氧甲基唑啉和羟甲基唑啉的抗氧化作用

Gerrit-Jan Westerveld , Robert A. Scheeren , Ingrid Dekker , Désirée H. Griffionen , Hans-Peter Voss , Aalt Bast
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引用次数: 17

摘要

通过测定氧甲基唑啉和羟甲基唑啉对微粒体脂质过氧化和羟基自由基清除活性的抑制作用,研究了其抗氧化作用。氧甲基唑啉对脂质过氧化有较强的抑制作用(15 min时IC50 = 4.9 μM, IC50 = 81)。μM at t = 30 min),对比木甲基唑啉。这两种化合物都是良好的羟基自由基清除剂。它们的速率常数(氧甲唑啉kS = 1.1 × 1012 M−1s−1,木甲基唑啉kS = 4.7 × 1010 M−1s−1)超过了已知的强效清除剂西咪替丁的速率常数(kS = 1.8 × 1010 M−1s−1)。在抑制脂质过氧化反应方面的差异可能是由于只有氧甲基唑啉有一个羟基,它可以提供一个氢原子并终止脂质过氧化的链式反应。其清除羟基自由基的作用机制尚不清楚。此外,氧甲基唑啉在清除羟基自由基方面的作用方式似乎与氧甲基唑啉和西咪替丁不同,这导致了极高的速率常数。由于氧化剂在炎症中的组织损伤中起作用,人们假设,特别是氧甲基唑啉和在较小程度上的木甲基唑啉,由于它们的抗氧化特性,在局部治疗鼻腔炎症方面可能具有额外的有益作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-oxidant actions of oxymethazoline and xylomethazoline

Anti-oxidant actions of oxymethazoline and xylomethazoline were investigated by measuring inhibition io microsomal lipid peroxidation and hydroxyl radical scavenging activity. Oxymethazoline was shown to be potent inhibitir of lipid peroxidation (IC50 = 4.9 μM at t = 15 min, IC50 = 81. μM at t = 30 min), in contrast to xylomethazoline. Both compounds were excellent hydroxyl radical scavengers. Their rate constants (kS = 1.1 × 1012 M−1s−1 for oxymethozoline and kS = 4.7 × 1010 M−1s−1 for xylomethazoline) exceeded the rate constant of a known powerful scavenger cimetidine (kS = 1.8 × 1010 M−1S−1). The difference in inhibiting lipid peroxidation might be explained by the fact that only oxymethazoline has a hydroxy group which can donate a hydrogen atom and terminate the chain reaction of lipid peroxidation. The mechanism of hydroxyl radical scavenging activity is still unclear. Moreover oxymethazoline seems to have a different mode of action in scavenging hydroxyl radicals than oxylomethazoline and cimetidine which results in an extremely high rate constant. Because oxidants play a role in tissue damage in inflammation, it was hypothesized that especially oxymethazoline and to a lesser extent xylomethazoline may have an additional beneficial effect, due to their anti-oxidant properties, in the topical treatment of nasal inflammation.

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