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Lipoic acid and vitamin C potentiate nitric oxide synthesis in human aortic endothelial cells independently of cellular glutathione status

机译:硫辛酸和维生素C增强人主动脉内皮细胞中一氧化氮的合成,而与细胞谷胱甘肽状态无关

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摘要

Vitamin C and thiol agents improve vasomotor function. To determine whether these compounds directly affect endothelial function, nitric oxide (NO) synthesis was measured in human aortic endothelial cells treated with ascorbic acid or the thiol modulating agents lipoic acid or L-2-oxothiazolidine-4-carboxylic acid (OTC). A dose-dependent increase in A23187-stimulated NO synthesis and elevated cGMP levels were observed in all cases except for OTC. Cellular GSH levels were not significantly increased, and the GSH/GSSG ratio was not significantly affected by treatment of the cells with lipoic acid, OTC, or ascorbic acid. Thus, vitamin C and lipoic acid potentiate endothelial NO synthesis and bioactivity by mechanisms that appear to be independent of cellular GSH levels and redox environment.
机译:维生素C和硫醇剂可改善血管舒缩功能。为了确定这些化合物是否直接影响内皮功能,在抗坏血酸或硫醇调节剂硫辛酸或L-2-氧噻唑烷-4-羧酸(OTC)处理的人的主动脉内皮细胞中测量了一氧化氮(NO)的合成。除OTC外,在所有情况下均观察到A23187刺激的NO合成的剂量依赖性增加和cGMP水平升高。用硫辛酸,OTC或抗坏血酸处理细胞后,细胞中GSH的水平没有显着增加,GSH / GSSG的比率也没有显着影响。因此,维生素C和硫辛酸通过似乎独立于细胞GSH水平和氧化还原环境的机制增强了内皮一氧化氮的合成和生物活性。

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  • 来源
    《Redox Report》 |2002年第4期|223-227|共5页
  • 作者单位

    Linus Pauling Institute, Oregon State University, Corvallis, Oregon, USA Department of Pharmacological Sciences, University of Milan, Italy and the College of Pharmacy, Oregon State University, Oregon, USA;

    Linus Pauling Institute, Oregon State University, Corvallis, Oregon, USA;

    Linus Pauling Institute, Oregon State University, Corvallis, Oregon, USA;

    Whitaker Cardiovascular Institute, Evans Memorial Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA;

    Linus Pauling Institute, Oregon State University, Corvallis, Oregon, USA;

    Linus Pauling Institute, Oregon State University, Corvallis, Oregon, USA;

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