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Antioxidant mechanisms of ascorbate and (R)-alpha-lipoic acid in aging and transition metal ion-mediated oxidative stress.

机译:抗坏血酸和(R)-α-硫辛酸在老化和过渡金属离子介导的氧化应激中的抗氧化机理。

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摘要

Oxidative stress is the major driving force behind the aging process and many age-related diseases. However, direct experimental evidence of whether antioxidants, such as ascorbate (AA) and lipoic acid (LA) can slow the progression of aging process and/or reduce risks of developing degenerative disease is largely absent. This suggests a better understanding of the precise mechanism of how dietary micronutrient affect parameters of involved in cellular redox balance and aging are warranted. In this dissertation, young and old rats were used as our model to understand potential pro-oxidant events that contribute to increases in oxidative stress in various tissues and how antioxidants such as ascorbate and lipoic acid influence these events. Our major findings are that the age-related impairment of mitochondria and increased deposition of iron contribute significantly to heighten levels of oxidative stress, as evidenced by the resultant increases in the rates of oxidant appearance and in the levels of oxidative damage to DNA, lipids and proteins. We find that AA and LA strongly protected against transition metal-ion dependent increases in oxidative stress. AA effectively inhibited transition metal-mediated lipide peroxidation in human plasma. LA in its reduced form effectively binds iron and copper in a redox inactive manner and reversed chronically elevated levels of iron in the brain without removing enzyme bound transition metal ions. LA also significantly attenuated the age-related increase in oxidative stress associated with mitochondrial decay in the heart, as evidenced by the improvements in AA levels and glutathione redox status. The declines in tissue GSH levels in aged rats were strongly associated with the diminished γ-GCL activity (in parallel with decreased expression of the catalytic and modulatory subunits), and lowered Nrf2 expression and binding to ARE sequence in rat liver. Remarkably, all these events were effectively reversed by the administration of LA, modulating the parameters to return to the observed in young animals. The implications of this work open new avenues not only for further understanding of the aging process but also for possible strategies in its modulation by the micronutrients.
机译:氧化应激是衰老过程和许多与年龄有关的疾病的主要驱动力。但是,几乎没有关于抗氧化剂如抗坏血酸(AA)和硫辛酸(LA)是否能减缓衰老过程的进展和/或降低发生退行性疾病风险的直接实验证据。这表明需要更好地了解饮食中微量营养素如何影响细胞氧化还原平衡和衰老相关参数的精确机制。本文以成年和成年大鼠为模型,了解可能促进多种组织氧化应激的潜在促氧化剂事件,以及抗氧化剂如抗坏血酸和硫辛酸如何影响这些事件。我们的主要发现是,与年龄相关的线粒体损伤和铁沉积的增加显着促进了氧化应激水平的升高,这证明了氧化剂的出现速率以及对DNA,脂质和脂肪的氧化损伤水平的提高。蛋白质。我们发现,AA和LA可以有效地防止依赖过渡金属离子的氧化应激增加。 AA有效抑制人体血浆中过渡金属介导的脂质过氧化。还原形式的LA以氧化还原非活性方式有效结合铁和铜,并在不去除酶结合的过渡金属离子的情况下逆转了大脑中铁的长期升高水平。洛杉矶还显着减轻了与心脏线粒体衰变相关的氧化应激与年龄相关的增加,这可通过AA水平和谷胱甘肽氧化还原状态的改善来证明。老年大鼠组织中GSH水平的下降与γ-GCL活性的降低密切相关(与催化亚基和调节性亚基的表达降低),以及Nrf2的表达降低以及与大鼠肝脏ARE序列的结合。值得注意的是,所有这些事件都可以通过服用LA来有效逆转,调节参数使其恢复到幼小动物身上观察到的效果。这项工作的意义不仅为进一步了解衰老过程提供了新途径,而且为微量营养素调节衰老过程的可能策略开辟了新途径。

著录项

  • 作者

    Suh, Jung Hyuk.;

  • 作者单位

    Oregon State University.;

  • 授予单位 Oregon State University.;
  • 学科 Chemistry Biochemistry.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 198 p.
  • 总页数 198
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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