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强效血管舒张和鸟苷酸环化酶激活剂二亚硝酰基铁(II)配合物以蛋白质结合形式储存在血管组织中,并由硫醇释放。

The potent vasodilating and guanylyl cyclase activating dinitrosyl-iron(II) complex is stored in a protein-bound form in vascular tissue and is released by thiols.

作者信息

Mülsch A, Mordvintcev P, Vanin A F, Busse R

机构信息

Department of Applied Physiology, University of Freiburg, Germany.

出版信息

FEBS Lett. 1991 Dec 9;294(3):252-6. doi: 10.1016/0014-5793(91)81441-a.

Abstract

We studied the biological activity, stability and interaction of dinitrosyl-iron(II)-L-cysteine with vascular tissue. Dinitrosyl-iron(II)-L-cysteine was a potent activator of purified soluble guanylyl cyclase (EC50 10 nM with and 100 nM without superoxide dismutase) and relaxed noradrenaline-precontracted segments of endothelium-denuded rabbit femoral artery (EC50 10 nM superoxide dismutase). Pre-incubation (5 min; 310 K) of endothelium-denuded rabbit aortic segments with dinitrosyl-iron(II)-L-cysteine (0.036-3.6 mM) resulted in a concentration-dependent formation of a dinitrosyl-iron(II) complex with protein thiol groups, as detected by ESR spectroscopy. While the complex with proteins was stable for 2 h at 310 K, dinitrosyl-iron(II)-L-cysteine in aqueous solution (36-360 microM) decomposed completely within 15 min, as indicated by disappearance of its isotropic ESR signal at gav = 2.03 (293 K). Aortic segments pre-incubated with dinitrosyl-iron(II)-L-cysteine released a labile vasodilating and guanylyl cyclase activating factor. Perfusion of these segments with N-acetyl-L-cysteine resulted in the generation of a low molecular weight dinitrosyl-iron(II)-dithiolate from the dinitrosyl-iron(II) complex with proteins, as revealed by the shape change of the ESR signal at 293 K. The low molecular weight dinitrosyl-iron(II)-dithiolate accounted for an enhanced guanylyl cyclase activation and vasodilation induced by the aortic effluent. We conclude that nitric oxide (NO) produced by, or acting on vascular cells can be stabilized and stored as a dinitrosyl-iron(II) complex with protein thiols, and can be released from cells in the form of a low molecular weight dinitrosyl-iron(II)-dithiolate by intra- and extracellular thiols.

摘要

我们研究了二亚硝酰基铁(II)-L-半胱氨酸与血管组织的生物活性、稳定性及相互作用。二亚硝酰基铁(II)-L-半胱氨酸是纯化的可溶性鸟苷酸环化酶的强效激活剂(有超氧化物歧化酶时EC50为10 nM,无超氧化物歧化酶时为100 nM),并能使去内皮的兔股动脉中去甲肾上腺素预收缩的节段舒张(超氧化物歧化酶存在时EC50为10 nM)。用二亚硝酰基铁(II)-L-半胱氨酸(0.036 - 3.6 mM)对去内皮的兔主动脉节段进行预孵育(5分钟;310 K),通过电子顺磁共振光谱检测发现,会形成一种与蛋白质硫醇基团结合的二亚硝酰基铁(II)复合物,且呈浓度依赖性。虽然该蛋白质复合物在310 K下可稳定存在2小时,但水溶液中的二亚硝酰基铁(II)-L-半胱氨酸(36 - 360 μM)在15分钟内完全分解,这可通过其在gav = 2.03(293 K)处的各向同性电子顺磁共振信号消失来表明。用二亚硝酰基铁(II)-L-半胱氨酸预孵育的主动脉节段会释放一种不稳定的血管舒张和鸟苷酸环化酶激活因子。用N-乙酰-L-半胱氨酸灌注这些节段会导致从与蛋白质结合的二亚硝酰基铁(II)复合物生成一种低分子量的二亚硝酰基铁(II)-二硫醇盐,这可通过293 K时电子顺磁共振信号的形状变化来揭示。低分子量的二亚硝酰基铁(II)-二硫醇盐导致主动脉流出液诱导的鸟苷酸环化酶激活增强和血管舒张。我们得出结论,由血管细胞产生或作用于血管细胞的一氧化氮(NO)可以作为与蛋白质硫醇结合的二亚硝酰基铁(II)复合物被稳定和储存,并可通过细胞内和细胞外的硫醇以低分子量二亚硝酰基铁(II)-二硫醇盐的形式从细胞中释放出来。

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