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以谷胱甘肽作为一氧化氮(NO)和亚硝酰阳离子(NO⁺)供体的二亚硝酰铁配合物。

Dinitrosyl iron complexes with glutathione as NO and NO⁺ donors.

作者信息

Borodulin Rostislav R, Kubrina Lyudmila N, Mikoyan Vasak D, Poltorakov Alexander P, Shvydkiy Vyacheslav О, Burbaev Dosymzhan Sh, Serezhenkov Vladimir A, Yakhontova Elena R, Vanin Anatoly F

机构信息

N.N. Semyonov Institute of Chemical Physics, Russian Academy of Sciences, Moscow, Russia.

出版信息

Nitric Oxide. 2013 Feb 28;29:4-16. doi: 10.1016/j.niox.2012.11.001. Epub 2012 Dec 5.

Abstract

It has been found that heating of solutions of the binuclear form of dinitrosyl iron complexes (B-DNIC) with glutathione in a degassed Thunberg apparatus (рН 1.0, 70°С, 6 h) results in their decomposition with a concomitant release of four gaseous NO molecules per one B-DNIC. Further injection of air into the Thunberg apparatus initiates fast oxidation of NO to NO₂ and formation of two GS-NO molecules per one B-DNIC. Under similar conditions, the decomposition of B-DNIC solutions in the Thunberg apparatus in the presence of air is complete within 30-40 min and is accompanied by formation of four GS-NO molecules per one B-DNIC. It is suggested that the latter events are determined by oxidation of B-DNIC iron and concominant release of four nitrosonium ions (NO⁺) from each complex. Binding of NO⁺ to thiol groups of glutathione provokes GS-NO synthesis. At neutral рН, decomposition of B-DNIC is initiated by strong iron chelators, viz., о-phenanthroline and N-methyl-d-glucamine dithiocarbamate (MGD). In the former case, the reaction occurs under anaerobic conditions (degassed Thunberg apparatus) and is accompanied by a release of four NO molecules from B-DNIC. Under identical conditions, MGD-induced decomposition of B-DNIC gives two EPR-active mononuclear mononitrosyl iron complexes with MGD (MNIC-MGD) able to incorporate two iron molecules and two NO molecules from each B-DNIC. The other two NO molecules released from B-DNIC (most probably, in the form of nitrosonium ions) bind to thiol groups of MGD to give corresponding S-nitrosothiols. Acidification of test solutions to рН 1.0 initiates hydrolysis of MGD and, as a consequence, decomposition of MNIC-MGD and the S-nitrosated form of MGD; the gaseous phase contains four NO molecules (as calculated per each B-DNIC). The data obtained testify to the ability of B-DNIC with glutathione (and, probably, of B-DNIC with other thiol-containing ligands) to release both NO molecules and nitrosonium ions upon their decomposition. As far as nitrosyl iron complexes with non-thiol-containing ligands predominantly represented by the mononuclear mononitrosyl iron form (MNIC) are concerned, their decomposition yields exclusively NO molecules.

摘要

已经发现,在脱气的桑伯格仪器中(pH 1.0,70℃,6小时),将双核形式的二亚硝基铁配合物(B-DNIC)与谷胱甘肽的溶液加热,会导致其分解,每个B-DNIC伴随释放出四个气态NO分子。进一步向桑伯格仪器中注入空气会引发NO快速氧化为NO₂,并每个B-DNIC形成两个GS-NO分子。在类似条件下,在空气中时,桑伯格仪器中B-DNIC溶液的分解在30 - 40分钟内完成,且每个B-DNIC伴随形成四个GS-NO分子。据推测,后一过程是由B-DNIC铁的氧化以及每个配合物伴随释放出四个亚硝鎓离子(NO⁺)所决定的。NO⁺与谷胱甘肽的巯基结合引发GS-NO的合成。在中性pH条件下,B-DNIC的分解由强铁螯合剂即邻菲罗啉和N-甲基-d-葡糖胺二硫代碳酸盐(MGD)引发。在前一种情况下,反应在厌氧条件下(脱气的桑伯格仪器)发生,且B-DNIC释放出四个NO分子。在相同条件下,MGD诱导的B-DNIC分解产生两个具有EPR活性的与MGD形成的单核单亚硝基铁配合物(MNIC-MGD),每个MNIC-MGD能够结合来自每个B-DNIC的两个铁原子和两个NO分子。从B-DNIC释放出的另外两个NO分子(很可能以亚硝鎓离子的形式)与MGD的巯基结合生成相应的S-亚硝基硫醇。将测试溶液酸化至pH 1.0会引发MGD的水解,结果导致MNIC-MGD和MGD的S-亚硝基化形式分解;气相中含有四个NO分子(按每个B-DNIC计算)。所获得的数据证明了B-DNIC与谷胱甘肽(可能还有B-DNIC与其他含硫醇配体)在分解时释放NO分子和亚硝鎓离子的能力。就主要以单核单亚硝基铁形式(MNIC)存在的与非含硫醇配体形成的亚硝基铁配合物而言,它们的分解仅产生NO分子。

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