Altindağ Z Z, Sahin G, Inanici F, Hasçelik Z
Hacettepe University, Faculty of Pharmacy, Department of Pharmaceutical Toxicology, Ankara, Turkey.
Rheumatol Int. 1998;18(3):107-11. doi: 10.1007/s002960050067.
Neopterin and biopterin are two products of the pteridine pathway. Even though their roles and interrelationships have not been exactly clarified, neopterin is known as a biomarker of cell-mediated immunity. In this case, the highly elevated neopterin levels are parallel to the slightly elevated biopterin levels. On the other hand, the reduced form of biopterin-tetrahydrobiopterin is an essential cofactor of aromatic monoxygenases that leads to synthesis of tyrosine, tryptophan and dopamine neurotransmitters and its concentration in body fluids and tissues is maintained by the enzyme dihydropteridine reductase (DHPR). Increased numbers of activated lymphocytes can be found in peripheral blood, in the synovial fluid and synovial membranes or patients with rheumatoid arthritis (RA). Since the present study was undertaken to evaluate the role of the pteridine pathway in RA, we measured urine neopterin levels and dried blood DHPR activities in 36 patients with RA and in 20 healthy volunteers, in parallel with other clinical parameters. We found that neopterin excretion was significantly increased in RA patients compared with controls. The means were 433 +/- 216, 153 +/- 43 and 111 +/- 34 mumol/mol creatinine for patients in active stage, in remission and controls, respectively. Our results suggest that urine neopterin levels were strongly dependent on the stage and activity of RA. Either as an effect of the disease itself or of drug administration, slightly reduced DHPR activities were detected (3.484 +/- 0.304 for control, 2.974 +/- 0.255 in active stage RA, and 3.048 +/- 0.302 red cytochrome C/min/5 mm disc in remission).
新蝶呤和生物蝶呤是蝶啶途径的两种产物。尽管它们的作用和相互关系尚未完全阐明,但新蝶呤被认为是细胞介导免疫的生物标志物。在这种情况下,新蝶呤水平的大幅升高与生物蝶呤水平的轻微升高是平行的。另一方面,生物蝶呤的还原形式——四氢生物蝶呤是芳香族单加氧酶的一种必需辅助因子,它参与酪氨酸、色氨酸和多巴胺神经递质的合成,其在体液和组织中的浓度由二氢蝶啶还原酶(DHPR)维持。在类风湿关节炎(RA)患者的外周血、滑液和滑膜中可发现活化淋巴细胞数量增加。由于本研究旨在评估蝶啶途径在RA中的作用,我们测量了36例RA患者和20名健康志愿者的尿新蝶呤水平和干血DHPR活性,并同时检测了其他临床参数。我们发现,与对照组相比,RA患者的新蝶呤排泄量显著增加。活动期、缓解期患者及对照组的均值分别为433±216、153±43和111±34 μmol/mol肌酐。我们的结果表明,尿新蝶呤水平强烈依赖于RA的分期和活动度。无论是疾病本身还是药物治疗的影响,均检测到DHPR活性略有降低(对照组为3.484±0.304,活动期RA为2.974±0.255,缓解期为3.048±0.302 还原型细胞色素C/分钟/5毫米圆盘)。