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Sumatriptan scavenges superoxide, hydroxyl, and nitric oxide radicals: in vitro electron spin resonance study.

机译:苏门曲普坦清除超氧化物,羟基和一氧化氮自由基:体外电子自旋共振研究。

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摘要

Background.-The molecular mechanisms of migraine have not yet been clarified. Oxygen free radicals have been implicated in the genesis of many pathological processes, including migraine. Sumatriptan succinate is known to be a very effective drug for acute relief of migraine attack. Objective.-To investigate the direct scavenging activities of sumatriptan for superoxide, hydroxyl, and nitric oxide (NO) radicals using electron spin resonance (ESR) spectroscopy. Methods.-Measurement of superoxide and hydroxyl radical scavenging activities was performed by ESR using 5,5-dimethyl-1-pyrroline-N-oxide as a spin trap. NO was generated from 1-hydroxy-2-oxo-3-(N-3-methyl-3-aminopropyl)-3-methyl-1-triazene and analyzed by 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl produced from the reaction between 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide and NO. Results.-The ESR study demonstrated that sumatriptan scavenged superoxide, hydroxyl, and NO in a dose-dependent manner. Conclusion.-Sumatriptan has direct scavenging activity on free radicals and NO. Acute migraine drugs with antioxidant properties may provide heretofore unheralded benefits via this mechanism.
机译:背景-偏头痛的分子机制尚未阐明。氧自由基与许多病理过程的发生有关,包括偏头痛。已知舒马曲坦琥珀酸盐是一种有效缓解急性偏头痛发作的药物。目的-使用电子自旋共振(ESR)光谱法研究舒马普坦对超氧化物,羟基和一氧化氮(NO)自由基的直接清除活性。方法:使用5,5-二甲基-1-吡咯啉-N-氧化物作为自旋阱,通过ESR测量超氧化物和羟基自由基清除活性。从1-羟基-2-氧代-3-(N-3-甲基-3-氨基丙基)-3-甲基-1-三氮烯生成NO,并通过2-(4-羧基苯基)-4,4,5分析, 2-(4-羧基苯基)-4,4,5,5-四甲基咪唑啉-1-氧基-3-氧化物与NO反应生成的5-四甲基咪唑啉-1-氧基。结果:-ESR研究表明舒马普坦以剂量依赖性方式清除了超氧化物,羟基和NO。结论:舒马曲坦对自由基和NO具有直接清除作用。具有这种抗氧化特性的急性偏头痛药物可能通过这种机制提供前所未有的益处。

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