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[一种以半胱氨酸为血管内皮舒张因子候选物质的二亚硝酰基铁配合物的稳定性]

[Stability of a dinitrosyl iron complex with cysteine as a candidate for the role of blood vessel endothelial relaxation factor].

作者信息

Vanin A F

出版信息

Biokhimiia. 1995 Feb;60(2):308-14.

PMID:7718671
Abstract

EPR evidence is presented that stability of the dinitrosyl iron complex (DNIC) with cysteine [(cys)2Fe(NO+)2] which determines its capability to produce NO depends on the redox state of the complex. The complex is maximally stable in the oxidized state characterized by the d6 electron configuration of iron. The reducing effect of dithionite, cysteine or GSH on this particular form of DNIC results in its transformation into unstable paramagnetic, NO-releasing forms. The effect of thiols is concentration-dependent. At low cysteine concentrations (1-5 mM and 20 microM of DNIC), thiols destabilize DNIC, acting as reducing agents. However, higher thiol concentrations (10 mM) added to DNIC stabilize the reduced forms of the complex, acting as ligands. The data obtained suggest that those authors who studied the vasodilatory activity of DNIC on isolated blood vessels, dealt with a stable oxidized form of DNIC. This form may arise due to oxidation of the unstable paramagnetic form of DNIC (DNIC 1:20) resulting from dilution of its aqueous solutions.

摘要

电子顺磁共振(EPR)证据表明,二亚硝基铁配合物(DNIC)与半胱氨酸形成的配合物[(cys)2Fe(NO+)2]的稳定性决定了其产生一氧化氮(NO)的能力,而这种稳定性取决于配合物的氧化还原状态。该配合物在以铁的d6电子构型为特征的氧化态下最为稳定。连二亚硫酸盐、半胱氨酸或谷胱甘肽(GSH)对这种特定形式的DNIC的还原作用会导致其转变为不稳定的顺磁性、释放NO的形式。硫醇的作用具有浓度依赖性。在低半胱氨酸浓度(1-5 mM以及相对于DNIC为20 microM)下,硫醇作为还原剂使DNIC不稳定。然而,向DNIC中加入更高浓度的硫醇(10 mM)会使配合物的还原形式稳定,此时硫醇作为配体。所获得的数据表明,那些研究DNIC对离体血管舒张活性的作者所研究的是DNIC的稳定氧化形式。这种形式可能是由于DNIC水溶液稀释产生的不稳定顺磁性形式(DNIC 1:20)被氧化所致。

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