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Peroxiredoxin 6, a Novel Player in the Pathogenesis of Diabetes

机译:Peroxiredoxin 6,糖尿病发病机理中的新成员

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摘要

Enhanced oxidative stress contributes to the pathogenesis of diabetes and its complications. Peroxiredoxin 6 (PRDX6) is a key regulator of cellular redox balance, with the peculiar ability to neutralize peroxides, peroxynitrite, and phospholipid hydroperoxides. In the current study, we aimed to define the role of PRDX6 in the pathophys-iology of type 2 diabetes (T2D) using PRDX6 knockout (-/-) mice. Glucose and insulin responses were evaluated respectively by irrtraperitoneal glucose and insulin tolerance tests. Peripheral insulin sensitivity was analyzed by euglycemic-hyperinsulinemic clamp, and molecular tools were used to investigate insulin signaling. Moreover, inflammatory and lipid parameters were evaluated. We demonstrated that PRDX6~(-/-) mice developed a phenotype similar to early-stage T2D caused by both reduced glucose-dependent insulin secretion and increased insulin resistance. Impaired insulin signaling was present in PRDX6~(-/-) mice, leading to reduction of muscle glucose uptake. Morphological and ultrastructural changes were observed in islets of Lang-erhans and livers of mutant animals, as well as altered plasma lipid profiles and inflammatory parameters. In conclusion, we demonstrated that PRDX6 is a key mediator of overt hyperglycemia in T2D glucose metabolism, opening new perspectives for targeted therapeutic strategies in diabetes care.
机译:氧化应激增强导致糖尿病及其并发症的发病机理。 Peroxiredoxin 6(PRDX6)是细胞氧化还原平衡的关键调节剂,具有中和过氧化物,过氧亚硝酸盐和磷脂氢过氧化物的独特能力。在当前的研究中,我们旨在使用PRDX6基因敲除(-/-)小鼠定义PRDX6在2型糖尿病(T2D)病理学中的作用。葡萄糖和胰岛素反应分别通过腹膜内葡萄糖和胰岛素耐受性测试进行评估。通过正常血糖-高胰岛素钳夹分析外周胰岛素敏感性,并使用分子工具研究胰岛素信号传导。此外,评估了炎症和脂质参数。我们证明PRDX6〜(-/-)小鼠表现出类似于早期T2D的表型,这是由于葡萄糖依赖性胰岛素分泌减少和胰岛素抵抗增加所致。 PRDX6〜(-/-)小鼠体内胰岛素信号传导异常,导致肌肉葡萄糖摄取减少。在朗格汉斯岛和突变动物肝脏中观察到形态学和超微结构变化,以及血浆脂质谱和炎症参数改变。总之,我们证明PRDX6是T2D葡萄糖代谢中明显的高血糖的关键介体,为糖尿病护理的靶向治疗策略开辟了新的前景。

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  • 来源
    《Diabetes》 |2014年第10期|3210-3220|共11页
  • 作者单位

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Division of Endocrinology and Metabolic Diseases, Universita Cattolica del Sacro Cuore, Rome, Italy,Diabetic Care Clinics, Associazione dei Cavalieri Italiani Sovrano Militare Ordine di Malta, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Anatomic Pathology, Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy,Institute of Translational Pharmacology, National Research Council, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy,Institute of Translational Pharmacology, National Research Council, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy,Istituto di Ricovero e Cura a Carattere Scientifico San Raffaele Pisana, Rome, Italy;

    Division of Endocrinology and Metabolic Diseases, Universita Cattolica del Sacro Cuore, Rome, Italy,Fondazione Don Carlo Gnocchi, Milan, Italy;

    Anatomic Pathology, Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy;

    Department of System Medicine, University of Rome Tor Vergata, Rome, Italy;

  • 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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