Davì Giovanni, Falco Angela, Patrono Carlo
Center of Excellence on Aging, University of Chieti "G. D'Annunzio" School of Medicine, Chieti, Italy.
Antioxid Redox Signal. 2005 Jan-Feb;7(1-2):256-68. doi: 10.1089/ars.2005.7.256.
There is considerable evidence that hyperglycemia represents the main cause of complications of diabetes mellitus (DM), and oxidative stress resulting from increased generation of reactive oxygen species plays a crucial role in their pathogenesis. In fact, in the absence of an appropriate response from endogenous antioxidant mechanisms, the redox imbalance causes the activation of stress-sensitive intracellular signaling pathways. The latter play a key role in the development of late complications of DM, as well as in mediating insulin resistance (i.e., resistance to insulin-mediated glucose uptake by some cells) and impaired insulin secretion. This review, focused on lipid peroxidation in DM, will examine the mechanisms and clinical readouts of oxidative stress in this setting, the relationship between lipid peroxidation and antioxidant status in type 1 and type 2 DM, the effects of hyperglycemia and metabolic control on in vivo markers of lipid peroxidation (i.e., isoprostanes), and the association between isoprostane formation and platelet activation. Finally, possible targets of antioxidant therapy for diabetic vascular complications will be discussed.
有大量证据表明,高血糖是糖尿病(DM)并发症的主要原因,活性氧生成增加所导致的氧化应激在其发病机制中起关键作用。事实上,在内源性抗氧化机制未做出适当反应的情况下,氧化还原失衡会导致应激敏感型细胞内信号通路的激活。后者在糖尿病晚期并发症的发展以及介导胰岛素抵抗(即某些细胞对胰岛素介导的葡萄糖摄取的抵抗)和胰岛素分泌受损方面起关键作用。本综述聚焦于糖尿病中的脂质过氧化,将探讨这种情况下氧化应激的机制和临床指标、1型和2型糖尿病中脂质过氧化与抗氧化状态之间的关系、高血糖和代谢控制对脂质过氧化体内标志物(即异前列腺素)的影响,以及异前列腺素形成与血小板活化之间的关联。最后,将讨论糖尿病血管并发症抗氧化治疗的可能靶点。