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Uncoupling Endothelial Nitric Oxide Synthase Is Ameliorated by Green Tea in Experimental Diabetes by Re-establishing Tetrahydrobiopterin Levels

机译:通过重新建立四氢生物蝶呤的水平,绿茶可改善实验性糖尿病中非偶联内皮型一氧化氮合酶的水平。

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摘要

The current study investigated the potential of green tea (GT) to improve uncoupling of endothelial nitric oxide synthase (eNOS) in diabetic conditions. In rats with streptozotocin-induced diabetes, nitric oxide (NO) bioavailability was reduced by uncoupling eNOS, characterized by a reduction in tetrahydrobiopterin (BH4) levels and a decrease in the eNOS dimer-to-monomer ratio. GT treatment ameliorated these abnormalities. Moreover, immortalized human mesangial cells (ihMCs) exposed to high glucose (HG) levels exhibited a rise in reactive oxygen species (ROS) and a decline in NO levels, which were reversed with GT. BH_4 and the activity of guanosine triphosphate cyclohydrolase I decreased in ihMCs exposed to HG and was normalized by GT. Exogenous administration of BH_4 in ihMCs reversed the HG-induced rise in ROS and the decline in NO production. However, coadministra-tion of GT with BH_4 did not result in a further reduction in ROS production, suggesting that reduced ROS with GT was indeed secondary to uncoupled eNOS. In summary, GT reversed the diabetes-induced reduction of BH4 levels, ameliorating uncoupling eNOS, and thus increasing NO bioavailability and reducing oxi-dative stress, two abnormalities that are involved in the path-ogenesis of diabetic nephropathy.
机译:当前的研究调查了绿茶(GT)在糖尿病条件下改善内皮型一氧化氮合酶(eNOS)解偶联的潜力。在患有链脲佐菌素诱导的糖尿病的大鼠中,解偶联eNOS会降低一氧化氮(NO)的生物利用度,其特征是四氢生物蝶呤(BH4)水平降低和eNOS二聚体与单体比例降低。 GT治疗改善了这些异常。此外,暴露于高葡萄糖(HG)水平的永生化人肾小球膜细胞(ihMC)表现出活性氧(ROS)升高和NO水平下降,而GT则相反。在暴露于HG的ihMC中,BH_4和鸟嘌呤三磷酸鸟苷环水解酶I的活性降低,并被GT标准化。在ihMC中外源给予BH_4可逆转HG诱导的ROS升高和NO生成的降低。但是,GT与BH_4的共同给药并未导致ROS的进一步降低,这表明与GT结合的ROS的减少确实是eNOS脱钩的继发因素。总之,GT逆转了糖尿病引起的BH4水平降低,改善了未偶联的eNOS,从而增加了NO的生物利用度并降低了氧化应激,这是糖尿病性肾病发病机理中的两个异常现象。

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  • 来源
    《Diabetes》 |2012年第7期|p.1838-1847|共10页
  • 作者单位

    Renal Pathophysiology Laboratory, Investigation on Diabetes Complications, Faculty of Medical Sciences, State University of Campinas (Uni-camp), Campinas, Sao Paulo, Brazil;

    Renal Pathophysiology Laboratory, Investigation on Diabetes Complications, Faculty of Medical Sciences, State University of Campinas (Uni-camp), Campinas, Sao Paulo, Brazil;

    Renal Pathophysiology Laboratory, Investigation on Diabetes Complications, Faculty of Medical Sciences, State University of Campinas (Uni-camp), Campinas, Sao Paulo, Brazil;

    Renal Pathophysiology Laboratory, Investigation on Diabetes Complications, Faculty of Medical Sciences, State University of Campinas (Uni-camp), Campinas, Sao Paulo, Brazil;

    Renal Pathophysiology Laboratory, Investigation on Diabetes Complications, Faculty of Medical Sciences, State University of Campinas (Uni-camp), Campinas, Sao Paulo, Brazil;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:46:27

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