Preisz Zsolt, Hartvig Nóra, Bognár Balázs, Kálai Tamás, Kunsági-Máté Sándor
Institute of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Pécs, Szigeti 12, H-7624 Pécs, Hungary.
Department of General and Physical Chemistry, Faculty of Sciences, University of Pécs, Ifjúság 6, H-7624 Pécs, Hungary.
Pharmaceuticals (Basel). 2021 Jul 11;14(7):665. doi: 10.3390/ph14070665.
The scavenging effect of the antimetabolite dihydrofolate reductase inhibitor methotrexate (MTX) and the isomers of its photoswitchable derivate, - and -phototrexate (PHX), have been compared by ESR spectroscopy, with the application of a cyclic hydroxylamine spin probe. The results showed the most pronounced scavenging effect in the presence of -phototrexate (-PHX). At a low concentration (100 µM) -PHX also showed a greater scavenging effect than the parent molecule MTX. Direct antioxidant properties of the investigated molecules were measured by ABTS scavenging assay, which showed no significant difference between -PHX and -PHX, but both of the isomers of PHX showed a higher antioxidant capacity than MTX. These findings imply that -PHX may have more pronounced anti-inflammatory and tissue-protective effects than MTX, despite the lack of its cytotoxic, antineoplastic effect.
通过电子自旋共振光谱法,应用环状羟胺自旋探针,比较了抗代谢物二氢叶酸还原酶抑制剂甲氨蝶呤(MTX)及其光开关衍生物的异构体α-和β-光甲氨蝶呤(PHX)的清除作用。结果表明,在α-光甲氨蝶呤(α-PHX)存在的情况下,清除作用最为明显。在低浓度(100μM)时,α-PHX的清除作用也比母体分子MTX更强。通过ABTS清除试验测定了所研究分子的直接抗氧化性能,结果表明α-PHX和β-PHX之间没有显著差异,但两种PHX异构体的抗氧化能力均高于MTX。这些发现表明,尽管α-PHX缺乏细胞毒性和抗肿瘤作用,但它可能比MTX具有更明显的抗炎和组织保护作用。