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抗病毒化合物膦甲酸钠(膦甲酸)产生羟基自由基。

Generation of hydroxyl radicals by the antiviral compound phosphonoformic acid (foscarnet).

作者信息

Lindqvist C, Nordström T

机构信息

Department of Biology, Abo Akademi University, BioCity, Turku, Finland.

出版信息

Pharmacol Toxicol. 2001 Jul;89(1):49-55. doi: 10.1034/j.1600-0773.2001.d01-135.x.

Abstract

Phosphonoformic acid (foscarnet) is an antiviral agent that is used to treat severe cytomegalovirus infections in AIDS patients. We demonstrate by using the ferrous iron indicator Ferrozine and ascorbic acid (vitamin C) that foscarnet can chelate ferric iron and form a redox-active iron complex. By using the hydroxyl radical indicator coumarin-3-carboxylic acid we found that the foscarnet-Fe3 complex formed can readily catalyze hydroxyl radical (.OH) generation by the Fenton reaction: (Fe2+ + H2O2-4Fe3+ + .OH + -OH) if hydrogen peroxide and ascorbic acid are present. Hydroxylation of coumarin-3-carboxylic acid could be blocked by addition of known hydroxyl radical scavengers such as mannitol, sucrose, glucose and dimethyl sulfoxide. Moreover, by using a DNA nicking assay, we found that foscarnet catalyzed hydroxyl radicals can induce single strand brakes in DNA. The potency of the hydroxyl radicals formed to induce damage could also be demonstrated in a phosphate-free buffer where the hydroxyl radicals formed attacked and liberated phosphate from the foscarnet molecule. Our results indicate that foscarnet catalyzed hydroxyl radical formation might take place during conditions where a peroxide generating system(s), vitamin C and transitions metals are present.

摘要

膦甲酸(膦甲酸钠)是一种抗病毒药物,用于治疗艾滋病患者的严重巨细胞病毒感染。我们通过使用亚铁指示剂菲洛嗪和抗坏血酸(维生素C)证明,膦甲酸可以螯合三价铁并形成具有氧化还原活性的铁络合物。通过使用羟基自由基指示剂香豆素-3-羧酸,我们发现形成的膦甲酸-Fe3络合物可以通过芬顿反应轻易催化羟基自由基(·OH)的产生:(Fe2+ + H2O2 → Fe3+ + ·OH + -OH),前提是存在过氧化氢和抗坏血酸。香豆素-3-羧酸的羟基化可以通过添加已知的羟基自由基清除剂如甘露醇、蔗糖、葡萄糖和二甲基亚砜来阻断。此外,通过使用DNA切口试验,我们发现膦甲酸催化产生的羟基自由基可以诱导DNA单链断裂。在无磷酸盐缓冲液中也可以证明形成的羟基自由基诱导损伤的能力,在该缓冲液中,形成的羟基自由基攻击膦甲酸分子并从中释放出磷酸盐。我们的结果表明,在存在过氧化物生成系统、维生素C和过渡金属的条件下,可能会发生膦甲酸催化的羟基自由基形成。

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