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首页> 外文期刊>Free Radical Biology and Medicine: The Official Journal of the Oxygen Society >Kinetics of reaction of peroxynitrite with selenium- and sulfur-containing compounds: Absolute rate constants and assessment of biological significance
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Kinetics of reaction of peroxynitrite with selenium- and sulfur-containing compounds: Absolute rate constants and assessment of biological significance

机译:含硒和含硫化合物的过氧硝酸盐反应动力学:绝对速率常数和生物学意义的评估

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Peroxynitrite (the physiological mixture of ONOOH and its anion, ONOO-) is a powerful biologically-relevant oxidant capable of oxidizing and damaging a range of important targets including sulfides, thiols, lipids, proteins, carbohydrates and nucleic acids. Excessive production of peroxynitrite is associated with several human pathologies including cardiovascular disease, ischemic-reperfusion injury, circulatory shock, inflammation and neurodegeneration. This study demonstrates that low-molecularmass selenols (RSeH), selenides (RSeR') and to a lesser extent diselenides (RSeSeR') react with peroxynitrite with high rate constants. Low molecular mass selenols react particularly rapidly with peroxynitrite, with second order rate constants k(2) in the range 5.1 x 10(5)-1.9 x 10(6) M-1 s(-1), and 250-830 fold faster than the corresponding thiols (RSH) and many other endogenous biological targets. Reactions of peroxynitrite with selenides, including selenosugars are approximately 15-fold faster than their sulfur homologs with k(2) approximately 2.5 x 10(3) M-1 s(-1). The rate constants for diselenides and sulfides were slower with k(2) 0.72-1.3 x 10(3) M-1 s(-1) and approximately 2.1 x 10(2) M-1 s(-1) respectively. These studies demonstrate that both endogenous and exogenous selenium-containing compounds may modulate peroxynitrite-mediated damage at sites of acute and chronic inflammation, with this being of particular relevance at extracellular sites where the thiol pool is limited. (C) 2015 Elsevier Inc. All rights reserved.
机译:过氧硝酸盐(OnoOH及其阴离子的生理混合物,ONOO-)是一种强大的生物相关氧化剂,能够氧化和损害一系列重要的靶标,包括硫化物,硫醇,脂质,蛋白质,碳水化合物和核酸。过氧基酯的过量生产与包括心血管疾病,缺血再灌注损伤,循环冲击,炎症和神经变性的几种人类病理有关。该研究表明,低分子蛋白酶硒(RSEH),硒化物(RSER')和较小程度的二烯醇(RSESER')与具有高速率常数的过氧硝酸盐反应。低分子质量硒醇用过氧硝酸盐反应特别快,二阶速率常数K(2),范围为5.1×10(5)-1.9×10(6)m-1s(-1),更快地折叠250-830倍比相应的硫醇(RSH)和许多其他内源生物靶标。与硒核苷酸在内的过氧化硒酸酯的反应比与K(2)约2.5×10(3)m-1s(-1)的硫同源物快约15倍。二烯烃和硫化物的速率常数分别较慢,k(2)0.72-1.3×10(3)m-1s(-1)和约2.1×10(2)m-1s(-1)。这些研究表明,含内源性和外源性硒化合物可以调节急性和慢性炎症部位的过氧族介导的损伤,这在硫醇池受限的细胞外位点具有特殊相关性。 (c)2015 Elsevier Inc.保留所有权利。

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