首页> 外文期刊>The Biochemical Journal >PEROXYNITRITE-MEDIATED FORMATION OF FREE RADICALS IN HUMAN PLASMA - EPR DETECTION OF ASCORBYL, ALBUMIN-THIYL AND URIC ACID-DERIVED FREE RADICALS
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PEROXYNITRITE-MEDIATED FORMATION OF FREE RADICALS IN HUMAN PLASMA - EPR DETECTION OF ASCORBYL, ALBUMIN-THIYL AND URIC ACID-DERIVED FREE RADICALS

机译:过氧亚硝酸盐介导的人血浆中自由基的形成-EPR检测抗坏血酸,白蛋白-硫辛酸和尿酸衍生的自由基

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Formation of peroxynitrite by the fast reaction between nitric oxide and superoxide anion may represent a critical control point in cells producing both species, leading to either down-regulation of the physiological effects of superoxide anion and nitric oxide by forming an inert product, nitrate, or to potentiation of their toxic effects by oxidation of nearby molecules by peroxynitrite. (The term peroxynitrite is used to refer to the sum of all possible forms of peroxynitrite anion and peroxynitrous acid unless otherwise specified.) In this report we demonstrate that, in spite of all the antioxidant defences present in human plasma, its interaction with peroxynitrite leads to generation of free radical intermediates such as (i) the ascorbyl radical, detected by direct EPR, (ii) the albumin-thiyl radical, detected by spin-trapping experiments with both N-tert-butyl-alpha-phenylnitrone and 5,5-dimethyl-1-pyrroline N-oxide (DMPO), and (iii) a uric acid-derived free radical, detected as the DMPO radical adduct in plasma whose thiol groups were previously blocked with 5,5-dithiobis-(2-nitrobenzoic acid). The identity of the latter adduct was confirmed by parallel experiments demonstrating that it is not detectable in plasma pretreated with uricase, whereas it is formed in incubations of peroxynitrite with uric acid. Peroxynitrite-mediated oxidations were also followed by oxygen consumption and ascorbate and plasma-thiol depletion. Our results support the view that peroxynitrite-mediated one-electron oxidation of biomolecules may be an important event in its cytotoxic mechanism. In addition, the data have methodological implications by providing support for the use of EPR methodologies for monitoring both free radical reactions and ascorbate concentrations in biological fluids. [References: 57]
机译:一氧化氮和超氧阴离子之间快速反应形成的过氧亚硝酸盐可能代表了产生这两种物质的细胞中的关键控制点,从而导致通过形成惰性产物硝酸盐或通过调节超氧阴离子和一氧化氮的生理作用而产生下调。通过过亚硝酸盐氧化附近的分子来增强其毒性作用。 (除非另有说明,否则术语过氧亚硝酸盐用于表示过氧亚硝酸盐阴离子和过氧亚硝酸的所有可能形式的总和。)在本报告中,我们证明,尽管人体血浆中存在所有抗氧化剂防御作用,但其与过氧亚硝酸盐铅的相互作用生成自由基中间体,例如(i)通过直接EPR检测的抗坏血酸基,(ii)通过N-叔丁基-α-苯基硝酮和5,5的自旋捕获实验检测的白蛋白-噻吩基-二甲基-1-吡咯啉N-氧化物(DMPO)和(iii)尿酸衍生的自由基,在血浆中的DMPO自由基加合物中被检测出,该血浆中的巯基先前已被5,5-二硫代双-(2-硝基苯甲酸)阻断酸)。后者的加合物的身份通过平行实验证实,证明在尿酸酶预处理的血浆中无法检测到,而在过氧亚硝酸盐与尿酸的孵育中形成了。过氧亚硝酸盐介导的氧化还伴随着氧气的消耗,抗坏血酸盐和血浆硫醇的消耗。我们的结果支持这样的观点,即过氧亚硝酸盐介导的生物分子的单电子氧化可能是其细胞毒性机制中的重要事件。此外,这些数据还通过支持EPR方法用于监测自由基反应和生物流体中抗坏血酸的浓度而具有方法学意义。 [参考:57]

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