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过氧亚硝酸盐介导的丙酮酸脱羧生成二氧化碳和二氧化碳自由基阴离子。

Peroxynitrite-mediated decarboxylation of pyruvate to both carbon dioxide and carbon dioxide radical anion.

作者信息

Vásquez-Vivar J, Denicola A, Radi R, Augusto O

机构信息

Departamento de Bioquímica, Universidade de São Paulo, Brazil.

出版信息

Chem Res Toxicol. 1997 Jul;10(7):786-94. doi: 10.1021/tx970031g.

Abstract

There has been a recent renewal of interest in the antioxidant properties of pyruvate which are usually attributed to its capacity to undergo oxidative decarboxylation in the presence of hydrogen peroxide. The interaction of pyruvate with other oxidizing biological intermediates, however, has been scarcely considered in the literature. Here we report that peroxynitrite, the oxidant produced by the reaction between superoxide anion and nitric oxide, reacts with pyruvate with an apparent second-order rate constant of 88 +/- 7 M-1 s-1 at pH 7.4 and 37 degrees C. Kinetic studies indicated that pyruvate reacts with peroxynitrite anion (k = 100 +/- 7 M-1 s-1, peroxynitrous acid (k = 49 +/- 7 M-1 s-1, and a highly oxidizing species derived from peroxynitrous acid. Pyruvate decarboxylation was proved by anion exchange chromatography detection of acetate in incubations of peroxynitrite and pyruvate at pH 7.4 and 5.5. Formation of carbon dioxide radical anion was ascertained by EPR spin-trapping studies in the presence of GSH and the spin-trap 5,5-dimethyl-1-pyrroline N-oxide (DMPO). The use of pyruvate labeled with 13C at the 1-position led to the detection of the labeled DMPO carbon dioxide radical anion adduct. In the absence of GSH, oxygen consumption studies confirmed that peroxynitrite mediates the decarboxylation of pyruvate to free radical intermediates. Comparing the yields of acetate and free radicals estimated from the oxygen uptake studies, it is concluded that pyruvate is oxidized by both one- and two-electron oxidation pathways, the latter being preponderant. Hydrogen peroxide-mediated pyruvate oxidation does not produce detectable levels of carbon dioxide radical anion except in the presence of iron(II)-ethylenediamine-N,N,N',N'-tetraacetate (EDTA). The apparent second-order rate constant of the reaction between pyruvate and hydrogen peroxide was determined to be 1 order of magnitude lower than that of the reaction between pyruvate and peroxynitrite. The latter process may contribute to the antioxidant properties of pyruvate.

摘要

最近,人们对丙酮酸的抗氧化特性重新产生了兴趣,其抗氧化特性通常归因于它在过氧化氢存在下进行氧化脱羧的能力。然而,丙酮酸与其他氧化性生物中间体的相互作用在文献中几乎未被考虑。在此,我们报告,超氧阴离子与一氧化氮反应产生的氧化剂过氧亚硝酸根,在pH 7.4和37℃下与丙酮酸反应,表观二级速率常数为88±7 M⁻¹ s⁻¹。动力学研究表明,丙酮酸与过氧亚硝酸根阴离子(k = 100±7 M⁻¹ s⁻¹)、过氧亚硝酸(k = 49±7 M⁻¹ s⁻¹)以及一种源自过氧亚硝酸的高氧化性物种反应。在pH 7.4和5.5条件下,通过阴离子交换色谱法检测过氧亚硝酸根与丙酮酸孵育液中的乙酸盐,证实了丙酮酸的脱羧反应。在谷胱甘肽(GSH)和自旋捕获剂5,5 - 二甲基 - 1 - 吡咯啉N - 氧化物(DMPO)存在下,通过电子顺磁共振(EPR)自旋捕获研究确定了二氧化碳自由基阴离子的形成。使用在1位标记有¹³C的丙酮酸,导致检测到标记的DMPO二氧化碳自由基阴离子加合物。在没有GSH的情况下,耗氧研究证实过氧亚硝酸根介导丙酮酸脱羧生成自由基中间体。比较从耗氧研究估计的乙酸盐和自由基产率,可以得出结论,丙酮酸通过单电子和双电子氧化途径被氧化,后者占主导。除了在存在亚铁离子 - 乙二胺 - N,N,N',N'-四乙酸(EDTA)的情况下,过氧化氢介导的丙酮酸氧化不会产生可检测水平的二氧化碳自由基阴离子。丙酮酸与过氧化氢反应的表观二级速率常数被确定比丙酮酸与过氧亚硝酸根反应的速率常数低1个数量级。后一过程可能有助于丙酮酸的抗氧化特性。

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