of Rheumatology, University of Birmingham, UK.
Lancet (London, England)
|January 4, 1992
概括
系统性红斑狼 (SLE) 患者表现出S-氧化受损,这是一个关键的硫代谢途径. 这项研究强调了SLE和类风湿性关节炎之间硫代谢的明显生化差异.
科学领域:
- 生物化学 生物化学
- 免疫学 免疫学 免疫学
- 代谢途径 代谢途径
背景情况:
- 硫代谢在生物系统中起着至关重要的作用.
- 代谢途径的改变与像SLE这样的自身免疫性疾病有关.
- 了解SLE中的硫代谢可以揭示疾病特定的生物标志物.
研究的目的:
- 研究系统性红斑狼 (SLE) 患者中硫代谢的S-氧化途径的活性.
- 将SLE患者的硫代谢与健康对照进行比较.
- 为了区分SLE和类风湿性关节炎 (RA) 之间的硫代谢概况.
主要方法:
- 使用S-carboxy-L-methylcysteine作为一个探测器来评估S-氧化活性.
- 测量了囊氧酶 (血囊/硫酸盐) 的基质/产品比.
- 评估了由硫甲基转移酶催化的S-甲基化途径.
主要成果:
- 显著的大多数SLE患者 (71%) 显示硫酸化受损.
- 25%的SLE患者几乎没有硫氧化物产生,而对照组只有4%.
- 在SLE患者中,囊氧化酶途径显著上调 (p < 0.00001).
- 在SLE患者中,S-甲基化途径保持不变.
结论:
- SLE的特点是S-氧化受损,这是硫代谢的关键途径.
- 在SLE患者中,S-甲基化途径不受影响.
- 硫代谢在SLE和RA之间表现出明显的差异,在RA中,这两种途径都受到损害.
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